Logan McLeod, Basil G Bereza, Minsup Shim, Paul Grootendorst
Background: Commentaries on the adequacy of insurance coverage for prescription drugs available to Canadians have emphasized differences in the coverage provided by different provincial governments. Less is known about the actual financial burden of prescription drug spending and how this burden varies by province of residence, affluence and source of primary drug coverage.
Methods: We used data from a nationally representative household expenditure survey to analyze the financial burden of prescription drugs. We focused on the drug budget share (defined as the share of the household budget spent on prescription drugs), considering how it varied by province, total household budget and likely primary source of drug insurance coverage (i.e., provincial government plan for senior citizens, social assistance plan or private coverage). We examined both "typical" households (at the median of the distribution of the drug budget share) and households with relatively large shares (in the top 5%). Finally, we estimated the percentage of households with catastrophic drug expenditures (defined as a drug budget share of 10% or more) and the average catastrophic drug expenditures.
Results: Senior, social assistance and general population households accounted for 21.1%, 8.9% and 69.9% of the sample of 14,430 respondents to the 2006 Survey of Household Spending, respectively. The median drug budget share in Canada was 1.1% for senior households (range 0.4% [Ontario] to 3.6% [Saskatchewan]) and 0.1% for both social assistance households and general population households, with little appreciable variation across provinces for these latter 2 categories. The 95th percentile drug budget share in Canada was 7.4% for senior households (range 3.5% [Ontario] to 12.7% [Saskatchewan]), 5.4% for social assistance households (range 2.3% [British Columbia] to 13.0% [Prince Edward Island]) and 2.6% for general population households (range 2.1% [Ontario] to 5.4% [Prince Edward Island]). The interprovincial range of the 95th percentile drug budget share was 10.7 percentage points for social assistance households, 9.2 percentage points for senior households and 3.3 percentage points for general population households.
Interpretation: For most households, the financial burden of prescription drug expenditures appeared to be relatively small, with little interprovincial variation. However, a small number of households incurred catastrophic drug costs. These households were concentrated in the groups that traditionally benefit from provincial government drug plans. It is likely that some households did not purchase needed prescription drugs because of the expense, so our estimates of the financial burden of catastrophic prescription drug expenditures therefore represent a lower bound.
{"title":"Financial burden of household out-of-pocket expenditures for prescription drugs: cross-sectional analysis based on national survey data.","authors":"Logan McLeod, Basil G Bereza, Minsup Shim, Paul Grootendorst","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Commentaries on the adequacy of insurance coverage for prescription drugs available to Canadians have emphasized differences in the coverage provided by different provincial governments. Less is known about the actual financial burden of prescription drug spending and how this burden varies by province of residence, affluence and source of primary drug coverage.</p><p><strong>Methods: </strong>We used data from a nationally representative household expenditure survey to analyze the financial burden of prescription drugs. We focused on the drug budget share (defined as the share of the household budget spent on prescription drugs), considering how it varied by province, total household budget and likely primary source of drug insurance coverage (i.e., provincial government plan for senior citizens, social assistance plan or private coverage). We examined both \"typical\" households (at the median of the distribution of the drug budget share) and households with relatively large shares (in the top 5%). Finally, we estimated the percentage of households with catastrophic drug expenditures (defined as a drug budget share of 10% or more) and the average catastrophic drug expenditures.</p><p><strong>Results: </strong>Senior, social assistance and general population households accounted for 21.1%, 8.9% and 69.9% of the sample of 14,430 respondents to the 2006 Survey of Household Spending, respectively. The median drug budget share in Canada was 1.1% for senior households (range 0.4% [Ontario] to 3.6% [Saskatchewan]) and 0.1% for both social assistance households and general population households, with little appreciable variation across provinces for these latter 2 categories. The 95th percentile drug budget share in Canada was 7.4% for senior households (range 3.5% [Ontario] to 12.7% [Saskatchewan]), 5.4% for social assistance households (range 2.3% [British Columbia] to 13.0% [Prince Edward Island]) and 2.6% for general population households (range 2.1% [Ontario] to 5.4% [Prince Edward Island]). The interprovincial range of the 95th percentile drug budget share was 10.7 percentage points for social assistance households, 9.2 percentage points for senior households and 3.3 percentage points for general population households.</p><p><strong>Interpretation: </strong>For most households, the financial burden of prescription drug expenditures appeared to be relatively small, with little interprovincial variation. However, a small number of households incurred catastrophic drug costs. These households were concentrated in the groups that traditionally benefit from provincial government drug plans. It is likely that some households did not purchase needed prescription drugs because of the expense, so our estimates of the financial burden of catastrophic prescription drug expenditures therefore represent a lower bound.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 1","pages":"e1-9"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/1e/8b/OpenMed-05-e1.PMC3205811.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40123025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Margaret J McGregor, Marcy Cohen, Catherine-Rose Stocks-Rankin, Michelle B Cox, Kia Salomons, Kimberlyn M McGrail, Charmaine Spencer, Lisa A Ronald, Michael Schulzer
Background: Nursing homes provide long-term housing, support and nursing care to frail elders who are no longer able to function independently. Although studies conducted in the United States have demonstrated an association between for-profit ownership and inferior quality, relatively few Canadian studies have made performance comparisons with reference to type of ownership. Complaints are one proxy measure of performance in the nursing home setting. Our study goal was to determine whether there is an association between facility ownership and the frequency of nursing home complaints.
Methods: We analyzed publicly available data on complaints, regulatory measures, facility ownership and size for 604 facilities in Ontario over 1 year (2007/08) and 62 facilities in British Columbia (Fraser Health region) over 4 years (2004-2008). All analyses were carried out at the facility level. Negative binomial regression analysis was used to assess the association between type of facility ownership and frequency of complaints.
Results: The mean (standard deviation) number of verified/substantiated complaints per 100 beds per year in Ontario and Fraser Health was 0.45 (1.10) and 0.78 (1.63) respectively. Most complaints related to resident care. Complaints were more frequent in facilities with more citations, i.e., violations of the legislation or regulations governing a home, (Ontario) and inspection violations (Fraser Health). Compared with Ontario's for-profit chain facilities, adjusted incident rate ratios and 95% confidence intervals of verified complaints were 0.56 (0.27-1.16), 0.58 (0.34-1.00), 0.43 (0.21- 0.88), and 0.50 (0.30- 0.84) for for-profit single-site, non-profit, charitable, and public facilities respectively. In Fraser Health, the adjusted incident rate ratio of substantiated complaints in non-profit facilities compared with for-profit facilities was 0.18 (0.07-0.45).
Interpretation: Compared with for-profit chain facilities, non-profit, charitable and public facilities had significantly lower rates of complaints in Ontario. Likewise, in British Columbia's Fraser Health region, non-profit owned facilities had significantly lower rates of complaints compared with for-profit owned facilities.
{"title":"Complaints in for-profit, non-profit and public nursing homes in two Canadian provinces.","authors":"Margaret J McGregor, Marcy Cohen, Catherine-Rose Stocks-Rankin, Michelle B Cox, Kia Salomons, Kimberlyn M McGrail, Charmaine Spencer, Lisa A Ronald, Michael Schulzer","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Nursing homes provide long-term housing, support and nursing care to frail elders who are no longer able to function independently. Although studies conducted in the United States have demonstrated an association between for-profit ownership and inferior quality, relatively few Canadian studies have made performance comparisons with reference to type of ownership. Complaints are one proxy measure of performance in the nursing home setting. Our study goal was to determine whether there is an association between facility ownership and the frequency of nursing home complaints.</p><p><strong>Methods: </strong>We analyzed publicly available data on complaints, regulatory measures, facility ownership and size for 604 facilities in Ontario over 1 year (2007/08) and 62 facilities in British Columbia (Fraser Health region) over 4 years (2004-2008). All analyses were carried out at the facility level. Negative binomial regression analysis was used to assess the association between type of facility ownership and frequency of complaints.</p><p><strong>Results: </strong>The mean (standard deviation) number of verified/substantiated complaints per 100 beds per year in Ontario and Fraser Health was 0.45 (1.10) and 0.78 (1.63) respectively. Most complaints related to resident care. Complaints were more frequent in facilities with more citations, i.e., violations of the legislation or regulations governing a home, (Ontario) and inspection violations (Fraser Health). Compared with Ontario's for-profit chain facilities, adjusted incident rate ratios and 95% confidence intervals of verified complaints were 0.56 (0.27-1.16), 0.58 (0.34-1.00), 0.43 (0.21- 0.88), and 0.50 (0.30- 0.84) for for-profit single-site, non-profit, charitable, and public facilities respectively. In Fraser Health, the adjusted incident rate ratio of substantiated complaints in non-profit facilities compared with for-profit facilities was 0.18 (0.07-0.45).</p><p><strong>Interpretation: </strong>Compared with for-profit chain facilities, non-profit, charitable and public facilities had significantly lower rates of complaints in Ontario. Likewise, in British Columbia's Fraser Health region, non-profit owned facilities had significantly lower rates of complaints compared with for-profit owned facilities.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 4","pages":"e183-92"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ee/4f/OpenMed-05-e183.PMC3345377.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30601603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Practice pattern variations are often attributed to physician decision-making with no accounting for patient preferences.
Objective: To test whether a mass media television broadcast unrelated to health was associated with changes in the rate and characteristics of visits for acute emergency care.
Design: Time-series analysis of emergency department visits for any reason.
Subjects: Population-based sample of all patients seeking emergency care in Ontario, Canada.
Measures: The broadcast day was defined as the Olympic men's gold medal ice hockey game final. The control days were defined as the 6 Sundays before and after the broadcast day.
Results: A total of 99 447 visits occurred over the 7 Sundays, of which 13 990 occurred on the broadcast day. Comparing the broadcast day with control days, we found no significant difference in the hourly rate of visits before the broadcast (544 vs 537, p = 0.41) or after the broadcast (647 vs 639, p = 0.55). In contrast, we observed a significant reduction in hourly rate of visits during the broadcast (647 vs 783, p < 0.001), equal to an absolute decrease of 409 patients, a relative decrease of 17% (95% confidence interval 13-21), or about 136 fewer patients per hour. The relative decrease during the broadcast was particularly large for adult men with low triage severity. The greatest reductions were for patients with abdominal, musculoskeletal or traumatic disorders.
Conclusion: Mass media television broadcasts can influence patient preferences and thereby lead to a decrease in emergency department visits.
背景:实践模式的变化通常归因于医生的决策,而没有考虑到患者的偏好。目的:检验与健康无关的大众媒体电视广播是否与急症急诊就诊率和特征的变化有关。设计:任何原因急诊就诊的时间序列分析。研究对象:以人群为基础的加拿大安大略省所有寻求急诊治疗的患者样本。衡量标准:转播日被定义为奥运会男子冰球金牌决赛。对照日定义为广播日前后的6个周日。结果:7个周日共访问99 447人次,其中广播日访问13 990人次。将广播日与对照日进行比较,我们发现广播前(544 vs 537, p = 0.41)和广播后(647 vs 639, p = 0.55)的每小时访问率没有显著差异。相比之下,我们观察到广播期间每小时就诊率显著降低(647 vs 783, p < 0.001),相当于绝对减少409例患者,相对减少17%(95%置信区间13-21),或每小时减少约136例患者。在广播期间,分诊严重程度较低的成年男性的相对下降幅度尤其大。减少最多的是腹部、肌肉骨骼或创伤性疾病的患者。结论:大众传媒电视广播可影响患者的偏好,从而导致急诊科就诊次数减少。
{"title":"Emergency department visits during an Olympic gold medal television broadcast.","authors":"Donald A Redelmeier, Marian J Vermeulen","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Practice pattern variations are often attributed to physician decision-making with no accounting for patient preferences.</p><p><strong>Objective: </strong>To test whether a mass media television broadcast unrelated to health was associated with changes in the rate and characteristics of visits for acute emergency care.</p><p><strong>Design: </strong>Time-series analysis of emergency department visits for any reason.</p><p><strong>Subjects: </strong>Population-based sample of all patients seeking emergency care in Ontario, Canada.</p><p><strong>Measures: </strong>The broadcast day was defined as the Olympic men's gold medal ice hockey game final. The control days were defined as the 6 Sundays before and after the broadcast day.</p><p><strong>Results: </strong>A total of 99 447 visits occurred over the 7 Sundays, of which 13 990 occurred on the broadcast day. Comparing the broadcast day with control days, we found no significant difference in the hourly rate of visits before the broadcast (544 vs 537, p = 0.41) or after the broadcast (647 vs 639, p = 0.55). In contrast, we observed a significant reduction in hourly rate of visits during the broadcast (647 vs 783, p < 0.001), equal to an absolute decrease of 409 patients, a relative decrease of 17% (95% confidence interval 13-21), or about 136 fewer patients per hour. The relative decrease during the broadcast was particularly large for adult men with low triage severity. The greatest reductions were for patients with abdominal, musculoskeletal or traumatic disorders.</p><p><strong>Conclusion: </strong>Mass media television broadcasts can influence patient preferences and thereby lead to a decrease in emergency department visits.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 2","pages":"e112-9"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4d/8a/OpenMed-05-e112.PMC3148000.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30139966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Enlist in our MASH unit: an invitation to join the Meaningful Analogies in Sports and Health network.","authors":"Steven Lewis, Mark Wahba, Mary Smillie","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 4","pages":"e175-6"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f8/3c/OpenMed-05-e175.PMC3345373.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30601601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Carl van Walraven, Jenna Wong, Kareem Morant, Alison Jennings, Peter C Austin, Prasad Jetty, Alan J Forster
Background: An abdominal aortic aneurysm (AAA) that is identified when the abdomen is imaged for some other reason is known as an incidental AAA. No population-based studies have assessed the management of incidental AAAs. The objective of this study was to measure the completeness of radiographic monitoring of incidental AAAs by means of a population-based analysis.
Methods: We linked a cohort of patients with incidental AAA (defined as a previously unidentified aortic enlargement exceeding 30 mm in diameter found in an imaging study performed for another reason) to various population-based databases. We followed the patients to elective repair or rupture of the aneurysm, death or 31 Mar. 2009. We used evidence-based monitoring guidelines to calculate the proportion of observation time during which each incidental AAA was incompletely monitored. We used negative binomial regression to determine the association of patient-related factors with this outcome.
Results: For the period between January 1996 and September 2008, we identified 191 patients with incidental AAA (mean diameter 37.6 mm, 95% confidence interval [CI] 36.6-38.6 mm; median follow-up 4.4 [range 0.6-12.7] years). Fifty-six of these patients (29.3%) had no radiographic monitoring of the aneurysm. Overall, patients spent one-fifth of their time with incomplete monitoring of the AAA (median 19.4%, interquartile range 0.3%-44.0%). Factors independently associated with incomplete monitoring included older age (relative rate [change in proportion of time with incomplete monitoring] [RR] 1.27, 95% CI 1.10-1.47, per decade), larger size (RR 1.65, 95% CI 1.38-2.01, per 10-mm increase) and detection of the aneurysm while the patient was in hospital or the emergency department (RR 1.34, 95% CI 1.00-1.79). Comorbidities were not associated with monitoring.
Interpretation: Radiographic monitoring of incidental AAAs was incomplete, and almost one-third of patients underwent no monitoring at all. Incomplete monitoring did not appear to be related to patients' comorbidity.
{"title":"Radiographic monitoring of incidental abdominal aortic aneurysms: a retrospective population-based cohort study.","authors":"Carl van Walraven, Jenna Wong, Kareem Morant, Alison Jennings, Peter C Austin, Prasad Jetty, Alan J Forster","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>An abdominal aortic aneurysm (AAA) that is identified when the abdomen is imaged for some other reason is known as an incidental AAA. No population-based studies have assessed the management of incidental AAAs. The objective of this study was to measure the completeness of radiographic monitoring of incidental AAAs by means of a population-based analysis.</p><p><strong>Methods: </strong>We linked a cohort of patients with incidental AAA (defined as a previously unidentified aortic enlargement exceeding 30 mm in diameter found in an imaging study performed for another reason) to various population-based databases. We followed the patients to elective repair or rupture of the aneurysm, death or 31 Mar. 2009. We used evidence-based monitoring guidelines to calculate the proportion of observation time during which each incidental AAA was incompletely monitored. We used negative binomial regression to determine the association of patient-related factors with this outcome.</p><p><strong>Results: </strong>For the period between January 1996 and September 2008, we identified 191 patients with incidental AAA (mean diameter 37.6 mm, 95% confidence interval [CI] 36.6-38.6 mm; median follow-up 4.4 [range 0.6-12.7] years). Fifty-six of these patients (29.3%) had no radiographic monitoring of the aneurysm. Overall, patients spent one-fifth of their time with incomplete monitoring of the AAA (median 19.4%, interquartile range 0.3%-44.0%). Factors independently associated with incomplete monitoring included older age (relative rate [change in proportion of time with incomplete monitoring] [RR] 1.27, 95% CI 1.10-1.47, per decade), larger size (RR 1.65, 95% CI 1.38-2.01, per 10-mm increase) and detection of the aneurysm while the patient was in hospital or the emergency department (RR 1.34, 95% CI 1.00-1.79). Comorbidities were not associated with monitoring.</p><p><strong>Interpretation: </strong>Radiographic monitoring of incidental AAAs was incomplete, and almost one-third of patients underwent no monitoring at all. Incomplete monitoring did not appear to be related to patients' comorbidity.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 2","pages":"e67-76"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ce/2f/OpenMed-05-e67.PMC3147999.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30139967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tara Gomes, David N Juurlink, Irfan A Dhalla, Angela Mailis-Gagnon, J Michael Paterson, Muhammad M Mamdani
Background: Opioid therapy for patients with chronic nonmalignant pain remains controversial, primarily because of safety concerns and the potential for abuse. The objective of this study was to examine trends in opioid utilization for nonmalignant pain among recipients of social assistance and to explore the relation between dose of analgesic and mortality.
Methods: Using a cross-sectional study design, we characterized annual trends in prescriptions for and daily dose of opioid analgesics between 2003 and 2008 for beneficiaries (aged 15 to 64 years) of Ontario's public drug plan. We defined moderate, high and very high dose thresholds as daily doses of up to 200, 201 to 400, and more than 400 mg oral morphine (or equivalent), respectively. In an exploratory cohort study, we followed, over a 2-year period, patients who received at least one prescription for an opioid in 2004 to investigate the relation between opioid dose and opioid-related mortality.
Results: Over the study period, opioid prescribing rates rose by 16.2%, and 180 974 individuals received nearly 1.5 million opioid prescriptions in 2008. Also by 2008, the daily dose dispensed exceeded 200 mg morphine equivalent for almost a third (32.6%) of recipients of long-acting oxycodone but only 20.3% of those treated with fentanyl or other long-acting opioids. Among patients for whom high or very high doses of opioids were dispensed in 2004, 19.3% of deaths during the subsequent 2 years were opioid-related, occurring at a median age of 46 years. Two-year opioid-related mortality rates were 1.63 per 1000 population (95% confidence interval [CI] 1.42-1.85) among people with moderate-dose prescriptions, 7.92 per 1000 population (95% CI 5.25-11.49) among those with high-dose prescriptions, and 9.94 per 1000 population (95% CI 2.78-25.12) among those with very-high-dose prescriptions.
Interpretation: Among socio-economically disadvantaged patients in Ontario, the use and dose of opioids for nonmalignant pain has increased substantially, driven primarily by the use of long-acting oxycodone and, to a lesser extent, fentanyl. The findings of our exploratory study suggested a strong association between opioid-related mortality and the dose of opioid dispensed.
背景:阿片类药物治疗慢性非恶性疼痛患者仍然存在争议,主要是因为安全性问题和滥用的可能性。本研究的目的是研究阿片类药物在社会救助接受者中用于治疗非恶性疼痛的趋势,并探讨止痛药剂量与死亡率之间的关系。方法:采用横断面研究设计,我们描述了2003年至2008年安大略省公共药物计划受益人(15至64岁)阿片类镇痛药处方和日剂量的年度趋势。我们将中度、高剂量和极高剂量阈值分别定义为每日口服吗啡剂量高达200mg、201至400mg和超过400mg(或同等剂量)。在一项探索性队列研究中,我们对2004年至少接受过一次阿片类药物处方的患者进行了为期2年的随访,以调查阿片类药物剂量与阿片类药物相关死亡率之间的关系。结果:在研究期间,阿片类药物处方率上升了16.2%,2008年有180974人获得了近150万张阿片类药物处方。同样,到2008年,近三分之一(32.6%)长效羟考酮接受者的日剂量超过200毫克吗啡当量,而芬太尼或其他长效阿片类药物接受者的日剂量仅为20.3%。在2004年使用高剂量或非常高剂量阿片类药物的患者中,在随后的2年中,19.3%的死亡与阿片类药物有关,发生的中位年龄为46岁。在中等剂量处方人群中,两年阿片类药物相关死亡率为1.63 / 1000(95%可信区间[CI] 1.42-1.85),在高剂量处方人群中为7.92 / 1000 (95% CI 5.25-11.49),在高剂量处方人群中为9.94 / 1000 (95% CI 2.78-25.12)。解释:在安大略省社会经济条件较差的患者中,阿片类药物治疗非恶性疼痛的使用和剂量大幅增加,主要是由于长效羟考酮的使用,芬太尼的使用程度较低。我们的探索性研究结果表明,阿片类药物相关死亡率与阿片类药物的剂量有很强的相关性。
{"title":"Trends in opioid use and dosing among socio-economically disadvantaged patients.","authors":"Tara Gomes, David N Juurlink, Irfan A Dhalla, Angela Mailis-Gagnon, J Michael Paterson, Muhammad M Mamdani","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Opioid therapy for patients with chronic nonmalignant pain remains controversial, primarily because of safety concerns and the potential for abuse. The objective of this study was to examine trends in opioid utilization for nonmalignant pain among recipients of social assistance and to explore the relation between dose of analgesic and mortality.</p><p><strong>Methods: </strong>Using a cross-sectional study design, we characterized annual trends in prescriptions for and daily dose of opioid analgesics between 2003 and 2008 for beneficiaries (aged 15 to 64 years) of Ontario's public drug plan. We defined moderate, high and very high dose thresholds as daily doses of up to 200, 201 to 400, and more than 400 mg oral morphine (or equivalent), respectively. In an exploratory cohort study, we followed, over a 2-year period, patients who received at least one prescription for an opioid in 2004 to investigate the relation between opioid dose and opioid-related mortality.</p><p><strong>Results: </strong>Over the study period, opioid prescribing rates rose by 16.2%, and 180 974 individuals received nearly 1.5 million opioid prescriptions in 2008. Also by 2008, the daily dose dispensed exceeded 200 mg morphine equivalent for almost a third (32.6%) of recipients of long-acting oxycodone but only 20.3% of those treated with fentanyl or other long-acting opioids. Among patients for whom high or very high doses of opioids were dispensed in 2004, 19.3% of deaths during the subsequent 2 years were opioid-related, occurring at a median age of 46 years. Two-year opioid-related mortality rates were 1.63 per 1000 population (95% confidence interval [CI] 1.42-1.85) among people with moderate-dose prescriptions, 7.92 per 1000 population (95% CI 5.25-11.49) among those with high-dose prescriptions, and 9.94 per 1000 population (95% CI 2.78-25.12) among those with very-high-dose prescriptions.</p><p><strong>Interpretation: </strong>Among socio-economically disadvantaged patients in Ontario, the use and dose of opioids for nonmalignant pain has increased substantially, driven primarily by the use of long-acting oxycodone and, to a lesser extent, fentanyl. The findings of our exploratory study suggested a strong association between opioid-related mortality and the dose of opioid dispensed.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"5 1","pages":"e13-22"},"PeriodicalIF":0.0,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ad/85/OpenMed-05-e13.PMC3205807.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40123027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"To test or not to test? Self-monitoring of blood glucose in patients with type 2 diabetes managed without insulin.","authors":"Sonia Butalia, Doreen M Rabi","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"4 2","pages":"e114-6"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c2/f4/OpenMed-04-e114.PMC3116684.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30248937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Keeping the GINA in the bottle: assessing the current need for genetic non-discrimination legislation in Canada.","authors":"Daryl Pullman, Trudo Lemmens","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"4 2","pages":"e95-7"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/17/f8/OpenMed-04-e95.PMC3116686.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30248940","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Extracts from the meeting of the Standing Committee on Health on the appointment of Dr. Prigent to the governing council of the Canadian Institutes of Health Research.","authors":"","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"4 1","pages":"e31-9"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/55/c3/OpenMed-04-e31.PMC3116677.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29947016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dean T Eurich, Sumit R Majumdar, Finlay A McAlister, Ross T Tsuyuki, Yutaka Yasui, Jeffrey A Johnson
Background: Composite outcomes that weight each component equally are commonly used to study treatment effects. We hypothesized that each component of a composite outcome would differentially affect patients' overall health-related quality of life (HRQL).
Methods: We tested our hypothesis using data from 2 published clinical studies of treatment for heart failure, one comparing metformin and sulfonylurea and the other comparing digoxin and placebo. We applied the quality-adjusted survival (QAS) approach, which incorporates HRQL data to accommodate differential weights for 2 components (in this analysis, death or admission to hospital) of a commonly used composite end point. For each of the 2 studies, the composite outcome was partitioned into its components, to which utility weights derived from the literature were assigned. Total QAS time determined for each treatment by the QAS analysis was compared with the results from traditional survival analyses based on Cox proportional hazards regression.
Results: In the observational study of metformin in heart failure, the risk of the composite outcome of death or admission to hospital was lower for those receiving metformin therapy than for those who received sulfonylurea (event rate 160 [77%] v. 658 [85%]; hazard ratio [HR] 0.83, 95% confidence interval [CI] 0.70-0.99). With traditional survival analysis, the net gain was 0.82 years (95% CI 0.26-1.37), whereas the difference in QAS time was less, at 0.54 years (95% CI 0.20-0.89). In the randomized trial of digoxin therapy, the risk of the composite outcome was lower for those receiving the intervention than for those receiving placebo (event rate 1291 [38%] v. 1041 [31%]; HR 0.75, 95% CI 0.69-0.82). With traditional survival analysis, the net gain was 0.06 years (95% CI 0.02-0.16), whereas the difference in QAS time was greater, at 0.11 years (95% CI 0.06-0.16).
Interpretation: Studies that assume equal weights for the components of composite outcomes may overestimate or underestimate treatment effects. By incorporating HRQL into survival analyses, the impact of the various components of the outcome can be assessed more directly.
背景:平均加权各成分的综合结局通常用于研究治疗效果。我们假设复合结局的每个组成部分会不同地影响患者的总体健康相关生活质量(HRQL)。方法:我们使用两项已发表的治疗心力衰竭的临床研究数据来检验我们的假设,一项比较二甲双胍和磺脲类药物,另一项比较地高辛和安慰剂。我们采用了质量调整生存(QAS)方法,该方法结合了HRQL数据,以适应常用复合终点的2个组成部分(在本分析中,死亡或住院)的差异权重。对于这两项研究中的每一项,将综合结果划分为其组成部分,并为其分配来自文献的效用权重。通过QAS分析确定的每个治疗的总QAS时间与基于Cox比例风险回归的传统生存分析结果进行比较。结果:在二甲双胍治疗心力衰竭的观察性研究中,接受二甲双胍治疗的患者死亡或住院的复合结局风险低于接受磺脲治疗的患者(事件率160[77%]比658 [85%];风险比[HR] 0.83, 95%可信区间[CI] 0.70-0.99)。在传统的生存分析中,净获益为0.82年(95% CI 0.26-1.37),而QAS时间的差异较小,为0.54年(95% CI 0.20-0.89)。在地高辛治疗的随机试验中,接受干预的患者发生复合结局的风险低于接受安慰剂的患者(事件率1291 [38%]vs 1041 [31%];Hr 0.75, 95% ci 0.69-0.82)。在传统的生存分析中,净增益为0.06年(95% CI 0.02-0.16),而QAS时间的差异更大,为0.11年(95% CI 0.06-0.16)。解释:假设复合结果各组成部分权重相等的研究可能高估或低估了治疗效果。通过将HRQL纳入生存分析,可以更直接地评估结果的各个组成部分的影响。
{"title":"Analyzing composite outcomes in cardiovascular studies: traditional Cox proportional hazards versus quality-of-life-adjusted survival approaches.","authors":"Dean T Eurich, Sumit R Majumdar, Finlay A McAlister, Ross T Tsuyuki, Yutaka Yasui, Jeffrey A Johnson","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Composite outcomes that weight each component equally are commonly used to study treatment effects. We hypothesized that each component of a composite outcome would differentially affect patients' overall health-related quality of life (HRQL).</p><p><strong>Methods: </strong>We tested our hypothesis using data from 2 published clinical studies of treatment for heart failure, one comparing metformin and sulfonylurea and the other comparing digoxin and placebo. We applied the quality-adjusted survival (QAS) approach, which incorporates HRQL data to accommodate differential weights for 2 components (in this analysis, death or admission to hospital) of a commonly used composite end point. For each of the 2 studies, the composite outcome was partitioned into its components, to which utility weights derived from the literature were assigned. Total QAS time determined for each treatment by the QAS analysis was compared with the results from traditional survival analyses based on Cox proportional hazards regression.</p><p><strong>Results: </strong>In the observational study of metformin in heart failure, the risk of the composite outcome of death or admission to hospital was lower for those receiving metformin therapy than for those who received sulfonylurea (event rate 160 [77%] v. 658 [85%]; hazard ratio [HR] 0.83, 95% confidence interval [CI] 0.70-0.99). With traditional survival analysis, the net gain was 0.82 years (95% CI 0.26-1.37), whereas the difference in QAS time was less, at 0.54 years (95% CI 0.20-0.89). In the randomized trial of digoxin therapy, the risk of the composite outcome was lower for those receiving the intervention than for those receiving placebo (event rate 1291 [38%] v. 1041 [31%]; HR 0.75, 95% CI 0.69-0.82). With traditional survival analysis, the net gain was 0.06 years (95% CI 0.02-0.16), whereas the difference in QAS time was greater, at 0.11 years (95% CI 0.06-0.16).</p><p><strong>Interpretation: </strong>Studies that assume equal weights for the components of composite outcomes may overestimate or underestimate treatment effects. By incorporating HRQL into survival analyses, the impact of the various components of the outcome can be assessed more directly.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"4 1","pages":"e40-8"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b7/da/OpenMed-04-e40.PMC3116673.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29947017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}