Evidence map›Paper›PMID 35615033›Full record

ArticleFrontiers in public health2022

Study on the Economic Burden of Neurodevelopmental Diseases on Patients With Genetic Diagnosis.

Donghua Xie, Ruoyu Duan, Chen Li, Zhiqun Xie, Aihua Wang, Lili Xiong, Jianhui Wei, Hui Xi, Junqu Fang, Huifang Yan and 5 more

Abstract read
In one paragraph

Article in Frontiers in public health, 2022. 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
–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

2 citing papers in PubMed.

  1. Review
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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.

Donghua XieDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Ruoyu DuanDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Chen LiChildren Health Hospital of Shenzhen City, Shenzhen, China.
Zhiqun XieDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Aihua WangDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Lili XiongDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Jianhui WeiXiangya School of Public Health, Central South University, Changsha, China.
Hui XiDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Junqu FangDepartment of Information Management, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Huifang YanDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Junyu WangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Yu ZhangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Xiao MaoNHC Key Laboratory of Birth Defect for Research and Prevention (Maternal and Child Health Hospital of Hunan Province), Changsha, China.
Jingmin WangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Hua WangNHC Key Laboratory of Birth Defect for Research and Prevention (Maternal and Child Health Hospital of Hunan Province), Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To study the burden of neurodevelopmental diseases (NDDs) via cost-of-illness analysis of Chinese patients with genetic diagnosis. Methods: We recruited NDD patients (0-18 years old) with genetic diagnosis (GD) from September 1, 2020 to January 30, 2021. We gathered basic information on the details of diagnosis, as well as the direct medical cost, direct non-healthcare cost and indirect cost before and after receiving GD. We corrected the cost for time biases by calculating the cost per day for each patient. Results: For the 502 patients with NDDs, the mean age was 4.08 ± 3.47. The household income was 0.6 (0.4, 1.0) 10,000 CNY per-month on average. The direct medical cost, direct non-healthcare cost and indirect cost were 12.27 (7.36, 22.23) 10,000 CNY, 1.45 (0.73, 2.69)10,000 CNY and 14.14(4.80, 28.25) 10,000 CNY per patient, respectively. Every patient received 1.20 (0.34, 3.60) 10,000 CNY on average (15.91%) from insurance. The daily total cost after receiving GD were ~62.48% lower than those before GD (191.59 CNY vs. 71.45 CNY). The descend range of lab cost (95.77%, Conclusions: Early genetic diagnosis is crucial for to reducing the burden of disease because of the amount of money spent was lower when they are diagnosed at younger age. Patients with NDDs can incur a heavy economic burden, especially in rehabilitation cost and indirect cost, because the insurance coverage for patients is low, so it is urgent for governments to pay more attention to these issues.

Indexed as

Financial StressHospitalizationAdolescentChildChild, PreschoolCosts and Cost AnalysisHumansInfantInfant, Newborncosteconomic burdengenetic diagnosisinsuranceneurodevelopmental disease

Identifiers

PMID35615033
PMCPMC9126321

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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.