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Cefepime induced bone marrow suppression in a child with osteomyelitis.


Cefepime, a fourth generation cephalosporin fourth generation cephalosporin Cefepime, Maxipime® Infectious disease A cephalosporin active against a broader range of bacteria than 3rd generation cephalosporins. See Cephalosporin.  is known to cause headaches (2.4%), nausea (1.8%), rash (1.8%) and diarrhea (1.7%). Cefepime is not known to cause neutropenia and is indicated as monotherapy for empiric treatment of febrile neutropenic patients. After an exhaustive search of the medical literature and discussion with cefepime's sole manufacturers, we report the first case of cefepime induced bone marrow suppression Bone marrow suppression
A decrease in cells responsible for providing immunity, carrying oxygen, and those responsible for normal blood clotting.

Mentioned in: Cancer Therapy, Definitive

bone marrow suppression 
. A 4-year-old white male was admitted with 5 days of intermittent fevers with a T max 105.4[degrees]F. His history included hospitalization for 8 days, a month before for low grade fevers and left groin pain. After an extensive workup, he was diagnosed to have osteomyelitis of L5 disc and pelvic ramus ramus /ra·mus/ (ra´mus) pl. ra´mi   [L.] a branch, as of a nerve, vein, or artery.

ramus articula´ris
. His medications included ibuprofen and Lortab for pain and intravenous nafcillin nafcillin /naf·cil·lin/ (naf-sil´in) a semisynthetic, acid- and penicillinase-resistant penicillin that is effective against staphylococcal infections; used as the sodium salt.  for 3 days. He was discharged on a course of oral azithromycin for 5 days and intravenous cefepime for 1 month. His CBC (1) (Cell Broadcast Center) See cell broadcast.

(2) (Cipher Block Chaining) In cryptography, a mode of operation that combines the ciphertext of one block with the plaintext of the next block.
 a week after discharge was WBC 6.3 K/cmm; Hgb 11.3 g/dl; Hct 33%; MCV 83 cmic; Plt 378 K/cmm. Examination revealed an active child with an unremarkable physical examination except for mild limited range of motion of his left hip. Current admission investigations: WBC 2.6 K/cmm; ANC 26; Hgb 10 g/dl; Hct 29.3%; MCV 76.4 cmic; Plt 144 K/cmm. Peripheral blood: Severe neutropenia, normoblastic anemia with reticulocytopenia and mild thrombocytopenia. Bone marrow studies: Hypocellular marrow with myeloid hypoplasia hypoplasia /hy·po·pla·sia/ (-pla´zhah) incomplete development or underdevelopment of an organ or tissue.hypoplas´tic

enamel hypoplasia
 with no phenotypic evidence of abnormal lymphoid or blast population. Course in hospital: Cefepime was discontinued and vancomycin started. A single dose of subcutaneous filgrastim (G-CSF G-CSF granulocyte colony-stimulating factor.

G-CSF

granulocyte-colony stimulating factor.

G-CSF Granulocyte colony-stimulating factor Molecular therapeutics A biological response modifier, the recombinant DNA form of
) improved his CBC; WBC 4.1 K/cmm; ANC 700. He was discharged on vancomycin with his CBC showing WBC 5.5 K/cmm; ANC 1595, 1 week later. Cefepime induced bone marrow suppression is a possibility that resolves with its discontinuation and responds to G-CSF.

Jaideep Shenoi, MD, and B. Bhushan Sharma, MD. Department of Medicine-Pediatrics and Department of Pediatrics, University of Oklahoma-College of Medicine, Tulsa, OK.
COPYRIGHT 2004 Southern Medical Association
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Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:Section on Pediatric and Adolescent Medicine
Author:Sharma, B. Bhushan
Publication:Southern Medical Journal
Date:Oct 1, 2004
Words:337
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