What are the recommendations for managing cardiac risks in patients with Glucose-6-phosphate dehydrogenase (G6PD) deficiency?

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Last updated: June 8, 2025View editorial policy

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From the Guidelines

Managing cardiac risks in patients with Glucose-6-phosphate dehydrogenase (G6PD) deficiency requires careful medication selection and monitoring to avoid triggering hemolysis. The primary concern in these patients is the potential for certain medications to cause oxidative stress, leading to hemolytic anemia, which can worsen cardiac conditions by reducing oxygen delivery to the heart and other tissues.

Key Considerations

  • Avoid medications known to trigger hemolysis in G6PD-deficient patients, such as quinidine, procainamide, and high-dose aspirin 1.
  • Nitrates (like nitroglycerin, isosorbide dinitrate) and most beta-blockers (such as metoprolol, atenolol) are generally safe for cardiac management.
  • ACE inhibitors (like enalapril, lisinopril) and ARBs (such as losartan, valsartan) can also be used safely for hypertension and heart failure.
  • For antiplatelet therapy, clopidogrel is preferred over high-dose aspirin.

Monitoring and Education

  • Regular monitoring of complete blood counts is essential when initiating new cardiac medications.
  • Patients should be educated about symptoms of hemolysis (fatigue, jaundice, dark urine) and instructed to seek immediate medical attention if these occur. Given the recommendations for screening and managing G6PD deficiency, particularly in the context of starting oxidant drugs 1, it's crucial to prioritize the avoidance of medications that could exacerbate the condition, focusing on the use of safe alternatives for cardiac management.

From the Research

Cardiac Risks in G6PD Deficiency

The management of cardiac risks in patients with Glucose-6-phosphate dehydrogenase (G6PD) deficiency requires careful consideration of the potential for hemolysis and oxidative stress.

  • Aspirin, a common medication for cardiovascular disease, may be contraindicated in patients with G6PD deficiency due to the risk of hemolytic anemia 2.
  • However, some studies suggest that aspirin may be safe in certain cases, such as in patients with class II G6PD deficiency undergoing percutaneous coronary interventions (PCI) 3.
  • Perioperative management of patients with severe G6PD deficiency undergoing open heart surgery requires careful planning to reduce the formation of free radicals and prevent hemolysis 4.

Treatment Strategies

Treatment strategies for G6PD deficiency are limited, and there are currently no therapeutics available to treat the condition 5.

  • Potential pharmacological pathways, including glutathione metabolism and compensatory NADPH production routes, may offer future therapeutic targets 5.
  • Transcriptional upregulation of the G6PD gene may also be a potential therapeutic approach 5.

Clinical Considerations

G6PD deficiency is a global health issue, and patients with the condition may be asymptomatic or develop severe jaundice and acute hemolytic anemia in response to certain triggers 6.

  • Clinicians should be aware of the potential risks and benefits of aspirin therapy in patients with G6PD deficiency and carefully weigh the decision to prescribe the medication 2.
  • Patients with G6PD deficiency undergoing cardiac surgery or other procedures should receive careful perioperative management to minimize the risk of hemolysis and oxidative stress 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Aspirin Therapy in Cardiovascular Disease with Glucose-6-Phosphate Dehydrogenase Deficiency, Safe or Not?

American journal of cardiovascular drugs : drugs, devices, and other interventions, 2021

Research

Glucose-6-Phosphate Dehydrogenase Deficiency.

Hematology/oncology clinics of North America, 2016

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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