Evidence map›Paper›PMID 29131156›Full record

ArticleBone marrow transplantation2018

Impact of choice, timing, sequence and combination of broad-spectrum antibiotics on the outcome of allogeneic haematopoietic stem cell transplantation.

F Farowski, V Bücker, J J Vehreschild, L Biehl, R Cruz-Aguilar, C Scheid, U Holtick, N Jazmati, H Wisplinghoff, O A Cornely and 1 more

Open access · bronzeAbstract read
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In one paragraph

Article in Bone marrow transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Oral Vancomycin Prophylaxis Is Highly Effective in Preventing Clostridium difficile Infection in Allogeneic Hematopoietic Cell Transplant Recipients.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
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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

11 authors at 2 institutions in 1 country.

F FarowskiDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
V BückerDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
J J VehreschildDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
L BiehlDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
R Cruz-AguilarDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
C ScheidDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
U HoltickDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
N JazmatiGerman Centre for Infection Research (DZIF), Partner Site Bonn-Cologne, Cologne, Germany.
H WisplinghoffInstitute for Medical Microbiology, Immunology and Hygiene, University Hospital of Cologne, Cologne, Germany.
O A CornelyDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
M J G T VehreschildDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
University Hospital Cologne · DEGerman Center for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent data link the incidence of intestinal GvHD (iGvHD) after allogeneic haematopoietic stem cell transplantation (aSCT) to exposure with piperacillin-tazobactam or imipenem-cilastatin. To assess relevance of timing, duration, sequence and combination of antibiotic treatment in this setting, we applied a time-dependent model to our aSCT cohort. Patients from the prospective Cologne Cohort of Neutropenic Patients (CoCoNut) undergoing aSCT from January 2007 to April 2013 were included into a time-dependent multivariate Cox proportional hazards regression model with backward-stepwise selection. In 399 eligible patients, cumulative antibiotic exposure (hazard ratio (HR) 2.46; 95% confidence interval (95% CI) 1.59-3.81; P<0.001) and exposure to sequential treatment with penicillin derivatives and carbapenems (HR 6.22, 95% CI 1.27-30.31), but not to the individual classes, were associated with iGvHD at day 100. Glycopeptides were assessed as a risk factor (HR 3.73, 95% CI 1.51-9.19), but not considered independent, since their use was dependent on previous exposure to penicillin derivatives and carbapenems. Patients with iGvHD presented with increased non-relapse mortality at day 365 (HR 3.51; 95% CI 2.10-5.89; P<0.001). We identified sequential exposure to penicillin derivatives and carbapenems as well as overall exposure to antibiotics as independent risk factors for iGVHD. Confirmation of these findings in larger, prospective cohorts is necessary.

Indexed as

AdolescentAdultAgedAnti-Bacterial AgentsFemaleHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedTransplantation ConditioningTransplantation, HomologousTreatment OutcomeYoung AdultAnti-Bacterial Agents

Identifiers

PMID29131156
OpenAlexW2768197039

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.