For a 48‑year‑old man with type 2 diabetes, recent hypoglycaemic seizure, alcohol‑dependence syndrome, COPD, mild chronic small‑vessel cerebrovascular disease, splenomegaly with ascites, bilateral pleural effusions, mild renal impairment, hypokalaemia, urinary infection, and currently receiving 25 % dextrose IV, levipil 500 mg IV, veloz 20 mg IV, ceftriaxone 1 g IV, ondansetron 4 mg IV three times daily, thiamine 100 mg IV, optineuron IV, acetylcysteine 600 mg orally, and furosemide 20 mg IV, what drug‑related problems are present and what actions should be taken to resolve them?

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Drug Therapy Review: Identified Drug-Related Problems and Resolutions

Problem 1: Hypoglycemia Risk from Inappropriate Dextrose Administration

The 25% dextrose IV "SOS" (as needed) regimen is inappropriate for a patient with recurrent hypoglycemia and must be replaced with scheduled glucose monitoring and a structured prevention strategy. 1

  • The patient presented with hypoglycemic seizure (FBS 67 mg/dl) and HbA1c of 6.7%, indicating his glucose-lowering regimen is too aggressive 1
  • Immediate action: Discontinue "SOS" dextrose orders and implement scheduled blood glucose monitoring every 4-6 hours 1
  • The American Diabetes Association recommends medication reduction when HbA1c is substantially below target (<6.5%) to prevent recurrent hypoglycemia 1, 2
  • Critical pitfall: Reactive dextrose administration treats symptoms but fails to address the underlying medication-induced hypoglycemia 1

Root Cause Analysis Required:

  • Identify which antidiabetic medications the patient was taking prior to admission (sulfonylureas, insulin, or other agents) 1
  • If sulfonylureas were used: discontinue immediately due to high hypoglycemia risk, especially in alcohol-dependent patients with irregular oral intake 1, 3
  • If insulin was used: reduce dose by 20-25% initially and reassess based on glucose trends 2
  • Alcohol dependence syndrome significantly increases hypoglycemia risk through impaired hepatic gluconeogenesis 1, 4

Problem 2: Hypokalemia Exacerbated by Furosemide

The patient's potassium of 3.3 mEq/L is dangerously low and will worsen with continued furosemide, creating risk for cardiac arrhythmias and seizure recurrence. 5

  • Furosemide causes potassium depletion, especially with brisk diuresis, and the FDA label explicitly warns that hypokalemia may develop with inadequate oral electrolyte intake 5
  • Immediate action: Administer IV potassium chloride to correct to >4.0 mEq/L before continuing diuretics 5
  • The combination of hypokalemia and levipil (levetiracetam) may reduce seizure threshold 5
  • Ongoing management: Add oral potassium supplementation (20-40 mEq twice daily) and monitor serum potassium every 2-3 days 5

Additional Electrolyte Concerns:

  • Furosemide may also cause hypomagnesemia and hypocalcemia, both of which lower seizure threshold 5
  • Check magnesium and ionized calcium levels immediately given the seizure history 5
  • The FDA label states that all patients receiving furosemide should be observed for signs of electrolyte imbalance including muscle cramps, weakness, and arrhythmia 5

Problem 3: Inappropriate Proton Pump Inhibitor Use

Veloz (rabeprazole) 20 mg IV daily lacks clear indication and should be discontinued to reduce polypharmacy burden. 1

  • No evidence of active gastrointestinal bleeding, peptic ulcer disease, or NSAID use is documented 1
  • The American Diabetes Association emphasizes reducing medication complexity when regimen burden becomes an obstacle to adherence 1
  • Action: Discontinue veloz unless specific indication emerges (e.g., stress ulcer prophylaxis if mechanical ventilation required) 1
  • Common pitfall: Reflexive PPI prescription in hospitalized patients without reassessment of necessity 1

Problem 4: Ceftriaxone Dosing in Renal and Hepatic Impairment

While ceftriaxone 1 gram IV twice daily is appropriate for urinary tract infection, monitoring is required given splenomegaly, ascites, and pleural effusions suggesting hepatic dysfunction. 6

  • Ceftriaxone undergoes both renal (40-70%) and biliary (30-60%) elimination 6
  • Patients with ascites show significant changes in volume of distribution but not substantially different half-lives (9.7 vs 8 hours) 6
  • The patient's creatinine of 0.66 mg/dl suggests preserved renal function, but ascites indicates possible hepatic impairment 6
  • Action: Continue current dose but monitor for drug accumulation if hepatic function worsens (rising bilirubin, worsening coagulopathy) 6
  • Duration: Limit to 7-10 days for uncomplicated UTI (albumin 3+, pus cells 6-8) 6

Problem 5: Thiamine Dosing Inadequate for Alcohol Dependence Syndrome

Thiamine 100 mg IV once daily is insufficient for a patient with alcohol dependence syndrome at risk for Wernicke's encephalopathy, especially given slurred speech and neurological symptoms. 1

  • Slurred speech and involuntary jerking movements may represent early Wernicke's encephalopathy or alcohol withdrawal 1
  • Immediate action: Increase thiamine to 500 mg IV three times daily for 3-5 days, then transition to 100 mg IV/PO daily 1
  • Thiamine must be administered before any glucose-containing solutions to prevent precipitating Wernicke's encephalopathy 1
  • Critical error in current regimen: Dextrose is being given without adequate thiamine coverage 1

Problem 6: Missing Cardiovascular and Renal Protective Therapy

The patient has multiple cardiovascular risk factors (diabetes, chronic small vessel disease, bilateral carotid/vertebral narrowing) but is not receiving guideline-recommended cardioprotective medications. 1

  • MRI shows chronic small vessel disease and atherosclerotic narrowing, indicating high cardiovascular risk 1
  • The American Diabetes Association recommends that patients with established ASCVD receive agents that reduce cardiorenal risk 1
  • Action upon discharge: Initiate SGLT2 inhibitor (e.g., empagliflozin 10 mg daily) or GLP-1 receptor agonist for cardiovascular protection 1
  • Also required: Statin therapy (high-intensity) and antiplatelet agent given atherosclerotic disease 1
  • Metformin should be considered as first-line glucose-lowering therapy given cardiovascular benefits, unless contraindicated 1

Problem 7: Acetylcysteine Indication Unclear

Acetylcysteine 600 mg orally twice daily for COPD with whitish expectoration is reasonable as a mucolytic, but efficacy should be reassessed after 5-7 days. 1

  • Acetylcysteine may help with mucus clearance in COPD exacerbations 1
  • Action: Continue for acute exacerbation but discontinue if no symptomatic improvement after one week 1
  • Consider adding inhaled bronchodilators (short-acting beta-agonist and anticholinergic) if not already prescribed 1

Problem 8: Ondansetron Dosing and QT Prolongation Risk

Ondansetron 4 mg IV three times daily is appropriate for nausea, but ECG monitoring is required given hypokalemia and potential QT prolongation. 5

  • Ondansetron can prolong QT interval, especially with electrolyte abnormalities 5
  • The patient's hypokalemia (3.3 mEq/L) significantly increases risk of torsades de pointes 5
  • Action: Obtain baseline ECG and repeat after potassium correction 5
  • Reduce to twice daily dosing once nausea controlled to minimize QT risk 5

Problem 9: Polypharmacy and Medication Reconciliation

The current regimen includes 9 medications without documentation of home medications, creating risk for drug interactions and duplication. 1, 7

  • Immediate action: Obtain complete home medication list including all antidiabetic agents, antihypertensives, and supplements 7
  • Alcohol dependence increases risk of medication non-adherence and drug-alcohol interactions 7
  • Discharge planning must include medication reconciliation and simplification where possible 1
  • Fixed-dose combinations should be considered to improve adherence 1

Summary Algorithm for Resolution

  1. Correct hypokalemia immediately (IV KCl to >4.0 mEq/L) before continuing furosemide 5
  2. Increase thiamine to 500 mg IV TID for 3-5 days 1
  3. Replace "SOS" dextrose with scheduled glucose monitoring every 4-6 hours 1
  4. Identify and discontinue/reduce hypoglycemia-causing medications (sulfonylureas first, then insulin dose reduction) 1, 2
  5. Discontinue veloz unless specific indication identified 1
  6. Check magnesium, calcium, and obtain ECG given seizure history and ondansetron use 5
  7. Plan discharge medications: SGLT2i or GLP-1 RA, statin, antiplatelet, and appropriate glucose-lowering therapy 1
  8. Monitor ceftriaxone duration (7-10 days maximum for UTI) 6

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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