🔴 SGLT2I inhibitors and acute decompensate Heart failure
🛑Before starting SGLT2I Inhibitors during an Acute Heart Fallus(AHF)
✅The patient should be clinically and hemodynamically stable and able to tolerate oral intake. According to recent clinical trials regarding in-hospital initiation of SGLT2 inhibitors, five criteria have to be fulfilled
1❇️-Patients should have a systolic blood pressure above 100 mmHg. and should not have developed any symptoms of hypotension in the preceding 6 hour
2-❇️Progressive and effective decongestion must have been verified, with no need of increasing
the intravenous diuretic dose during the last 6 hours
3-❇️No prescription of intravenous vasodilators including nitrates within the last fi hours
4❇️-No administration of intravenous Inotropic drugs in the last 24 hours is required
5-❇️Patients should have a minimally preserved renal function, with an eGFR superior to 20
mL/min/m
🛑Before starting SGLT2I Inhibitors during an Acute Heart Fallus(AHF)
✅The patient should be clinically and hemodynamically stable and able to tolerate oral intake. According to recent clinical trials regarding in-hospital initiation of SGLT2 inhibitors, five criteria have to be fulfilled
1❇️-Patients should have a systolic blood pressure above 100 mmHg. and should not have developed any symptoms of hypotension in the preceding 6 hour
2-❇️Progressive and effective decongestion must have been verified, with no need of increasing
the intravenous diuretic dose during the last 6 hours
3-❇️No prescription of intravenous vasodilators including nitrates within the last fi hours
4❇️-No administration of intravenous Inotropic drugs in the last 24 hours is required
5-❇️Patients should have a minimally preserved renal function, with an eGFR superior to 20
mL/min/m
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✅تذكر
أعلى جرعه ل Ampicillin-sulbactam قد نشوفها في حاله الاصابه ب Acinetobacter infection الجرعه قد تصل إلى 27 جرام في اليوم في حاله كانت العدوى Moderate to severe infections
#UPToDate
أعلى جرعه ل Ampicillin-sulbactam قد نشوفها في حاله الاصابه ب Acinetobacter infection الجرعه قد تصل إلى 27 جرام في اليوم في حاله كانت العدوى Moderate to severe infections
#UPToDate
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#remember
✅COPD is a major risk factor for CVD, especially ASCVD, stroke, and HE
✅COPD patients are prone to antythmias AF and ventricular tachycardia) ant cardiac death
✅All COPD patients should be investigated for CVD.
✅Common COPD medications are usually safe in terms of CV adverse events
#tips and tricks in cardiology
✅COPD is a major risk factor for CVD, especially ASCVD, stroke, and HE
✅COPD patients are prone to antythmias AF and ventricular tachycardia) ant cardiac death
✅All COPD patients should be investigated for CVD.
✅Common COPD medications are usually safe in terms of CV adverse events
#tips and tricks in cardiology
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🛑Do not use NOAC (ex rivaroxaban)in the following conditions
✅Prosthetic heart valves or moderate to severe mitral stenosis
✅Pediatric patients (age < 18 years)
✅Pregnant or lactating
✅Antiphospholipid syndrome
✅Active GIT malignancy
✅Prosthetic heart valves or moderate to severe mitral stenosis
✅Pediatric patients (age < 18 years)
✅Pregnant or lactating
✅Antiphospholipid syndrome
✅Active GIT malignancy
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Clinical Notes
🛑Do not use NOAC (ex rivaroxaban)in the following conditions ✅Prosthetic heart valves or moderate to severe mitral stenosis ✅Pediatric patients (age < 18 years) ✅Pregnant or lactating ✅Antiphospholipid syndrome ✅Active GIT malignancy
بنسبه ل رقم واحد من خلال الدراسات وجدوا بأن المرضى الذين ياخذون NOAC
highest risk of thromboembolic events
مقارنه ب warfarin لذا مازال warfarin الخيار الأول هنا
رقم اثنين وثلاثه مافيش دراسات كافيه بخصوص efficacy and safety
رقم اربعه
increased risk of recurrent thrombotic events
مقارنه ب warfarin
لذا يظل ال warfarin مع الهيبارين الخيار الأول هنا
رقم خمسه
Increase risk of GIT bleeding
highest risk of thromboembolic events
مقارنه ب warfarin لذا مازال warfarin الخيار الأول هنا
رقم اثنين وثلاثه مافيش دراسات كافيه بخصوص efficacy and safety
رقم اربعه
increased risk of recurrent thrombotic events
مقارنه ب warfarin
لذا يظل ال warfarin مع الهيبارين الخيار الأول هنا
رقم خمسه
Increase risk of GIT bleeding
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🛑Use of erythropoiesis-stimulating agent in Management of anemia in critically ill patient
✅Erythropoiesis-stimulating agents are reommended to be used in critically ill anemic (Hb≤ 10.0-12.0 g/dL) and/or trauma patients in the absence of contraindication.
✅The recommended dose is 40,000 IU by subcutaneous injection once weekly in combination with an iron supplement
✅It is not recommended to administer iron to reduce red blood cell utilisation
or morbidity and mortality in critical care patients, except in combination with erythropoiesis-stimulating agents.
✅Erythropoiesis-stimulating agents are reommended to be used in critically ill anemic (Hb≤ 10.0-12.0 g/dL) and/or trauma patients in the absence of contraindication.
✅The recommended dose is 40,000 IU by subcutaneous injection once weekly in combination with an iron supplement
✅It is not recommended to administer iron to reduce red blood cell utilisation
or morbidity and mortality in critical care patients, except in combination with erythropoiesis-stimulating agents.
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🛑Recommendations for the management of venous thromboembolism (VTE) in patients receiving anticancer treatment
✅Apixaban, edoxaban, or rivaroxaban are recommended for the treatment of symptomatic or incidental VTE in patients with cancer without contraindications (class 1).
✅Low molecular weight heparin (LMWH) are recommended for the treatment of symptomatic or incidental VTE in patients with cancer with platelet count>50 000/μL (class I).
✅In patients with cancer with platelet counts of 25 000-50 000/μL, anticoagulation with half-dose LMWH may be considered after a multidisciplinary discussion (class Ilb).
✅Prolongation of anticoagulation therapy beyond 6 months should be considered in selected patients with active cancer including metastatic disease (class lla).
#tips and tricks in cardiology
✅Apixaban, edoxaban, or rivaroxaban are recommended for the treatment of symptomatic or incidental VTE in patients with cancer without contraindications (class 1).
✅Low molecular weight heparin (LMWH) are recommended for the treatment of symptomatic or incidental VTE in patients with cancer with platelet count>50 000/μL (class I).
✅In patients with cancer with platelet counts of 25 000-50 000/μL, anticoagulation with half-dose LMWH may be considered after a multidisciplinary discussion (class Ilb).
✅Prolongation of anticoagulation therapy beyond 6 months should be considered in selected patients with active cancer including metastatic disease (class lla).
#tips and tricks in cardiology
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🛑Vasopressors in septic shock
✅After the first two boluses of fluid challenges assess the diastolic pressure (DP) and/or mean arterial pressure
✅If DP < 50 mmHg or MAP < 65 mmHg start norepinephrine within the first hour of resuscitation @ 0.1 ug/kg/min
✅If central access is not available, consider initiating vasopressor peripherally
✅Vasopressors peripherally should be administered for short period not more than 6 hours
❇️The concentration should not exceed 60 ug/ml
✅Consider echocardiography to assess cardiac function
🛑Assess MAP
✅If MAP < 65 mmHg, titrate norepinephrine up to 0.7 ug/kg/min
✅Consider adding vasopressin @ 0.03 units/min if MAP < 65 mmHg and norepinephrine dose reached 0.25-0.5 ug/kg/min
✅Consider adding epinephrine if MAP<65 mmHg despite norepinephrine and vasopressin
❇️If MAP cannot be achieved with vasopressors, the following measures can be used
✅Minimize sedation and use of midazolam instead of propofol
✅IV hydrocortisone 50 mg every 6 hours or as continuous infusion. Hydrocortisone is suggested to be initiated when the dose of norepinephrine or epinephrine ≥ 0.25 ug/kg/min at least 4 hours of initiation.
✅Terlipressin is NOT recommended as a vasopressor in septic shock patient
#ICU basic
✅After the first two boluses of fluid challenges assess the diastolic pressure (DP) and/or mean arterial pressure
✅If DP < 50 mmHg or MAP < 65 mmHg start norepinephrine within the first hour of resuscitation @ 0.1 ug/kg/min
✅If central access is not available, consider initiating vasopressor peripherally
✅Vasopressors peripherally should be administered for short period not more than 6 hours
❇️The concentration should not exceed 60 ug/ml
✅Consider echocardiography to assess cardiac function
🛑Assess MAP
✅If MAP < 65 mmHg, titrate norepinephrine up to 0.7 ug/kg/min
✅Consider adding vasopressin @ 0.03 units/min if MAP < 65 mmHg and norepinephrine dose reached 0.25-0.5 ug/kg/min
✅Consider adding epinephrine if MAP<65 mmHg despite norepinephrine and vasopressin
❇️If MAP cannot be achieved with vasopressors, the following measures can be used
✅Minimize sedation and use of midazolam instead of propofol
✅IV hydrocortisone 50 mg every 6 hours or as continuous infusion. Hydrocortisone is suggested to be initiated when the dose of norepinephrine or epinephrine ≥ 0.25 ug/kg/min at least 4 hours of initiation.
✅Terlipressin is NOT recommended as a vasopressor in septic shock patient
#ICU basic
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🛑Bicarbonate therapy in septic shock
✅For adults with septic shock, severe metabolic acidemia (pH s 7.2) and AKI (AKIN score 2 or 3), NaHCO3 can be given
✅75-125 ml NaHCO3 8.4% in 30 min, maximum 500 ml in 24 hours.
✅NaHCO3 should not be used to improve hemodynamics or to reduce vasopressor requirements.
✅For adults with septic shock, severe metabolic acidemia (pH s 7.2) and AKI (AKIN score 2 or 3), NaHCO3 can be given
✅75-125 ml NaHCO3 8.4% in 30 min, maximum 500 ml in 24 hours.
✅NaHCO3 should not be used to improve hemodynamics or to reduce vasopressor requirements.
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من مشاركه الزميل الدكتور مسعود في اول مؤتمر للصيادلة السريرية في اليمن مناقشه case report كانت بعنون
Medication-Related Challenges in Managing Diabetic Foot Complications: A Case Report
Medication-Related Challenges in Managing Diabetic Foot Complications: A Case Report
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Clinical Notes
من مشاركه الزميل الدكتور مسعود في اول مؤتمر للصيادلة السريرية في اليمن مناقشه case report كانت بعنون Medication-Related Challenges in Managing Diabetic Foot Complications: A Case Report
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VIEW IN TELEGRAM
الحاله التي تم مشاركتها المؤتمر
الوقت كان ضيق وفيه نقص اشياء وكانت تركز على ال
Drugs Related Problems
الوقت كان ضيق وفيه نقص اشياء وكانت تركز على ال
Drugs Related Problems
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🛑OPIOID ANALGESICS in treatment pain in critically ill adult patients
✅Patients with bronchospasm – For patients with known or active bronchospasm, fentanyl or hydromorphone is preferred rather than morphine because little histamine is released by these synthetic opioids
✅Patients requiring fluid restriction – Hydromorphone may be useful in fluid-restricted patients with high opioid requirements since it is available in a highly concentrated preparation (10 mg/mL)
✅Patients with hemodynamic instability – For patients with hemodynamic instability, we use shorter-acting agents such as fentanyl rather than morphine, which has a slightly longer duration of action. Morphine also causes more histamine release, which can exacerbate hypotension.
✅Patients with renal and/or hepatic insufficiency – For critically ill patients with renal and/or hepatic insufficiency, we typically select intravenous fentanyl or hydromorphone, with dose adjustments as needed.
Morphine should be avoided due to its renal clearance.
✅In patients with severe multiorgan failure, remifentanil is occasionally selected because its metabolism is not dependent on renal or hepatic function
#UPTODATE2025
✅Patients with bronchospasm – For patients with known or active bronchospasm, fentanyl or hydromorphone is preferred rather than morphine because little histamine is released by these synthetic opioids
✅Patients requiring fluid restriction – Hydromorphone may be useful in fluid-restricted patients with high opioid requirements since it is available in a highly concentrated preparation (10 mg/mL)
✅Patients with hemodynamic instability – For patients with hemodynamic instability, we use shorter-acting agents such as fentanyl rather than morphine, which has a slightly longer duration of action. Morphine also causes more histamine release, which can exacerbate hypotension.
✅Patients with renal and/or hepatic insufficiency – For critically ill patients with renal and/or hepatic insufficiency, we typically select intravenous fentanyl or hydromorphone, with dose adjustments as needed.
Morphine should be avoided due to its renal clearance.
✅In patients with severe multiorgan failure, remifentanil is occasionally selected because its metabolism is not dependent on renal or hepatic function
#UPTODATE2025
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🛑NSAIDs analgesics and AKI
✅NSAID use in at-risk patients – We avoid systemic NSAIDs for pain or inflammation in patients with the following:
•✅Volume depletion
•✅Nephrotic syndrome
•✅Heart failure
•✅Cirrhosis
•✅Hypercalcemia
#UPTODATE2025
✅NSAID use in at-risk patients – We avoid systemic NSAIDs for pain or inflammation in patients with the following:
•✅Volume depletion
•✅Nephrotic syndrome
•✅Heart failure
•✅Cirrhosis
•✅Hypercalcemia
#UPTODATE2025
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🛑sulfamethoxazole/trimethoprim and hyperkalemia
✅Hyperkalemia may occur with sulfamethoxazole/trimethoprim and be life threatening usually reversible following discontinuation
✅Hyperkalemia may occur with sulfamethoxazole/trimethoprim and be life threatening usually reversible following discontinuation
✅Onset: Varied; usually occurs within 5 to 10 days after sulfamethoxazole/trimethoprim is initiated
✅Risk factors:
• High doses (trimethoprim 20 mg/kg/day)
• Kidney impairment
• Older patients
• Hypoaldosteronism
• Concomitant use of medications causing or exacerbating hyperkalemia
#UPTODATE2025
✅Hyperkalemia may occur with sulfamethoxazole/trimethoprim and be life threatening usually reversible following discontinuation
✅Hyperkalemia may occur with sulfamethoxazole/trimethoprim and be life threatening usually reversible following discontinuation
✅Onset: Varied; usually occurs within 5 to 10 days after sulfamethoxazole/trimethoprim is initiated
✅Risk factors:
• High doses (trimethoprim 20 mg/kg/day)
• Kidney impairment
• Older patients
• Hypoaldosteronism
• Concomitant use of medications causing or exacerbating hyperkalemia
#UPTODATE2025
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🛑SGLT2I inhibitors drugs and surgery
✅Sodium-glucose cotransporter 2 (SGLT2) inhibitors – SGLT2 inhibitors (eg, empagliflozin, dapagliflozin, canagliflozin, ertugliflozin, bexagliflozin) should be stopped three to four days before surgery
✅ These agents increase the risk of urinary tract infections and hypovolemia
✅Sodium-glucose cotransporter 2 (SGLT2) inhibitors – SGLT2 inhibitors (eg, empagliflozin, dapagliflozin, canagliflozin, ertugliflozin, bexagliflozin) should be stopped three to four days before surgery
✅ These agents increase the risk of urinary tract infections and hypovolemia
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