Evidence map›Paper›PMID 29980189›Full record

ArticleBMC infectious diseases2018

Clinical course and significance of nontuberculous mycobacteria and its subtypes in cystic fibrosis.

Maxine S Eikani, Melodee Nugent, Arash Poursina, Pippa Simpson, Hara Levy

Abstract read
In one paragraph

Article in BMC infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Non-Tuberculous Mycobacterial Diseases in Children.Pathogens (Basel, Switzerland) · 2020
    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.

Maxine S EikaniNovant Health Pediatric Pulmonology, Novant Health Hemby Children's Hospital, Charlotte, NC, USA.
Melodee NugentChildren's Research Institute, Children's Hospital of Wisconsin, Milwaukee, WI, USA.
Arash PoursinaPiedmont Medical Center Infectious Disease, Piedmont Medical Center, Rock Hill, SC, USA.
Pippa SimpsonChildren's Research Institute, Children's Hospital of Wisconsin, Milwaukee, WI, USA.
Hara LevyDivision of Pulmonary, MedicineNorthwestern University Feinberg School of Medicine, Ann and Robert H. Lurie Children's Hospital, Chicago, IL, USA. HLevy@luriechildrens.org.ORCID 0000-0002-3784-0711

Funding

Children's Hospital of Wisconsin & Health System grant; Children's Research Institute Pilot Innovative Research;NIH/NHLBI Director's New Innovator Award 1DP2 OD 00703
6 · The paper itself

Abstract

backgroundNontuberculous mycobacteria (NTM) infections in patients with cystic fibrosis (CF) is increasing globally. However, the related epidemiology, comorbidities, and clinical impact of NTM infection remains unclear in the progress of CF lung disease and patient survival.

methodsWe performed a retrospective, case-control, cohort study (10 years), comparing NTM culture-positive CF patients (N = 28) to matched controls (N = 26). NTM positive patients were divided in to two groups of slow-growing (N = 17) and rapid- growing NTM (N = 8). Three patients were positive for both slow and rapid NTM. For independent group comparisons, a non-parametric Mann-Whitney test (Kruskal-Wallis test for more than two groups) was used to compare the continuous variables, and a Fisher's exact test was used for the categorical variables. Paired comparisons were performed using a Wilcoxon signed-rank test.

resultsThe prevalence of NTM isolation was 8%. The age at CF diagnosis was significantly lower in the slow-growing NTM group compared to the rapidly growing NTM group (P = 0.04). The median percent predicted forced expiratory flow of 25% - 75% (FEF25-75) was significantly higher before NTM acquisition in slow-growing (P = 0.013) and rapidly growing NTM group (P = 0.028). The slow-growing NTM group received significantly more penicillin/beta lactamase (P = 0.010) and rifampin (P = 0.042) following isolation. Macrolide use was significantly higher after isolation in both the slow-growing NTM (P = 0.018) and rapidly growing NTM groups (P = 0.042).

conclusionsAn earlier CF diagnosis was associated with a higher isolation of slow-growing NTM and greater antimicrobial use after infection. NTM acquisition is associated with a worsening of FEF25-75. Thus, both the early diagnosis and treatment of an NTM infection in patients with CF may positively impact lung function.

Indexed as

AdolescentAnti-Bacterial AgentsCase-Control StudiesChildChild, PreschoolCohort StudiesComorbidityCystic FibrosisFemaleHumansInfantMacrolidesMaleMycobacterium Infections, NontuberculousNontuberculous MycobacteriaPrevalenceAnti-Bacterial AgentsMacrolidesCystic fibrosisForced expiratory volumeInfectious diseaseNontuberculous mycobacteriaPulmonary function test

Identifiers

PMID29980189
PMCPMC6035392

What OpenQuestion holds

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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.