Evidence map›Paper›PMID 11781649›Full record

ArticleBone marrow transplantation2001

Cidofovir as primary pre-emptive therapy for post-transplant cytomegalovirus infections.

S Chakrabarti, K E Collingham, H Osman, C D Fegan, D W Milligan

Abstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Outcomes of transplant recipients treated with cidofovir for resistant or refractory cytomegalovirus infection.Transplant infectious disease : an official journal of the Transplantation Society · 2021
    Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

S ChakrabartiDepartment of Haematology, Birmingham Heartlands Hospital, Birmingham, UK.
K E Collingham
H Osman
C D Fegan
D W Milligan
Heartlands Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pre-emptive antiviral therapy for CMV infection following allogeneic stem cell transplantation is an effective strategy for preventing CMV disease. This entails the logistic difficulty of daily intravenous therapy with ganciclovir or foscarnet to clinically asymptomatic patients. Cidofovir (CDV) is effective against CMV in vitro and has the practical advantage of weekly administration. However, there are limited data on the pre-emptive use of CDV in CMV infections. We carried out a pilot study exploring the efficacy and toxicity of CDV as primary pre-emptive therapy for CMV infections monitored by PCR-based assays. CDV was used at 5 mg/kg with probenecid and hydration, weekly for a maximum of 4 weeks, followed by fortnightly maintenance treatment. Four patients were treated with CDV and two of them responded. Both the non-responders developed CMV disease. There was no renal toxicity noted in any of the patients, but three patients had severe vomiting and one developed uveitis, which precluded maintenance treatment in the two responders. Following failure of CDV, foscarnet was effective in controlling the CMV infection in both patients, although the infection recurred in both. Thus, larger randomised studies are required before CDV can be recommended as a primary pre-emptive therapy for post-transplant CMV infections.

Indexed as

Hematopoietic Stem Cell TransplantationOrganophosphonatesAdultAntiviral AgentsCidofovirCyclosporineCytomegalovirusCytomegalovirus InfectionsCytosineDNA, ViralDrug EvaluationEye Infections, ViralFemaleFoscarnetGraft vs Host DiseaseHematologic NeoplasmsAntiviral AgentsCidofovirCyclosporineCytosineDNA, ViralFoscarnetOrganophosphonatesOrganophosphorus CompoundsProbenecid

Identifiers

PMID11781649
OpenAlexW2324172217

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.