Evidence map›Paper›PMID 27417464›Full record

ArticleChildren (Basel, Switzerland)2014

Uptake and Diagnostic Yield of Chromosomal Microarray in an Australian Child Development Clinic.

Dylan Mordaunt, Michael Gabbett, Melanie Waugh, Karen O'Brien, Helen Heussler

Abstract read
In one paragraph

Article in Children (Basel, Switzerland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Screening forBioMed research international · 2021
    Article
  4. Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.American journal of medical genetics. Part A · 2018
    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

5 authors.

Dylan MordauntMater Children's Hospital, Raymond Terrace, South Brisbane, QLD 4101, Australia. d.a.mordaunt@gmail.com.
Michael GabbettGenetic Health Queensland, Back Street, off Bramston Terrace, Herston, QLD 4029, Australia. michael.gabbett@health.qld.gov.au.
Melanie WaughMater Children's Hospital, Raymond Terrace, South Brisbane, QLD 4101, Australia. mlwgmo@gmail.com.
Karen O'BrienMater Children's Hospital, Raymond Terrace, South Brisbane, QLD 4101, Australia. k.obrien@psy.uq.edu.au.
Helen HeusslerMater Children's Hospital, Raymond Terrace, South Brisbane, QLD 4101, Australia. Honey.Heussler@mater.org.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism is an etiologically heterogeneous developmental disorder for which the range of genetic investigations has expanded considerably over the past decade. Introduction of chromosomal microarray (CMA) to clinical practice has expanded the range of conditions which pediatricians are able to detect. This study reviewed the utilization, yield and cost of genetic investigations in a sample of children with pervasive developmental disorders (PDD) in an Australian metropolitan child development service. Six hundred and ninety eight patients with PDD were identified from the clinic population. One hundred and ten (15.7%) of the clinic population had undergone investigation with chromosomal microarray, 140 (20.0%) with karyotype (KT), and 167 (23.9%) with Fragile X testing (FRGX). Twelve (10.9%) CMA findings were reported, of which seven (6.3%) were felt to be the likely cause of the child's clinical features. Five (3.5%) KT findings were reported, of which four (2.9%) were felt to be the likely cause of the child's clinical features. Two patients (1.2%) were identified with Fragile X expansions. One fifth of the clinic's recent PDD population had undergone testing with CMA. CMA appears to have increased the diagnostic yield of the genetic investigation of autism, in line with internationally reported levels. Number needed to test (NNT) and cost per incremental diagnosis, were also in line with internationally reported levels.

Indexed as

Asperger syndromeautismautistic disorderchildhood disintegrative disorderchromosomal microarraypervasive developmental disorder-not otherwise specifiedRett syndrome

Identifiers

PMID27417464
PMCPMC4939515

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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.