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š Quick note
Indicattions of blood transfusion in patient with G6PD deficiency:
š Hb less than 7g/dl
š Hb less than 9g/dl with concurrent hemolysis
š Hb less than 9g/dl with persistent hemoglobinuria
While
In patient with Hb 7-9g/dl without hemolysis or hemoglobinuria, carefully manage fluid and monitor the urine colour for 48hr
#hematology
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What are the surgical landmarks for the tympanic segment of 7th N?
šCochleariform process, oval window, pyramidal process, semicanal for the tensor tympani, vertical groove on promontory for the tympanic nerve.
What are the landmarks of the tympanic segment of VII from the mastoid approach?
šLateral semicircular canal (SCC) and the cog.
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Treatment itching associated with chronic liver diseases is treated by
Cholestyramine
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Cardiology Note:
In *men or women* who are ā„65 years of age who have ever smoked, *or* have first-degree relatives of patients with AAA, ultrasound screening for detection of AAA is recommended/reasonable
(Now it inculdes both men and women, ages at least 65, not limited to ages less than 75 years, history of family AAA is inculded)
Reference:
2022 ACC/AHA Guideline for the Diagnosis and Management of Aortic Disease
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MC phobia encountered in clinical practise - Agoraphobia-60%
MC psychiatric symptom in clinical practise - Anxiety
Prosopagnosia is - Inability to recognise Face
Sexual arousal due to exposure of one's genitalia - Exhibitionism
Necrophilia - Sexual arousal with corpses
Klismaphilia - sexual arousal with Enemas
MC OCD is - Washers - Unmarried males
MC ECG change seen with Anti psychotic drug - QT Prolongation
Inability to experience pressure is known as - Anhedonia
Auditory hallucinations are found in - Schizophrenia
What is normal MMSE(mini mental state examination)score - >24
Dellusion is a disorder ofĀ - thought
Which is the primary symptom of Mania - Over activity
Hallucination is a disorder of - Perception
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Right suprarenal vein drain into IVC ; and left suprarenal vein drain into left Renal vein
Suprarenal gland is supplied by suprarenal, renal, inferior phrenic artery and aorta
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β-hCG is a vital sign in women withĀ
acute abdomen.
ā β-hCG in the setting of shock is a ruptured ectopic pregnancy until proven otherwise.
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Helicobacter pylori
Management
eradication may be achieved with a 7-day course ofa proton pump inhibitor + amoxicillin +(clarithromycin OR metronidazole)
if penicillin-allergic: a proton pump inhibitor + metronidazole + clarithromycin
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#CV_manifastations_of_Sjorens_syn
*myocarditis
*pericarditis, /pericardial effusion
*valvular abnormalities
*cardiac arrhythmias including prolonged QT interval.
*heart failure
*pulmonary hypertension/ pulmonary arterial hypertension (Ph and PAH impact both heart and lungs)
*Congenital heart block occurs in about 2% of babies born to SSA positive mothers
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signs of pulmonary hypertension
As follows:
⢠Low volume pulse.
⢠Prominent āaā wave in JVP.
⢠Palpable P2.
⢠Left parasternal heave (indicates RVH).
⢠Epigastric pulsation (indicates RVH).
⢠Loud P2 on auscultation.
⢠EDM (Graham Steell murmur due to pulmonary regurgitation).
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#remember
patients with low HDL (ā¤40 mg/dL) and high triglyceride (Ā ā„200 mg/dL) levels associatedĀ with risk of AF and its complications
#EHRA
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AHA/ASA Guideline for Spontaneous ICH :
⢠If SBP = 150 - 220 mm Hg and no contraindication to acute BP treatment, acute lowering to SBP 140 mm Hg is safe (Class I )
⢠If SBP >220 mm Hg, it is reasonable to consider aggressive reduction of BP with continuous IV infusion (Class IIb )
Subarachnoid Hemorrhage :
⢠Treat pain with analgesics
⢠Consider effects of nimodipine
⢠Control BP until aneurysm obliterated
⢠A decrease in SBP to <160 mm Hg is reasonable
⢠Agents: nicardipine, labetalol,esmolol, clevidipine
Ischemic Stroke Guideline :
⢠Eligible for reperfusion therapy
ā Lower BP if >185/110 mm Hg
⢠During and after reperfusion therapy
ā Maintain BP less than 180/105 mm Hg
⢠Others: lower BP if >220/120 mm Hg or another indication exists; lower by 15%
⢠Suggested agents: Labetalol, nicardipine
Antihypertensive in Acute Intracranial Events :
⢠Nicardipine
⢠Labetalol
⢠Esmolol
⢠Caution with nitroprusside and nitroglycerin May increase cerebral blood flow
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Felty syndrome
āŖClinical features
Rheumatoid arthritis
Severe erosive joint disease & deformity
Rheumatoid nodules
Vasculitis (mononeuritis multiplex, necrotizing skin lesions)
Neutropenia (ANC <2000/µL)
Splenomegaly
āŖDiagnosis
Anti-CCP & RF are positive in >90% of patients
Markedly elevated ESR, often >85 mm/hr
Peripheral smear & bone marrow biopsy to rule out other causes of neutropenia
ANC = absolute neutrophil count; anti-CCP = anticyclic citrullinated peptide; ESR = erythrocyte sedimentation rate; RF = rheumatoid factor.
This patient with swollen, deformed hand joints and an elevated erythrocyte sedimentation rate likely has untreated inflammatory polyarthritis. The presence of concurrent neutropenia and splenomegaly raise strong suspicion for Felty syndrome, an uncommon but serious complication of long-standing, erosive rheumatoid arthritis (RA).
Felty syndrome is marked by the formation of autoantibodies against neutrophil components and granulocyte colony-stimulating factor, leading to neutropenia (ie, absolute neutrophil count <2,000/mm3) and an increased risk of recurrent bacterial infection (particularly of the skin and sinuses). Neutrophils coated with antibodies are also trapped in the spleen, which usually results in splenomegaly. Most patients also have extraarticular manifestations of RA such as lymphadenopathy, rheumatoid nodules, and/or necrotizing skin lesions.
The diagnosis is made based on clinical features but is supported by the presence of high-titer rheumatoid factor and anticitrullinated peptide antibodies (both of which are usually elevated in RA). Most patients are also HLA-DR4 positive (indicating a genetic susceptibility). Other causes of neutropenia should be ruled out with bone marrow biopsy and peripheral smear prior to establishing the diagnosis. Symptoms generally improve with treatment of the underlying RA.
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āļøHbA1c Is Affected By Many Factors:
āŖļøElevated HbA1c
Can occur in Iron Deficiency, Vitamin B12 Deficiency, Alcohol Dependence, Chronic Renal Failure, Hyperbilirubinaemia, Splenectomy.
āŖļøReduced HbA1c
Can occur in Chronic Liver Disease, Hypertriglyceridaemia, Some Haemoglobinopathies, Splenomegaly, Rheumatoid Arthritis.
š
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The most common cause of unilatral pulm.edema is
Prolonged unilatral depandant position
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#Pneumonia
Rusty-colored sputum: found in streptococcus pneumonia infection
Currant jellylike sputum: found in klebsiella pneumonia infection
Foul-smelling sputum: found in patients with aspiration pneumonia
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Marfan Syndrome
"MARFANS"
š·Mitral Valve Prolapse
š·Aortic Dissection
š·Regurgitant Aortic Valve
š·Fingers Long ( Arachnodactyly )
š·Arm Span>Height
š·Nasal Voice ( High Arched Palate )
š·Sternal Excavation
#notes
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āļøSVT: Management
ā
Acute managementā
ā¾Vagal manoeuvres: eg. Valsalva manoeuvre, Carotid sinus massage
ā¾I/V Adenosine: 6mgā12mgā12mg, contraindicated in Asthmatics (Verapamil is a preferable option)
ā¾Electrical cardioversion
ā
Prevention of episodesā
ā¾Ī²-blockers
ā¾Radio-frequency ablation
#med
#cardio
(FCPS, MRCP)
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Classical triad of carotid artery dissection include
1- partial Horner syndrome
2- headache
3- contralateral weakness .
Partial Horner syndrome mean miosis and ptosis but without anhidrosis
