Evidence map›Paper›PMID 25822836›Full record

ArticlePloS one2015

Home mechanical ventilation in childhood-onset hereditary neuromuscular diseases: 13 years' experience at a single center in Korea.

Young Joo Han, June Dong Park, Bongjin Lee, Yu Hyeon Choi, Dong In Suh, Byung Chan Lim, Jong-Hee Chae

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Young Joo HanDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
June Dong ParkDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Bongjin LeeDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Yu Hyeon ChoiDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Dong In SuhDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Byung Chan LimDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea; Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital, Seoul, Korea.
Jong-Hee ChaeDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea; Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital, Seoul, Korea.
Seoul National University · KRSeoul National University Children's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChildren with hereditary neuromuscular diseases (NMDs) are at a high risk of morbidity and mortality related to respiratory failure. The use of home mechanical ventilation (HMV) has saved the lives of many children with NMD but, due to a lack of studies, dependable guidelines are not available. We drew upon our experience to compare the various underlying NMDs and to evaluate HMV with regard to respiratory morbidity, the proper indications and timing for its use, and to develop a policy to improve the quality of home noninvasive ventilation (NIV).

methodsWe retrospectively analyzed the medical records of 57 children with childhood-onset hereditary NMDs in whom HMV was initiated between January 2000 and May 2013 at Seoul National University Children's Hospital. The degree of respiratory morbidity was estimated by the frequency and duration of hospitalizations caused by respiratory distress.

resultsThe most common NMD was spinal muscular atrophy (SMA, n = 33). Emergent mechanical ventilation was initiated in 44% of the patients before the confirmed diagnosis, and the indicators of pre-HMV respiratory morbidity (e.g., extubation trials, hypoxia, hospitalizations, and intensive care unit stay) were greater in these patients than in others. The proportion of post-HMV hospitalizations (range, 0.00-0.52; median, 0.01) was lower than that of pre-HMV hospitalizations (0.02-1.00; 0.99) (P < 0.001). Eight patients were able to maintain home NIV. The main causes of NIV failure were air leakage and a large amount of airway secretions.

conclusionsThe application of HMV helped reduce respiratory morbidity in children with childhood-onset hereditary NMD. Patients with SMA type I can benefit from an early diagnosis and the timely application of HMV. The choice between invasive and noninvasive HMV should be based on the patient's age and NIV trial tolerance. Systematic follow-up guidelines provided by a multidisciplinary team are needed.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleHome Care ServicesHospitalizationHumansInfantMaleNeuromuscular DiseasesNoninvasive VentilationRepublic of KoreaRespiration, ArtificialRespiratory InsufficiencyRetrospective Studies

Identifiers

PMID25822836
PMCPMC4379105
OpenAlexW2017671346

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.