Mortality among older Spanish people with hip fractures: a population-based matched cohort study

2021 ◽  
Author(s):  
Alicia Gutiérrez-Misis ◽  
Rocío Queipo ◽  
María Victoria Castell ◽  
Teresa Alarcón ◽  
Rocío Menéndez-Colino ◽  
...  
Keyword(s):  
Cohort Study ◽  
Hip Fractures ◽  
Population Based ◽  
Matched Cohort ◽  
Matched Cohort Study

PO-19 Initiation of low-dose aspirin and risk of colorectal neoplasms: a population-based matched cohort study in Denmark

2021 ◽  
Vol 200 ◽  
pp. S26
Author(s):  
E. Schønfeldt Troelsen ◽  
D. Körmendiné Farkas ◽  
R. Erichsen ◽  
T. Sørensen
Keyword(s):  
Cohort Study ◽  
Colorectal Neoplasms ◽  
Low Dose ◽  
Population Based ◽  
Matched Cohort ◽  
Matched Cohort Study ◽  
Dose Aspirin ◽  
Low Dose Aspirin

Quality of life before and after sinonasal surgery: a population-based matched cohort study

2016 ◽  
Vol 274 (2) ◽  
pp. 795-802 ◽  
Author(s):  
Antti I. Alakärppä ◽  
Timo J. Koskenkorva ◽  
Petri T. Koivunen ◽  
Olli-Pekka Alho
Keyword(s):  
Quality Of Life ◽  
Cohort Study ◽  
Population Based ◽  
Matched Cohort ◽  
Matched Cohort Study ◽  
Before And After

Increased risk of adhesive capsulitis among patients with gout: A nationwide population-based matched-cohort study

2018 ◽  
Vol 21 (9) ◽  
pp. 1716-1722 ◽  
Author(s):  
Kao-Chih Hsu ◽  
Chia-Hung Sun ◽  
Yin-Yin Wu ◽  
Liang-Cheng Chen ◽  
Yung-Tsan Wu ◽  
...  
Keyword(s):  
Cohort Study ◽  
Adhesive Capsulitis ◽  
Population Based ◽  
Matched Cohort ◽  
Matched Cohort Study ◽  
Increased Risk

scholarly journals Severe maternal morbidity and postpartum mental health-related outcomes in Sweden: a population-based matched-cohort study

2018 ◽  
Vol 22 (4) ◽  
pp. 519-526 ◽  
Author(s):  
Elizabeth Wall-Wieler ◽  
Suzan L. Carmichael ◽  
Marcelo L. Urquia ◽  
Can Liu ◽  
Anders Hjern
Keyword(s):  
Mental Health ◽  
Cohort Study ◽  
Maternal Morbidity ◽  
Population Based ◽  
Severe Maternal Morbidity ◽  
Matched Cohort ◽  
Matched Cohort Study ◽  
Postpartum Mental Health ◽  
Health Related

scholarly journals Differential cerebrovascular risks in glioblastoma and meningioma patients: a population-based matched cohort study in Wales (United Kingdom)

2021 ◽  
Vol 23 (Supplement_4) ◽  
pp. iv12-iv12
Author(s):  
Michael T C Poon ◽  
Kai Jin ◽  
Paul M Brennan ◽  
Jonine Figueroa ◽  
Cathie Sudlow
Keyword(s):  
Cohort Study ◽  
General Population ◽  
Ischaemic Stroke ◽  
Population Based ◽  
Parametric Models ◽  
Matched Cohort ◽  
Matched Cohort Study ◽  
Hazard Ratios ◽  
History Of

Abstract Aims There is limited evidence on cerebrovascular risks in glioblastoma and meningioma patients. We aimed to compare cerebrovascular risks of these patients with the general population. Method We used population-based routine healthcare and administrative data linkage in this matched cohort study. Cases were adult glioblastoma and meningioma patients diagnosed in Wales 2000-2014 identified in the cancer registry. Controls from cancer-free general population were matched to cases (5:1 ratio) on age (±5 years), sex and GP practice. Factors included in multivariable models were age, sex, index of multiple deprivation, hypertension, diabetes, high cholesterol, history of cardiovascular disease, and medications for cardiovascular diseases. Outcomes were fatal and non-fatal haemorrhagic and ischaemic stroke. We used flexible parametric models adjusting for confounders to calculate the hazard ratios (HR). Results Final analytic population was 16,921 participants, of which 1,340 had glioblastoma and 1,498 had meningioma. The median follow-up time was 0.5 year for glioblastoma patients, 4.9 years for meningioma patients, and 6.6 years for controls. The number of haemorrhage and ischaemic stroke was 154 and 374 in the glioblastoma matched cohort, respectively, and 180 and 569 in the meningioma matched cohort, respectively. The adjusted HRs for haemorrhagic and ischaemic stroke were 3.74 (95%CI 1.87-6.57) and 5.62 (95%CI 2.56-10.42) in glioblastoma patients, respectively, and were 2.42 (95%CI 1.58-3.52) and 1.86 (95%CI 1.54-2.23) in meningioma patients compared with their controls. Conclusion Glioblastoma and meningioma patients had higher cerebrovascular risks; these risks were even higher for glioblastoma patients. Further assessment of these potentially modifiable risks may improve survivorship.

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