Question From (1 To 50
1. An 8 year old child has low-grade fever, arthritis, colicky abdominal pain and a purpuric rash llocalized on the lower extremities. laboratory studies reveal a guaiac-positive stool, urinalysis with red blood cell (RBC) casts and mild proteinuria, and a normal platelet count. The most likely diagnosis is:
A. Henoch-Schonlein’s vasculitis
B. Systemic lupus erythematosus (SLE)
C. Rocky Mountain spotted fever
D. Idiopathic thrombocytopenic purpura
E. Poststreptococcal glomerulonephritis
Answer: Henoch-Schonlein’s vasculitis
Explanation
Henoch-Schonlein’s vasculitis is a type of vasculitis that affects small blood vessels, primarily in children. It is characterized by a purpuric rash, joint pain and swelling (arthritis), abdominal pain, and sometimes kidney involvement. The purpuric rash is typically located on the lower extremities and may also be present on the buttocks and ankles. The guaiac-positive stool and presence of red blood cell casts and mild proteinuria on urinalysis suggest gastrointestinal and renal involvement, which are common in Henoch-Schonlein’s vasculitis. The normal platelet count distinguishes this condition from other forms of thrombocytopenic purpura. Systemic lupus erythematosus (SLE) (B) is a chronic autoimmune disease that can affect various organs, including the skin, joints, and kidneys, but it is less likely to present with a purpuric rash and gastrointestinal symptoms. Rocky Mountain spotted fever (C) is a bacterial infection transmitted by ticks that can cause fever, rash, and other symptoms, but it is less likely to present with joint pain and gastrointestinal symptoms. Idiopathic thrombocytopenic purpura (D) is a condition characterized by low platelet count and purpura, but it is less likely to present with joint pain and gastrointestinal symptoms. Poststreptococcal glomerulonephritis (E) is a type of glomerulonephritis that can occur after a streptococcal infection, but it is less likely to present with a purpuric rash and joint pain. Therefore, based on the information provided, the most likely diagnosis for the child is Henoch-Schonlein’s vasculitis. It is important to seek prompt medical attention and treatment for this condition, which may include supportive care, nonsteroidal anti-inflammatory drugs (NSAIDs), and sometimes corticosteroids or other immunosuppressive drugs. |
2. A woman complains of having slight dark bloody discharges and mild pains in the lower part of abdomen for several days. Last menses were 7 weeks ago. The pregnancy test is positive. Bimanual investigation: the body of the uterus indicates for about 5-6 weeks of pregnancy, it is soft, painless. In the left appendage there is a retort-like formation, 7 х 5 cm large, mobile, painless. What examination is necessary for detection of fetus localization?
A. Ultrasound
B. Hysteroscopy
C. Hromohydrotubation
D. Colposcopy
E. Cystoscopy
Answer: Ultrasound
Explanation
Ultrasound is a non-invasive imaging technique that uses high-frequency sound waves to create images of the inside of the body. It is a safe and effective method for detecting the location of the fetus in early pregnancy. In this case, the woman has a positive pregnancy test and is experiencing slight dark bloody discharges and mild pains in the lower part of the abdomen. Bimanual investigation reveals a uterus indicating about 5-6 weeks of pregnancy, but there is also a retort-like formation in the left appendage, 7 x 5 cm large, mobile, and painless. An ultrasound can be used to determine the location of the fetus, whether it is in the uterus or outside of it (such as in an ectopic pregnancy), and to evaluate the size and condition of the uterus and any other pelvic organs. Hysteroscopy (B) is an invasive procedure that involves inserting a thin, lighted tube through the cervix to examine the inside of the uterus. It is not typically used to determine the location of the fetus in early pregnancy. Hromohydrotubation (C) is a diagnostic procedure that involves injecting a contrast material into the uterus and fallopian tubes to evaluate their patency. It is not typically used to determine the location of the fetus in early pregnancy. Colposcopy (D) is a procedure that involves examining the cervix and vagina with a special instrument called a colposcope. It is used to evaluate abnormal cervical cells, but it is not typically used to determine the location of the fetus in early pregnancy. Cystoscopy (E) is a procedure that involves inserting a thin, lighted tube through the urethra to examine the inside of the bladder. It is not typically used to determine the location of the fetus in early pregnancy. Therefore, based on the information provided, the most appropriate examination for detection of fetus localization in this case is ultrasound. It is important to consult with a qualified medical professional for an accurate diagnosis and appropriate treatment plan. |
3. A pregnant woman in her 40th week of pregnancy undergoes obstetric examination: the cervix of uterus is undeveloped. The oxytocin test is negative. Examination at 32 weeks revealed: AP 140/90 mm Hg, proteinuria 1 g/l, peripheral edemata. Reflexes are normal. Choose the most correct tactics:
A. Labour stimulation after preparation
B. Absolute bed rest for 1 month
C. Complex therapy of gestosis for 2 days
D. Caesarian section immediately
E. Complex therapy of gestosis for 7 days
Answer: Labour stimulation after preparation
Explanation
The woman is in her 40th week of pregnancy and the cervix is undeveloped. The negative oxytocin test indicates that the woman is not yet ready for labor. At 32 weeks, the woman had elevated blood pressure, proteinuria, and peripheral edema, which are signs of preeclampsia or gestosis. Based on this information, the most appropriate tactic is to prepare the woman for labor and then initiate labor stimulation. This may involve cervical ripening with prostaglandin medications and then induction of labor with oxytocin. This approach can help to avoid complications associated with prolonged pregnancy, such as fetal distress or placental insufficiency, while also monitoring and managing the preeclampsia or gestosis. Absolute bed rest for 1 month (B) is not appropriate in this case as it may increase the risk of thromboembolic events and other complications associated with prolonged bed rest. Moreover, the woman is already at 40 weeks of pregnancy and waiting for another month is not advisable. Complex therapy of gestosis for 2 days (C) or 7 days (E) may not be sufficient to manage the preeclampsia or gestosis and prepare the woman for labor. Moreover, delaying labor induction may increase the risk of complications for both the mother and the baby. Caesarean section immediately (D) is not recommended in this case as it may not be necessary and may increase the risk of complications associated with surgery. Therefore, based on the information provided, the most appropriate tactic in this case is labor stimulation after preparation. It is important to consult with a qualified obstetrician for an accurate diagnosis and appropriate treatment plan. |
4. A 26 year old woman had the second labour within the last 2 years with oxytocin application. The child’s weight is 4080 gr. After the placent birth there were massive bleeding, signs of hemorrhagic shock. Despite the introduction of contractive agents, good contraction of the uterus and absence of any cervical and vaginal disorders, the bleeding proceeds. Choose the most probable cause of bleeding:
A. Atony of the uterus
B. Injury of cervix of the uterus
C. Hysterorrhexis
D. Delay of the part of placenta
E. Hypotonia of the uterus
Answer: Atony of the uterus
Explanation
Atony of the uterus refers to the failure of the uterus to properly contract after childbirth, which can lead to postpartum hemorrhage. This condition can be caused by a variety of factors, including prolonged labor, multiple pregnancies, oxytocin administration, and large fetal size. In this case, the woman had her second labor within the last 2 years with oxytocin application and delivered a large baby weighing 4080 grams. After the delivery of the placenta, there was massive bleeding with signs of hemorrhagic shock, despite the introduction of contractive agents and good contraction of the uterus. Atony of the uterus is the most likely cause of bleeding in this scenario, even in the absence of any cervical and vaginal disorders. Injury of cervix of the uterus (B) and hysterorrhexis (C) can also result in bleeding, but they are less likely in this case as there are no cervical or vaginal disorders reported. Delay of the part of placenta (D) can cause bleeding, but it would typically occur before the delivery of the placenta and would be unlikely to continue after the placenta has been delivered. Hypotonia of the uterus (E) is a less severe form of uterine atony and can also lead to postpartum hemorrhage, but it is less likely to cause massive bleeding and hemorrhagic shock. Therefore, based on the information provided, the most probable cause of bleeding in this case is atony of the uterus. It is important to seek prompt medical attention and treatment for postpartum hemorrhage, which may include medications, uterine massage, and sometimes surgical intervention. |
5. On the first day after labour a woman had the rise of temperature up to 39oC. Rupture of fetal membranes took place 36 hours before labour. Examination of the bacterial flora of cervix of the uterus revealed hemocatheretic streptococcus of A group. The uterus body is soft, tender. Discharges are bloody, with admixtures of pus. Specify the most probable postnatal complication:
A. Metroendometritis
B. Thrombophlebitis of veins of the pelvis
C. Infectious hematoma
D. Infective contamination of the urinary system
E. Apostasis of sutures after the episiotomy
Answer: Metroendometritis
Explanation
Metroendometritis is an infection of the endometrium and myometrium of the uterus that can occur after childbirth. Risk factors for metroendometritis include prolonged labor, premature rupture of membranes, and maternal infection. In this case, the woman had a temperature rise up to 39oC on the first day after labor. The examination of the bacterial flora of the cervix of the uterus revealed hemocatheretic streptococcus of A group. The uterus body is soft, tender, and discharges are bloody with admixtures of pus. These symptoms and findings are consistent with metroendometritis. Thrombophlebitis of veins of the pelvis (B) is a less likely complication in this case, as there is no mention of symptoms such as pain, swelling, or redness in the legs. Infectious hematoma (C) is also a less likely complication in this case, as there is no mention of a palpable mass or swelling in the pelvic area. Infective contamination of the urinary system (D) is a less likely complication, as there is no mention of symptoms such as dysuria, urinary frequency, or urgency. Apostasis of sutures after the episiotomy (E) is a less likely complication, as there is no mention of a perineal wound or sutures. Therefore, based on the information provided, the most probable postnatal complication in this case is metroendometritis. It is important to seek prompt medical attention and treatment for this condition, which may include antibiotics, pain management, and supportive care. |
6. A woman of a high-risk group (chronic pyelonephritis in anamnesis) had vaginal delivery. The day after labour she complained of fever and loin pains, frequent urodynia. Specify the most probable complication:
A. Infectious contamination of the urinary system
B. Thrombophlebitis of veins of the pelvis
C. Infectious hematoma
D. Endometritis
E. Apostasis of sutures after episiotomy
Answer: Infectious contamination of the urinary system
Explanation
Women with a history of chronic pyelonephritis are at increased risk for urinary tract infections (UTIs) during pregnancy and after delivery. UTIs can lead to complications such as pyelonephritis, which is a kidney infection that can cause fever, loin pain, and frequent urination. In this case, the woman complained of fever and loin pains, as well as frequent urination, the day after delivery. These symptoms are consistent with pyelonephritis or a UTI. Therefore, infectious contamination of the urinary system is the most probable complication in this case. Thrombophlebitis of veins of the pelvis (B) is a less likely complication in this case, as loin pain and frequent urination are not typical symptoms of this condition. Infectious hematoma (C) is also a less likely complication in this case, as there is no mention of a palpable mass or swelling in the pelvic area. Endometritis (D) is a less likely complication in this case, as the symptoms are more consistent with a UTI than with an infection of the uterus. Apostasis of sutures after the episiotomy (E) is not likely to cause fever or loin pain, and is therefore a less likely complication. Therefore, based on the information provided, the most probable complication in this case is infectious contamination of the urinary system. It is important to seek prompt medical attention and treatment for UTIs and pyelonephritis, which may include antibiotics, pain management, and supportive care. |
7. A woman in her 39th week of pregnancy, the second labour, has regular birth activity. Uterine contractions take place every 3 minutes. What criteria describe the beginning of the II labor stage the most precisely?
A. Cervical dilatation by no less than 4 cm
B. Cervical smoothing over 90%
C. Duration of uterine contractions over 30 seconds
D. Presenting part is in the lower region of small pelvis
E. Rupture of fetal bladder
Answer: Cervical dilatation by no less than 4 cm
Explanation
The second stage of labor begins when the cervix is fully dilated (10 cm) and ends with the delivery of the baby. Therefore, the beginning of the second stage of labor is defined by the onset of complete cervical dilation. In this case, the woman is in her 39th week of pregnancy and is experiencing regular uterine contractions every 3 minutes. However, the information provided does not specify the degree of cervical dilation, so it cannot be assumed that the second stage of labor has begun. Cervical smoothing over 90% (B) is a less precise criterion for the beginning of the second stage of labor, as it depends on the subjective assessment of the healthcare provider and may vary. Duration of uterine contractions over 30 seconds (C) is not a precise criterion for the beginning of the second stage of labor, as uterine contractions can vary in duration and intensity throughout labor. The presenting part being in the lower region of the small pelvis (D) is a sign that the baby is descending and progressing through the birth canal, but it does not necessarily indicate the beginning of the second stage of labor. Rupture of the fetal bladder (E) is not a criterion for the beginning of the second stage of labor, as the onset of the second stage is defined by cervical dilation, not the rupture of membranes. Therefore, based on the information provided, the criteria that describe the beginning of the second stage of labor most precisely is cervical dilation by no less than 4 cm. It is important to monitor the progress of labor and consult with a qualified healthcare provider for an accurate assessment and management. |
8. A 24 years old primipara was hospitalised with complaints about discharge of the amniotic waters. The uterus is tonic on palpation. The position of the fetus is longitudinal, it is pressed with the head to pelvic outlet. Palpitation of the fetus is rhythmical, 140 bpm, auscultated on the left below the navel. Internal examination: cervix of the uterus is 2,5 cm long, dense, the external os is closed, light amniotic waters out of it. Point a correct component of the diagnosis:
A. Antenatal discharge of the amniotic waters
B. Early discharge of the amniotic waters
C. The beginning of the 1st stage of labour
D. The end of the 1st stage of labour
E. Pathological preterm labour
Answer: Antenatal discharge of the amniotic waters
Explanation
Antenatal discharge of the amniotic waters refers to the rupture of the amniotic sac before the onset of labor. In this case, the 24-year-old primipara was hospitalized with complaints about the discharge of the amniotic waters, and internal examination revealed a 2.5 cm long, dense cervix with a closed external os and light amniotic fluid leakage. The fact that the uterus is tonic on palpation and the position of the fetus is longitudinal with the head in the pelvic outlet suggests that labor may not have yet started. The rhythmical palpitation of the fetus at 140 bpm, auscultated on the left below the navel, is consistent with a normal fetal heart rate. Early discharge of the amniotic waters (B) refers to the rupture of the amniotic sac before 37 weeks of gestation, which can lead to preterm labor. However, there is no information in this case to suggest that the patient is less than 37 weeks pregnant. The beginning of the 1st stage of labor (C) is characterized by the onset of regular uterine contractions and cervical dilation. However, there is no mention of uterine contractions or cervical dilation in this case. The end of the 1st stage of labor (D) is characterized by complete cervical dilation (10 cm) and the transition to the second stage of labor. However, there is no information in this case to suggest that the patient has completed the first stage of labor. Pathological preterm labor (E) is labor that begins before 37 weeks of gestation and is associated with various maternal and fetal complications. However, there is no information in this case to suggest that labor has begun or that the patient is less than 37 weeks pregnant. Therefore, based on the information provided, the correct component of the diagnosis is antenatal discharge of the amniotic waters. It is important to monitor the patient closely for signs of infection or preterm labor and to provide appropriate management and care. |
9. A 29 year old patient underwent surgical treatment because of the benign serous epithelial tumour of an ovary. The postoperative period has elapsed without complications. What is it necessary to prescribe for the rehabilitational period:
A. Hormonotherapy and proteolytic enzymes
B. Antibacterial therapy and adaptogens
C. Lasertherapy and enzymotherapy
D. Magnitotherapy and vitamin therapy
E. The patient does not require further care
Answer: Hormonotherapy and proteolytic enzymes
Explanation
Hormonotherapy may be necessary to regulate hormonal imbalances that may have been caused by the tumor or the surgery. Proteolytic enzymes may be prescribed to aid in the healing process and to reduce inflammation. Antibacterial therapy (B) may be necessary if there is an infection present, but there is no information in this case to suggest that the patient has an infection. Laser therapy and enzymotherapy (C) are not typically prescribed for the rehabilitational period following surgery for a benign ovarian tumor. Magnitotherapy and vitamin therapy (D) may be helpful in certain cases, but there is no information in this case to suggest that the patient requires these therapies. The patient does require further care (E) after surgical treatment for a benign ovarian tumor, but the specific care required will depend on the individual patient’s needs and the details of their case. Therefore, based on the information provided, it is necessary to prescribe hormonotherapy and proteolytic enzymes for the rehabilitational period following surgical treatment for a benign serous epithelial tumor of an ovary. It is important to consult with a qualified healthcare provider for an individualized treatment plan and appropriate management. |
10. A patient was delivered to a surgical department after a road accident with a closed trauma of chest and right-sided rib fracture. The patient was diagnosed with right-sided pneumothorax, it is indicated to perform drainage of pleural cavity. Pleural puncture should be made in:
A. In the 2nd intercostal space along the middle clavicular line
B. In the 6th intercostal space along the posterior axillary line
C. In the 7th intercostal space along the scapular line
D. In the projection of pleural sinus
E. In the point of the greatest dullness on percussion
Answer: In the 2nd intercostal space along the middle clavicular line
Explanation
The middle clavicular line is an imaginary line that runs vertically down the center of the clavicle. The 2nd intercostal space is located just below the 2nd rib. This site is the recommended location for pleural puncture to drain the pleural cavity in cases of pneumothorax. The other options listed are not the recommended locations for pleural puncture in this case: B) In the 6th intercostal space along the posterior axillary line is a location that may be used for chest tube insertion in some cases of pleural effusion, but is not the recommended location for pleural puncture in pneumothorax due to rib fracture. C) In the 7th intercostal space along the scapular line is a location that may be used for chest tube insertion in some cases of pleural effusion, but is not the recommended location for pleural puncture in pneumothorax due to rib fracture. D) In the projection of pleural sinus is not a specific location for pleural puncture and may not be appropriate for drainage in pneumothorax due to rib fracture. E) In the point of the greatest dullness on percussion is not a specific location for pleural puncture and may not be appropriate for drainage in pneumothorax due to rib fracture. Therefore, based on the information provided, the pleural puncture for drainage of pleural cavity in this patient with right-sided pneumothorax due to rib fracture should be made in the 2nd intercostal space along the middle clavicular line. It is important to consult with a qualified healthcare provider for appropriate management and care. |
11. A primagravida with pregnancy of 37- 38 weeks complains of headache, nausea, pain in epigastrium. Objective: the skin is acyanotic. Face is hydropic, there is short fibrillar twitching of blepharons, muscles of the face and the inferior extremities. The look is fixed. AP- 200/110 mm Hg; sphygmus of 92 bpm, intense. Respiration rate is 32/min. Heart activity is rhythmical. Appreciable edemata of the inferior extremities are present. Urine is cloudy. What medication should be administered?
A. Droperidolum of 0,25% – 2,0 ml
B. Dibazolum of 1% – 6,0 ml
C. Papaverine hydrochloride of 2% – 4,0 ml
D. Hexenalum of 1% – 2,0 ml
E. Pentaminum of 5% – 4,0 ml
Answer: Droperidolum of 0,25% – 2,0 ml
Explanation
The clinical presentation described in this case is consistent with severe preeclampsia, a potentially life-threatening complication of pregnancy. The appropriate medication to administer in this case is A) Droperidolum of 0.25% – 2.0 ml. Droperidolum is an antipsychotic medication that can be used to manage the neurological symptoms associated with severe preeclampsia, such as headache and seizures. The dosage of 0.25% – 2.0 ml is appropriate for this patient based on the information provided. Dibazolum (B) is a vasodilator that can lower blood pressure, but it is not the first-line treatment for severe preeclampsia. Papaverine hydrochloride (C) is also a vasodilator that is not typically used for the management of severe preeclampsia. Hexenalum (D) is a sedative that is not typically used for the management of severe preeclampsia. Pentaminum (E) is a medication used for the treatment of heart failure and is not appropriate for the management of severe preeclampsia. Therefore, based on the information provided, the appropriate medication to administer in this case is droperidolum of 0.25% – 2.0 ml to manage the neurological symptoms associated with severe preeclampsia. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of severe preeclampsia. |
12. A 40 year old woman has changes of mammary gland. What are the most often symtomps that precede the malignization?
A. Skin induration with inverted nipple
B. Painful movable induration
C. Painless movable induration
D. Bloody discharges from the nipple
E. Pure discharges from the nipple
Answer: Skin induration with inverted nipple
Explanation
The most often symptoms that precede the malignization in changes of the mammary gland in a 40-year-old woman is A) skin induration with inverted nipple. Skin induration or thickening, along with an inverted nipple, can be early signs of breast cancer. Inverted nipple means that the nipple, which normally protrudes outwards, is pulled inwards or pointed inwards. Painful movable induration (B) and painless movable induration (C) are also symptoms that can occur in breast cancer, but they are not necessarily early signs that precede malignization. Bloody discharges from the nipple (D) are typically a later sign of breast cancer and may not occur until the cancer has progressed. Pure discharges from the nipple (E) are more commonly associated with benign breast conditions, such as fibrocystic breast changes, and are not necessarily an early sign of breast cancer. Therefore, based on the information provided, the most often symptom that precedes the malignization in changes of the mammary gland in a 40-year-old woman is skin induration with inverted nipple. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of breast changes. |
13. A patient who takes diuretics has developed arrhythmia as a result of cardiac glycoside overdose. What is the treatment tactics in this case?
A. Increased potassium concentration in blood
B. Increased sodium consentration in blood
C. Reduced magnesium concentration in blood
D. Increased calcium concentration in blood
E. –
Answer: Increased potassium concentration in blood
Explanation
In a patient who takes diuretics and has developed arrhythmia as a result of cardiac glycoside overdose, the appropriate treatment tactic is to increase potassium concentration in the blood. Therefore, the correct answer is A) Increased potassium concentration in blood. Cardiac glycosides, such as digoxin, work by increasing the force and efficiency of heart contractions. However, they can also cause arrhythmias, especially when taken in excess. Diuretics can exacerbate this effect by reducing potassium levels in the blood. Increasing potassium levels in the blood can help counteract the effects of cardiac glycoside overdose and reduce the risk of arrhythmias. This can be done by administering potassium supplements or increasing the patient’s intake of potassium-rich foods. Increased sodium concentration in blood (B) is not an appropriate treatment tactic in this case, as it can exacerbate the effects of cardiac glycoside overdose. Reduced magnesium concentration in blood (C) is also not an appropriate treatment tactic, as magnesium is necessary for proper heart function and reducing magnesium levels can worsen arrhythmias. Increased calcium concentration in blood (D) is also not an appropriate treatment tactic, as it can exacerbate the effects of cardiac glycoside overdose and increase the risk of arrhythmias. Therefore, based on the information provided, the appropriate treatment tactic in a patient who takes diuretics and has developed arrhythmia as a result of cardiac glycoside overdose is to increase potassium concentration in the blood. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of cardiac glycoside overdose and arrhythmias. |
14. An onset of severe preeclampsia at 16 weeks gestation might be caused by:
A. Hydatidiform mole
B. Anencephaly
C. Twin gestation
D. Maternal renal disease
E. Interventricular defect of the fetus
]
Answer: Hydatidiform mole
Explanation
The onset of severe preeclampsia at 16 weeks gestation might be caused by A) hydatidiform mole. A hydatidiform mole is a type of gestational trophoblastic disease that occurs when the fertilized egg develops into a mass of abnormal cells in the uterus instead of a normal embryo and placenta. This can cause early-onset severe preeclampsia. Anencephaly (B), twin gestation (C), maternal renal disease (D), and interventricular defect of the fetus (E) are not typically associated with early-onset severe preeclampsia. Therefore, based on the information provided, the onset of severe preeclampsia at 16 weeks gestation might be caused by a hydatidiform mole. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of severe preeclampsia. |
15. A 9 year old girl with a history of intermittent wheezing for several years is brought to the pediatrician. The child has been taking no medications for some time. Physical examination reveals agitation and perioral cyanosis. Intercostal and suprasternal retractions are present. The breath sounds are quiet, and wheezing is audible bilaterally. The child is admitted to the hospital. Appropriate interventions might include all of the following EXCEPT:
A. Prescribe nebulized cromolyn sodium
B. Prescribe intravenous aminophylline
C. Administer supplemental oxygen
D. Prescribe intravenous corticosteroids
E. Prescribe nebulized metaproterenol
Answer: Prescribe nebulized cromolyn sodium
Explanation
In a 9-year-old girl with a history of intermittent wheezing who presents with agitation, perioral cyanosis, intercostal and suprasternal retractions, and bilateral wheezing, appropriate interventions might include all of the following except A) prescribe nebulized cromolyn sodium. Cromolyn sodium is a medication used for the prevention of asthma attacks and is not recommended for the treatment of acute severe asthma attacks. Therefore, it would not be an appropriate intervention in this case. Intravenous aminophylline (B), supplemental oxygen (C), intravenous corticosteroids (D), and nebulized metaproterenol (E) are appropriate interventions for the treatment of acute severe asthma attacks. Intravenous aminophylline is a bronchodilator that can be used to relax the smooth muscles of the airways and improve breathing. Supplemental oxygen can help increase the oxygen saturation in the blood and reduce the risk of complications. Intravenous corticosteroids can help reduce inflammation in the airways and improve breathing. Nebulized metaproterenol is a bronchodilator that can help relax the smooth muscles of the airways and improve breathing. Therefore, based on the information provided, the inappropriate intervention in this case would be to prescribe nebulized cromolyn sodium. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of acute severe asthma attacks. |
16. Routine examination of an otherwise healthy child with a history of bronchial asthma reveals AP of 140/90 mm Hg. The most likely cause of the hypertension is:
A. Renal disease
B. Theophylline toxicity
C. Chronic lung disease
D. Coarctation of the aorta
E. Obesity
Answer: Renal disease
Explanation
In an otherwise healthy child with a history of bronchial asthma who presents with a blood pressure of 140/90 mm Hg, the most likely cause of the hypertension is A) renal disease. Hypertension in children is usually secondary to an underlying medical condition. The most common cause of hypertension in children is renal disease, which can be due to a variety of conditions such as renal artery stenosis, glomerulonephritis, or polycystic kidney disease. Theophylline toxicity (B) can cause a variety of symptoms, including nausea, vomiting, tremors, and seizures, but it is not typically associated with hypertension. Chronic lung disease (C) such as asthma can cause pulmonary hypertension, but this is not typically associated with systemic hypertension. Coarctation of the aorta (D) can cause hypertension in children, but it is usually associated with other symptoms such as leg cramping, cold feet, and a weak or absent pulse in the legs. Obesity (E) can also cause hypertension in children, but it would not be the most likely cause in an otherwise healthy child with a history of bronchial asthma. Therefore, based on the information provided, the most likely cause of hypertension in an otherwise healthy child with a history of bronchial asthma and a blood pressure of 140/90 mm Hg is renal disease. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of hypertension in children. |
17. The average body lenth of newborn boys is 50,9 cm at a sigma 1,66; and average mass – 3432 at a sigma 5,00. What criterion is necessary to compare degree of variability of these signs?
A. Coefficient of variation
B. Sigma
C. Limit
D. Amplitude
E. Coefficient of association
Answer: Coefficient of variation
Explanation
To compare the degree of variability of the signs, the appropriate criterion is A) coefficient of variation. The coefficient of variation (CV) is a statistical measure that compares the standard deviation of a variable to its mean. It is often used to compare the variability of different variables, such as body length and mass in this case, because it allows for the comparison of variables with different units of measurement. The formula for calculating the coefficient of variation is: CV = (standard deviation / mean) x 100% By calculating the coefficient of variation for both body length and mass, we can compare the degree of variability of these signs. Sigma (B) is a symbol used to represent the standard deviation in statistics, but it is not a criterion for comparing the variability of different signs. Limit (C) is not a statistical measure used to compare the variability of different signs. Amplitude (D) is a measure of the range of values for a variable, but it does not take into account the mean or standard deviation and is not suitable for comparing the variability of different signs. Coefficient of association (E) is a measure of the strength and direction of the relationship between two variables, but it is not used to compare the variability of different signs. Therefore, based on the information provided, the appropriate criterion for comparing the degree of variability of body length and mass in newborn boys is the coefficient of variation. |
18. What method is applied to establish rate of correlation between age of men and their mortality due to myocardial infarction?
A. Method of grade correlation (Spirman)
B. Correlation ratio
C. The quadrate method (Pirson)
D. The Indirect method (Student)
E. Method of graduated correlation (Armler)
Answer: Method of grade correlation (Spirman)
Explanation
The appropriate method to establish the rate of correlation between age of men and their mortality due to myocardial infarction is A) Method of grade correlation (Spearman). The method of grade correlation, also known as the Spearman rank correlation coefficient, is a statistical measure used to assess the strength and direction of the relationship between two variables. It is a nonparametric measure that does not require the assumption of a linear relationship between the variables and is often used when the data is not normally distributed. In this case, the age of men and their mortality due to myocardial infarction are two variables that may have a non-linear relationship. The Spearman rank correlation coefficient would be an appropriate method to establish the rate of correlation between these variables. Correlation ratio (B), the quadrate method (C), the indirect method (D), and the graduated correlation method (E) are not appropriate methods for establishing the rate of correlation between these variables. Therefore, based on the information provided, the appropriate method to establish the rate of correlation between age of men and their mortality due to myocardial infarction is the method of grade correlation (Spearman). |
19. Adenosine triphosphate may be expected to convert which of the following arrhythmias to sinus rhythm?
A. Paroxysmal supraventricular tachycardia
B. Paroxysmal ventricular tachycardia
C. Atrial fibrillation
D. Atrial flutter
E. Ventricular fibrillation
Answer: Paroxysmal supraventricular tachycardia
Explanation
Adenosine triphosphate (ATP) may be expected to convert A) paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm. PSVT is a type of arrhythmia that originates above the ventricles, usually in the atria. It is often caused by reentry circuits or accessory pathways within the atrioventricular node or atrial tissue. Adenosine is a medication that works by blocking the atrioventricular node and interrupting the reentry circuits, which can convert PSVT to sinus rhythm. Paroxysmal ventricular tachycardia (B) is a type of arrhythmia that originates in the ventricles, and it is not typically responsive to adenosine. Atrial fibrillation (C) and atrial flutter (D) are types of arrhythmias that originate in the atria and are not typically responsive to adenosine. Ventricular fibrillation (E) is a life-threatening arrhythmia that originates in the ventricles, and it is not typically treated with adenosine. Therefore, based on the information provided, adenosine triphosphate may be expected to convert paroxysmal supraventricular tachycardia to sinus rhythm. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of arrhythmias. |
20. A 48 year old man complains of fatique and shortness of breath. His Ht is 32%, and Hb – 103 g/l. Peripheral blood smear reveals macrocytosis. Serum vitamin B12 level is 90 pg/ml (normal is 170 to 940); serum folate level is 6 ng/ml (normal is 2 to 14). Possible causes to consider include all of the following EXCEPT:
A. Colonic diverticulitis
B. Vegetarianism
C. Regional enteritis
D. Pancreatitis
E. Fish tapeworm infection
Answer: Colonic diverticulitis
Explanation
The possible causes to consider in a 48-year-old man with fatigue, shortness of breath, macrocytosis, low hemoglobin, low serum vitamin B12 level, and low serum folate level include all of the following except A) colonic diverticulitis. Colonic diverticulitis (A) is not typically associated with vitamin B12 or folate deficiencies. Vegetarianism (B) can lead to vitamin B12 deficiency if the individual is not consuming adequate amounts of vitamin B12 from fortified foods or supplements. Regional enteritis (C), also known as Crohn’s disease, is a type of inflammatory bowel disease that can cause malabsorption of vitamin B12 and folate. Pancreatitis (D) can lead to malabsorption of nutrients, including vitamin B12 and folate. Fish tapeworm infection (E) can cause vitamin B12 deficiency due to competition for the nutrient and subsequent malabsorption. Therefore, based on the information provided, the possible causes to consider in this case include vegetarianism, regional enteritis, pancreatitis, and fish tapeworm infection. Colonic diverticulitis is not typically associated with vitamin B12 or folate deficiencies. It is important to consult with a qualified healthcare provider for appropriate diagnosis and management of these conditions. |
21. A 56 year old man complains of fatigue, dyspnea on exertion and palpitations. He has had a murmur since childhood. Examination reveals a lift at the left sternal border, split S1, and fixed splitting of S2. There is a grade 3/6 midsystolic pulmonic murmur and a 1/6 middiastolic tricuspid murmur at the lower left sternal border. Chest x-ray shows right ventricular enlargement and prominent pulmonary arteries. ECG demonstrates atrial fibrillation with a right bundle branch block. The most likely diagnosis is:
A. Arterial septal defect
B. Coarctation of the aorta
C. Patent ductus arteriosus
D. Tetralogy of Fallot
E. Ventricular septal defect
Answer: Arterial septal defect
Explanation
Based on the clinical presentation and findings, the most likely diagnosis for the 56-year-old man is A) arterial septal defect (ASD). ASD is a congenital heart defect that results in an opening between the left and right atria of the heart. The symptoms of ASD may not appear until adulthood, and they can include fatigue, dyspnea on exertion, and palpitations. The murmur heard in ASD is typically a grade 2-3/6 mid-systolic ejection murmur heard at the left upper sternal border. In addition, ASD may cause right ventricular enlargement and prominent pulmonary arteries seen on a chest x-ray. The fixed splitting of S2 is a characteristic finding in ASD due to the increased blood flow across the pulmonary valve. Coarctation of the aorta (B), patent ductus arteriosus (C), tetralogy of Fallot (D), and ventricular septal defect (E) are other congenital heart defects that can cause murmurs and other symptoms, but they would not typically present with the same clinical findings as seen in this case. Therefore, based on the information provided, the most likely diagnosis for the 56-year-old man is arterial septal defect (ASD). It is important to consult with a qualified healthcare provider for appropriate management and care in cases of congenital heart defects. |
22. Generalized low voltage on an ECG (QRS deflection < 5 mm in limb leads and < 10 mm in precordial leads) may be a marker for all of the following disorders EXCEPT:
A. Hyperthyroidism
B. Pericardial effusion
C. Cardiac transplant rejection
D. Amyloidosis
E. Coronary artery disease
Answer: Hyperthyroidism
Explanation
Generalized low voltage on an ECG (QRS deflection < 5 mm in limb leads and < 10 mm in precordial leads) may be a marker for all of the following disorders EXCEPT A) hyperthyroidism. Generalized low voltage on an ECG is a finding that can be seen in a variety of conditions that affect the heart or the body as a whole. Some of the conditions that can cause this finding include pericardial effusion (B), cardiac transplant rejection (C), amyloidosis (D), and coronary artery disease (E). Hyperthyroidism (A) is not typically associated with generalized low voltage on an ECG, and this finding would not be considered a marker for this condition. Therefore, based on the information provided, generalized low voltage on an ECG may be a marker for pericardial effusion, cardiac transplant rejection, amyloidosis, and coronary artery disease, but it would not typically be associated with hyperthyroidism. It is important to consult with a qualified healthcare provider for appropriate diagnosis and management of these conditions. |
23. Five days after a total hip replacement a 72 year old woman becomes acutely short of breath, diaphoretic and hypotensive. Both lung fields are clear to auscultation and percussion, but examination of the neck reveals mild jugular venous distension with prominent A waves. Heart sounds are normal. ECG shows sinus tachycardia with a new right bundle branch block and minor nonspecific ST − T wave changes. The most likely diagnosis is:
A. Pulmonary thromboembolism
B. Acute myocardial infarction
C. Aortic dissection
D. Pericarditis
E. Aspiration
Answer: Pulmonary thromboembolism
Explanation
Based on the clinical presentation and findings, the most likely diagnosis for the 72-year-old woman is A) pulmonary thromboembolism (PTE). PTE is a serious condition in which a blood clot blocks one or more pulmonary arteries in the lungs, leading to acute shortness of breath, hypotension, and diaphoresis. The physical examination finding of mild jugular venous distension with prominent A waves is consistent with right heart strain due to the increased resistance from the blocked pulmonary arteries. The ECG findings of sinus tachycardia with a new right bundle branch block and minor nonspecific ST-T wave changes are also consistent with right heart strain. Acute myocardial infarction (B) typically presents with chest pain or discomfort, and the ECG findings would show ST-segment elevation or new Q waves. Aortic dissection (C) can present with sudden onset of severe chest or back pain, and the physical examination findings may include differences in blood pressure between the arms and potentially aortic regurgitation or murmur. Pericarditis (D) can cause chest pain, but it would not typically present with acute shortness of breath and hypotension. The physical examination findings may include a pericardial friction rub. Aspiration (E) can cause respiratory symptoms, but it would not typically present with acute hypotension and diaphoresis. Therefore, based on the information provided, the most likely diagnosis for the 72-year-old woman is pulmonary thromboembolism (PTE). It is important to consult with a qualified healthcare provider for appropriate management and care in cases of PTE. |
24. A child is 6 years old. Within one year of observation he had URI that lasted 8 days. Physical state is satisfactory. Specify hi health group:
A. I
B. II
C. III (a)
D. III (b)
E. III (c)
Answer: I
Explanation
The child is 6 years old and had a URI (upper respiratory infection) that lasted 8 days within the past year, but their physical state is currently satisfactory. According to the World Health Organization’s classification system for child health, this child would fall under group I, which represents children with no signs of any nutritional deficiencies or chronic diseases. Groups II, III (a), III (b), and III (c) are used to classify children with varying degrees of malnutrition, chronic diseases, or disabilities, and the child in this scenario does not meet the criteria for any of these groups. Therefore, based on the information provided, the child’s health group can be classified as I. It is important to continue monitoring the child’s health and seeking appropriate medical attention as needed. |
25. Which of the following IS NOT TYPICAL for Addison’s disease?
A. High serum Na+
B. High serum K+
C. Elevated BUN
D. Dilute urine
E. Elevated hematocrit
Answer: High serum Na+
Explanation
Addison’s disease is a disorder that occurs when the adrenal glands do not produce enough cortisol and aldosterone. The symptoms of Addison’s disease can vary, but some common features include fatigue, weakness, weight loss, and low blood pressure. In addition, the following laboratory abnormalities are typically seen in Addison’s disease: A. High serum Na+: This is NOT typical for Addison’s disease. Instead, hyponatremia (low serum sodium) is commonly seen due to the loss of salt in the urine. B. High serum K+: This is a typical finding in Addison’s disease, as the lack of aldosterone can lead to hyperkalemia (high serum potassium). C. Elevated BUN: This is a typical finding in Addison’s disease, as dehydration and decreased renal perfusion can lead to increased blood urea nitrogen (BUN). D. Dilute urine: This is a typical finding in Addison’s disease, as the lack of aldosterone can impair the ability of the kidneys to concentrate urine. E. Elevated hematocrit: This is a typical finding in Addison’s disease, as the lack of cortisol can lead to an increase in erythropoietin production, which stimulates the bone marrow to produce more red blood cells. Therefore, based on the information provided, the laboratory abnormality that is NOT typical for Addison’s disease is A) high serum Na+. |
26. A 38 year old man, previously in good health, suddenly develops severe abdominal pain radiating from the left loin to groin and accompanied by nausea, perspiration and the need for frequent urination. He is restless, tossing in bed but has no abnormal findings. The most likely diagnosis is:
A. Leftsided renal colic
B. Herpes zoster
C. Sigmoid diverticulitis
D. Torsion of the left testicle
E. Retroperitoneal haemorrhage
Answer: Leftsided renal colic
Explanation
Based on the clinical presentation and findings, the most likely diagnosis for the 38-year-old man is A) left-sided renal colic. Renal colic is a condition in which a kidney stone becomes lodged in the ureter, causing severe pain that can radiate from the back or flank to the groin. The pain is typically accompanied by other symptoms, such as nausea, sweating, and the need for frequent urination. The restlessness and tossing in bed that the patient is experiencing are also typical of renal colic.
Therefore, based on the information provided, the most likely diagnosis for the 38-year-old man is left-sided renal colic. It is important to consult with a qualified healthcare provider for appropriate management and care in cases of renal colic. |
27. A 40 year old woman has a selfdetected hard breast mass. The procedure of choice for confirming the diagnosis is:
A. Excision biopsy
B. Mammography
C. Thermography
D. Ultrasonography
E. Aspiration biopsy with cytology
Answer: Excision biopsy
Explanation
Based on the clinical presentation, the procedure of choice for confirming the diagnosis of a self-detected hard breast mass in a 40-year-old woman is A) excision biopsy. Excision biopsy is the gold standard for diagnosing breast cancer, as it involves removing the entire mass and examining it under a microscope for the presence of cancerous cells. This procedure is typically performed under local anesthesia in an outpatient setting. Mammography (B) and ultrasonography (D) are imaging studies that can help detect breast abnormalities, but they cannot definitively diagnose breast cancer. These studies may be used in conjunction with other diagnostic tests, such as biopsy, to help confirm the diagnosis. Thermography (C) is a non-invasive imaging test that uses infrared technology to detect changes in temperature on the skin surface of the breast. However, it is not considered a reliable diagnostic tool for breast cancer. Aspiration biopsy with cytology (E) involves using a needle to extract a small sample of cells from the breast mass and examining them under a microscope for the presence of cancerous cells. While this procedure can be useful in some cases, it is not as reliable as excision biopsy for diagnosing breast cancer. Therefore, based on the information provided, the procedure of choice for confirming the diagnosis of a self-detected hard breast mass in a 40-year-old woman is excision biopsy. It is important to consult with a qualified healthcare provider for appropriate diagnosis and management of breast abnormalities. |
28. A 38 year old man was admitted to a hospital from his working place on July 19 because of hip fracture. He was invalid till November 19. Requires prolongation of treatment. Who decides on the issue of further temporary invalidity?
A. Specialized (traumatologic) MSEC
B. DCC
C. The head physician of a polyclinic
D. Interregional general MSEC
E. Regional MSEC
Answer: Specialized (traumatologic) MSEC
Explanation
Based on the information provided, the decision regarding the further temporary invalidity of the 38-year-old man would be made by A) specialized (traumatologic) MSEC (Medical and Social Expertise Commission). MSEC is a medical institution responsible for evaluating the degree of disability and the need for social protection measures for individuals with health impairments. In this case, the man suffered a hip fracture and was invalid until November 19, and now requires prolongation of treatment. Therefore, he would need to undergo a medical and social expertise evaluation to determine the extent of his disability and the need for further temporary invalidity. The specialized (traumatologic) MSEC is a specific type of MSEC that deals with disabilities related to trauma and injuries. As such, this would be the appropriate authority to evaluate the man’s temporary invalidity and determine whether it should be prolonged. The DCC (B) is the District Clinical Committee that oversees the provision of healthcare services in a particular district, but it is not responsible for determining the degree of disability or the need for social protection measures. The head physician of a polyclinic (C) is responsible for the management of a polyclinic, but would not typically be involved in the determination of disability or social protection measures. The interregional general MSEC (D) and the regional MSEC (E) are other types of MSECs that evaluate disability and the need for social protection measures, but the specialized (traumatologic) MSEC would be the appropriate authority in this case due to the nature of the man’s injury. Therefore, based on the information provided, the decision regarding the further temporary invalidity of the 38-year-old man would be made by the specialized (traumatologic) MSEC. |
29. During investigation for chronic, severe, epigastric pain, a 40 year old alcoholic man is found to have multiple areas of narrowing alternating with dilatation (“chain of lakes”appearance) of the main pancreatic duct. The operation of choice is:
A. Lateral pancreaticojejunostomy
B. Distal pancreaticojejunostomy
C. Sphincterotomy
D. Distal pancreatectomy
E. Total pancreatectomy
Answer: Lateral pancreaticojejunostomy
Explanation
The description of “multiple areas of narrowing alternating with dilatation (‘chain of lakes’ appearance) of the main pancreatic duct” is characteristic of chronic pancreatitis, which is a chronic inflammation of the pancreas that can lead to scarring, fibrosis, and narrowing of the pancreatic ducts. Lateral pancreaticojejunostomy, also known as the Puestow procedure, is the operation of choice for patients with chronic pancreatitis who have a dilated pancreatic duct. It involves creating a side-to-side anastomosis between the dilated pancreatic duct and a loop of jejunum, which allows pancreatic juice to drain more easily into the small intestine and can improve symptoms such as abdominal pain, nausea, and vomiting. This procedure is typically reserved for patients who have not responded to conservative management, including avoiding alcohol and smoking cessation. Distal pancreaticojejunostomy and distal pancreatectomy are not appropriate procedures in this case, as they involve removing the tail of the pancreas and would not address the issues with the main pancreatic duct. Sphincterotomy, which involves cutting the sphincter muscle at the end of the pancreatic duct to allow better drainage of pancreatic juice, is more commonly used for patients with sphincter of Oddi dysfunction rather than chronic pancreatitis. Total pancreatectomy is typically only considered as a last resort in patients with severe, intractable pain who have not responded to other treatments, as it can lead to lifelong diabetes and other complications. |
30. The treatment of choice for duodenal obstruction caused by secondary duodenal hematoma that developed a few days after blunt abdominal injury is:
A. Nasogastric decompression and parenteral alimentation
B. Retrocolic gastrojejunostomy
C. Duodenojejunostomy
D. Immediate exploration
E. Tube duodenostomy
Answer: Nasogastric decompression and parenteral alimentation
Explanation
Duodenal obstruction caused by a secondary duodenal hematoma that developed a few days after blunt abdominal injury is a relatively rare condition, but it can be a serious and potentially life-threatening complication. The initial management typically involves supportive measures to stabilize the patient and relieve the obstruction. Nasogastric decompression, which involves placing a tube through the nose and into the stomach to remove air and fluid, can help to relieve the obstruction and reduce nausea and vomiting. Parenteral alimentation, which involves providing nutrition through an intravenous line, can help to maintain the patient’s nutrition while the obstruction is being managed. Surgical intervention may be necessary if conservative measures are unsuccessful, but the specific procedure chosen depends on the severity of the obstruction and the patient’s overall condition. Retrocolic gastrojejunostomy and duodenojejunostomy are surgical procedures that can be used to bypass the obstructed portion of the duodenum, but they are typically reserved for cases where conservative measures have failed or the obstruction is severe. Immediate exploration and tube duodenostomy are also surgical options that may be considered in certain cases, but they are not the first-line treatment for this condition. |
31. A 25 year old man has a sudden onset of chest pain on the right and dyspnea. His trachea is deviated to the left. All of the following would be anticipated EXCEPT:
A. Pleural friction rub on the left
B. Absence of rhonchi
C. Absence of rales
D. Hyperresonance over the right chest
E. Distant breath sounds on the right
Answer: Pleural friction rub on the left
Explanation
The clinical presentation described in the question is suggestive of a tension pneumothorax, which is a medical emergency that requires prompt recognition and treatment. A tension pneumothorax occurs when air enters the pleural space and cannot escape, causing increasing pressure on the lung and mediastinum, which can lead to respiratory distress, hypoxia, and cardiovascular collapse. When a tension pneumothorax is present, the trachea is typically deviated away from the affected side due to the increased pressure in the pleural space. Other physical exam findings may include hyperresonance over the affected side, absent or diminished breath sounds on the affected side, and absence of rhonchi or rales. A pleural friction rub is a sound heard on auscultation that is caused by the rubbing together of inflamed pleural surfaces, and it is not typically associated with a tension pneumothorax. In this case, the presence of a pleural friction rub on the left would be unexpected, as it suggests an unrelated condition such as pleurisy or pneumonia on the contralateral side. The other findings described in the answer choices are consistent with the clinical presentation of a tension pneumothorax. |
32. A 5 tons milk batch was sampled. The lab analysis revealed: fat content 2%, specific density – 1,04 g/cm3, acidity – 210Т, reductase probe – weak-positive. What way is the product to be used in?
A. Sell but inform customers about milk quality
B. Discard for animal feeding
C. Technical utilization
D. Sell without limitations
E. Do the product away
Answer: Sell but inform customers about milk quality
Explanation
The lab analysis results indicate that the milk batch has a low fat content (2%) and high acidity (210T), which suggest that it may not meet the standard quality criteria for milk. Additionally, the weak-positive result on the reductase probe test may indicate that the milk has been partially oxidized, which can affect its flavor and nutritional value. However, the specific density of the milk is within the normal range (1.04 g/cm3), which suggests that it has not been significantly diluted with water. Based on these results, the milk can still be sold, but it is important to inform customers about its quality and potential issues. Depending on the regulations in the specific region, it may be necessary to label the milk as “low quality” or “substandard” to ensure that consumers are aware of its condition. Discarding the milk for animal feeding or technical utilization may be appropriate if the milk is found to be unsafe for human consumption due to contamination or other factors. However, based solely on the lab analysis results provided in the question, there is no indication that the milk is unsafe for human consumption. Doing the product away, or throwing it out, would be an excessive and unnecessary waste if the milk is still safe for human consumption. |
33. What guarantees against the preconceived attitude to the physician in cases of professional law violations do you know?
A. Sanction of public prosecutor, inquiry by preliminary investigator of prosecutor’s office, committee of experts
B. Draw up a statement about forensic medical examination
C. Conduct an inquiry by preliminary investigator of police department
D. Utilisation copy of medical documents
E. Conduct forensic medical examination by district forensic medicine expert
Answer: Sanction of public prosecutor, inquiry by preliminary investigator of prosecutor’s office, committee of experts
Explanation
In cases of professional law violations by a physician, there are several measures in place to help ensure that any preconceived attitudes or biases do not unfairly influence the outcome of the investigation. These measures typically involve a combination of legal and medical procedures designed to provide independent scrutiny and oversight of the investigation process. One such measure is the sanction of the public prosecutor, which involves a legal authority issuing a penalty or punishment for the violation that has been committed. This can help to ensure that the investigation is conducted in a fair and impartial manner, without any preconceived attitudes towards the physician or the situation. Another measure is the inquiry by the preliminary investigator of the prosecutor’s office, which involves an independent investigator examining the evidence and conducting interviews to determine the facts of the case. This can help to ensure that the investigation is conducted thoroughly and impartially, without any biases or preconceptions. Additionally, a committee of experts may be convened to review the evidence and provide an independent assessment of the situation. This can help to ensure that the investigation is conducted with a high degree of scientific rigor and expertise, and that any potential biases or preconceptions are identified and addressed. Other measures, such as drawing up a statement about forensic medical examination, conducting an inquiry by the preliminary investigator of the police department, or utilizing a copy of medical documents, may also be used in some cases, but they are typically not sufficient on their own to provide the necessary level of independent oversight and scrutiny. A forensic medical examination by a district forensic medicine expert may also be conducted as part of the investigation, but this is typically only one aspect of a broader investigation process. |
34. If a child has adherent fingers on his right hand, then what will be your diagnosis?
A. Syndactyly
B. Polydactyly
C. Macrodactyly
D. Ectrodactyly
E. Ectromelia
Answer: Syndactyly
Explanation
Syndactyly is a congenital condition in which two or more fingers or toes are fused together. It is caused by incomplete separation of the digits during fetal development and can affect one or both hands or feet. The degree of fusion can vary, ranging from partial fusion at the base of the digits to complete fusion throughout the entire length of the digits. In the case described, the child has adherent fingers on their right hand, which is suggestive of syndactyly. This condition can be diagnosed through physical examination and imaging studies such as X-rays or CT scans. Polydactyly, on the other hand, is a condition in which a person has extra fingers or toes. Macrodactyly is a condition in which one or more digits are abnormally large. Ectrodactyly is a condition in which one or more digits are missing or underdeveloped. Ectromelia is a rare congenital disorder that affects the development of the limbs and can result in partial or complete absence of one or more limbs. Therefore, based on the description given in the question, syndactyly is the most likely diagnosis. However, a definitive diagnosis would require further evaluation by a medical professional. |
35. A 16 year old patient with complaints of frequent pain in the abdomen was diagnosed with melanoma, examination revealed also pigmentation of the mucosa and skin, polyp in the stomach and large intestine. It is know that the patient’s mother has an analogous pigmentation and has been often treated for anemia. What disease is suspected?
A. Peytz-Egers’s polyposis
B. Chron’s disease
C. Tuberculosis of the intestine
D. Adolescent polyposis
E. Hirschprung’s disease
Answer: Peytz-Egers’s polyposis
Explanation
Peutz-Jeghers syndrome is a rare genetic disorder characterized by the development of hamartomatous polyps in the gastrointestinal tract, as well as mucocutaneous pigmentation. The polyps can occur throughout the gastrointestinal tract, but are most commonly found in the small intestine and colon. Patients with Peutz-Jeghers syndrome are at an increased risk of developing gastrointestinal cancers, including colorectal, pancreatic, and gastric cancers. In the case described, the 16-year-old patient has complaints of frequent abdominal pain, as well as pigmentation of the mucosa and skin, and polyps in the stomach and large intestine. These symptoms are consistent with the diagnosis of Peutz-Jeghers syndrome. The fact that the patient’s mother has a similar pigmentation and has been treated for anemia also suggests a genetic component to the condition. Crohn’s disease, tuberculosis of the intestine, adolescent polyposis, and Hirschsprung’s disease are all conditions that can cause abdominal pain and gastrointestinal symptoms, but they are not typically associated with mucocutaneous pigmentation or the development of hamartomatous polyps. Therefore, based on the symptoms described in the question, Peutz-Jeghers syndrome is the most likely diagnosis. Confirmation of the diagnosis would require further evaluation by a medical professional, including genetic testing and endoscopic examination of the gastrointestinal tract. |
36. A 41 year old patient was admitted to the intensive care unit with haemorrhagic shock due to gastric bleeding. He has a history of hepatitis B during the last 5 years. The source of bleeding are esophageal veins. What is the most effective method for control of the bleeding?
A. Introduction of obturator nasogastric tube
B. Intravenous administration of pituitrin
C. Hemostatic therapy
D. Operation
E. Administration of plasma
Answer: Introduction of obturator nasogastric tub
Explanation
Esophageal varices are enlarged veins in the lower esophagus that can cause life-threatening bleeding in patients with liver disease, such as hepatitis B. Hemostatic therapy is the most effective method for controlling bleeding from esophageal varices. This may involve endoscopic treatment, such as band ligation or sclerotherapy, or pharmacological therapy, such as the use of vasopressin or octreotide to reduce blood flow to the varices. The introduction of an obturator nasogastric tube is not an effective method for controlling bleeding from esophageal varices. This procedure involves inserting a tube through the nose and into the stomach to help remove fluids and air, but it does not address the underlying cause of the bleeding. Intravenous administration of pituitrin, a medication used to stimulate uterine contractions during childbirth, is not effective for controlling bleeding from esophageal varices and may have serious side effects. Surgery may be necessary in some cases of esophageal varices, particularly if other treatments have failed or the patient is experiencing life-threatening bleeding. However, surgery is generally considered a last resort and is not the first-line treatment for this condition. Administration of plasma may be used in some cases to replace clotting factors and help control bleeding, but it is typically used in conjunction with other treatments such as hemostatic therapy. Therefore, based on the information given in the question, hemostatic therapy is the most effective method for controlling bleeding from esophageal varices caused by hepatitis B. |
37. It is suspected that a 34 year old patient has an abscess of Douglas pouches. What diagnostic method is to be chosen?
A. Digital examination of rectum
B. Rectoromanoscopy
C. Laparoscopy
D. Percussion and auscultation of stomach
E. R-scopy of abdominal cavity
Answer: Digital examination of rectum
Explanation
Douglas pouch, also known as the rectouterine pouch or the cul-de-sac of Douglas, is a space located between the rectum and the uterus in females. An abscess in this area is known as a Douglas abscess and can cause symptoms such as pelvic pain, fever, and vaginal discharge. Digital examination of the rectum is a common diagnostic method for evaluating Douglas abscesses. During this procedure, a healthcare provider inserts a gloved and lubricated finger into the rectum to feel for any abnormalities, such as swelling or tenderness in the area of the Douglas pouch. Rectoromanoscopy, which involves inserting a flexible tube with a camera into the rectum and lower colon, may also be used to evaluate the area and identify the presence of an abscess. However, this procedure is more invasive and may not be necessary for the initial diagnosis of a Douglas abscess. Laparoscopy, a minimally invasive surgical procedure that involves inserting a camera through a small incision in the abdomen, may be used to evaluate the pelvic area and identify the extent of the abscess. However, this procedure is typically reserved for cases where the diagnosis is unclear or the abscess is particularly large or complex. Percussion and auscultation of the stomach and R-scopy of the abdominal cavity are not typically used to diagnose a Douglas abscess, as they do not provide direct visualization or palpation of the affected area. Therefore, based on the information given in the question, digital examination of the rectum is the most appropriate diagnostic method for evaluating a suspected Douglas abscess. |
38. A 52 year old man has recurrent transient ischemic attacks. Auscultation of the carotid arteries detected murmur. What diagnostic method is to be applied in the first place?
A. Ultrasound dopplerography
B. CT of the brain
C. MRI of the brain
D. Cerebral angiography
E. Electroencephalography
Answer: Ultrasound dopplerography
Explanation
Transient ischemic attacks (TIAs) are brief episodes of neurological dysfunction caused by temporary disruption of blood flow to the brain. They are often caused by atherosclerotic disease in the carotid arteries, which are the major blood vessels that supply blood to the brain. A carotid artery bruit or murmur detected on auscultation is a common finding in patients with carotid artery disease. Ultrasound dopplerography is a non-invasive diagnostic method that uses high-frequency sound waves to create images of the blood vessels. It is the most appropriate initial diagnostic method for evaluating carotid artery disease. The test can detect the presence of plaque in the carotid arteries and assess the degree of stenosis or narrowing of the arteries. This information can help determine the patient’s risk of stroke and guide treatment decisions. CT and MRI of the brain are imaging studies that can help evaluate the extent of brain damage caused by a TIA or stroke, but they are not the first-line diagnostic methods for evaluating carotid artery disease. Cerebral angiography is a more invasive test that involves injecting contrast dye into the blood vessels to create detailed images of the blood flow in the brain. It is typically reserved for cases where other diagnostic methods have been inconclusive or when intervention is being considered. Electroencephalography (EEG) is a test that measures electrical activity in the brain and is typically used to evaluate seizures or other neurological conditions that affect brain function. It is not a first-line diagnostic method for evaluating carotid artery disease. Therefore, based on the information given in the question, ultrasound dopplerography is the most appropriate initial diagnostic method for evaluating the carotid arteries in a patient with recurrent TIAs and a carotid artery murmur. |
39. A 34 year old woman in the 10th week of gestation (the second pregnancy) consulted a doctor of antenatal clinic in order to be registered there. In the previous pregnancy hydramnion was observed, the child’s birth weight was 4086 g. What examination method should be applied in the first place?
A. The test for tolerance to glucose
B. Determination of the contents of fetoproteinum
C. Bacteriological examination of discharges from vagina
D. A cardiophonography of fetus
E. US of fetus
Answer: The test for tolerance to glucose
Explanation
Hydramnios, also known as polyhydramnios, is a condition in which there is an excessive amount of amniotic fluid surrounding the fetus. It can be associated with a range of fetal and maternal complications, including preterm labor, premature rupture of membranes, and fetal malpresentation. In the case described, the patient had hydramnios in her previous pregnancy and delivered a large baby. These factors increase the risk of gestational diabetes mellitus (GDM), a type of diabetes that develops during pregnancy and can lead to complications for both the mother and fetus. The test for tolerance to glucose, also known as the glucose tolerance test (GTT), is a screening test used to diagnose GDM. During this test, the patient drinks a sugary solution and blood samples are taken at timed intervals to measure the body’s response to the glucose. Abnormal results may indicate the presence of GDM and further evaluation and treatment may be necessary. Determination of the contents of fetoproteinum and bacteriological examination of discharges from the vagina are not appropriate methods for evaluating the risk of GDM or hydramnios. A cardiophonography of the fetus may be used to evaluate the fetal heart rate and rhythm and detect any abnormalities, but it is not the first-line test for evaluating the risk of hydramnios or GDM. US of the fetus is a valuable diagnostic method in pregnancy, but it is not the first-line test for evaluating the risk of GDM or hydramnios. However, ultrasound examination may be used to monitor the amount of amniotic fluid around the fetus and detect any abnormalities. Therefore, based on the information given in the question, the test for tolerance to glucose is the most appropriate initial diagnostic method for evaluating the risk of GDM in a patient with a history of hydramnios and a large baby in a previous pregnancy. |
40. A patient with acute purulent otitis media complicated by mastoiditis was admitted to a hospital. Roentgenogram of mastoid processes showed the shadiowing of the cellular system on the lesion, absence of bone septa was present. What are the necessary therapeutic +actions at the second stage of mastoiditis?
A. Mastoidotomy
B. Paracentesis of the drum
C. Radical operation on the middle ear
D. Tympanoplasty
E. Cateterization of the Eustachian tube
Answer: Mastoidotomy
Explanation
Mastoiditis is a bacterial infection of the mastoid bone in the skull, which is located behind the ear. It can occur as a complication of acute otitis media, an infection of the middle ear. In severe cases, mastoiditis can cause destruction of the mastoid bone and surrounding tissues, leading to serious complications such as meningitis, brain abscess, or hearing loss. In the case described, the patient has acute purulent otitis media complicated by mastoiditis, and a roentgenogram of the mastoid processes shows the shadowing of the cellular system on the lesion, with an absence of bone septa. This suggests that the infection has caused destruction of the mastoid bone and the formation of a mastoid abscess. Mastoidotomy is a surgical procedure that involves making an incision in the mastoid bone to drain the abscess and remove infected tissue. It is the necessary therapeutic action at the second stage of mastoiditis when there is evidence of a mastoid abscess. Paracentesis of the drum, tympanoplasty, and catheterization of the Eustachian tube are not appropriate treatments for mastoiditis, as they do not address the underlying infection in the mastoid bone. Radical operation on the middle ear may be necessary in some cases of chronic otitis media with extensive damage to the middle ear structures, but it is not typically indicated in cases of mastoiditis. Therefore, based on the information given in the question, mastoidotomy is the necessary therapeutic action at the second stage of mastoiditis with evidence of a mastoid abscess. |
41. A 22 year old patient was admitted to trauma center with complaints of pain in the left ankle joint that was getting worse during moving and weight bearing. On the clinical examination it was found that the patient had the closed fracture of medial malleolus without displacement. In which position should the foot be fixed in plaster cast?
A. At right angle with varus positioning of the foot
B. In position of planter flexion of foot
C. In position of pronation
D. In position of supination
E. In position of dorsal flexion of foot
Answer: At right angle with varus positioning of the foot
Explanation
A closed fracture of the medial malleolus is a type of ankle fracture in which the bony prominence on the inner side of the ankle is broken but the skin is not broken. This type of fracture can often be treated with a plaster cast. When applying a cast for a fracture of the medial malleolus, the foot should be fixed at a right angle with varus positioning. Varus positioning means that the foot is turned inward, with the sole of the foot tilted toward the midline of the body. This position helps to align the fractured bone and prevent displacement. Positioning the foot in plantar flexion, pronation, supination, or dorsal flexion is not appropriate for a fracture of the medial malleolus, as it does not provide the necessary support and alignment for the fractured bone. Therefore, based on the information given in the question, the foot should be fixed in a plaster cast at a right angle with varus positioning for a closed fracture of the medial malleolus without displacement. |
42. A patient with acute respiratory viral infection (3rd day of disease) complains of pain in lumbar region, nausea, dysuria, oliguria. Urinalysis – hematuria (100-200 RBC in eyeshot spot), specific gravity – 1002. The blood creatinin level is 0,18 millimole/l, potassium level – 6,4 millimole/l. Make the diagnosis:
A. Acute interstitial nephritis
B. Acute renal failure
C. Acute glomerylonephritis
D. Acute cystitis
E. Acute renal colic
Answer: Acute interstitial nephritis
Explanation
Acute interstitial nephritis (AIN) is an inflammation of the renal interstitium, which is the space between the kidney tubules. It can be caused by a variety of factors, including medications, infections, and autoimmune disorders. Patients with AIN may present with symptoms such as flank pain, nausea, vomiting, dysuria, and oliguria. In the case described, the patient has an acute respiratory viral infection and presents with pain in the lumbar region, nausea, dysuria, and oliguria. Urinalysis shows hematuria, with 100-200 red blood cells in the eyeshot spot, and a specific gravity of 1002. The blood creatinine level is slightly elevated, and the potassium level is elevated. These findings suggest the presence of AIN, as hematuria, low specific gravity, and mild elevations in creatinine and potassium levels are common features of this condition. The fact that the patient has an acute respiratory viral infection also supports the diagnosis of AIN, as viral infections can be a cause of AIN. Acute renal failure, acute glomerulonephritis, acute cystitis, and acute renal colic are all possible diagnoses in this patient, but they are less likely based on the clinical presentation and laboratory findings. Therefore, based on the information given in the question, the most likely diagnosis for this patient is acute interstitial nephritis. |
43. A 3 month old infant suffering from acute segmental pneumonia has dyspnea (respiration rate – 80 per minute), paradoxical breathing, tachycardia, total cyanosis. Respiration / pulse ratio is 1:2. The heart dullness under normal size. Such signs characterise:
A. Respiratory failure of III degree
B. Respiratory failure of I degree
C. Respiratory failure of II degree
D. Myocarditis
E. Congenital heart malformation
Answer: Respiratory failure of III degree
Explanation
The clinical presentation described in the question suggests severe respiratory distress in a 3-month-old infant with acute segmental pneumonia. The infant is experiencing dyspnea with a respiratory rate of 80 breaths per minute, paradoxical breathing, tachycardia, and total cyanosis. The respiratory/pulse ratio is 1:2, indicating that the respiratory rate is twice the heart rate. The heart dullness is normal. These findings suggest that the infant is in respiratory failure of III degree, which is the most severe degree of respiratory failure. This is characterized by severe respiratory distress with a respiratory rate greater than 60 breaths per minute, paradoxical breathing, cyanosis, and altered consciousness. Myocarditis, congenital heart malformation, and respiratory failure of I or II degree are less likely diagnoses based on the clinical presentation and symptoms described in the question. Therefore, based on the information given in the question, the most likely diagnosis for this infant is respiratory failure of III degree due to acute segmental pneumonia. Immediate medical intervention is necessary to manage the respiratory distress and improve oxygenation. |
44. A 3 year old child has been suffering from fever, cough, coryza, conjunctivitis for 4 days. He has been taking sulfadimethoxine. Today it has fever up to 39oC and maculopapular rash on its face. Except of rash the child’s skin has no changes. What is your diagnosis?
A. Measles
B. Allergic rash
C. Rubella
D. Scarlet fever
E. Pseudotuberculosis
Answer: Measles
Explanation
Measles is a highly contagious viral infection that spreads through respiratory droplets. It typically begins with symptoms such as fever, cough, coryza (inflammation of the mucous membranes in the nose), and conjunctivitis (redness and swelling of the eyes). These symptoms last for several days before a maculopapular rash appears on the face and then spreads to the trunk and extremities. In the case described, the 3-year-old child has been experiencing fever, cough, coryza, and conjunctivitis for 4 days and has been taking sulfadimethoxine. Today, the child has a fever of up to 39°C and a maculopapular rash on the face. These symptoms are consistent with the diagnosis of measles. Allergic rash, rubella, scarlet fever, and pseudotuberculosis are all possible diagnoses in this case, but they are less likely based on the clinical presentation and symptoms described in the question. Therefore, based on the information given in the question, the most likely diagnosis for this child is measles. It is important to confirm the diagnosis with laboratory testing and provide appropriate treatment and supportive care to manage the symptoms and prevent complications. |
45. A 2 year old girl has been ill for 3 days. Today she has low grade fever, severe catarrhal presentations, slight maculopapular rash on her buttocks and enlarged occipital lymph nodes. What is your diagnosis?
A. Rubella
B. Scarlet fever
C. Measles
D. Adenoviral infection
E. Pseudotuberculosis
Answer: Rubella
Explanation
Rubella, also known as German measles, is a viral infection that is commonly seen in children. It is characterized by symptoms such as low-grade fever, catarrhal symptoms (inflammation of the mucous membranes in the nose and throat), and a maculopapular rash that typically begins on the face and spreads to the trunk and extremities. Enlarged occipital lymph nodes are also commonly seen in rubella. In the case described, the 2-year-old girl has been ill for 3 days and presents with low-grade fever, severe catarrhal symptoms, and a slight maculopapular rash on her buttocks. Enlarged occipital lymph nodes are also present. These symptoms are consistent with the diagnosis of rubella. Scarlet fever, measles, adenoviral infection, and pseudotuberculosis are all possible diagnoses, but they are less likely based on the clinical presentation and symptoms described in the question. Therefore, based on the information given in the question, the most likely diagnosis for this 2-year-old girl is rubella. It is important to confirm the diagnosis with laboratory testing and provide appropriate treatment and supportive care to manage the symptoms and prevent complications. |
46. A 3 year old boy fell ill abruptly: fever up to 39oC, weakness, vomitng. Haemorrhagic rash of various size appeared on his lower limbs in 5 hours. Meningococcemia with infective – toxic shock of the 1 degree was diagnosed. What medications should be administered?
A. Chloramphenicol succinate and prednisone
B. Penicillin and prednisone
C. Penicillin and immunoglobulin
D. Chloramphenicol succinate and interferon
E. Ampicillin and immunoglobulin
Answer: Chloramphenicol succinate and prednisone
Explanation
Meningococcemia is a serious bacterial infection caused by Neisseria meningitidis. It can present with symptoms such as fever, weakness, vomiting, and a hemorrhagic rash that spreads rapidly. Infective-toxic shock is a complication that can occur in severe cases. In the case described, a 3-year-old boy has developed symptoms of meningococcemia with infective-toxic shock of the 1 degree. The presence of a hemorrhagic rash on the lower limbs is highly suggestive of this diagnosis. Immediate medical intervention is necessary to manage the infection and prevent complications. The recommended treatment for meningococcemia includes antibiotics such as chloramphenicol or a third-generation cephalosporin, which should be administered as soon as possible after diagnosis. Prednisone is a corticosteroid that can be used to reduce inflammation and improve outcomes in patients with severe meningococcal disease. Therefore, based on the information given in the question, the most appropriate medications to administer to this 3-year-old boy with meningococcemia and infective-toxic shock of the 1 degree are chloramphenicol succinate and prednisone. It is important to closely monitor the child’s condition and provide supportive care as needed, including intravenous fluids, oxygen, and other interventions to manage shock. |
47. A 7 year old girl has mild form of varicella. Headache, weakness, vertigo, tremor of her limbs, ataxia, then mental confusion appeared on the 5th day of illness. Meningeal signs are negative. Cerebrospinal fluid examination is normal. How can you explain these signs?
A. Encephalitis
B. Meningitis
C. Meningoencephalitis
D. Myelitis
E. Neurotoxic syndrome
Answer: Encephalitis
Explanation
Varicella, also known as chickenpox, is a viral infection that is usually mild and self-limited in children. However, in rare cases, it can lead to complications such as encephalitis, which is inflammation of the brain. In the case described, a 7-year-old girl has a mild form of varicella, but on the 5th day of illness, she develops symptoms such as headache, weakness, vertigo, tremor of her limbs, ataxia, and mental confusion. These symptoms are suggestive of encephalitis, as they indicate inflammation and dysfunction of the brain. Meningeal signs are negative, and cerebrospinal fluid examination is normal, which suggests that the inflammation is primarily affecting the brain and not the meninges. This is consistent with the diagnosis of encephalitis. Meningitis, meningoencephalitis, myelitis, and neurotoxic syndrome are all possible diagnoses, but they are less likely based on the clinical presentation and symptoms described in the question. Therefore, based on the information given in the question, the most likely diagnosis for this 7-year-old girl is encephalitis due to varicella. It is important to confirm the diagnosis with laboratory testing and provide appropriate treatment and supportive care to manage the symptoms and prevent complications. |
48. A 14 year old patient complains of chest pain, temperature up to 38, 5oC, breathlessness. He had acute tonsillitis 2 weeks ago. He is in grave condition. The skin is pale. Heart borders are dilated, heart sounds are quiet. Above total heart area you can hear pericardium friction sound. Electrocardiogram: the descent of QRS voltage, the inversion T. The liver is enlarged by 3 cm. ESR – 4 mm/h, ASL – 0 – 1260, C-reactive protein +++. Your diagnosis:
A. Rheumatic pancarditis
B. Rheumatic pericarditis
C. Rheumatic myocarditis
D. Rheumatic endocarditis
E. Septic endocarditis
Answer: Rheumatic pancarditis
Explanation
Rheumatic fever is a serious inflammatory disease that can develop after a streptococcal infection, such as acute tonsillitis. It can affect different parts of the heart, including the pericardium, myocardium, and endocardium. When all three layers of the heart are involved, it is called pancarditis. In the case described, the 14-year-old patient presents with chest pain, high fever, and breathlessness, which are suggestive of cardiac involvement. The physical examination reveals pale skin, dilated heart borders, quiet heart sounds, and a pericardial friction rub above the total heart area. The electrocardiogram shows a descent of QRS voltage and T wave inversion, which are common findings in pancarditis. The enlarged liver and elevated inflammatory markers, such as ESR and C-reactive protein, are also consistent with rheumatic fever. Based on these findings, the most likely diagnosis for this patient is rheumatic pancarditis. Rheumatic pericarditis, myocarditis, and endocarditis are also possible diagnoses, but the involvement of all three layers of the heart suggests pancarditis. Septic endocarditis is less likely in this case, as there is no evidence of a bacterial infection and the patient has a history of acute tonsillitis, which is more consistent with rheumatic fever. Therefore, based on the information given in the question, the most likely diagnosis for this 14-year-old patient is rheumatic pancarditis. Urgent medical intervention is necessary to manage the cardiac complications and prevent further damage to the heart. |
49. A woman born a child. It was her fith pregnancy but the first delivery. Mother’s blood group is A(II)Rh−, newborn’s – A(II)Rh+. The level of indirect bilirubin in umbilical blood was 58 micromole/l, hemoglobin – 140 g/l, RBC- 3, 8·1012/l. In 2 hours the level of indirect bilirubin turned 82 micromole/l. The hemolytic disease of newborn (icteric-anemic type, Rhincompatibility) was diagnosed. Choose the therapeutic tactics:
A. Replacement blood transfusion (conservative therapy)
B. Conservative therapy
C. Blood transfusion (conservative therapy)
D. Symptomatic therapy
E. Antibiotics
Answer: Replacement blood transfusion (conservative therapy)
Explanation
The newborn in this case has hemolytic disease of the newborn (HDN) due to Rh incompatibility between the mother and the baby. This occurs when the mother is Rh-negative and the baby is Rh-positive, and the mother has developed antibodies against the Rh factor from a previous pregnancy or blood transfusion. These antibodies can cross the placenta and attack the baby’s red blood cells, leading to hemolysis and the release of bilirubin into the bloodstream. The level of indirect bilirubin in the umbilical blood is already high at 58 micromole/l, and it has increased to 82 micromole/l within 2 hours, indicating that the baby is at risk for developing severe hyperbilirubinemia and bilirubin encephalopathy, which can cause permanent brain damage or even death. The recommended treatment for severe HDN is replacement blood transfusion, which involves replacing the baby’s blood with Rh-negative blood to reduce the level of circulating antibodies and prevent further hemolysis. This is a form of conservative therapy, which aims to manage the underlying cause of the disease rather than simply treating the symptoms. Conservative therapy may also include phototherapy to help break down the excess bilirubin in the bloodstream and prevent its accumulation in the brain. Symptomatic therapy, such as fluids and electrolytes, may also be necessary to manage any complications that arise. Antibiotics are not indicated in this case, as there is no evidence of bacterial infection. Therefore, the most appropriate therapeutic tactic for this newborn with hemolytic disease of the newborn due to Rh incompatibility is replacement blood transfusion (conservative therapy). |
50. A mother consulted a pediatrician about her son. Her son was born with body mass of 3 kg and length of 48 cm. He’s 1 year old now. What is the required normal mass?
A. 10,5 kg
B. 9,0 kg
C. 11,0 kg
D. 12,0 kg
E. 15,0 kg
Answer: 10,5 kg
Explanation
The normal weight for a 1-year-old child can vary depending on various factors such as gender, genetics, and growth patterns. However, on average, a 1-year-old child should weigh around three times their birth weight. In the case described, the child was born with a weight of 3 kg. Therefore, the expected weight at 1 year of age would be around 9 kg. However, since the child has likely grown in length and muscle mass over the past year, a more accurate estimate would be around 10.5 kg. Therefore, based on the information given in the question, the required normal weight for this 1-year-old child is approximately 10.5 kg. However, it is important to note that this is just an estimate, and each child’s growth and development should be monitored by a pediatrician to ensure that they are growing appropriately. |