Evidence map›Paper›PMID 37301973›Full record

ArticleBMC pregnancy and childbirth2023

Experience in prenatal genetic testing and reproductive decision-making for monogenic disorders from a single tertiary care genetics clinic in a low-middle income country.

Amna Hanif, Fizza Akbar, Salman Kirmani, Amyna Jaffarali, Ghulam Zainab, Ayesha Malik, Zeeshan Ansar, Bushra Afroze

Open access · goldAbstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Amna HanifDepartment of Paediatrics & Child Health, Aga Khan University (AKU) Hospital, Stadium Road, Karachi, Pakistan.
Fizza AkbarDepartment of Paediatrics & Child Health, Aga Khan University (AKU) Hospital, Stadium Road, Karachi, Pakistan.
Salman KirmaniDepartment of Paediatrics & Child Health, Aga Khan University (AKU) Hospital, Stadium Road, Karachi, Pakistan.
Amyna JaffaraliDepartment of Paediatrics & Child Health, Aga Khan University (AKU) Hospital, Stadium Road, Karachi, Pakistan.
Ghulam ZainabDepartment of Obstetrics & Gynaecology, Aga Khan University (AKU) Hospital, Karachi, Pakistan.
Ayesha MalikDepartment of Obstetrics & Gynaecology, Aga Khan University (AKU) Hospital, Karachi, Pakistan.
Zeeshan AnsarSection of Molecular Pathology, Department of Pathology and Laboratory Medicine, Aga Khan University (AKU) Hospital, Karachi, Pakistan.
Bushra AfrozeDepartment of Paediatrics & Child Health, Aga Khan University (AKU) Hospital, Stadium Road, Karachi, Pakistan. bushra.afroze@aku.edu.
Aga Khan University Hospital · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesExplore health-care seeking behaviour among couples with pregnancies at-risk of monogenic disorders and compare time duration for obtaining Prenatal Genetic Test (PGT) results based on (i) amniocentesis and Chorionic Villus Sampling (CVS) (ii) in-house testing and out-sourced testing. Report the spectrum of monogenic disorders in our cohort.

methodsMedical records of women consulting prenatal genetic counselling clinic at Aga Khan University Hospital, Karachi from December-2015 to March-2021 with history of miscarriage or a monogenic disorder in previous children were reviewed.

resultsForty-three pregnancies in 40 couples were evaluated, 37(93%) were consanguineous. Twenty-five (63%) couples consulted before and 15(37%) after conception. Thirty-one (71%) pregnancies underwent CVS at the mean gestational age of 13-weeks and 6-days ± 1-week and 3-days and amniocentesis at 16-weeks and 2-days ± 1-week and 4-days. PGT for 30 (70%) pregnancies was outsourced. The mean number of days for in-house PGT was 16.92 ± 7.80 days whereas for outsourced was 25.45 ± 7.7 days. Mean duration from procedure to PGT result was 20.55 days after CVS compared to 28.75 days after amniocentesis. Eight (18%) fetuses were homozygous for disease-causing variant for whom couples opted for termination of pregnancy (TOP). Twenty-six monogenetic disorders were identified in 40 families.

conclusionProactive health-care seeking behaviour and TOP acceptance is present amongst couples who have experienced a genetic disorder.

Indexed as

AmniocentesisDeveloping CountriesChildChorionic Villi SamplingFemaleGenetic TestingHumansInfantPregnancyTertiary Health CareGenetic testingInformed reproductive decision makingLMICsPrenatal diagnosisRare disease burden

Identifiers

PMID37301973
PMCPMC10257259
OpenAlexW4380077708

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.