| Literature DB >> 31262329 |
Xinmiao Shi1, Hui Liu2, Siyan Zhan3, Zhaoxia Wang4, Lin Wang5, Chongya Dong6, Yanfang Wang7, Chen Yao6,7, Jie Ding8, Yan Li9.
Abstract
BACKGROUND: There are many public health issues to resolve regarding rare diseases, including a lack of data from large-scale studies. The objective of this study was to explore fundamental data for a list of rare diseases in China, based on a hospitalization summary reports (HSRs) database. The Target Rare Diseases List (TRDL) 2017 was generated using an expert consensus method in which experts listed diseases according to research priorities. Using codes of the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) and key search terms of rare diseases in English and Chinese, data were obtained from HSRs of 96 hospitals, covering a population of over 15 million in China from 2014 to 2015. We extracted and analyzed information on demographics, hospitalizations, and readmissions.Entities:
Keywords: Database; Hospitalization; Rare diseases
Year: 2019 PMID: 31262329 PMCID: PMC6604331 DOI: 10.1186/s13023-019-1137-y
Source DB: PubMed Journal: Orphanet J Rare Dis ISSN: 1750-1172 Impact factor: 4.123
Fig. 1Flowchart of TRDL 2017 development and data capture. TRDL, Target Rare Diseases List
General characteristics of the top 10 rare diseases with most cases on the Target Rare Diseases List 2017
| Disease | Total No. | 2014 | 2015 | ||||
|---|---|---|---|---|---|---|---|
| N | Male | Age (yr, mean ± SD) | N | Male | Age (yr, mean ± SD) | ||
| Thalassemia | 14,855 | 6782 | 1761 (25.97%) | 28.5 ± 17.0 | 8073 | 1836 (22.74%) | 29.4 ± 16.5 |
| IPAH | 9536 | 4661 | 1837 (39.41%) | 46.7 ± 24.7 | 4875 | 1934 (39.67%) | 51.6 ± 23.9 |
| PLCH | 7657 | 3302 | 2114 (64.02%) | 7.1 ± 10.5 | 4355 | 2799 (64.27%) | 7.7 ± 11.5 |
| Moyamoya disease | 7419 | 3441 | 1642 (47.72%) | 41.0 ± 15.3 | 3978 | 1834 (46.10%) | 42.3 ± 15.1 |
| MND | 4057 | 2030 | 1331 (65.57%) | 55.8 ± 13.9 | 2027 | 1347 (66.45%) | 56.7 ± 12.8 |
| IPF | 3764 | 1470 | 1001 (68.10%) | 67.3 ± 12.8 | 2294 | 1579 (68.83%) | 69.0 ± 13.1 |
| SSc | 3252 | 1522 | 286 (18.80%) | 51.5 ± 13.8 | 1730 | 335 (19.36%) | 51.2 ± 14.2 |
| HLD | 3000 | 1433 | 773 (53.94%) | 23.9 ± 13.3 | 1567 | 887 (56.60%) | 24.9 ± 14.2 |
| CoA | 2654 | 1269 | 865 (68.16%) | 9.2 ± 14.8 | 1385 | 893 (64.48%) | 10.7 ± 16.4 |
| TGA | 2221 | 1082 | 707 (65.34%) | 6.6 ± 13.1 | 1139 | 757 (66.46%) | 7.8 ± 14.4 |
CoA coarctation of the aorta, HLD hepatolenticular degeneration, IPAH idiopathic pulmonary arterial hypertension, IPF idiopathic pulmonary fibrosis, MND motor neuron disease, PLCH pulmonary Langerhans cell histiocytosis, SSc systemic sclerosis, TGA transposition of the great arteries
Fig. 2The percentage of the top 10 rare diseases with most cases and other diseases on the Target Rare Diseases List 2017
Fig. 3Age distribution of the top 10 rare diseases with most cases on the Target Rare Diseases List 2017. CoA: coarctation of the aorta; HLD: hepatolenticular degeneration; IPAH: idiopathic pulmonary arterial hypertension; IPF: idiopathic pulmonary fibrosis; MND: motor neuron disease; PLCH: pulmonary Langerhans cell histiocytosis; SSc: systemic sclerosis; TGA: transposition of the great arteries
Fig. 4City distribution of cases for the 281 rare disease on the Target Rare Diseases List 2017 (during 2014–2015)
Fig. 5Age distribution of cases for the 281 rare disease on the Target Rare Diseases List 2017 (during 2014–2015)
The 10 rare diseases on the Target Rare Diseases List 2017 with the highest rates of readmission (2014–2015)
| Name of disease | No. of readmission | No. of hospitalizations | Readmission ratea |
|---|---|---|---|
| PLCH | 4968 | 7657 | 64.88% |
| Arginase deficiency | 9 | 14 | 64.29% |
| BS | 22 | 40 | 55.00% |
| Osteopetrosis | 115 | 211 | 54.50% |
| XHIM | 1 | 2 | 50.00% |
| XLA | 44 | 109 | 40.37% |
| WAS | 2 | 5 | 40.00% |
| HUS | 205 | 532 | 38.53% |
| CD | 111 | 301 | 36.88% |
| XP | 19 | 54 | 35.19% |
BS Blau syndrome, CD Castleman disease, HUS hemolytic uremic syndrome, PLCH pulmonary Langerhans cell histiocytosis, WAS Wiskott–Aldrich syndrome, XHIM X-linked hyper IgM syndrome, XLA X-linked agammaglobulinemia, XP xeroderma pigmentosum
aProportion with rehospitalization in the same hospital