Evidence map›Paper›PMID 32059709›Full record

ArticleBMC pregnancy and childbirth2020

Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.

Claudia Ching Yan Chung, Kelvin Yuen Kwong Chan, Pui Wah Hui, Patrick Kwok Cheung Au, Wai Keung Tam, Samuel Kai Man Li, Gordon Ka Chun Leung, Jasmine Lee Fong Fung, Marcus Chun Yin Chan, Ho Ming Luk and 5 more

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Article in BMC pregnancy and childbirth, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

15 authors.

Claudia Ching Yan ChungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Special Administrative Region, China.
Kelvin Yuen Kwong ChanDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China.
Pui Wah HuiDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China.
Patrick Kwok Cheung AuDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China.
Wai Keung TamDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China.
Samuel Kai Man LiDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China.
Gordon Ka Chun LeungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Special Administrative Region, China.
Jasmine Lee Fong FungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Special Administrative Region, China.
Marcus Chun Yin ChanDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Special Administrative Region, China.
Ho Ming LukDepartment of Health, Clinical Genetic Service, Hong Kong, Special Administrative Region, China.
Annisa Shui Lam MakDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong, Special Administrative Region, China.
Kwok Yin LeungDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong, Special Administrative Region, China.
Mary Hoi Yin TangPrenatal Diagnostic Laboratory, Tsan Yuk Hospital, Hong Kong, Special Administrative Region, China.
Brian Hon Yin ChungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, Special Administrative Region, China. bhychung@hku.hk.
Anita Sik Yau KanDepartment of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong, Special Administrative Region, China. kansya@hku.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChromosomal microarray (CMA) has been shown to be cost-effective over karyotyping in invasive prenatal diagnosis for pregnancies with fetal ultrasound anomalies. Yet, information regarding preceding and subsequent tests must be considered as a whole before the true cost-effectiveness can emerge. Currently in Hong Kong, karyotyping is offered free as the standard prenatal test while genome-wide array comparative genome hybridization (aCGH), a form of CMA, is self-financed. A new algorithm was proposed to use aCGH following quantitative fluorescent polymerase chain reaction (QF-PCR) as primary test instead of karyotyping. This study aims to evaluate the cost-effectiveness of the proposed algorithm versus the current algorithm for prenatal diagnosis in Hong Kong.

methodsBetween November 2014 and February 2016, 129 pregnant women who required invasive prenatal diagnosis at two public hospitals in Hong Kong were prospectively recruited. The proposed algorithm was performed for all participants in this demonstration study. For the cost-effectiveness analysis, cost and outcome (diagnostic rate) data were compared with that of a hypothetical scenario representing the current algorithm. Further analysis was performed to incorporate women's willingness-to-pay for the aCGH test. Impact of government subsidies on the aCGH test was explored as a sensitivity analysis.

resultsThe proposed algorithm dominated the current algorithm for prenatal diagnosis. Both algorithms were equally effective but the proposed algorithm was significantly cheaper (p ≤ 0.05). Taking into account women's willingness-to-pay for an aCGH test, the proposed algorithm was more effective and less costly than the current algorithm. When the government subsidy reaches 100%, the maximum number of diagnoses could be made.

conclusionBy switching to the proposed algorithm, cost saving can be achieved whilst maximizing the diagnostic rate for invasive prenatal diagnosis. It is recommended to implement aCGH as a primary test following QF-PCR to replace the majority of karyotyping for prenatal diagnosis in Hong Kong.

Indexed as

Cost-Benefit AnalysisAlgorithmsAneuploidyComparative Genomic HybridizationFemaleHong KongHumansKaryotypingPolymerase Chain ReactionPregnancyPrenatal DiagnosisPublic HealthChromosomal microarray - prenatal diagnosis - cost effectiveness analysis - cost saving - Hong KongKaryotyping

Identifiers

PMID32059709
PMCPMC7023733

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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.