Evidence map›Paper›PMID 22875462›Full record

ArticlePediatric surgery international2012

Pulmonary artery size as an indication for thoracoscopic repair of congenital diaphragmatic hernia in neonates.

Tadaharu Okazaki, Kinya Nishimura, Hiroyuki Koga, Go Miyano, Manabu Okawada, Hiromichi Shoji, Toshiaki Shimizu, Shintaro Makino, Satoru Takeda, Eiichi Inada and 2 more

Abstract readComparative Study
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In one paragraph

Article in Pediatric surgery international, 2012. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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.

  1. Review
  2. Article
  3. Article
  4. [Indication: scientific and ethical basis of medical practice].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2014
    Article
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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

12 authors.

Tadaharu OkazakiDepartment of Pediatric General and Urogenital Surgery, Juntendo University School of Medicine, Tokyo, Japan. okazakit@juntendo.ac.jp
Kinya Nishimura
Hiroyuki Koga
Go Miyano
Manabu Okawada
Hiromichi Shoji
Toshiaki Shimizu
Shintaro Makino
Satoru Takeda
Eiichi Inada
Geoffrey J Lane
Atsuyuki Yamataka

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe reviewed 24 consecutive cases of prenatally or immediately postnatally diagnosed left-sided congenital diaphragmatic hernia (CDH) to evaluate pulmonary artery (PA) size as an indication for thoracoscopic repair (TR).

methodsCDH repair is planned once echocardiography confirms improvement in pulmonary hypertension. TR is chosen if cardiopulmonary status is stable more than 10 min in the decubitus position in the neonatal intensive care unit (NICU) under conventional mechanical or high frequency oscillatory ventilation (HFOV) with/without nitric oxide (NO) and the patient appears likely to tolerate manual ventilation during transfer to the operating room. Otherwise open repair (OR) is performed in NICU. Proximal right PA (RPA) and left PA (LPA) diameters measured at birth were assessed with respect to the type of repair.

results10/24 had TR and 14/24 had OR. TR cases had significantly larger RPA/LPA diameters (3.52 ± 0.23 vs. 3.10 ± 0.56 mm, p < 0.05 for RPA; 3.04 ± 0.26 vs. 2.48 ± 0.37, p < 0.01 for LPA), and significantly less requirement for HFOV (70 vs. 100 %, p < 0.05) and NO (20 vs. 86 %, p < 0.01). Four TR required conversion to OR for technical reasons (n = 3) and cardiopulmonary instability (n = 1).

conclusionsTR can be considered when RPA/LPA diameters are larger than 3.0/2.5 mm, respectively, and cardiopulmonary status is stable without NO.

Indexed as

Hernias, Diaphragmatic, CongenitalEchocardiography, Doppler, ColorFemaleFollow-Up StudiesHernia, DiaphragmaticHerniorrhaphyHumansInfant, NewbornMalePreoperative PeriodPrognosisPulmonary ArteryRetrospective StudiesThoracoscopy

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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.