因舒巴坦/氨苄西林引起的特异性药物性粒细胞缺乏症1例

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL
Kazuya Toda MD, Kaku Kuroda MD, CAS, Moe Kuroda MD, MPH, Kota Kawai MD, Yukihiro Sato MD
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引用次数: 0

摘要

特异性药物性粒细胞缺乏症是一种罕见但危及生命的疾病,需要立即进行医疗干预。虽然舒巴坦/氨苄西林(SBT/ABPC)是一种广泛使用的抗生素,但在我们的叙述性文献回顾中,没有发现其相关的粒细胞缺乏症的病例报告。我们报告了一例85岁的男性患者,他在接受SBT/ABPC治疗压疮感染和吸入性肺炎后出现粒细胞缺乏症,并附有叙述性文献综述。认识到这种情况,及时停用可疑药物,并密切监测白细胞总数,对于早期发现和管理这种危及生命的并发症至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A case of idiosyncratic drug-induced agranulocytosis because of sulbactam/ampicillin

A case of idiosyncratic drug-induced agranulocytosis because of sulbactam/ampicillin

Idiosyncratic drug-induced agranulocytosis is a rare but life-threatening condition that requires immediate medical intervention. Although sulbactam/ampicillin (SBT/ABPC) is a widely used antibiotic, no prior case reports of its associated agranulocytosis were identified in our narrative literature review. We present a case of an 85-year-old man who developed agranulocytosis following SBT/ABPC treatment for pressure ulcer infection and aspiration pneumonia, accompanied by a narrative literature review. Awareness of this condition, prompt discontinuation of the suspected agent, and close monitoring of total white blood cell counts are essential for early detection and management of this life-threatening complication.

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来源期刊
Journal of General and Family Medicine
Journal of General and Family Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
6.20%
发文量
79
审稿时长
48 weeks
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