Efficacy of ceftriaxone or meropenem as initial therapies in Whipple's disease

Gerhard E Feurle1, Natascha S Junga, Thomas Marth

  • 1DRK Krankenhaus, Neuwied, Germany. g.e.feurle@t-online.de

Gastroenterology
|November 3, 2009
PubMed
Abstract

Insights

This randomized controlled trial found that ceftriaxone or meropenem followed by trimethoprim-sulfamethoxazole effectively treats Whipple's disease, achieving long-term remission in most patients. One patient with cerebrospinal fluid infection required additional therapy.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Clinical Trials

Background:

  • Whipple's disease is a chronic infection caused by Tropheryma whipplei.
  • Effective antimicrobial therapy is crucial for managing this rare condition.
  • Identifying treatments that cross the blood-brain barrier is important for comprehensive care.

Purpose of the Study:

  • To evaluate the efficacy of ceftriaxone and meropenem in treating Whipple's disease.
  • To compare the long-term remission rates of two distinct antimicrobial regimens.
  • To assess the safety and effectiveness of antimicrobials crossing the blood-brain barrier.

Main Methods:

  • A randomized controlled trial involving 40 treatment-naive patients from Central Europe.
  • Two groups received 14-day infusions of either ceftriaxone (2g daily) or meropenem (3g daily).
  • All patients subsequently received 12 months of oral trimethoprim-sulfamethoxazole, with a 3-year follow-up for remission.

Main Results:

  • All 40 patients achieved clinical and laboratory remission.
  • Remission was sustained throughout the follow-up period for all patients, barring two unrelated deaths.
  • One patient with asymptomatic cerebrospinal fluid infection, resistant to initial treatments, responded to chloroquine and minocycline.

Conclusions:

  • Ceftriaxone or meropenem, followed by trimethoprim-sulfamethoxazole, provides a curative treatment for Whipple's disease.
  • The study demonstrates high efficacy and sustained remission rates.
  • Additional targeted therapy may be necessary for specific cases, such as asymptomatic cerebrospinal fluid infections.

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