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A case report of tigecycline induced acute pancreatitis in a renal transplant patient and review of the literature: Should we avoid tigecycline in patients on calcineurin inhibitors?
Author(s) -
Yazirli Bercemhan,
Kara Emre,
Inkaya Ahmet Cagkan,
Maden Sarpcan,
Ozberk Ugur,
Yildirim Tolga,
Parlak Erkan,
Uzun Omrum,
Yilmaz Seref Rahmi,
Arici Mustafa
Publication year - 2021
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1111/tid.13593
Subject(s) - tigecycline , medicine , pancreatitis , adverse effect , acute pancreatitis , transplantation , surgery , antibiotics , microbiology and biotechnology , biology
Tigecycline has been approved by the US (United States) Food and Drug Administration in a variety of complicated infections due to its broad‐spectrum antibiotic activity. Following phase III trials, the product label was revised and acute pancreatitis was listed as an adverse effect. Its safety profile in special groups such as renal transplant patients is not exactly known. We report the first case of unintentional rechallenge of tigecycline induced pancreatitis in a renal transplant patient. Ten days following the renal transplantation, a 35‐year‐old patient presented to the clinic with acute rejection. He received anti‐thymocyte globulin (ATG) and pulse steroid treatments for rejection. Following the treatment, he developed perianal cellulitis and tigecycline was started. Nine days following initiation of tigecycline he received thrombectomy for his incidental cardiac thrombus. One day after thrombectomy, he developed acute pancreatitis (AP). Thrombectomy was suspected to be the cause of AP. During hospitalization for transplant rejection, tigecycline was re‐started for a newly developed complicated abdominal infection. On the third day of the tigecycline re‐treatment, he developed a second episode of AP. Following tigecycline withdrawal, his symptoms resolved and serum pancreatic enzymes returned to normal, thus AP was ultimately attributed to tigecycline. This lethal side effect should be kept in mind while treating severe infections in renal transplant recipients.