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Article: Macrovascular and microvascular disease in obese patients with type 2 diabetes attending structured diabetes education program: a population-based propensity-matched cohort analysis of Patient Empowerment Programme (PEP)

TitleMacrovascular and microvascular disease in obese patients with type 2 diabetes attending structured diabetes education program: a population-based propensity-matched cohort analysis of Patient Empowerment Programme (PEP)
Authors
KeywordsMacrovascular disease
Microvascular disease
Type 2 diabetes
Structured education
Self-management
Primary care
Issue Date2016
PublisherHumana Press, Inc. The Journal's web site is located at http://www.springer.com/humana+press/journal/12020
Citation
Endocrine, 2016, v. 53 n. 2, p. 412-422 How to Cite?
AbstractPatient Empowerment Programme (PEP) in primary care was effective in preventing diabetes-related complications in patients with diabetes. Nevertheless, the effect of PEP on glycaemic control, weight control, and complications was unclear in obese type 2 diabetic patients. We aimed to assess whether PEP reduced all-cause mortality, first macrovascular and microvascular disease events. A cohort of 6372 obese type 2 diabetic patients without prior occurrence of macrovascular or microvascular disease events on or before baseline study recruitment date was linked to the administrative database from 2008 to 2013. Non-PEP participants were matched one-to-one with the PEP participants using propensity score method with respect to their baseline covariates. Cox proportional hazard regressions were performed to estimate the associations of the PEP intervention with the occurrence of first macrovascular or microvascular disease events and death from any cause, controlling for demographic and clinical characteristics. During a median 31.5 months of follow-up, 350 (PEP/non-PEP: 151/199) patients suffered from a first macrovascular or microvascular disease event while 95 patients (PEP/non-PEP: 34/61) died from any cause. After adjusting for confounding variables, PEP participants had lower incidence rates of all-cause mortality [hazard ratio (HR): 0.589, 95 % confidence interval (CI) 0.380–0.915, P = 0.018] and first macrovascular or microvascular disease events (HR: 0.782, 95 % CI 0.632–0.968, P = 0.024) than those with PEP. Enrolment to PEP was an effective approach in reducing all-cause mortality and first macrovascular or microvascular disease events in obese patients with type 2 diabetes.
Persistent Identifierhttp://hdl.handle.net/10722/223214
ISSN
2023 Impact Factor: 3.0
2023 SCImago Journal Rankings: 0.844
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWong, CKH-
dc.contributor.authorWong, WCW-
dc.contributor.authorWan, EYF-
dc.contributor.authorChan, AKC-
dc.contributor.authorChan, FWK-
dc.contributor.authorLam, CLK-
dc.date.accessioned2016-02-23T01:55:33Z-
dc.date.available2016-02-23T01:55:33Z-
dc.date.issued2016-
dc.identifier.citationEndocrine, 2016, v. 53 n. 2, p. 412-422-
dc.identifier.issn1355-008X-
dc.identifier.urihttp://hdl.handle.net/10722/223214-
dc.description.abstractPatient Empowerment Programme (PEP) in primary care was effective in preventing diabetes-related complications in patients with diabetes. Nevertheless, the effect of PEP on glycaemic control, weight control, and complications was unclear in obese type 2 diabetic patients. We aimed to assess whether PEP reduced all-cause mortality, first macrovascular and microvascular disease events. A cohort of 6372 obese type 2 diabetic patients without prior occurrence of macrovascular or microvascular disease events on or before baseline study recruitment date was linked to the administrative database from 2008 to 2013. Non-PEP participants were matched one-to-one with the PEP participants using propensity score method with respect to their baseline covariates. Cox proportional hazard regressions were performed to estimate the associations of the PEP intervention with the occurrence of first macrovascular or microvascular disease events and death from any cause, controlling for demographic and clinical characteristics. During a median 31.5 months of follow-up, 350 (PEP/non-PEP: 151/199) patients suffered from a first macrovascular or microvascular disease event while 95 patients (PEP/non-PEP: 34/61) died from any cause. After adjusting for confounding variables, PEP participants had lower incidence rates of all-cause mortality [hazard ratio (HR): 0.589, 95 % confidence interval (CI) 0.380–0.915, P = 0.018] and first macrovascular or microvascular disease events (HR: 0.782, 95 % CI 0.632–0.968, P = 0.024) than those with PEP. Enrolment to PEP was an effective approach in reducing all-cause mortality and first macrovascular or microvascular disease events in obese patients with type 2 diabetes.-
dc.languageeng-
dc.publisherHumana Press, Inc. The Journal's web site is located at http://www.springer.com/humana+press/journal/12020-
dc.relation.ispartofEndocrine-
dc.rightsThis is a post-peer-review, pre-copyedit version of an article published in Endocrine. The final authenticated version is available online at: http://dx.doi.org/10.1007/s12020-015-0843-z.-
dc.subjectMacrovascular disease-
dc.subjectMicrovascular disease-
dc.subjectType 2 diabetes-
dc.subjectStructured education-
dc.subjectSelf-management-
dc.subjectPrimary care-
dc.titleMacrovascular and microvascular disease in obese patients with type 2 diabetes attending structured diabetes education program: a population-based propensity-matched cohort analysis of Patient Empowerment Programme (PEP)-
dc.typeArticle-
dc.identifier.emailWong, CKH: carlosho@hku.hk-
dc.identifier.emailWong, WCW: wongwcw@hku.hk-
dc.identifier.emailWan, EYF: yfwan@hku.hk-
dc.identifier.emailChan, AKC: kcchanae@hku.hk-
dc.identifier.emailLam, CLK: clklam@hku.hk-
dc.identifier.authorityWong, CKH=rp01931-
dc.identifier.authorityWong, WCW=rp01457-
dc.identifier.authorityWan, EYF=rp02518-
dc.identifier.authorityLam, CLK=rp00350-
dc.description.naturepostprint-
dc.identifier.doi10.1007/s12020-015-0843-z-
dc.identifier.pmid26785847-
dc.identifier.scopuseid_2-s2.0-84954533667-
dc.identifier.hkuros256860-
dc.identifier.volume53-
dc.identifier.issue2-
dc.identifier.spage412-
dc.identifier.epage422-
dc.identifier.isiWOS:000380140800009-
dc.publisher.placeUnited States-
dc.identifier.issnl1355-008X-

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