Evidence map›Paper›PMID 27179533›Full record

Observational studyChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016

Factors associated with the timeliness of postnatal surgical repair of spina bifida.

Elizabeth Radcliff, Cynthia H Cassell, Sarah B Laditka, Judy K Thibadeau, Jane Correia, Scott D Grosse, Russell S Kirby

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Female monozygotic twins with sacral myelomeningocele.Surgical neurology international · 2023
    Article
  5. Article
  6. Perspectives on urological care in spina bifida patients.Intractable & rare diseases research · 2021
    Review
  7. Observational
  8. Article
  9. Article
  10. Article
  11. Congenital lumbar kyphosis with skin ulceration and osteomyelitis in a myelomeningocele child: a case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
  12. A comparison of the MOMS trial results to a contemporaneous, single-institution, postnatal closure cohort.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017
    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

7 authors at 6 institutions in 1 country.

Elizabeth RadcliffSouth Carolina Rural Health Research Center, Arnold School of Public Health, University of South Carolina, 220 Stoneridge Drive, Suite 204, Columbia, SC, 29210, USA. radclife@mailbox.sc.edu.
Cynthia H CassellNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Sarah B LaditkaDepartment of Public Health Sciences, College of Health and Human Services, University of North Carolina at Charlotte, Charlotte, North Carolina, USA.
Judy K ThibadeauNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jane CorreiaBureau of Epidemiology, Division of Disease Control and Health Protection, Florida Department of Health, Florida Birth Defects Registry, Tallahassee, Florida, USA.
Scott D GrosseNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Russell S KirbyBirth Defects Surveillance Program, Department of Community and Family Health, College of Public Health, University of South Florida, Tampa, Florida, USA.
Centers for Disease Control and Prevention · USFlorida Department of Health · USNational Center on Birth Defects and Developmental Disabilities · USUniversity of North Carolina at Charlotte · USUniversity of South Carolina · USUniversity of South Florida · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

purposeClinical guidelines recommend repair of open spina bifida (SB) prenatally or within the first days of an infant's life. We examined maternal, infant, and health care system factors associated with time-to-repair among infants with postnatal repair.

methodsThis retrospective, statewide, population-based study examined infants with SB born in Florida 1998-2007, ascertained by the Florida Birth Defects Registry. We used procedure codes from hospital discharge records to identify the first recorded myelomeningocele repair (ICD-9 CM procedure code 03.52) among infants with birth hospitalizations. Using Poisson multivariable regression, we examined time-to-repair by hydrocephalus, SB type (isolated [no other coded major birth defect] versus non-isolated), and other selected factors.

resultsOf 199 infants with a recorded birth hospitalization and coded myelomeningocele repair, 87.9 % had hydrocephalus and 19.6 % had non-isolated SB. About 76.4 % of infants had repair by day 2 of life. In adjusted analyses, infants with hydrocephalus were more likely to have timely repair (adjusted prevalence ratio (aPR) = 1.48, 95 % confidence interval (CI) 1.02-2.14) than infants without hydrocephalus. SB type was not associated with repair timing. Infants born in lower level nursery care hospitals with were less likely to have timely repairs (aPR = 0.71, 95 % CI 0.52-0.98) than those born in higher level nursery care hospitals.

conclusionsMost infants with SB had surgical repair in the first 2 days of life. Lower level birth hospital nursery care was associated with later repairs. Prenatal diagnosis can facilitate planning for a birth hospital with higher level of nursery care, thus improving opportunities for timely repair.

Indexed as

Prenatal DiagnosisAdolescentAdultAge FactorsChildCommunity Health PlanningFemaleHumansHydrocephalusMaleRetrospective StudiesSpinal DysraphismTime FactorsTreatment OutcomeYoung AdultBirth defectsPediatric surgerySpina bifidaTimeliness

Identifiers

PMID27179533
PMCPMC5007061
OpenAlexW2356860340

What OpenQuestion holds

Textmetadata
LicenceTDM
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.