What home medications should a patient with Hyperosmolar Hyperglycemic State (HHS) and diabetes continue after hospital management?

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Last updated: January 30, 2026View editorial policy

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Home Medications After HHS Management

Continue metformin and basal insulin at adjusted doses, while holding SGLT2 inhibitors, GLP-1 agonists, and sulfonylureas until the patient is stable and euvolemic. 1

Medications to Continue

Metformin

  • Resume metformin once the patient is clinically stable, euvolemic, and renal function has normalized (creatinine returned to baseline, eGFR stable) 1, 2
  • Metformin should be continued as the foundation of type 2 diabetes therapy unless contraindicated 1, 2
  • Hold metformin if there is ongoing acute illness, dehydration, or renal impairment (eGFR <30 mL/min/1.73m²) due to lactic acidosis risk 3, 4

Basal Insulin

  • Continue or initiate basal insulin (insulin glargine or detemir) as the cornerstone of glycemic management 1, 2
  • For patients previously on insulin: reduce home dose by 20% if they were on high-dose insulin (≥0.6 units/kg/day) to prevent hypoglycemia 2, 4
  • For insulin-naive patients: start at 10 units once daily or 0.1-0.2 units/kg/day 1, 2
  • Basal insulin must never be held completely, even in patients with poor oral intake, as it provides essential background glucose control 1, 2

Antihypertensive Medications

  • Resume ACE inhibitors, ARBs, and other antihypertensives once euvolemia is achieved and renal function is stable 1
  • These medications should be continued in the absence of hemodynamic instability or contraindications 1

Statins

  • Continue statin therapy throughout hospitalization and after discharge 1
  • No dose adjustment is typically needed unless there are specific contraindications 1

Medications to Hold or Discontinue

SGLT2 Inhibitors

  • Hold SGLT2 inhibitors during acute illness and for at least 3-7 days after HHS resolution 1, 5
  • These agents increase risk of euglycemic DKA and volume depletion 5
  • Can be cautiously restarted once the patient is stable, euvolemic, and eating normally 1

GLP-1 Receptor Agonists

  • Hold GLP-1 agonists during acute illness due to gastrointestinal side effects (nausea, vomiting) that can worsen dehydration 1
  • Resume once oral intake is adequate and the patient is clinically stable 1

Sulfonylureas

  • Discontinue sulfonylureas permanently or hold until glycemic control is reassessed 1, 2
  • These agents significantly increase hypoglycemia risk, especially when combined with insulin 1, 2
  • If restarted, use with extreme caution and only after insulin doses are stabilized 2

Thiazolidinediones (TZDs)

  • Hold TZDs during hospitalization due to fluid retention risk 1
  • Reassess need for these agents at outpatient follow-up 1

Discharge Insulin Regimen

Basal-Bolus Approach for Severe Hyperglycemia

  • For patients with HbA1c ≥9% or severe hyperglycemia during hospitalization, discharge on basal-bolus insulin at 80% of inpatient total daily dose 4
  • Split as 50% basal insulin once daily and 50% prandial insulin divided among three meals 2, 4

Basal-Only Approach for Moderate Hyperglycemia

  • For patients with HbA1c <9% and good glycemic control in hospital, discharge on basal insulin alone 1, 2
  • Start at 10 units once daily or 0.1-0.2 units/kg/day 2
  • Provide clear titration instructions: increase by 2 units every 3 days if fasting glucose >130 mg/dL 2

Critical Discharge Planning Elements

Medication Reconciliation

  • Cross-check all medications to ensure no chronic medications were inappropriately stopped 1
  • Provide written prescriptions for all new or changed medications before discharge 1
  • Review medication costs and insurance coverage to ensure adherence 4

Patient Education Requirements

  • Provide diabetes self-management education including glucose monitoring, insulin administration, hypoglycemia recognition and treatment, and sick day management 1, 4
  • Teach proper insulin injection technique and site rotation 2
  • Ensure patient has supplies: glucose meter, test strips, lancets, insulin syringes or pens 1

Follow-Up Scheduling

  • Schedule outpatient follow-up within 1-2 weeks of discharge for patients with medication changes or suboptimal glucose control 1
  • Earlier follow-up (within 1 week) is preferred for patients discharged on new insulin regimens 1
  • Arrange endocrinology referral if not already established 1

Common Pitfalls to Avoid

  • Never discharge patients on sliding scale insulin alone—this approach is ineffective and associated with poor outcomes 1, 3, 4
  • Never discontinue metformin when starting insulin unless contraindicated—the combination provides superior control with less weight gain 2
  • Never restart SGLT2 inhibitors immediately after HHS—wait until the patient is fully stable and euvolemic 5
  • Never discharge without clear written instructions for insulin titration—therapeutic inertia leads to prolonged hyperglycemia 2
  • Never assume patients can afford prescribed medications—discuss costs and alternatives before discharge 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Initial Dosing for Lantus (Insulin Glargine) in Patients Requiring Insulin Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Insulin Intensification Plan Assessment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Inpatient Hyperglycemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

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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