House of medicine
ะกัะฐัะธััะธะบะฐHouse Of medicine for Medical collections and note: โช๏ธWelcome everyone(๐ฉโโ๏ธ,๐จโโ๏ธ) I am medical student . study in Sana'a university. โช๏ธBest Wishesโบ๐ @MedicineAiibot Twitter account:- https://x.com/Drhusy3nn
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ะัะตะฝะบะฐ ะฟะพ ะฟัะพัะผะพััะฐะผ ะฝะตะดะฐะฒะฝะธั ะฟะพััะพะฒ: ะฟะพัั ะฝะฐะฑะธัะฐะตั ะฟะพััะธ ะฒัั ะทะฐ ะฟะตัะฒัะต ัััะบะธ.
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Poor Prognostic Markers in Rheumatoid Arthritis High anti-CCP titre High RF titre High CRP / ESR Persistent high disease activity Early radiographic erosions Smoking Extra-articular manifestations Most specific prognostic antibody: Anti-CCP Best evidence of established structural damage: Radiographic erosions
๐ฉบ VASOPRESSIN IN SEPTIC SHOCK โ HIGH-YIELD ๐น Norepinephrine remains FIRST-LINE vasopressor in septic shock. ๐น If MAP remains inadequate or norepinephrine requirements are progressively increasing: โก๏ธ Add vasopressin rather than simply escalating norepinephrine indefinitely. ๐ Why Vasopressin? โข Acts mainly on V1a receptors โข โ Vasoconstriction โข โ โ SVR โข โ โ MAP โข Works through a non-adrenergic pathway ๐ Typical Dose โข Vasopressin: 0.03 units/min IV infusion โข Usually administered as a fixed-dose infusion โข Unlike norepinephrine, it is generally not aggressively titrated ๐ฏ Benefits โข Catecholamine-sparing effect โข โ Norepinephrine requirements โข Provides an alternative vasoconstrictor pathway โข Helps restore vascular tone and achieve target MAP โข May limit excessive catecholamine exposure โ ๏ธ Important Risks Excessive vasoconstriction may cause: โข ๐๏ธ Digital/limb ischemia โข ๐ฉธ Mesenteric ischemia โข โค๏ธ Myocardial ischemia โข Other ischemic complications โก๏ธ Higher doses = greater risk of ischemia. ๐จ Postgraduate Pearl Vasopressin treats vasoplegia โ NOT the underlying cause of septic shock. Always address: โข ๐ง Fluid status/resuscitation โข ๐ Appropriate antibiotics โข ๐ Rapid source control โข โค๏ธ Cardiac function โข ๐ฉธ Other causes of persistent hypotension ๐ง Remember Septic shock + increasing norepinephrine requirement โก๏ธ Norepinephrine + Vasopressin โ Not: endlessly escalating catecholamines Vasopressin = non-adrenergic vasoconstriction + catecholamine sparing.
HOW TO READ #BRAIN_CT STEP BY STEP #CTHead #CTBrain #CTScan #trending #viral #explorepage
D-dimer = helps rule out PE, not rule it in. D-dimer is sensitive but nonspecific.
๐ #CMV CYTOMEGALOVIRUS Treatment Protocol (Theory Only): First-Line Treatment: * Mild to Moderate: Valganciclovir 900 mg PO BD (dose adjust for GFR). * Severe/Life-Threatening/GI Malabsorption: Ganciclovir 5 mg/kg IV q12h (dose adjust for GFR). Second-Line Treatment: * For resistanceto valganciclovir or ganciclovir: โก๏ธ Foscarnet. Monitoring: * Check plasma CMV DNA weekly. * Do not change antiviral therapy in first few weeks if clinically improving despite DNA persistence/increase. * Reduce dose only if GFR worsens as underdosing increases the risk of treatment failure and antiviral resistance. * For leukopenia: Consider G-CSF, withhold myelosuppressive drugs, then consider antiviral change. Duration: * Minimum 2 weeks until clinical resolution and CMV DNAemia clearance (<200 IU/mL) on 1โ2 consecutive weekly samples. Additional: * In patients without concomitant rejection, reduction of immunosuppression may be considered in: - Severe CMV disease - Poor clinical response - High viral load - Cytopenia Adjunctive immunoglobulin therapy is not routinely recommended. Secondary CMV prophylaxis is not routinely recommended. Suspect ganciclovir resistance if: - Prior cumulative exposure to valganciclovir/ganciclovir is >6 weeks, and - There is clinical treatment failure after 2 weeks of therapy or persistent CMV DNAemia during prophylaxis. #MNA #MedicineNotesAcademy #Nephrology #CMV #KidneyTransplant #ExamPearls #WhatsAppAcademy
7 Knee Conditions You Must Know For USMLE 1๏ธโฃ ACL Tear ๐ฌ Non-contact pivot or valgus blow (the tibia slides forward) ๐ Pop + rapid swelling (hemarthrosis) + giving way ๐ Anterior drawer / Lachman. LAMP = Lateral condyle to Anterior tibia 2๏ธโฃ PCL Tear ๐ฌ Dashboard injury or a fall onto a bent knee ๐ Posterior drawer (the tibia sags back) 3๏ธโฃ Collateral Ligaments (MCL and LCL) ๐ฌ Valgus blow tears the MCL; varus blow tears the LCL ๐ Valgus stress opens the medial side = MCL; varus opens the lateral = LCL โ ๏ธ The MCL is attached to the medial meniscus (they tear together) 4๏ธโฃ Meniscal Tear ๐ฌ Twist on a planted foot; the medial meniscus is most common ๐ Joint-line tenderness + locking + effusion ๐ McMurray. LIME = Lateral tears on Internal rotation, Medial on External 5๏ธโฃ Unhappy Triad ๐ฌ Valgus blow to a planted foot -> ACL + MCL + meniscus โ ๏ธ Classically the medial meniscus, but the lateral is now more common 6๏ธโฃ Prepatellar Bursitis ๐ฌ Repeated kneeling (housemaid's knee) ๐ Swollen, tender lump over the front of the kneecap 7๏ธโฃ Baker (Popliteal) Cyst ๐ฌ Fluid in the bursa behind the knee; linked to OA and RA โ ๏ธ Rupture mimics a DVT (calf pain and swelling) Comment "NOTES" to get access to my USMLE 2026 Step 1, 2 & 3 notes #usmle #medstudent #medschool #medicalstudent #medicalschool
This does not mean the patient has failed. It means treatment must evolve. Therapy may progress from: ๐ฅ Lifestyle intervention โก๏ธ Metformin โก๏ธ Second medication โก๏ธ Third medication โก๏ธ Basal insulin โก๏ธ Prandial or combination insulin therapy Regular reassessment helps prevent years of uncontrolled hyperglycaemia. โโโโโโโโโโโโโโโโโโ ๐ฉบ 19. MONITORING AND FOLLOW-UP โโโโโโโโโโโโโโโโโโ Patients should be monitored for: ๐ฉธ A1C ๐ซ Kidney function ๐งช Electrolytes ๐ฉบ Blood pressure โ๏ธ Weight ๐งซ Albuminuria ๐๏ธ Retinopathy ๐ฆถ Neuropathy and foot disease โค๏ธ Cardiovascular risk ๐ Medication side effects ๐ง Depression and diabetes distress A1C is commonly reassessed every three months when therapy is changing or glucose is above target, and less frequently once stable. โโโโโโโโโโโโโโโโโโ ๐ KEY MESSAGE โโโโโโโโโโโโโโโโโโ The best diabetes medication is not the same for every patient. Treatment should be: โ Individualised โ Timely โ Cardiovascularly protective โ Kidney protective โ Weight conscious โ Affordable โ Safe โ Acceptable to the patient The ultimate goal is not only a lower A1C. It is to help patients live longer, healthier lives with fewer cardiovascular, kidney, neurological and eye complications. ๐ Educational content only. Treatment decisions should be individualised by a qualified healthcare professional. โค๏ธ Follow Cardiovascular Education for more evidence-based medical learning. #Type2Diabetes #DiabetesManagement #Metformin #GLP1 #SGLT2 #Insulin #CardiovascularDisease #HeartFailure #KidneyDisease #ASCVD #MedicalEducation #CardiovascularEducation #A1C #WeightManagement #DiabetesCare
In advanced nondialysis CKD, particularly eGFR <30 mL/min/1.73 mยฒ, treatment options may include: ๐ Insulin ๐ Linagliptin ๐ Carefully titrated GLP-1โbased therapy ๐ Repaglinide ๐ Low-dose short-acting sulfonylurea, such as glipizide Important considerations: โ ๏ธ Hypoglycaemia risk increases in advanced CKD โ ๏ธ Insulin requirements may decrease โ ๏ธ GLP-1 gastrointestinal effects may cause dehydration โ Linagliptin does not generally require renal dose adjustment โโโโโโโโโโโโโโโโโโ โ๏ธ 13. OBESITY OR OBESITY-RELATED COMORBIDITY โโโโโโโโโโโโโโโโโโ When substantial weight reduction is a primary treatment goal, GLP-1โbased therapy may be considered early. High-potency options include: ๐ฅ Tirzepatide ๐ฅ Subcutaneous semaglutide These therapies can provide: โ Significant weight loss โ Strong A1C reduction โ Cardiovascular benefit with selected agents โ Kidney protection with selected agents Cost, insurance coverage, tolerability and contraindications must be considered. โโโโโโโโโโโโโโโโโโ ๐จ 14. A1C >9% OR SYMPTOMATIC HYPERGLYCAEMIA โโโโโโโโโโโโโโโโโโ When A1C is markedly elevated or the patient has: ๐ฝ Polyuria ๐ฅค Polydipsia โ๏ธ Unintentional weight loss ๐ด Significant fatigue ๐ฅ Catabolic symptoms Treatment should be intensified promptly. Preferred options include: ๐ Insulin or ๐ GLP-1โbased therapy if type 1 diabetes is unlikely and the patient is not catabolic Insulin is preferred when there is insulin deficiency, severe hyperglycaemia or catabolism. Basal insulin options include: ๐ NPH ๐ Insulin glargine ๐ Insulin degludec Continuing metformin with insulin, when safe, may reduce insulin requirements and limit weight gain. โโโโโโโโโโโโโโโโโโ โ 15. WHEN TO ADD A SECOND AGENT โโโโโโโโโโโโโโโโโโ A second medication is usually added when A1C remains above the individualised target after approximately three months of metformin plus lifestyle intervention. Before intensifying therapy, review: ๐ Medication adherence ๐ Diet and physical activity ๐ Weight gain ๐ Intercurrent illness ๐ Glucocorticoid use ๐ Atypical antipsychotics ๐ Immunosuppressive therapy ๐ Possible latent autoimmune diabetes in adults ๐ Therapeutic inertia Treatment failure is not always medication failure. The underlying cause should be identified first. โโโโโโโโโโโโโโโโโโ ๐งฌ 16. CHOOSING THE SECOND AGENT โโโโโโโโโโโโโโโโโโ The best medication depends on the individual patient. Consider: โ ASCVD โ Heart failure โ Kidney disease โ Obesity โ A1C reduction needed โ Hypoglycaemia risk โ Weight effects โ Side effects โ Cost and access โ Patient preference Potential options include: ๐ GLP-1โbased therapy ๐ SGLT2 inhibitor ๐ Basal insulin ๐ DPP-4 inhibitor ๐ Short-acting sulfonylurea ๐ Repaglinide ๐ Pioglitazone โโโโโโโโโโโโโโโโโโ ๐ 17. COMPARING COMMON DRUG CLASSES โโโโโโโโโโโโโโโโโโ ๐ GLP-1โbased therapy โ Strong A1C reduction โ Weight loss โ Low hypoglycaemia risk โ Cardiovascular and kidney benefit with selected agents โ ๏ธ Gastrointestinal effects โ ๏ธ Cost and access concerns ๐ SGLT2 inhibitors โ Heart-failure and kidney protection โ Weight loss โ Low hypoglycaemia risk โ ๏ธ Genital infections โ ๏ธ Volume depletion โ ๏ธ Ketoacidosis risk โ ๏ธ Weaker glycaemic effect at low eGFR ๐ Basal insulin โ Powerful glucose lowering โ Effective at any A1C โ ๏ธ Hypoglycaemia โ ๏ธ Weight gain โ ๏ธ Requires education and titration ๐ Sulfonylureas โ Effective โ Inexpensive โ ๏ธ Hypoglycaemia โ ๏ธ Weight gain โก๏ธ Short-acting agents are generally preferred ๐ DPP-4 inhibitors โ Well tolerated โ Weight neutral โ Low hypoglycaemia risk โ ๏ธ Modest glucose-lowering effect ๐ Pioglitazone โ Improves insulin sensitivity โ Low hypoglycaemia risk โ ๏ธ Weight gain โ ๏ธ Fluid retention โ ๏ธ Heart-failure risk โ ๏ธ Fracture risk โโโโโโโโโโโโโโโโโโ ๐ 18. DIABETES IS PROGRESSIVE โโโโโโโโโโโโโโโโโโ Even after an initially successful response, glucose levels may rise over time because of progressive beta-cell dysfunction and insulin resistance.
Diabetes distress and depression can significantly interfere with self-care. Patients may feel overwhelmed by: ๐ Multiple medications ๐ฉธ Glucose monitoring ๐ฝ๏ธ Dietary restrictions ๐ Exercise expectations โ ๏ธ Fear of complications Psychological support and psychotherapy may improve both emotional wellbeing and glucose control. Mental health is part of diabetes care. โโโโโโโโโโโโโโโโโโ ๐ 7. WHEN SHOULD MEDICATION BE STARTED? โโโโโโโโโโโโโโโโโโ For most patients with A1C clearly above targetโapproximately >7.5โ8%โmedication should usually begin at diagnosis together with lifestyle intervention. For highly motivated patients with A1C close to target, a supervised lifestyle trial may be considered: โณ Approximately three months if modifiable dietary contributors are present โณ Three to six months in selected patients with A1C near target Treatment should not be delayed when hyperglycaemia is significant or symptoms are present. โโโโโโโโโโโโโโโโโโ ๐ 8. METFORMIN: COMMON FIRST-LINE THERAPY โโโโโโโโโโโโโโโโโโ In the absence of contraindications or a strong indication for another medication class, metformin remains a commonly preferred initial therapy. A practical initiation strategy: ๐ Start 500 mg once daily with the evening meal ๐ Add 500 mg with breakfast if tolerated ๐ Increase gradually every one to two weeks ๐ Usual maximum total dose: approximately 2000 mg/day Advantages: โ Effective glucose lowering โ Very low hypoglycaemia risk โ Usually weight neutral or modest weight loss โ Low cost โ Extensive clinical experience For gastrointestinal intolerance: โ๏ธ Take with food โ๏ธ Titrate more slowly โ๏ธ Consider extended-release metformin โโโโโโโโโโโโโโโโโโ โค๏ธ 9. WHEN ANOTHER DRUG CLASS MAY BE PREFERRED โโโโโโโโโโโโโโโโโโ Medication choice should be guided by comorbiditiesโnot only by A1C. ๐ซ Established ASCVD or high cardiovascular risk Consider a GLP-1โbased therapy with proven cardiovascular benefit, such as: ๐ Dulaglutide ๐ Liraglutide ๐ Semaglutide ๐ Tirzepatide SGLT2 inhibitors with cardiovascular benefit may also be appropriate: ๐ Empagliflozin ๐ Dapagliflozin ๐ Canagliflozin GLP-1โbased therapy is particularly attractive when: โ Weight loss is desired โ A1C reduction is a major priority โ ASCVD predominates โโโโโโโโโโโโโโโโโโ ๐ 10. HEART FAILURE OR DIABETIC KIDNEY DISEASE โโโโโโโโโโโโโโโโโโ When heart failure or diabetic kidney disease predominates, an SGLT2 inhibitor is generally prioritised because of proven cardiorenal protection. Examples include: ๐ Empagliflozin 10 mg ๐ Dapagliflozin 10 mg ๐ Canagliflozin 100 mg Potential benefits: โ Reduced heart-failure hospitalisation โ Slower kidney disease progression โ Reduced cardiovascular risk โ Reduced mortality in selected populations Important points: โ ๏ธ Glucose-lowering efficacy declines as eGFR falls โ Heart and kidney protection may continue even when glycaemic efficacy is reduced ๐ Additional glucose-lowering medication may still be required GLP-1โbased therapy may also provide kidney protection and remains effective for glucose lowering across a wider range of kidney function. โโโโโโโโโโโโโโโโโโ โ ๏ธ 11. SGLT2 INHIBITOR PRECAUTIONS โโโโโโโโโโโโโโโโโโ Use caution or avoid in selected patients with: โ Recurrent genital yeast infections โ Frequent urinary infections โ Active foot ulceration โ High risk of diabetic ketoacidosis โ Severe dehydration risk โ Significant alcohol or substance misuse โ Conditions causing pancreatic insulin deficiency SGLT2 inhibitors should generally be held: โธ๏ธ Three to four days before surgery โธ๏ธ Before colonoscopy preparation โธ๏ธ During prolonged fasting โธ๏ธ During poor oral intake or acute illness This helps reduce the risk of euglycaemic diabetic ketoacidosis. โโโโโโโโโโโโโโโโโโ ๐ซ 12. ADVANCED CHRONIC KIDNEY DISEASE โโโโโโโโโโโโโโโโโโ
๐ฉบ PRACTICE CHANGING UPDATES 2026 TYPE 2 DIABETES: A PRACTICAL GUIDE TO GLUCOSE-LOWERING THERAPY ๐ From lifestyle modification to metformin, GLP-1 therapy, SGLT2 inhibitors and insulin intensification Type 2 diabetes management is not only about lowering blood glucose. Effective treatment should also reduce cardiovascular risk, protect kidney function, support weight management, prevent complications and improve quality of life. โโโโโโโโโโโโโโโโโโ ๐ฏ 1. INDIVIDUALISE THE TREATMENT GOAL โโโโโโโโโโโโโโโโโโ For most nonpregnant adults: ๐ด Target A1C: <7% However, the goal should be individualised according to: โ Age โ Life expectancy โ Comorbidities โ Duration of diabetes โ Risk of hypoglycaemia โ Medication burden โ Patient preferences and treatment cost Older adults, people with multiple comorbidities or those with limited life expectancy may need less intensive targets. Common glucose targets include: ๐ฉธ Fasting glucose: 80โ130 mg/dL ๐ฉธ Post-meal glucose: <180 mg/dL, measured approximately 90โ120 minutes after eating Lowering A1C reduces the risk of microvascular complications such as: ๐๏ธ Retinopathy ๐ซ Kidney disease ๐ฆถ Neuropathy However, very aggressive glucose lowering may increase hypoglycaemia, adverse effects and polypharmacy. The goal is safe and sustainable controlโnot simply the lowest possible A1C. โโโโโโโโโโโโโโโโโโ โค๏ธ 2. CARDIOVASCULAR RISK REDUCTION IS ESSENTIAL โโโโโโโโโโโโโโโโโโ Every patient with type 2 diabetes should receive comprehensive cardiovascular risk management. This includes: ๐ญ Smoking cessation ๐ฉบ Blood pressure control ๐ Statin therapy when indicated ๐ฅ Healthy nutrition ๐ Regular physical activity โ๏ธ Weight reduction or maintenance ๐ Antiplatelet therapy for established ASCVD when appropriate Managing glucose alone is not enough. Blood pressure, cholesterol, weight, smoking and kidney health must also be addressed. โโโโโโโโโโโโโโโโโโ ๐ 3. DIABETES EDUCATION โโโโโโโโโโโโโโโโโโ Patients should participate in structured diabetes self-management education and support. Education should cover: โ Nutrition โ Exercise โ Medication adherence โ Glucose monitoring โ Prevention of hypoglycaemia โ Foot care โ Recognition of complications โ Sick-day management โ Emotional and psychological support Diabetes education, including mobile-based interventions, can meaningfully improve A1C. โโโโโโโโโโโโโโโโโโ ๐ฅ 4. NUTRITION AND WEIGHT MANAGEMENT โโโโโโโโโโโโโโโโโโ Weight management should be considered a major therapeutic goal alongside glucose control. Even modest weight loss can improve: โ Insulin resistance โ Glycaemic control โ Blood pressure โ Fatty liver disease โ Sleep apnoea โ Mobility and quality of life A body-weight reduction of approximately 5โ10% can provide important metabolic benefits. Patients should be encouraged to: ๐ฅฆ Choose nutrient-dense foods ๐ฅค Avoid sugar-sweetened drinks ๐ง Limit fruit juices ๐ฝ๏ธ Maintain consistent carbohydrate intake ๐ฅ Increase vegetables, fibre and lean protein ๐ Reduce excessive calorie intake โ๏ธ Aim for weight loss or at least prevention of further weight gain The most successful programmes combine nutrition, physical activity and behavioural support. โโโโโโโโโโโโโโโโโโ ๐ 5. EXERCISE RECOMMENDATIONS โโโโโโโโโโโโโโโโโโ Exercise improves insulin sensitivity even without significant weight loss. Recommended activity: ๐ถ At least 150 minutes/week of moderate-intensity aerobic exercise ๐ Spread over at least three days โณ Avoid more than two consecutive inactive days ๐๏ธ Resistance training at least twice weekly, when safe ๐ช Reduce prolonged sitting and sedentary time People with advanced retinopathy, severe coronary disease or other exercise-limiting conditions should receive individualised recommendations. โโโโโโโโโโโโโโโโโโ ๐ง 6. PSYCHOLOGICAL HEALTH โโโโโโโโโโโโโโโโโโ
ะฑะตะท ะฟะพะดะฟะธัะธ
ะฑะตะท ะฟะพะดะฟะธัะธ
๐ุฏูู 20 Drug interaction ู ูู ูู ุฌุฏุง 1๏ธโฃ SSRIs + Tramadol = Serotonin Syndrome + Seizures. 2๏ธโฃ Fluvoxamine + Tizanidine = Severe hypotension ู CNS depression. 3๏ธโฃ Clarithromycin + Apixaban/Rivaroxaban = Major bleeding. 4๏ธโฃ NSAIDs + ACEI/ARB + Diuretics = Triple Whammy ู Acute Kidney Injury. 5๏ธโฃ TMP-SMX + ACEI/ARB/Spironolactone = Life threatening hyperkalemia. 6๏ธโฃ PPIs + Methotrexate (high doses) = Toxicity 7๏ธโฃ Fluoroquinolones + Corticosteroids = Tendon rupture. 8๏ธโฃ Linezolid + SSRIs/SNRIs = Serotonin Syndrome. 9๏ธโฃ Amiodarone + DOACs = Increased bleeding risk. ๐ Fluconazole + Sulfonylureas = Severe hypoglycemia. 1๏ธโฃ1๏ธโฃ Verapamil/Diltiazem + Beta blockers = Severe bradycardia and heart block. 1๏ธโฃ2๏ธโฃ Levothyroxine + Iron/Calcium = Treatment failure. 1๏ธโฃ3๏ธโฃ Sildenafil + Nitrates = Catastrophic hypotension. 1๏ธโฃ4๏ธโฃ Spironolactone + Potassium supplements = Severe hyperkalemia. 1๏ธโฃ5๏ธโฃ Macrolides + Statins = Rhabdomyolysis. 1๏ธโฃ6๏ธโฃ NSAIDs + Lithium = Lithium toxicity. 1๏ธโฃ7๏ธโฃ Carbamazepine + DOACs = Treatment failure ุจุณุจุจ ุงูู CYP3A4 induction. 1๏ธโฃ8๏ธโฃ Rifampicin + Oral contraceptives = Contraceptive failure. 1๏ธโฃ9๏ธโฃ Metronidazole + Warfarin = Markedly elevated INR. 2๏ธโฃ0๏ธโฃ Colchicine + Clarithromycin = Fatal toxicity ุฎุตูุตุง ูู ูุจุงุฑ ุงูุณู ูู ุฑุถู ุงูููู. #๐๐ช๐ฑ๐ถ๐ธ๐พ๐ญ_๐ข๐ฑ๐ช๐ญ๐
ะฑะตะท ะฟะพะดะฟะธัะธ
ะฑะตะท ะฟะพะดะฟะธัะธ
ะฑะตะท ะฟะพะดะฟะธัะธ
ะฑะตะท ะฟะพะดะฟะธัะธ
#Ventricular fibrillation is characterized by: Regularity: Chaotic rhythm Rate: Unable to determine P Wave: Unable to determine PR Interval: Unable to determine QRS Complex: Unable to determine #ECG #CARDIOLOGY@HouseOfmedicinee
#Polymorphic ventricular tachycardia is characterized by: - Regularity: Usually irregular - Rate: Atrial rate not measurable; ventricular rate 150-250 bpm - P Wave: No P waves - PR Interval: No PRI - QRS Complex: Variable morphology with asymmetrical - QRS complexes; wide and bizarre โ usually > 0.12 seconds #ECG #CARDIOLOGY@HouseOfmedicinee
#Asystole is characterized by: - Regularity: None - Rate: None - P Wave: Flat line - PR Interval: None - QRS Complex: Flat line #ECG #CARDIOLOGY @HouseOfmedicinee