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Article: Prevalence, mortality and healthcare economic burden of tuberous sclerosis in Hong Kong: a population-based retrospective cohort study (1995–2018)

TitlePrevalence, mortality and healthcare economic burden of tuberous sclerosis in Hong Kong: a population-based retrospective cohort study (1995–2018)
Authors
KeywordsTuberous sclerosis
Epidemiology
Prevalence
Mortality
Survival
Treatment
mTOR inhibitor
Healthcare burden
Healthcare resources
Hong Kong
Issue Date2020
PublisherBioMed Central Ltd. The Journal's web site is located at http://www.ojrd.com
Citation
Orphanet Journal of Rare Diseases, 2020, v. 15, article no. 264 How to Cite?
AbstractBackground: We aim to elucidate the disease impact by accounting the prevalence, survival rate, genetics, mTOR inhibitor use and direct costs of tuberous sclerosis complex (TSC) in our local setting. TSC patients with documented visits to our local public hospitals in 1995–2018 were identified. The public hospitals captured most if not all local TSC patients. Demographics such as age, sex, death, genetic profiles were retrieved from the central electronic database. Data including prevalence, age distribution and survival rate were analysed. Direct cost was calculated with reference to the drug use and number of visits to various public hospital facilities. Results: We identified 284 surviving TSC patients (55.3% male) in Hong Kong. The age range was from 4.5 months to 89.9 years, with a median age of 27.2 years. Paediatrics (< 18 years) to adult (≥18 years) ratio was 1:2.84. The overall prevalence of TSC patients was 3.87 in 100,000 (i.e. 1 in 25,833). Genetically, TSC1:TSC2 ratio is 1:2.7. Thirty seven patients died within the study period. The age of death ranged from 7.6 years to 77.8 years, with a median age of death at 36.6 years (IQR: 24.7–51.1 years). Most patients survived till adulthood. Survival rate at 20 and 50 years follow-up was 98.6 and 79.5% respectively. Two hundred and twenty nine TSC patients (71.3%) had neurological manifestations, sixteen patients (5.0%) had chronic kidney diseases and five patients (1.6%) had pulmonary lymphangioleiomyomatosis. Forty seven (16.5%) TSC patients were prescribed with mTOR inhibitors within the study period. Healthcare facility utilization was further analysed in the 2008–2018 cohort. In particular, the mean number of specialist out-patient clinic visits per patient-year was 9.23 per patient-year, which was 4.91 times more than that of local general population. Conclusions: Prevalence of local TSC patients is within the range of that reported in the literature. Local TSC patients have fair long term survival, but they require disproportionally high healthcare cost when compared with the general population, particularly in terms of outpatient (OP) visits. Although effective disease-modifying agent (i.e. mTOR inhibitor) is available, it was not widely used yet in Hong Kong despite the fact that Government approved and supported its use recently. Further research on quality of life and setting up a comprehensive patient registry are necessary for more accurate assessment of cost and benefit.
Persistent Identifierhttp://hdl.handle.net/10722/306509
ISSN
2021 Impact Factor: 4.303
2020 SCImago Journal Rankings: 1.274
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChu, WCY-
dc.contributor.authorChiang, LLW-
dc.contributor.authorChan, DCC-
dc.contributor.authorWong, WHS-
dc.contributor.authorChan, GCF-
dc.date.accessioned2021-10-22T07:35:37Z-
dc.date.available2021-10-22T07:35:37Z-
dc.date.issued2020-
dc.identifier.citationOrphanet Journal of Rare Diseases, 2020, v. 15, article no. 264-
dc.identifier.issn1750-1172-
dc.identifier.urihttp://hdl.handle.net/10722/306509-
dc.description.abstractBackground: We aim to elucidate the disease impact by accounting the prevalence, survival rate, genetics, mTOR inhibitor use and direct costs of tuberous sclerosis complex (TSC) in our local setting. TSC patients with documented visits to our local public hospitals in 1995–2018 were identified. The public hospitals captured most if not all local TSC patients. Demographics such as age, sex, death, genetic profiles were retrieved from the central electronic database. Data including prevalence, age distribution and survival rate were analysed. Direct cost was calculated with reference to the drug use and number of visits to various public hospital facilities. Results: We identified 284 surviving TSC patients (55.3% male) in Hong Kong. The age range was from 4.5 months to 89.9 years, with a median age of 27.2 years. Paediatrics (< 18 years) to adult (≥18 years) ratio was 1:2.84. The overall prevalence of TSC patients was 3.87 in 100,000 (i.e. 1 in 25,833). Genetically, TSC1:TSC2 ratio is 1:2.7. Thirty seven patients died within the study period. The age of death ranged from 7.6 years to 77.8 years, with a median age of death at 36.6 years (IQR: 24.7–51.1 years). Most patients survived till adulthood. Survival rate at 20 and 50 years follow-up was 98.6 and 79.5% respectively. Two hundred and twenty nine TSC patients (71.3%) had neurological manifestations, sixteen patients (5.0%) had chronic kidney diseases and five patients (1.6%) had pulmonary lymphangioleiomyomatosis. Forty seven (16.5%) TSC patients were prescribed with mTOR inhibitors within the study period. Healthcare facility utilization was further analysed in the 2008–2018 cohort. In particular, the mean number of specialist out-patient clinic visits per patient-year was 9.23 per patient-year, which was 4.91 times more than that of local general population. Conclusions: Prevalence of local TSC patients is within the range of that reported in the literature. Local TSC patients have fair long term survival, but they require disproportionally high healthcare cost when compared with the general population, particularly in terms of outpatient (OP) visits. Although effective disease-modifying agent (i.e. mTOR inhibitor) is available, it was not widely used yet in Hong Kong despite the fact that Government approved and supported its use recently. Further research on quality of life and setting up a comprehensive patient registry are necessary for more accurate assessment of cost and benefit.-
dc.languageeng-
dc.publisherBioMed Central Ltd. The Journal's web site is located at http://www.ojrd.com-
dc.relation.ispartofOrphanet Journal of Rare Diseases-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectTuberous sclerosis-
dc.subjectEpidemiology-
dc.subjectPrevalence-
dc.subjectMortality-
dc.subjectSurvival-
dc.subjectTreatment-
dc.subjectmTOR inhibitor-
dc.subjectHealthcare burden-
dc.subjectHealthcare resources-
dc.subjectHong Kong-
dc.titlePrevalence, mortality and healthcare economic burden of tuberous sclerosis in Hong Kong: a population-based retrospective cohort study (1995–2018)-
dc.typeArticle-
dc.identifier.emailWong, WHS: whswong@hku.hk-
dc.identifier.emailChan, GCF: gcfchan@hku.hk-
dc.identifier.authorityChan, GCF=rp00431-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13023-020-01517-2-
dc.identifier.pmid32988393-
dc.identifier.pmcidPMC7523393-
dc.identifier.scopuseid_2-s2.0-85092062230-
dc.identifier.hkuros328479-
dc.identifier.volume15-
dc.identifier.spagearticle no. 264-
dc.identifier.epagearticle no. 264-
dc.identifier.isiWOS:000576285700001-
dc.publisher.placeUnited Kingdom-

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