Evidence map›Paper›PMID 29843675›Full record

ArticleBMC pulmonary medicine2018

Mixed pneumonic plague and nosocomial MDR-bacterial infection of lung: a rare case report.

Voahangy Andrianaivoarimanana, Eric Bertherat, Rojo Rajaonarison, Tiana Rakotondramaro, Christophe Rogier, Minoarisoa Rajerison

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC pulmonary medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. A Perilous Combination:Vector borne and zoonotic diseases (Larchmont, N.Y.) · 2023
    Review
  3. Article
  4. Article
  5. Trends of Human Plague, Madagascar, 1998-2016.Emerging infectious diseases · 2019
    Article
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

6 authors at 3 institutions in 3 countries.

Voahangy AndrianaivoarimananaPlague Unit- Institut Pasteur de Madagascar, BP1274 Ambatofotsikely, 101, Antananarivo, Madagascar.
Eric BertheratDepartment of Infectious Hazard Management, World Health Organization, Avenue Appia 20, CH-1211, 27, Geneva, Switzerland.
Rojo RajaonarisonCentre Hospitalier Anti-pesteux d'Ambohimiandra, 101, Antananarivo, Madagascar.
Tiana RakotondramaroCentre Hospitalier de District de Miarinarivo, Antananarivo, Madagascar.
Christophe RogierInstitut Pasteur de Madagascar, BP1274 Ambatofotsikely, 101, Antananarivo, Madagascar.
Minoarisoa RajerisonPlague Unit- Institut Pasteur de Madagascar, BP1274 Ambatofotsikely, 101, Antananarivo, Madagascar. mino@pasteur.mg.ORCID http://orcid.org/0000-0002-0389-9280
Institut Pasteur de Madagascar · MGService de Santé des Armées · FRWorld Health Organization · CH

Funding

Institut Pasteur de Madagascar PA 14.43World Health Organization 001
6 · The paper itself

Abstract

backgroundPlague is a life-threatening disease caused by the bacterium, Yersinia pestis. Madagascar is the leading country for human plague cases worldwide. Human plague is a serious disease, particularly in its septicaemic and pneumonic forms. We report a case of pneumonic plague co-infected by a MDR-Stenotrophomonas maltophilia. CASE PRESENTATION: A 24 year-old man originated from Soavinandriana, a plague focus, felt uneasy and developed high fever with chills. He started treatment by himself, by private medical care and by a traditional healer for nine days moving several times from place to place. His condition had deteriorated when he presented to a district hospital with a syndrome of dyspnea, bronchial rale and altered state of consciousness. Two days later, plague diagnosis, performed as a last resort, revealed a positive F1 antigen on rapid diagnostic test. Additional tests (pla PCR and plague serology) evidenced a Y. pestis infection. However, streptomycin treatment did not achieve a complete recovery as the course of disease was complicated by the presence of MDR-S. maltophilia in his lung. This opportunistic infection could have been favored by an immunosuppression due to Y. pestis pulmonary infection and probably been acquired during his stay at a District Hospital. He was treated with a combination of ciprofloxacin and gentamycin and recovered fully.

conclusionsPneumonic plague infection may promote another virulent or avirulent bacterial infection particularly when it is not initially suspected. However, coinfection is rarely described and its occurrence frequency is unknown. In middle or low resources areas, which is the case of most plague endemic countries, control and prevention of infections in health facilities is not optimal. Co-infection with an opportunistic pathogen agent, such as S. maltophilia, is a risk which must not be disregarded as demonstrated by this case report. When deciding of a national control strategy, it should be taken into account in the choice of the first line treatment.

Indexed as

Cross InfectionPlagueStenotrophomonas maltophiliaYersinia pestisAnti-Bacterial AgentsCiprofloxacinCoinfectionDrug Resistance, Multiple, BacterialGentamicinsGram-Negative Bacterial InfectionsHumansMaleStreptomycinTreatment OutcomeYoung AdultAnti-Bacterial AgentsCiprofloxacinGentamicinsStreptomycinMadagascarPneumoniaStenotrophomonas maltophiliaYersinia pestis

Identifiers

PMID29843675
PMCPMC5975559
OpenAlexW2806402339

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.