You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | RSS | Access Rights | Sign In


  Vol. 141 No. 2, February 2006 TABLE OF CONTENTS
  Online Only
 •  Online First Table of
Contents
  Original Article
 •Online Features
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (11)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Bacterial Infections
 •Critical Care/ Intensive Care Medicine
 •Adult Critical Care
 •Surgery
 •Surgical Interventions
 •Gastrointestinal/ Upper Foregut
 •Randomized Controlled Trial
 •Infectious Diseases
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Delicious Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter What's this?

Molgramostim (GM-CSF) Associated With Antibiotic Treatment in Nontraumatic Abdominal Sepsis

A Randomized, Double-blind, Placebo-Controlled Clinical Trial

Héctor Orozco, MD; Jorge Arch, MD, PhD; Heriberto Medina-Franco, MD; Juan P. Pantoja, MD; Quintín H. González, MD; Mario Vilatoba, MD; Carlos Hinojosa, MD; Florencia Vargas-Vorackova, MD, PhD; José Sifuentes-Osornio, MD

Arch Surg. 2006;141:150-153.

Hypothesis  The addition of molgramostim (recombinant human granulocyte-macrophage colony-stimulating factor) to antibiotic therapy for nontraumatic and generalized abdominal sepsis is effective and has a significant impact on length of hospitalization, direct medical costs, and mortality.

Design  Randomized, double-blind, placebo-controlled clinical trial.

Setting  Tertiary referral center.

Patients  Fifty-eight patients with abdominal sepsis.

Interventions  Patients were allocated to receive, in addition to ceftriaxone sodium, amikacin sulfate, and metronidazole, molgramostim in a daily dosage of 3 µg/kg for 4 days (group 1) or placebo (group 2). Antibiotics were administered for at least 5 days and discontinued after clinical improvement had occurred and white blood cell count had been normal for 48 hours.

Main Outcome Measures  Time to improvement, duration of antibiotic therapy, hospital stay, complications, mortality, and adverse reactions to drugs.

Results  Median time to improvement was 2 days in group 1 and 4 days in group 2 (P<.005). Median length of hospitalization was 9 and 13 days, respectively (P<.001), and median duration of antibiotic therapy was 9 and 13 days, respectively (P<.001). Numbers of infectious complications in the 2 groups were, respectively, 6 and 16 (P = .02); of residual abscesses, 3 and 5; and of deaths, 2 and 2. Costs per patient were $12 333 and $16 081 (US dollars), respectively.

Conclusion  Addition of molgramostim to antibiotic therapy reduces the rate of infectious complications, the length of hospitalization, and costs in patients with nontraumatic abdominal sepsis.


Author Affiliations: Departments of Surgery (Drs Orozco, Arch, Medina-Franco, Pantoja, González, Vilatoba, and Hinojosa), Gastroenterology (Dr Vargas-Vorackova), and Infectious Diseases (Dr Sifuentes-Osornio), Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Delicious Delicious   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

RELATED ARTICLE

Molgramostim (GM-CSF) Associated With Antibiotic Treatment in Nontraumatic Abdominal Sepsis: A Randomized, Double-blind, Placebo-Controlled Clinical Trial—Invited Critique
Alden H. Harken
Arch Surg. 2006;141(2):154.
EXTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Mouse Eosinophils Possess Potent Antibacterial Properties In Vivo
Linch et al.
Infect. Immun. 2009;77:4976-4982.
ABSTRACT | FULL TEXT  

Immature Dendritic Cell-Derived Exosomes Rescue Septic Animals Via Milk Fat Globule Epidermal Growth Factor VIII
Miksa et al.
J. Immunol. 2009;183:5983-5990.
ABSTRACT | FULL TEXT  

A Novel Biomarker-guided Immunomodulatory Approach for the Therapy of Sepsis
Trapnell
Am. J. Respir. Crit. Care Med. 2009;180:585-586.
FULL TEXT  

Update in Critical Care 2006
Milbrandt et al.
Am. J. Respir. Crit. Care Med. 2007;175:638-648.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | PHYSICIAN JOBS | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2006 American Medical Association. All Rights Reserved.