Alqahtani Saleh A, Kleiner David E, Ghabril Marwan, Gu Jiezhun, Hoofnagle Jay H, Rockey Don C
Division of Digestive and Liver Diseases, The University of Texas Southwestern, Dallas, Texas.
Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Clin Gastroenterol Hepatol. 2015 Jul;13(7):1328-1336.e2. doi: 10.1016/j.cgh.2014.11.036. Epub 2014 Dec 18.
BACKGROUND & AIMS: Cephalosporin antibiotics are popular because they have a broad spectrum of activity and are generally well tolerated; however, cephalosporin-induced liver injury is considered rare. We describe a new syndrome associated with a single intravenous dose of cefazolin and the clinical features of cephalosporin-induced liver injury.
The Drug-Induced Liver Injury (DILI) Network collected detailed clinical data on 1212 patients with DILI between 2004 and 2012. We analyzed data from 41 patients in whom cephalosporins were implicated as primary agents of liver disease; 33 formally were adjudicated as having cephalosporin-induced DILI.
Nineteen patients developed clinically apparent DILI after a single intravenous dose of cefazolin. All patients developed self-limited liver injury 3 to 23 days after receiving cefazolin during surgery-often during a minor outpatient procedure. The latency period was 20 days. Clinical features included itching, jaundice, nausea, fever, and rash. Laboratory abnormalities included a mixed or cholestatic pattern of serum enzyme increases. We identified 14 more patients with DILI attributed to other cephalosporins (5 first-generation, 2 second-generation, 6 third-generation, and 1 fourth-generation agent). Although latency and injury patterns were similar for cefazolin and other cephalosporins, the other cephalosporins were associated with more severe courses of injury, including 2 deaths from liver failure.
DILI can develop after a single dose of cefazolin. It is characterized by a latency period of 1 to 3 weeks after exposure, a cholestatic biochemical pattern, and a self-limited moderate to severe clinical course. Other cephalosporins can cause a similar but more severe injury.
头孢菌素类抗生素因其抗菌谱广且通常耐受性良好而广受欢迎;然而,头孢菌素引起的肝损伤被认为较为罕见。我们描述了一种与单次静脉注射头孢唑林相关的新综合征以及头孢菌素引起的肝损伤的临床特征。
药物性肝损伤(DILI)网络收集了2004年至2012年间1212例DILI患者的详细临床数据。我们分析了41例头孢菌素被认为是肝病主要病因的患者的数据;其中33例被正式判定为头孢菌素引起的DILI。
19例患者在单次静脉注射头孢唑林后出现临床明显的DILI。所有患者在手术期间(通常是在小型门诊手术期间)接受头孢唑林后3至23天出现自限性肝损伤。潜伏期为20天。临床特征包括瘙痒、黄疸、恶心、发热和皮疹。实验室异常包括血清酶升高的混合或胆汁淤积模式。我们又确定了14例由其他头孢菌素引起DILI的患者(5例第一代、2例第二代、6例第三代和1例第四代药物)。虽然头孢唑林和其他头孢菌素的潜伏期和损伤模式相似,但其他头孢菌素与更严重的损伤病程相关,包括2例因肝衰竭死亡。
单次注射头孢唑林后可发生DILI。其特征为接触后1至3周的潜伏期、胆汁淤积性生化模式以及自限性的中度至重度临床病程。其他头孢菌素可引起类似但更严重的损伤。