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π¨π¦ MCCQE1,2 | #Case_199 | #answer
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β C
π Explanation
Propranolol, like other nonspecific beta blockers, may cause bronchospasm by blocking the beta receptors in the bronchial tree. Beta stimulation in the lungs produces bronchodilation, and its blockade leads to bronchoconstriction. In fact, propranolol is contraindicated in patients with known asthma or chronic obstructive pulmonary disease (COPD)
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β C
π Explanation
Propranolol, like other nonspecific beta blockers, may cause bronchospasm by blocking the beta receptors in the bronchial tree. Beta stimulation in the lungs produces bronchodilation, and its blockade leads to bronchoconstriction. In fact, propranolol is contraindicated in patients with known asthma or chronic obstructive pulmonary disease (COPD)
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π¨π¦ MCCQE1,2 | #Case_200
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A 39-year-old man is brought to the emergency department by his same sex partner because of confusion, diplopia and mild right arm weakness. On examination the patient is somewhat agitated and shows confusion for recent events. There is decreased pupillary response on the left with some paresis of lateral gaze on the right. Temperature is 38.3Β°C (101.0Β°F). Peripheral leukocyte count is increased.
The most appropriate next step in evaluation of his neurologic signs and symptoms is:
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A 39-year-old man is brought to the emergency department by his same sex partner because of confusion, diplopia and mild right arm weakness. On examination the patient is somewhat agitated and shows confusion for recent events. There is decreased pupillary response on the left with some paresis of lateral gaze on the right. Temperature is 38.3Β°C (101.0Β°F). Peripheral leukocyte count is increased.
The most appropriate next step in evaluation of his neurologic signs and symptoms is:
a) Bilateral carotid arteriographyb) CT scan of the headc) Electroencephalographyd) Lumbar puncturee) Serum test for HIV antibodiesTelegram
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π¨π¦ MCCQE1,2 | #Case_200 | #answer
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β B
π Explanation
The patient is described as a homosexual male with both subacute and acute neurologic abnormalities. Furthermore, the neurologic signs and symptoms described clearly indicate focal findings as would be seen with a mass lesion. In a homosexual man, one would suspect the possibility of toxoplasmosis, and a CT scan of the head should be performed. Toxoplasmosis would be revealed as multiple ring-enhancing lesions.
β Bilateral carotid angiography and an electroencephalogram are not indicated at this time.
β A lumbar puncture would in fact be contraindicated given the possibility of a mass lesion and possible increased intracranial pressure.
β While order a serum test for HIV antibodies may be appropriate it will not be most useful in evaluating his current signs and symptoms
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β B
π Explanation
The patient is described as a homosexual male with both subacute and acute neurologic abnormalities. Furthermore, the neurologic signs and symptoms described clearly indicate focal findings as would be seen with a mass lesion. In a homosexual man, one would suspect the possibility of toxoplasmosis, and a CT scan of the head should be performed. Toxoplasmosis would be revealed as multiple ring-enhancing lesions.
β Bilateral carotid angiography and an electroencephalogram are not indicated at this time.
β A lumbar puncture would in fact be contraindicated given the possibility of a mass lesion and possible increased intracranial pressure.
β While order a serum test for HIV antibodies may be appropriate it will not be most useful in evaluating his current signs and symptoms
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π¨π¦ MCCQE1,2 | #Case_201
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An 80-year-old male presents with the chief complain of a βbone spurβ, describing mid-heel pain that worsens as the day progresses. The pain is not relieved with ibuprofen. Examination reveals tenderness in the central aspect of the heel and a radiograph of the foot is unremarkable. The most likely diagnosis is:
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An 80-year-old male presents with the chief complain of a βbone spurβ, describing mid-heel pain that worsens as the day progresses. The pain is not relieved with ibuprofen. Examination reveals tenderness in the central aspect of the heel and a radiograph of the foot is unremarkable. The most likely diagnosis is:
a) Multiple myelomab) Fat-pad atrophyc) Tarsal tunnel syndromed) S1 radiculopathye) Plantar fasciitisTelegram
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π¨π¦ MCCQE1,2 | #Case_201 | #answer
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β B
π Explanation
Fat-pad atrophy is a common cause of heel pain in the geriatric patient, and in contrast to plantar fasciitis, causes pain as the day progresses.
β Plantar fasciitis classically presents as morning pain.
β Tarsal tunnel syndrome causes neuropathic pain in the distribution of the posterior tibial nerve, radiating into the plantar aspect of the foot toward the toes.
β Lumbar radiculopathy involves pain radiating down the leg into the heel, and is usually associated with weakness of dorsiflexion of the big toe and a decreased ankle reflex.
β Multiple myeloma would be an extremely unusual cause of heel pain; heel pain associated with cancer more commonly presents nocturnally
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β B
π Explanation
Fat-pad atrophy is a common cause of heel pain in the geriatric patient, and in contrast to plantar fasciitis, causes pain as the day progresses.
β Plantar fasciitis classically presents as morning pain.
β Tarsal tunnel syndrome causes neuropathic pain in the distribution of the posterior tibial nerve, radiating into the plantar aspect of the foot toward the toes.
β Lumbar radiculopathy involves pain radiating down the leg into the heel, and is usually associated with weakness of dorsiflexion of the big toe and a decreased ankle reflex.
β Multiple myeloma would be an extremely unusual cause of heel pain; heel pain associated with cancer more commonly presents nocturnally
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π¨π¦ MCCQE1,2 | #Case_202
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A 32-year-old female presents with bilateral pretibial tender, mildly red nodules 2 - 4 cm in diameter. A nodule that appeared earlier resolved, leaving a βbruisedβ area. She had a similar problem once when she was pregnant but it resolved spontaneously. Her medications include lovastatin (Mevacor) for hyperlipidemia and a low-dose oral contraceptive prescribed 5 months earlier. Her past history and a review of systems are otherwise unremarkable. The most appropriate next step would be to:
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
A 32-year-old female presents with bilateral pretibial tender, mildly red nodules 2 - 4 cm in diameter. A nodule that appeared earlier resolved, leaving a βbruisedβ area. She had a similar problem once when she was pregnant but it resolved spontaneously. Her medications include lovastatin (Mevacor) for hyperlipidemia and a low-dose oral contraceptive prescribed 5 months earlier. Her past history and a review of systems are otherwise unremarkable. The most appropriate next step would be to:
a) Order a serum creatinine phosphokinase levelb) Obtain a cervical culture for gonorrheac) Discontinue her oral contraceptivesd) Discontinue lovastatine) Treat with glucocorticoidsTelegram
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π¨π¦ MCCQE1,2 | #Case_202 | #answer
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β C
π Explanation
Erythema nodosum (EN) is a panniculitis most often appearing on the shins. In 35% - 55% of cases, no cause is found. EN has been associated with pregnancy and oral contraceptives (choice C). Other drugs including sulfonamides, bromides, iodides, and omeprazole have been associated with EN. Statins have not been associated with EN. Infectious agents associated with EN include beta-hemolytic streptococci, Mycobacterium, Yersinia, fungi, syphilis, Campylobacter, hepatitis C, and Epstein-Barr virus. Inflammatory conditions associated with EN include inflammatory bowel disease, sarcoidosis, Lofgrenβs syndrome and BehΓ§etβs syndrome. EN is usually self-limited or resolves with treatment of the underlying disorder. Glucocorticoids are usually not necessary for idiopathic EN.
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β C
π Explanation
Erythema nodosum (EN) is a panniculitis most often appearing on the shins. In 35% - 55% of cases, no cause is found. EN has been associated with pregnancy and oral contraceptives (choice C). Other drugs including sulfonamides, bromides, iodides, and omeprazole have been associated with EN. Statins have not been associated with EN. Infectious agents associated with EN include beta-hemolytic streptococci, Mycobacterium, Yersinia, fungi, syphilis, Campylobacter, hepatitis C, and Epstein-Barr virus. Inflammatory conditions associated with EN include inflammatory bowel disease, sarcoidosis, Lofgrenβs syndrome and BehΓ§etβs syndrome. EN is usually self-limited or resolves with treatment of the underlying disorder. Glucocorticoids are usually not necessary for idiopathic EN.
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π¨π¦ MCCQE1,2 | #Case_203
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A 67-year-old female presents to your department with her husband and they report that she has been experiencing mood swings with unusually frequent irritability, decreased sleep need, racing thoughts, and excitation. The patient has a 4-year history of rheumatoid arthritis and was recently started on a new medication. Which of the following is the most likely medication the patient is being treated with?
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A 67-year-old female presents to your department with her husband and they report that she has been experiencing mood swings with unusually frequent irritability, decreased sleep need, racing thoughts, and excitation. The patient has a 4-year history of rheumatoid arthritis and was recently started on a new medication. Which of the following is the most likely medication the patient is being treated with?
a) Gold saltsb) Methotrexatec) Meloxicamd) Prednisonee) MinocyclineTelegram
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π¨π¦ MCCQE1,2 | #Case_203 | #answer
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β D
π Explanation
This patient presents with psychiatric symptoms suggestive of a mania. Moods swings, irritability, decreased need to sleep, racing thoughts, excitation, and other symptoms usually associated with bipolar disorder are seen in many patients treated with prednisone (choice D) or other corticosteroids, especially with doses higher than 40 mg per day. Psychiatric side effects associated with corticosteroids are reversible with discontinuation of the drug or significant reduction in dose. Other common side effects of corticosteroids to be aware of are hypertension, hirsutism, obesity, diabetes mellitus, peptic ulcer disease, fatty liver, leukocytosis, oral candidiasis, myopathy, osteoporosis, and cataracts.
β Gold salts (choice A) can cause coloring of the skin in shades of mauve to a purplish dark grey when exposed to
sunlight, if the salts are taken on a regular basis over a long period of time. They can also cause kidney damage, pruritus, and oral ulcers.
β Methotrexate (choice B) can cause ulcerative stomatitis, leukopenia with immunosuppression, pneumonitis, pulmonary fibrosis, dizziness, and kidney failure.
β Meloxicam (choice C) like most NSAIDs can cause peptic ulcers, tinnitus, and skin rash. However, compared to other NSAIDs its side effects profile is favourable.
β Minocycline (choice E) can cause diarrhea, photosensitivity, dizziness, lupus, blue-gray skin, and like other tetracyclines it can cause discoloration of teeth, especially in children.
π Key point:
High dose corticosteroids can cause psychiatric adverse effects, particularly mood changes, which are reversible with discontinuation of the drug or significant reduction in dose
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β D
π Explanation
This patient presents with psychiatric symptoms suggestive of a mania. Moods swings, irritability, decreased need to sleep, racing thoughts, excitation, and other symptoms usually associated with bipolar disorder are seen in many patients treated with prednisone (choice D) or other corticosteroids, especially with doses higher than 40 mg per day. Psychiatric side effects associated with corticosteroids are reversible with discontinuation of the drug or significant reduction in dose. Other common side effects of corticosteroids to be aware of are hypertension, hirsutism, obesity, diabetes mellitus, peptic ulcer disease, fatty liver, leukocytosis, oral candidiasis, myopathy, osteoporosis, and cataracts.
β Gold salts (choice A) can cause coloring of the skin in shades of mauve to a purplish dark grey when exposed to
sunlight, if the salts are taken on a regular basis over a long period of time. They can also cause kidney damage, pruritus, and oral ulcers.
β Methotrexate (choice B) can cause ulcerative stomatitis, leukopenia with immunosuppression, pneumonitis, pulmonary fibrosis, dizziness, and kidney failure.
β Meloxicam (choice C) like most NSAIDs can cause peptic ulcers, tinnitus, and skin rash. However, compared to other NSAIDs its side effects profile is favourable.
β Minocycline (choice E) can cause diarrhea, photosensitivity, dizziness, lupus, blue-gray skin, and like other tetracyclines it can cause discoloration of teeth, especially in children.
π Key point:
High dose corticosteroids can cause psychiatric adverse effects, particularly mood changes, which are reversible with discontinuation of the drug or significant reduction in dose
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π¨π¦ MCCQE1,2 | #Case_204
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A 56-year-old woman with a history of diabetes and proteinuria presents to the ED complaining of right groin pain and decreased urine output for the past day. She denies any trauma, fever, or history of kidney stones or urinary tract infections. Her temperature is 37.2Β°C(99.0Β°F), blood pressure is 146/90 mm Hg, pulse is 104/min, and respiratory rate is 16/min. Heart and lung examinations are normal; she has no visible rashes and no costovertebral angle tenderness. There is trace ankle edema bilaterally. Laboratory tests show:
Na+ 134 mEq/L
K+ 4.9 mEq/L
Clβ 100 mEq/L
HCO3β 24 mEq/L
Blood urea nitrogen 38 mg/dL
Creatinine 1.6 mg/dL
Albumin 2.2 g/dL
Urinalysis 3+ blood, 4+ protein, no WBCs, no stones
What is the most appropriate next step in management of this patientβs condition?
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A 56-year-old woman with a history of diabetes and proteinuria presents to the ED complaining of right groin pain and decreased urine output for the past day. She denies any trauma, fever, or history of kidney stones or urinary tract infections. Her temperature is 37.2Β°C(99.0Β°F), blood pressure is 146/90 mm Hg, pulse is 104/min, and respiratory rate is 16/min. Heart and lung examinations are normal; she has no visible rashes and no costovertebral angle tenderness. There is trace ankle edema bilaterally. Laboratory tests show:
Na+ 134 mEq/L
K+ 4.9 mEq/L
Clβ 100 mEq/L
HCO3β 24 mEq/L
Blood urea nitrogen 38 mg/dL
Creatinine 1.6 mg/dL
Albumin 2.2 g/dL
Urinalysis 3+ blood, 4+ protein, no WBCs, no stones
What is the most appropriate next step in management of this patientβs condition?
(A) Analgesics and angiotensin-converting enzyme inhibitors(B) Kidney biopsy and high-dose corticosteroids(C) Renal vein ultrasound and heparin(D) Thiazides and spiral CT of the pelvis(E) Urine culture and oral quinolonesTelegram
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π¨π¦ MCCQE1,2 | #Case_204 | #answer
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β C
π Explanation
This patient has diabetes with proteinuria and likely has nephrotic syndrome. Among the many sequelae of nephrotic syndrome is hypercoagulability secondary to the loss of antithrombotic proteins in the urine (protein C, S, and antithrombin). These patients are at increased risk for arterial and venous thrombotic complications, including myocardial infarction, pulmonary embolism, deep vein thrombosis, and, as is the case with this patient, unilateral renal vein thrombosis (RVT). Classically, patients with RVT present with flank pain (secondary to distention of the renal capsule), hematuria, and evidence of renal impairment. Timely diagnosis via renal ultrasound, CT, or direct venography, as well as treatment with heparin, is crucial. The disruption of renal blood flow can lead to permanent damage.
β Answer A is incorrect. Analgesics and angiotensin-converting enzyme (ACE) inhibitors would do little to address the underlying pathology in this patient. Moreover, ACE inhibition may worsen this patientβs renal failure by decreasing the contralateral kidneyβs hyper-filtration.
β Answer B is incorrect. These modalities are important tools for the diagnosis and treatment of nephrotic syndrome. High-dose corticosteroids are used to treat minimal change disease, among other causes of nephrotic syndrome, but they will do little to address this patientβs acute complication.
β Answer D is incorrect. Spiral CT is useful in diagnosing renal calculi, and administration of a thiazide diuretic is helpful in treating chronic stone formation by decreasing hypercalciuria. This patient does not have findings that are consistent with nephrolithiasis; thus,these treatments would not be helpful.
β Answer E is incorrect. Urine culture and antibiotics are appropriate diagnostic and treatment modalities to address acute pyelonephritis. This patient is afebrile, lacks costovertebral
angle tenderness, and does not have dysuria or pyuria
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β C
π Explanation
This patient has diabetes with proteinuria and likely has nephrotic syndrome. Among the many sequelae of nephrotic syndrome is hypercoagulability secondary to the loss of antithrombotic proteins in the urine (protein C, S, and antithrombin). These patients are at increased risk for arterial and venous thrombotic complications, including myocardial infarction, pulmonary embolism, deep vein thrombosis, and, as is the case with this patient, unilateral renal vein thrombosis (RVT). Classically, patients with RVT present with flank pain (secondary to distention of the renal capsule), hematuria, and evidence of renal impairment. Timely diagnosis via renal ultrasound, CT, or direct venography, as well as treatment with heparin, is crucial. The disruption of renal blood flow can lead to permanent damage.
β Answer A is incorrect. Analgesics and angiotensin-converting enzyme (ACE) inhibitors would do little to address the underlying pathology in this patient. Moreover, ACE inhibition may worsen this patientβs renal failure by decreasing the contralateral kidneyβs hyper-filtration.
β Answer B is incorrect. These modalities are important tools for the diagnosis and treatment of nephrotic syndrome. High-dose corticosteroids are used to treat minimal change disease, among other causes of nephrotic syndrome, but they will do little to address this patientβs acute complication.
β Answer D is incorrect. Spiral CT is useful in diagnosing renal calculi, and administration of a thiazide diuretic is helpful in treating chronic stone formation by decreasing hypercalciuria. This patient does not have findings that are consistent with nephrolithiasis; thus,these treatments would not be helpful.
β Answer E is incorrect. Urine culture and antibiotics are appropriate diagnostic and treatment modalities to address acute pyelonephritis. This patient is afebrile, lacks costovertebral
angle tenderness, and does not have dysuria or pyuria
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π¨π¦ MCCQE1,2 | #Case_205
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A 6-month-old girl presents with vomiting and diarrhea of acute onset. Her systolic blood pressure is 40 mm Hg, pulse is 160/minute, she has poor peripheral circulation and is very lethargic. Her serum sodium concentration is 158 mmol/L. Which one of the following is the best initial management?
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A 6-month-old girl presents with vomiting and diarrhea of acute onset. Her systolic blood pressure is 40 mm Hg, pulse is 160/minute, she has poor peripheral circulation and is very lethargic. Her serum sodium concentration is 158 mmol/L. Which one of the following is the best initial management?
a) Intravenous 0.9% saline in aliquots of 20 mL/kgb) Intravenous 5% D/W/0.3% to 0.45% saline solutionc) Oral solution containing 50 mmol sodium per literd) Septic workupe) Hydrocortisone 200 mg intravenouslyTelegram
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π¨π¦ MCCQE1,2 | #Case_205 | #answer
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β A
π Explanation
Hypernatremia is plasma Na concentration > 145 mEq/L caused by a deficit of water relative to solute. A major symptom is thirst; other clinical manifestations are primarily neurologic (due to an osmotic shift of water out of cells), including confusion, neuromuscular excitability, seizures, and coma. Diagnosis is by measuring serum Na. Severely dehydrated infants must have their circulating blood volume restored first, usually with 0.9% saline in aliquots of 20 mL/kg IV. Treatment is then with 5% D/W/0.3% to 0.45% saline solution IV in volumes equal to the calculated fluid deficit, given over 2 to 3 days to avoid a rapid fall in serum osmolality, which would cause rapid movement of water into cells and potentially lead to cerebral edema. Maintenance fluids should be provided concurrently. The goal of treatment is to decrease serum Na by about 10 mEq/L/day
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β A
π Explanation
Hypernatremia is plasma Na concentration > 145 mEq/L caused by a deficit of water relative to solute. A major symptom is thirst; other clinical manifestations are primarily neurologic (due to an osmotic shift of water out of cells), including confusion, neuromuscular excitability, seizures, and coma. Diagnosis is by measuring serum Na. Severely dehydrated infants must have their circulating blood volume restored first, usually with 0.9% saline in aliquots of 20 mL/kg IV. Treatment is then with 5% D/W/0.3% to 0.45% saline solution IV in volumes equal to the calculated fluid deficit, given over 2 to 3 days to avoid a rapid fall in serum osmolality, which would cause rapid movement of water into cells and potentially lead to cerebral edema. Maintenance fluids should be provided concurrently. The goal of treatment is to decrease serum Na by about 10 mEq/L/day
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π¨π¦ MCCQE1,2 | #Case_206
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A 40-year-old patient with AIDS presents to the clinic with fatigue and weakness. X-ray of the chest is shown in the image. A methenamine silver stain of a bronchoalveolar lavage specimen reveals multiple organisms. Treatment with trimethoprim-sulfamethoxazole is contraindicated because the patient has a sulfa allergy. Which of the following agents should be used to treat this patientβs infection?
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
A 40-year-old patient with AIDS presents to the clinic with fatigue and weakness. X-ray of the chest is shown in the image. A methenamine silver stain of a bronchoalveolar lavage specimen reveals multiple organisms. Treatment with trimethoprim-sulfamethoxazole is contraindicated because the patient has a sulfa allergy. Which of the following agents should be used to treat this patientβs infection?
a) Ivermectinb) Metronidazolec) Penicillind) Pentamidinee) Protamineπ€1
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π¨π¦ MCCQE1,2 | #Case_206 | #answer
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β D
π Explanation
Diffuse, patchy infiltrate is consistent with Pneumocystis jiroveci pneumonia, which is confirmed by methenamine silver stain of lavage or biopsy sample. The first-line treatment of this condition is trimethoprim-sulfamethoxazole for patients with no contraindications to sulfa drugs. In the case of a patient with a sulfa allergy, the firstline treatment is pentamidine.
β Answer A is incorrect. Ivermectin is used to treat onchocerciasis (river blindness). It is thought to block the release of microfilariae from gravid female worms. One dose reduces microfilarial counts by up to 95%.
β Answer B is incorrect. Metronidazole is used to treat a wide variety of anaerobic bacterial infections. It is also effective against parasitic infections such as Giardia lamblia, Entamoeba
histolytica, Gardnerella vaginalis, and Trichomonas vaginalis.
β Answer C is incorrect. Penicillin is used to treat a variety of bacterial infections but is not effective in the treatment of Pneumocystis jiroveci pneumonia.
β Answer E is incorrect. Protamine is used to treat heparin overdose. It binds to heparin to form a stable complex that has no anticoagulant activity. Used alone, protamine has anticoagulant properties
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β D
π Explanation
Diffuse, patchy infiltrate is consistent with Pneumocystis jiroveci pneumonia, which is confirmed by methenamine silver stain of lavage or biopsy sample. The first-line treatment of this condition is trimethoprim-sulfamethoxazole for patients with no contraindications to sulfa drugs. In the case of a patient with a sulfa allergy, the firstline treatment is pentamidine.
β Answer A is incorrect. Ivermectin is used to treat onchocerciasis (river blindness). It is thought to block the release of microfilariae from gravid female worms. One dose reduces microfilarial counts by up to 95%.
β Answer B is incorrect. Metronidazole is used to treat a wide variety of anaerobic bacterial infections. It is also effective against parasitic infections such as Giardia lamblia, Entamoeba
histolytica, Gardnerella vaginalis, and Trichomonas vaginalis.
β Answer C is incorrect. Penicillin is used to treat a variety of bacterial infections but is not effective in the treatment of Pneumocystis jiroveci pneumonia.
β Answer E is incorrect. Protamine is used to treat heparin overdose. It binds to heparin to form a stable complex that has no anticoagulant activity. Used alone, protamine has anticoagulant properties
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π2
Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_207
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A 35-year-old male presents to your department with severe abdominal pain. He had similar complaints 3 months ago and after evaluation he was prescribed omeprazole for peptic ulcer disease. He says that the drug seemed to help a bit initially, but currently he feels his pain is getting worse. He says that the pain is associated with food. His father died at the age of 51 in a car accident. His mother is 58 years old and healthy. He has an older brother with a history of kidney stones. On physical examination he has pain in the epigastric region. Laboratory tests show:
Sodium: 140 mmol/L
Chloride: 116 mmol/L
Potassium: 4.8 mmol/L
Bicarbonate: 19 mmol/L
Magnesium: 0.85 mmol/L
Calcium: 3 mmol/L
BUN: 7 mmol/L
Creatinine: 200 microg/L
Glucose: 5.5 mmol/L
Gastrin: 1.1 ng/mL (normal < 100pg/mL)
If MEN is suspected, which of the following would be the best choice to arrive at the correct diagnosis?
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A 35-year-old male presents to your department with severe abdominal pain. He had similar complaints 3 months ago and after evaluation he was prescribed omeprazole for peptic ulcer disease. He says that the drug seemed to help a bit initially, but currently he feels his pain is getting worse. He says that the pain is associated with food. His father died at the age of 51 in a car accident. His mother is 58 years old and healthy. He has an older brother with a history of kidney stones. On physical examination he has pain in the epigastric region. Laboratory tests show:
Sodium: 140 mmol/L
Chloride: 116 mmol/L
Potassium: 4.8 mmol/L
Bicarbonate: 19 mmol/L
Magnesium: 0.85 mmol/L
Calcium: 3 mmol/L
BUN: 7 mmol/L
Creatinine: 200 microg/L
Glucose: 5.5 mmol/L
Gastrin: 1.1 ng/mL (normal < 100pg/mL)
If MEN is suspected, which of the following would be the best choice to arrive at the correct diagnosis?
a) Abdominal CT scanb) Endoscopic ultrasound with biopsyc) 24-hour urine vanillylmandelic acidd) Head MRIe) Serum calcitoninTelegram
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π2β€1π€1
Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_207 | #answer
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β D
π Explanation
This patientβs abdominal pain is most likely caused by peptic ulcer disease. His history of abdominal pain, minimal relief with omeprazole, and the laboratory test results that reveal excessive levels of gastrin point to a gastrinoma (i.e.Zollinger Ellison syndrome) as the most likely cause. This patient also has elevated levels of calcium and a family history of nephrolithiasis, which are suggestive of hyperparathyroidism. When all of this is taken into account, we must suspect multiple endocrine neoplasia type I (MEN I). This condition is a constellation of pituitary adenomas, parathyroid tumors, and pancreatic islet cell tumors. Pituitary adenomas secrete prolactin in 25% of patients and growth hormone in 5% of patients. Large pituitary adenomas may cause bitemporal hemianopsia, which is a risk factor for motor vehicle accidents in these patients. Head MRI (choice D) is considered the screening test of choice for pituitary adenomas.
β Abdominal CT scan (choice A) in the study of Zollinger-Ellison syndrome is used in the staging of cancer lesion. At this point, it would not be the best next step.
β Endoscopic ultrasound with biopsy (choice B) is an invasive study that should not be considered as the next step in the evaluation of this patient. Somatostatin receptor scintigraphy would be the best next step in the evaluation of Zollinger-Ellison syndrome but it was not among the choices offered.
β 24-hour urine vanillylmandelic acid (choice C) is useful in evaluating patients suspected of pheochromocytoma. This would be considered in a patient suspected of MEN II. MEN II a is a constellation of pheochromocytoma, parathyroid neoplasia, and medullary carcinoma of the thyroid, while MEN IIb includes pheochromocytoma, medullary thyroid carcinoma, and intestinal neuromas.
β Serum calcitonin (choice E) is also useful in the evaluation of medullary carcinoma of the thyroid in patients with MEN II.
π Key point:
Multiple endocrine neoplasia type I is a constellation of pituitary adenomas, parathyroid tumors, and pancreatic islet cell tumors. In a patient who presents with Zollinger-Ellison syndrome and hypercalcemia, a head MRI is indicated to screen the patient for pituitary adenoma
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β D
π Explanation
This patientβs abdominal pain is most likely caused by peptic ulcer disease. His history of abdominal pain, minimal relief with omeprazole, and the laboratory test results that reveal excessive levels of gastrin point to a gastrinoma (i.e.Zollinger Ellison syndrome) as the most likely cause. This patient also has elevated levels of calcium and a family history of nephrolithiasis, which are suggestive of hyperparathyroidism. When all of this is taken into account, we must suspect multiple endocrine neoplasia type I (MEN I). This condition is a constellation of pituitary adenomas, parathyroid tumors, and pancreatic islet cell tumors. Pituitary adenomas secrete prolactin in 25% of patients and growth hormone in 5% of patients. Large pituitary adenomas may cause bitemporal hemianopsia, which is a risk factor for motor vehicle accidents in these patients. Head MRI (choice D) is considered the screening test of choice for pituitary adenomas.
β Abdominal CT scan (choice A) in the study of Zollinger-Ellison syndrome is used in the staging of cancer lesion. At this point, it would not be the best next step.
β Endoscopic ultrasound with biopsy (choice B) is an invasive study that should not be considered as the next step in the evaluation of this patient. Somatostatin receptor scintigraphy would be the best next step in the evaluation of Zollinger-Ellison syndrome but it was not among the choices offered.
β 24-hour urine vanillylmandelic acid (choice C) is useful in evaluating patients suspected of pheochromocytoma. This would be considered in a patient suspected of MEN II. MEN II a is a constellation of pheochromocytoma, parathyroid neoplasia, and medullary carcinoma of the thyroid, while MEN IIb includes pheochromocytoma, medullary thyroid carcinoma, and intestinal neuromas.
β Serum calcitonin (choice E) is also useful in the evaluation of medullary carcinoma of the thyroid in patients with MEN II.
π Key point:
Multiple endocrine neoplasia type I is a constellation of pituitary adenomas, parathyroid tumors, and pancreatic islet cell tumors. In a patient who presents with Zollinger-Ellison syndrome and hypercalcemia, a head MRI is indicated to screen the patient for pituitary adenoma
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Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_208
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A 72-year-old male presents to your department with complaints of prolonged constipation, early satiety, and gastroesophageal reflux. This has led to feeling bloated most of the time and weight loss. The patient was diagnosed with Parkinsonβs disease 5 years ago and is treated with Selegiiline and Levodopa-Carbidopa combination. He was recently evaluated by his neurologist and found to be in stage 4 of the Hoehn and Yahr scale of this disease. Which of the following medication is contraindicated in this patient?
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A 72-year-old male presents to your department with complaints of prolonged constipation, early satiety, and gastroesophageal reflux. This has led to feeling bloated most of the time and weight loss. The patient was diagnosed with Parkinsonβs disease 5 years ago and is treated with Selegiiline and Levodopa-Carbidopa combination. He was recently evaluated by his neurologist and found to be in stage 4 of the Hoehn and Yahr scale of this disease. Which of the following medication is contraindicated in this patient?
a) Ropiniroleb) Metoclopramidec) Pramipexoled) Domperidonee) IsradipineTelegram
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Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_208 | #answer
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β B
π Explanation
This patient presents with constipation and symptoms suggestive of gastroparesis or delayed gastric emptying. Gastrointestinal motility is reduced in Parkinsonβs disease; besides, the medications used to treat this condition can also cause constipation. Patients can have hard, dry stools that are painful to pass due to slowed motility, and delayed emptying of a full bowel due to incoordination of rectal muscles. This could lead to complications such as paralytic ileus, acute bowel obstruction secondary to impaction, volvulus, and Ogilvieβs syndrome. Generally, metoclopramide (choice B) can be used to treat gastroparesis but it is contraindicated in patients with severe Parkinsonβs disease such as this patient who was recently evaluated to be in stage 4 on the Hoehn and Yahr scale of this condition. Parkinsonβs disease is characterized by loss of pigmented dopaminergic neurons and since this medication is a dopamine antagonist that crosses the brain blood barrier, it would worsen the patientβs condition.
β Ropinirole (choice A) and Pramipexole (choice C) are non-ergoline dopamine agonists and they are used in the treatment of Parkinsonβs disease. They are not contraindicated in this patient.
β Domperidone (choice D) is a peripheral dopamine (D2) and (D3) receptor antagonist. Since it doesnβt cross the brain blood barrier like Metoclopramide, it is one of the few dopamine antagonists that can be used as prokinetic to increase gastrointestinal peristalsis and promote gastric emptying in this patient.
β Isradipine (choice E) is a calcium channel blocker used as an antihypertensive medication that has been recently studied for use in treating Parkinsonβs disease with promising initial results. It is not contraindicated in this patient.
πKey point:
Metoclopramide is a dopamine antagonist and should not be used in patients with severe Parkinson's disease.
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β B
π Explanation
This patient presents with constipation and symptoms suggestive of gastroparesis or delayed gastric emptying. Gastrointestinal motility is reduced in Parkinsonβs disease; besides, the medications used to treat this condition can also cause constipation. Patients can have hard, dry stools that are painful to pass due to slowed motility, and delayed emptying of a full bowel due to incoordination of rectal muscles. This could lead to complications such as paralytic ileus, acute bowel obstruction secondary to impaction, volvulus, and Ogilvieβs syndrome. Generally, metoclopramide (choice B) can be used to treat gastroparesis but it is contraindicated in patients with severe Parkinsonβs disease such as this patient who was recently evaluated to be in stage 4 on the Hoehn and Yahr scale of this condition. Parkinsonβs disease is characterized by loss of pigmented dopaminergic neurons and since this medication is a dopamine antagonist that crosses the brain blood barrier, it would worsen the patientβs condition.
β Ropinirole (choice A) and Pramipexole (choice C) are non-ergoline dopamine agonists and they are used in the treatment of Parkinsonβs disease. They are not contraindicated in this patient.
β Domperidone (choice D) is a peripheral dopamine (D2) and (D3) receptor antagonist. Since it doesnβt cross the brain blood barrier like Metoclopramide, it is one of the few dopamine antagonists that can be used as prokinetic to increase gastrointestinal peristalsis and promote gastric emptying in this patient.
β Isradipine (choice E) is a calcium channel blocker used as an antihypertensive medication that has been recently studied for use in treating Parkinsonβs disease with promising initial results. It is not contraindicated in this patient.
πKey point:
Metoclopramide is a dopamine antagonist and should not be used in patients with severe Parkinson's disease.
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π1
Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_209
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A full-term newborn, born 72 hours ago, is noted to be jaundiced. The pregnancy was uneventful and the delivery
uncomplicated. The mother has type A-positive blood and the child has type O-positive. The child is breastfed and has lost 9 ounces from a birth weight of 8 lb. He is feeding for 20 minutes every 4 hours, and except for being icteric, has a normal examination. Laboratory evaluation reveals a total serum bilirubin level of 16 mg/dL (N 1.4-8.7), with a conjugated bilirubin level of 1.0 mg/dL. His hemoglobin level is 17.8 g/dL (N 13.4-19.8), his hematocrit is 55% (N 41-65), and his reticulocyte count is 3% (N 3-7). Appropriate management would include:
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A full-term newborn, born 72 hours ago, is noted to be jaundiced. The pregnancy was uneventful and the delivery
uncomplicated. The mother has type A-positive blood and the child has type O-positive. The child is breastfed and has lost 9 ounces from a birth weight of 8 lb. He is feeding for 20 minutes every 4 hours, and except for being icteric, has a normal examination. Laboratory evaluation reveals a total serum bilirubin level of 16 mg/dL (N 1.4-8.7), with a conjugated bilirubin level of 1.0 mg/dL. His hemoglobin level is 17.8 g/dL (N 13.4-19.8), his hematocrit is 55% (N 41-65), and his reticulocyte count is 3% (N 3-7). Appropriate management would include:
a) Phototherapyb) Exchange transferc) Blood cultures and antibiotic therapyd) Dextrose and water supplementatione) A recommendation to increase feedings to 10 times a dayTelegram
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Forwarded from MohammaDJ
π¨π¦ MCCQE1,2 | #Case_209 | #answer
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β E
π Explanation
Hyperbilirubinemia can occur in up to 60% of term newborns during the first week of life. Early guidelines on
management of elevated bilirubin were based on studies of bilirubin toxicity in infants who had hemolytic disease. Current recommendations now support the use of less intensive therapy in term newborns with jaundice who are otherwise healthy. Phototherapy should be initiated when the bilirubin level is above 15 mg/dL for infants at age 29-48 hours old, at 18 mg/dL for infants 49-72, and at 20 mg/dL in infants older than 72 hours. Generally, this problem is not considered pathologic unless it presents during the first hours after birth and the total serum bilirubin rises by more than 5 mg/dL/day or is higher than 17 mg/dL, or if the infant has signs or symptoms suggestive of a serious underlying illness such as sepsis. Fortunately, very few term newborns with jaundice have serious underlying pathology. Physiologic jaundice follows a pattern, with the bilirubin level peaking on the third or fourth day of life and then declining over the first week after birth. Infants with multiple risk factors may develop an exaggerated form of physiologic jaundice, with the total bilirubin level rising as high as 17 mg/dL. Breastfed infants are at an increased risk for exaggerated physiologic jaundice because of relative caloric deprivation in the first few days of life. Compared with formula-fed infants, those who are breastfed are six times more likely to experience moderate jaundice, with the bilirubin rising above 12 mg/dL. For breastfed newborns who have an early onset of hyperbilirubinemia, the frequency of feeding should be increased to more than 10 times per day. If the newborn has a decrease in weight gain, delayed stooling, and continued poor intake, then formula supplementation may be necessary. Breastfeeding should be continued to maintain breast milk production. Supplemental water or dextrose and water should not be given, as this can decrease breast milk production and may place the infant at risk for iatrogenic hyponatremia
γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°γ°
β E
π Explanation
Hyperbilirubinemia can occur in up to 60% of term newborns during the first week of life. Early guidelines on
management of elevated bilirubin were based on studies of bilirubin toxicity in infants who had hemolytic disease. Current recommendations now support the use of less intensive therapy in term newborns with jaundice who are otherwise healthy. Phototherapy should be initiated when the bilirubin level is above 15 mg/dL for infants at age 29-48 hours old, at 18 mg/dL for infants 49-72, and at 20 mg/dL in infants older than 72 hours. Generally, this problem is not considered pathologic unless it presents during the first hours after birth and the total serum bilirubin rises by more than 5 mg/dL/day or is higher than 17 mg/dL, or if the infant has signs or symptoms suggestive of a serious underlying illness such as sepsis. Fortunately, very few term newborns with jaundice have serious underlying pathology. Physiologic jaundice follows a pattern, with the bilirubin level peaking on the third or fourth day of life and then declining over the first week after birth. Infants with multiple risk factors may develop an exaggerated form of physiologic jaundice, with the total bilirubin level rising as high as 17 mg/dL. Breastfed infants are at an increased risk for exaggerated physiologic jaundice because of relative caloric deprivation in the first few days of life. Compared with formula-fed infants, those who are breastfed are six times more likely to experience moderate jaundice, with the bilirubin rising above 12 mg/dL. For breastfed newborns who have an early onset of hyperbilirubinemia, the frequency of feeding should be increased to more than 10 times per day. If the newborn has a decrease in weight gain, delayed stooling, and continued poor intake, then formula supplementation may be necessary. Breastfeeding should be continued to maintain breast milk production. Supplemental water or dextrose and water should not be given, as this can decrease breast milk production and may place the infant at risk for iatrogenic hyponatremia
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