7 research outputs found

    Understanding the costs of cancer care before and after diagnosis for the 21 most common cancers in Ontario: a population-based descriptive study

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    Background: The first year after cancer diagnosis is a period of intensive treatment and high cost. We sought to estimate costs for the 21 most common cancers in Ontario in the 3-month period before and the first year after diagnosis. Methods: We used the Ontario Cancer Registry to select patients who received diagnoses between 1997 and 2007 at 19 years of age or older, with valid International Classification of Diseases for Oncology (ICD-O) and histology codes, who survived 30 days or longer after diagnosis and had no second cancer within 90 days of the initial cancer (n = 402 399). We used linked administrative data to calculate mean costs for each cancer during the pre- and postdiagnosis periods for patients who died within 1 year after diagnosis and patients who survived beyond 1 year after diagnosis. Results: Mean prediagnosis costs were 2060(952060 (95% confidence interval [CI] 2023–2098)forallpatientswithcancer.Costsrangedfrom2098) for all patients with cancer. Costs ranged from 890 (95% CI 795–795–985) for melanoma to 4128(954128 (95% CI 3591–4664)forlivercanceramongpatientswhosurvivedbeyond1yearafterdiagnosis,andrangedfrom4664) for liver cancer among patients who survived beyond 1 year after diagnosis, and ranged from 2188 (95% CI 2040–2040–2336) for esophageal cancer to 5142(955142 (95% CI 4664–5620)formultiplemyelomaamongpatientswhodiedwithin1year.Themeanpostdiagnosiscostforourcohortwas5620) for multiple myeloma among patients who died within 1 year. The mean postdiagnosis cost for our cohort was 25 914 (95% CI 25782–25 782–26 046). Mean costs were lowest for melanoma (8611[958611 [95% CI 8221–9001])andhighestforesophagealcancer(9001]) and highest for esophageal cancer (50 620 [95% CI 47677–47 677–53 562] among patients who survived beyond 1 year after diagnosis, and ranged from 27560(9527 560 (95% CI 25 747–29373)forlivercancerto29 373) for liver cancer to 81 655 (95% CI 58361–58 361–104 949) for testicular cancer among patients who died within 1 year. Interpretation Our research provides cancer-related cost estimates for the pre- and postdiagnosis phases and offers insight into the economic burden incurred by the Ontario health care system. These estimates can help inform policy-makers’ decisions regarding resource allocation for cancer prevention and control, and can serve as important input for economic evaluations

    Serious Infections in a Population-Based Cohort of 86,039 Seniors With Rheumatoid Arthritis

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    Objective. To assess risk and risk factors for serious infections in seniors with rheumatoid arthritis (RA) using a case-control study nested within an RA cohort. Methods. We assembled a retrospective RA cohort age >66 years from Ontario health administrative data across 1992-2010. Nested case-control analyses were done, comparing RA patients with a primary diagnosis of infection (based on hospital or emergency department records) to matched RA controls. We assessed independent effects of drugs, adjusting for demographics, comorbidity, and markers of RA severity. Results. A total of 86,039 seniors with RA experienced 20,575 infections, for a rate of 46.4 events/1,000 person-years. The most frequently occurring events included respiratory infections, herpes zoster, and skin/soft tissue infections. Factors associated with infection included higher comorbidity, rural residence, markers of disease severity, and history of previous infection. In addition, anti-tumor necrosis factor agents and disease-modifying antirheumatic drugs were associated with a several-fold increase in infections, with an adjusted odds ratio (OR) ranging from 1.2-3.5. The drug category with the greatest effect estimate was glucocorticoids, which exhibited a clear dose response with an OR ranging from 4.0 at low doses to 7.6 at high doses. Conclusion. Seniors with RA have significant morbidity related to serious infections, which exceeds previous reports among younger RA populations. Rural residence, higher comorbidity, markers of disease severity, and previous infection were associated with serious infections in seniors with RA. Our results emphasize that many RA drugs may increase the risk of infection, but glucocorticoids appear to confer a particular risk

    Atypical antipsychotic drugs and risk of ischaemic stroke: population based retrospective cohort study

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    Objective To compare the incidence of admissions to hospital for stroke among older adults with dementia receiving atypical or typical antipsychotics. Design Population based retrospective cohort study. Setting Ontario, Canada. Patients 32 710 older adults (≤ 65 years) with dementia (17 845 dispensed an atypical antipsychotic and 14 865 dispensed a typical antipsychotic). Main outcome measures Admission to hospital with the most responsible diagnosis (single most important condition responsible for the patient's admission) of ischaemic stroke. Observation of patients until they were either admitted to hospital with ischaemic stroke, stopped taking antipsychotics, died, or the study ended. Results After adjustment for potential confounders, participants receiving atypical antipsychotics showed no significant increase in risk of ischaemic stroke compared with those receiving typical antipsychotics (adjusted hazard ratio 1.01, 95% confidence interval 0.81 to 1.26). This finding was consistent in a series of subgroup analyses, including ones of individual atypical antipsychotic drugs (risperidone, olanzapine, and quetiapine) and selected subpopulations of the main cohorts. Conclusion Older adults with dementia who take atypical antipsychotics have a similar risk of ischaemic stroke to those taking typical antipsychotics
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