Evidence map›Paper›PMID 37707590›Full record

ArticleEuropean journal of pediatrics2023

Pediatric multi-drug-resistant tuberculosis in Germany - diagnostic and therapeutic challenges of an "orphan disease".

Hannah-Lena Schäfer, Michael Barker, Peter Follmann, Annette Günther, André Hörning, Petra Kaiser-Labusch, Sebastian Kerzel, Christoph Maier, Samra Roth, Christian Schmidt and 6 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 11 institutions in 1 country.

Hannah-Lena SchäferDepartment of Pediatric Pulmonology, Ruhr University Bochum, St. Josef Hospital, University Hospital of Pediatrics and Adolescent Medicine, Alexandrinenstraße 5, Bochum, 44791, Germany. Hannah-lena.schaefer@ruhr-uni-bochum.de.ORCID http://orcid.org/0000-0002-3235-858X
Michael BarkerDepartment of Pediatrics, Heckeshorn Lung Unit, Helios Klinikum Emil von Behring, Berlin, Germany.
Peter FollmannKlinik für Kinder- und Jugendmedizin, Westpfalz-Klinikum, Kaiserslautern, Germany.
Annette GüntherDepartment of Pediatrics, Heckeshorn Lung Unit, Helios Klinikum Emil von Behring, Berlin, Germany.
André HörningUniversity Hospital Erlangen, Pediatrics, Germany.
Petra Kaiser-LabuschProfessor-Hess-Children's Hospital, Bremen-Mitte, Germany.
Sebastian KerzelDepartment of Pediatric Pneumology and Allergy, University Children's Hospital Regensburg, Campus St. Hedwig, Regensburg, Germany.
Christoph MaierDepartment of Pediatric Pulmonology, Ruhr University Bochum, St. Josef Hospital, University Hospital of Pediatrics and Adolescent Medicine, Alexandrinenstraße 5, Bochum, 44791, Germany.
Samra RothDepartment of Pediatric Pneumology and Allergy, University Children's Hospital Regensburg, Campus St. Hedwig, Regensburg, Germany.
Christian SchmidtKlinik für Kinder- und Jugendmedizin, St. Vinzenz-Hospital, Dinslaken, Germany.
Katharina SchützKlinik für Pädiatrische Pneumologie, Allergologie und Neonatologie, Medizinische Hochschule Hannover, Hannover, Germany.
Florian StehlingCentre for Pediatrics, University Hospital Essen, Essen, Germany.
Marie StruffertDepartment of Pediatric Pulmonology, Ruhr University Bochum, St. Josef Hospital, University Hospital of Pediatrics and Adolescent Medicine, Alexandrinenstraße 5, Bochum, 44791, Germany.
Nina TimmesfeldDepartment of Medical Informatics, Biometry and Epidemiology, Ruhr University, Bochum, Germany.
Paul VöhringerFranz-Lust-Klinik für Kinder- und Jugendmedizin Städtisches Klinikum, Karlsruhe, Germany.
Folke BrinkmannDepartment of Pediatric Pulmonology, Ruhr University Bochum, St. Josef Hospital, University Hospital of Pediatrics and Adolescent Medicine, Alexandrinenstraße 5, Bochum, 44791, Germany.
St. Josef-Hospital · DEHelios Klinikum Emil von Behring · DEUniversity Hospital Regensburg · DEEssen University Hospital · DEGerman Center for Lung Research · DEMedizinische Hochschule Hannover · DEProf. Hess Kinderklinik · DEStädtisches Klinikum Karlsruhe · DEUniversitätsklinikum Erlangen · DEWestpfalz Klinikum · DEZimmer Biomet (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Delay in diagnosing multidrug-resistant tuberculosis (MDR-pTB) in children prolongs time to effective treatment. Data on risk factors for pediatric MDR from low-incidence countries are scarce. Retrospective nationwide case-control study to analyze MDR-pTB cases in Germany between 2010 and 2020 in comparison to a drug-susceptible (DS)-pTB group. We included 52 MDR cases (24 tuberculosis (TB), 28 TB infection (TBI); mean age 7.3 years) and 56 DS cases (31 TB, 26 TBI; mean age 7.9 years). Groups were similar for sex, household size, and migration background. Compared to the DS group, more children with MDR were born in the Commonwealth of Independent States (CIS) (22% MDR-pTB vs. 13% DS-pTB, n.s.) and had more MDR index cases (94% MDR-pTB, 5% DS-pTB, p < 0.001). The interval between first healthcare contact and initiation of effective therapy was significantly longer in MDR-pTB (47 days) than in DS-pTB (11 days, p < 0.001), correlating with disease progression. Treatment for MDR-pTB was successful in 74%, but 22% experienced long-term adverse effects (e.g., hepatopathy, hearing loss).

conclusionsClose contact to MDR cases or birth in MDR-TB-high-incidence countries are risk factors for MDR-pTB. Early identification of potential MDR index cases by contact investigation, and susceptibility testing in children from high-burden MDR-TB countries are essential for timely diagnosis and treatment, reducing the severity of disease and treatment side effects.

trial registrationDeutsches Register Klinischer Studien ( https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00023817 ), DRKS00023817, 2020-09-08. WHAT IS KNOWN: •Management of children with MDR-TB remains challenging due to difficulties in diagnosing MDR-TB (lack of information on MDR index case, lack of microbiological confirmation in paucibacillary disease). •Choice of treatment regimen and monitoring of side effects. WHAT IS NEW: •Children with an MDR-TB index or born in a MDR-TB-high-incidence country are at higher risk of developing MDR-TB in a low incidence country. •The time lag to initiate treatment in MDR-TB is longer than in DS-TB and MDR-TB treatment involves a higher risk of adverse effects in longer treatment regimens especially with injectables.

Indexed as

TuberculosisTuberculosis, Multidrug-ResistantAntitubercular AgentsCase-Control StudiesChildHumansRare DiseasesRetrospective StudiesRisk FactorsAntitubercular AgentsChildrenGermanyMulticenterMultidrug resistance (MDR)Tuberculosis

Identifiers

PMID37707590
PMCPMC10640426
OpenAlexW4386726586

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.