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[Drug-induced immune hemolytic anemia caused by cefmetazole]
Natsuki Shioji1, Minoru Mizutani1, Mariko Okayama1
1Department of Internal Medicine, Matsusaka Chuo General Hospital.
Insights
Cefmetazole (CMZ) can cause drug-induced immune hemolytic anemia (DIIHA), a rare but serious condition. Promptly stopping the drug and initiating steroid treatment can effectively manage DIIHA symptoms.
Area of Science:
- Internal Medicine
- Hematology
- Pharmacology
Background:
- Acute calculous cholecystitis is a common surgical indication.
- Antibiotic prophylaxis is standard in cholecystectomy procedures.
Observation:
- A 56-year-old female developed hematuria and anemia post-cholecystectomy.
- Laboratory findings included severe anemia, elevated LDH, and undetectable haptoglobin.
- Direct globulin test was positive for IgG, suggesting immune-mediated hemolysis.
Findings:
- Drug-induced immune hemolytic anemia (DIIHA) was diagnosed, linked to cefmetazole (CMZ).
- Discontinuation of CMZ and administration of steroids led to symptom resolution.
- Antibodies against CMZ-coated red blood cells confirmed the diagnosis.
Implications:
- DIIHA is a rare but potentially fatal adverse drug reaction.
- Early recognition and management, including drug cessation and steroid therapy, are crucial.
- This case highlights the importance of considering DIIHA in patients with unexplained hemolysis during antibiotic therapy.
Abstract:
A 56-year-old female who was diagnosed with acute calculous cholecystitis received intravenous administration of cefmetazole (CMZ) from the day of admission; she underwent laparoscopic cholecystectomy on the 13th hospital day. She was referred to our department because of hematuria that persisted for 3 days and progressive anemia on the day after the surgery. Laboratory data showed the following results: hemoglobin (Hb) level, 6.8 g/dl; reticulocyte count, 3.4%; serum lactate dehydrogenase, 1,505 IU/l; serum creatinine, 1.1 mg/dl; and undetectable haptoglobin. The direct globulin test showed that the patient was positive for IgG. Thus, drug-induced immune hemolytic anemia (DIIHA) was considered. All drugs, including CMZ, were immediately discontinued, and steroid was administered. The signs of hemolysis began to subside 3 days after the initiation of steroid therapy, and the administration of steroid was discontinued on the 5th day of the treatment. The patient's Hb level gradually increased, and the direct globulin test showed that the patient was negative for IgG on the 21st day from the onset of hematuria. Antibodies against CMZ-coated red blood cells were observed in the serum preserved at the onset of hemolysis. DIIHA is a rare but life-threatening disease. Immediate discontinuation of any suspected drugs and the initiation of steroid therapy as necessary are important in cases wherein DIIHA is suspected.
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