Late-onset aspirin-related hemolysis and subsequent subdural hemorrhage in patient with glucose-6-phosphate dehydrogenase deficiency.
Jianle LiYicong ChenWeisheng DengJinsheng ZengPublished in: Clinical case reports (2024)
Aspirin-related hemolysis in G6PD-deficient individuals was generally reported among patients who received high-dose supplements within several days after ingestion. The safety of long-term and low-dose (50-325 mg/day) aspirin in patients coexist G6PD deficiency and cardiovascular disease is neglected in clinical practice. In this case, we observed a late-onset hemolysis and subsequent fatal subdural hemorrhage in one G6PD-deficient individual who had received long-term and low-dose aspirin. An 83-year-old male was diagnosed with acute ischemic stroke and treated with 100 mg/day aspirin at the emergency room. After admission, the patient was diagnosed with severe G6PD deficiency based on enzyme activity, but no hemolysis occurred within 10-day aspirin therapy in the hospital. Hence, 100 mg/day aspirin was continued on discharge. Two months later, the patient presented acute hemolysis manifested as fatigue, dark urine, and moderate jaundice. Although hemolysis was self-limit in a few days, hemoglobin decline continued for 20 days until a fatal subdural hemorrhage occurred. Our study indicated aspirin-related hemolysis could be late-onset in G6PD-deficient individual even receiving low-dose treatment and is probably linked to subsequent major bleeding events.
Keyphrases
- low dose
- late onset
- high dose
- early onset
- red blood cell
- cardiovascular disease
- acute ischemic stroke
- cardiovascular events
- case report
- stem cell transplantation
- clinical practice
- emergency department
- end stage renal disease
- healthcare
- antiplatelet therapy
- type diabetes
- public health
- chronic kidney disease
- ejection fraction
- acute coronary syndrome
- liver failure
- percutaneous coronary intervention
- prognostic factors
- intensive care unit
- blood pressure
- metabolic syndrome
- physical activity
- hepatitis b virus
- adipose tissue
- bone marrow
- cardiovascular risk factors
- anti inflammatory drugs
- wild type
- patient reported outcomes