Background: Death or urgent readmission after hospital discharge is a common adverse event that can be used to compare outcomes of care between institutions. To accurately adjust for risk and to allow for interhospital comparisons of readmission rates, we used administrative data to derive and internally validate an extension of the LACE index, a previously validated index for 30-day death or urgent readmission.
Methods: We randomly selected 500 000 medical and surgical patients discharged to the community from any Ontario hospital between 1 April 2003 and 31 March 2009. We derived a logistic regression model on 250 000 randomly selected patients from this group and modified the final model into an index scoring system, the LACE+ index. We internally validated the LACE+ index using data from the remaining 250 000 patients and compared its performance with that of the original LACE index.
Results: Within 30 days of discharge to the community, 33 825 (6.8%) of the patients had died or had been urgently readmitted. In addition to the variables included in the LACE index (length of stay in hospital [L], acuity of admission [A], comorbidity [C] and emergency department utilization in the 6 months before admission [E]), the LACE+ index incorporated patient age and sex, teaching status of the discharge hospital, acute diagnoses and procedures performed during the index admission, number of days on alternative level of care during the index admission, and number of elective and urgent admissions to hospital in the year before the index admission. The LACE+ index was highly discriminative (C statistic 0.771, 95% confidence interval 0.767-0.775), was well calibrated across most of its range of scores and had a model performance that exceeded that of the LACE index.
Interpretation: The LACE+ index can be used to predict the risk of postdischarge death or urgent readmission on the basis of administrative data for the Ontario population. Its performance exceeds that of the LACE index, and it allows analysts to accurately estimate the risk of important postdischarge outcomes.
{"title":"LACE+ index: extension of a validated index to predict early death or urgent readmission after hospital discharge using administrative data.","authors":"Carl van Walraven, Jenna Wong, Alan J Forster","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Death or urgent readmission after hospital discharge is a common adverse event that can be used to compare outcomes of care between institutions. To accurately adjust for risk and to allow for interhospital comparisons of readmission rates, we used administrative data to derive and internally validate an extension of the LACE index, a previously validated index for 30-day death or urgent readmission.</p><p><strong>Methods: </strong>We randomly selected 500 000 medical and surgical patients discharged to the community from any Ontario hospital between 1 April 2003 and 31 March 2009. We derived a logistic regression model on 250 000 randomly selected patients from this group and modified the final model into an index scoring system, the LACE+ index. We internally validated the LACE+ index using data from the remaining 250 000 patients and compared its performance with that of the original LACE index.</p><p><strong>Results: </strong>Within 30 days of discharge to the community, 33 825 (6.8%) of the patients had died or had been urgently readmitted. In addition to the variables included in the LACE index (length of stay in hospital [L], acuity of admission [A], comorbidity [C] and emergency department utilization in the 6 months before admission [E]), the LACE+ index incorporated patient age and sex, teaching status of the discharge hospital, acute diagnoses and procedures performed during the index admission, number of days on alternative level of care during the index admission, and number of elective and urgent admissions to hospital in the year before the index admission. The LACE+ index was highly discriminative (C statistic 0.771, 95% confidence interval 0.767-0.775), was well calibrated across most of its range of scores and had a model performance that exceeded that of the LACE index.</p><p><strong>Interpretation: </strong>The LACE+ index can be used to predict the risk of postdischarge death or urgent readmission on the basis of administrative data for the Ontario population. Its performance exceeds that of the LACE index, and it allows analysts to accurately estimate the risk of important postdischarge outcomes.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 3","pages":"e80-90"},"PeriodicalIF":0.0,"publicationDate":"2012-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/77/28/OpenMed-06-e80.PMC3659212.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31449878","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: Between 5% and 10% of patients die or are urgently readmitted within 30 days of discharge from hospital. Readmission risk indexes have either excluded acute diagnoses or modelled them as multiple distinct variables. In this study, we derived and validated a score summarizing the influence of acute hospital diagnoses and procedures on death or urgent readmission within 30 days.
Methods: From population-based hospital abstracts in Ontario, we randomly sampled 200 000 discharges between April 2003 and March 2009 and determined who had been readmitted urgently or died within 30 days of discharge. We used generalized estimating equation modelling, with a sample of 100 000 patients, to measure the adjusted association of various case-mix groups (CMGs-homogenous groups of acute care inpatients with similar clinical and resource-utilization characteristics) with 30-day death or urgent readmission. This final model was transformed into a scoring system that was validated in the remaining 100 000 patients.
Results: Patients in the derivation set belonged to 1 of 506 CMGs and had a 6.8% risk of 30-day death or urgent readmission. Forty-seven CMG codes (more than half of which were directly related to chronic diseases) were independently associated with this outcome, which led to a CMG score that ranged from -6 to 7 points. The CMG score was significantly associated with 30-day death or urgent readmission (unadjusted odds ratio for a 1-point increase in CMG score 1.52, 95% confidence interval [CI] 1.49-1.56). Alone, the CMG score was only moderately discriminative (C statistic 0.650, 95% CI 0.644-0.656). However, when the CMG score was added to a validated risk index for death or readmission, the C statistic increased to 0.759 (95% CI 0.753-0.765). The CMG score was well calibrated for 30-day death or readmission.
Interpretation: In this study, we developed a scoring system for acute hospital diagnoses and procedures that could be used as part of a risk-adjustment methodology for analyses of postdischarge outcomes.
背景:5%至10%的患者在出院后30天内死亡或紧急再次入院。再入院风险指数要么排除急性诊断,要么将其建模为多个不同的变量。在这项研究中,我们推导并验证了一个评分,总结了急性医院诊断和程序对30天内死亡或紧急再入院的影响。方法:从安大略省以人口为基础的医院摘要中,我们随机抽取2003年4月至2009年3月期间的20万例出院患者,并确定出院后30天内紧急再入院或死亡的患者。我们使用广义估计方程模型,以10万例患者为样本,测量各种病例组合组(具有相似临床和资源利用特征的急性护理住院患者的cmgs -同质组)与30天死亡或紧急再入院的调整相关性。这个最终的模型被转化为一个评分系统,在剩下的10万名患者中得到验证。结果:衍生组患者属于506例cmg中的1例,30天死亡或紧急再入院的风险为6.8%。47种CMG编码(其中一半以上与慢性疾病直接相关)与该结果独立相关,这导致CMG评分范围为-6至7分。CMG评分与30天死亡或紧急再入院显著相关(CMG评分增加1分的未调整优势比为1.52,95%可信区间[CI] 1.49-1.56)。单独来看,CMG评分仅具有中度判别性(C统计量0.650,95% CI 0.644-0.656)。然而,当将CMG评分与死亡或再入院的有效风险指数相加时,C统计量增加到0.759 (95% CI 0.753-0.765)。CMG评分被很好地校准为30天死亡或再入院。解释:在这项研究中,我们开发了一个急性医院诊断和程序评分系统,可作为风险调整方法的一部分,用于分析出院后的结果。
{"title":"Derivation and validation of a diagnostic score based on case-mix groups to predict 30-day death or urgent readmission.","authors":"Carl van Walraven, Jenna Wong, Alan J Forster","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Between 5% and 10% of patients die or are urgently readmitted within 30 days of discharge from hospital. Readmission risk indexes have either excluded acute diagnoses or modelled them as multiple distinct variables. In this study, we derived and validated a score summarizing the influence of acute hospital diagnoses and procedures on death or urgent readmission within 30 days.</p><p><strong>Methods: </strong>From population-based hospital abstracts in Ontario, we randomly sampled 200 000 discharges between April 2003 and March 2009 and determined who had been readmitted urgently or died within 30 days of discharge. We used generalized estimating equation modelling, with a sample of 100 000 patients, to measure the adjusted association of various case-mix groups (CMGs-homogenous groups of acute care inpatients with similar clinical and resource-utilization characteristics) with 30-day death or urgent readmission. This final model was transformed into a scoring system that was validated in the remaining 100 000 patients.</p><p><strong>Results: </strong>Patients in the derivation set belonged to 1 of 506 CMGs and had a 6.8% risk of 30-day death or urgent readmission. Forty-seven CMG codes (more than half of which were directly related to chronic diseases) were independently associated with this outcome, which led to a CMG score that ranged from -6 to 7 points. The CMG score was significantly associated with 30-day death or urgent readmission (unadjusted odds ratio for a 1-point increase in CMG score 1.52, 95% confidence interval [CI] 1.49-1.56). Alone, the CMG score was only moderately discriminative (C statistic 0.650, 95% CI 0.644-0.656). However, when the CMG score was added to a validated risk index for death or readmission, the C statistic increased to 0.759 (95% CI 0.753-0.765). The CMG score was well calibrated for 30-day death or readmission.</p><p><strong>Interpretation: </strong>In this study, we developed a scoring system for acute hospital diagnoses and procedures that could be used as part of a risk-adjustment methodology for analyses of postdischarge outcomes.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 3","pages":"e90-e100"},"PeriodicalIF":0.0,"publicationDate":"2012-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e3/4f/OpenMed-06-e90.PMC3654506.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31534190","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}
In Canada, we place significant cultural and financial value on our healthcare system. As such, it is imperative we measure its quality. In this commentary, we highlight some of the potential benefits and harms associated with measuring quality using currently available indicators, such as hospital mortality rates, emergency department length of stays, and readmission rates. These measures tend to focus on provider and process issues rather than patient outcomes and also reflect what we can measure rather than what we should measure. We argue that the current approaches are inadequate and recommend a better understanding of the limitations of current indicators and more provider engagement. To meet these recommendations the health system needs to increased investment in performance measurement systems.
{"title":"The use of quality indicators to promote accountability in health care: the good, the bad, and the ugly.","authors":"Alan J Forster, Carl van Walraven","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In Canada, we place significant cultural and financial value on our healthcare system. As such, it is imperative we measure its quality. In this commentary, we highlight some of the potential benefits and harms associated with measuring quality using currently available indicators, such as hospital mortality rates, emergency department length of stays, and readmission rates. These measures tend to focus on provider and process issues rather than patient outcomes and also reflect what we can measure rather than what we should measure. We argue that the current approaches are inadequate and recommend a better understanding of the limitations of current indicators and more provider engagement. To meet these recommendations the health system needs to increased investment in performance measurement systems.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 2","pages":"e75-9"},"PeriodicalIF":0.0,"publicationDate":"2012-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/65/51/OpenMed-06-e75.PMC3659217.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31449877","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}
Brendan McIntosh, Chris Cameron, Sumeet R Singh, Changhua Yu, Lisa Dolovich, Robyn Houlden
Background: Metformin and a sulphonylurea are often used in combination for the treatment of type 2 diabetes mellitus. We conducted a systematic review and meta-analysis to evaluate the comparative safety and efficacy of all available classes of antihyperglycemic therapies in patients with type 2 diabetes inadequately controlled with metformin and sulphonylurea combination therapy.
Methods: MEDLINE, MEDLINE In-Process & Other Non-Indexed Citations, EMBASE, BIOSIS Previews, PubMed and the Cochrane Central Register of Controlled Trials were searched for randomized controlled trials published in English from 1980 to November 2009. Additional citations were obtained from the grey literature and conference proceedings and through stakeholder feedback. Two reviewers independently selected the studies, extracted the data and assessed risk of bias. Key outcomes of interest were hemoglobin A1c, body weight, hypoglycemia, patients' satisfaction with treatment, quality of life, long-term diabetes-related complications, withdrawals due to adverse events, serious adverse events and mortality. Mixed-treatment comparison meta-analyses were conducted to calculate mean differences between drug classes for changes in hemoglobin A1c and body weight. When appropriate, pairwise meta-analyses were used to estimate differences for other outcomes.
Results: We identified 33 randomized controlled trials meeting the inclusion criteria. The methodologic quality of the studies was generally poor. Insulins (basal, biphasic, bolus), dipeptidyl peptidase-4 (DPP-4) inhibitors, glucagon-like peptide-1 (GLP-1) analogues and thiazolidinediones (TZDs) all produced statistically significant reductions in hemoglobin A1c in combination with metformin and a sulphonylurea (-0.89% to -1.17%), whereas meglitinides and alpha-glucosidase inhibitors did not. Biphasic insulin, bolus insulin, and TZDs were associated with weight gain (1.85-5.00 kg), whereas DPP-4 inhibitors and alpha-glucosidase inhibitors were weight-neutral, and GLP-1 analogues were associated with modest weight loss. Treatment regimens containing insulin were associated with increased hypoglycemia relative to comparators, but severe hypoglycemia was rare across all treatments.
Interpretation: Third-line agents for the treatment of type 2 diabetes are similar in terms of glycemic control but differ in their propensity to cause weight gain and hypoglycemia. Longer-term studies with larger sample sizes are required to determine if any of the drug classes are superior with regard to reducing diabetes-related complications.
背景:二甲双胍和磺脲经常联合用于治疗2型糖尿病。我们进行了一项系统综述和荟萃分析,以评估二甲双胍和磺脲联合治疗控制不足的2型糖尿病患者中所有可用类别的抗高血糖治疗的相对安全性和有效性。方法:检索1980年至2009年11月期间以英文发表的随机对照试验,检索MEDLINE、MEDLINE In-Process&Other Non-Redexed Citation、EMBASE、BIOSIS Previews、PubMed和Cochrane Central Register of Controlled Trials。从灰色文献和会议记录以及利益相关者的反馈中获得了额外的引文。两名评审员独立选择研究,提取数据并评估偏倚风险。感兴趣的主要结果是血红蛋白A1c、体重、低血糖、患者对治疗的满意度、生活质量、长期糖尿病相关并发症、因不良事件退出、严重不良事件和死亡率。进行混合治疗比较荟萃分析,以计算血红蛋白A1c和体重变化的药物类别之间的平均差异。在适当的情况下,使用成对荟萃分析来估计其他结果的差异。结果:我们确定了33项符合纳入标准的随机对照试验。研究的方法学质量普遍较差。胰岛素(基础、双相、推注)、二肽基肽酶-4(DPP-4)抑制剂、胰高血糖素样肽-1(GLP-1)类似物和噻唑烷二酮(TZDs)与二甲双胍和磺酰脲联合使用均能显著降低血红蛋白A1c(-0.89%至-1.17%),而甲肝苷类和α-葡萄糖苷酶抑制剂则没有。双相胰岛素、推注胰岛素和TZD与体重增加有关(1.85-5.00 kg),而DPP-4抑制剂和α-葡萄糖苷酶抑制剂是体重中性的,GLP-1类似物与适度的体重减轻有关。与对照组相比,含有胰岛素的治疗方案与低血糖症增加有关,但在所有治疗中,严重低血糖症都很罕见。解释:治疗2型糖尿病的三线药物在血糖控制方面相似,但在导致体重增加和低血糖的倾向上不同。需要进行更大样本量的长期研究,以确定是否有任何药物类别在减少糖尿病相关并发症方面更优越。
{"title":"Choice of therapy in patients with type 2 diabetes inadequately controlled with metformin and a sulphonylurea: a systematic review and mixed-treatment comparison meta-analysis.","authors":"Brendan McIntosh, Chris Cameron, Sumeet R Singh, Changhua Yu, Lisa Dolovich, Robyn Houlden","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Metformin and a sulphonylurea are often used in combination for the treatment of type 2 diabetes mellitus. We conducted a systematic review and meta-analysis to evaluate the comparative safety and efficacy of all available classes of antihyperglycemic therapies in patients with type 2 diabetes inadequately controlled with metformin and sulphonylurea combination therapy.</p><p><strong>Methods: </strong>MEDLINE, MEDLINE In-Process & Other Non-Indexed Citations, EMBASE, BIOSIS Previews, PubMed and the Cochrane Central Register of Controlled Trials were searched for randomized controlled trials published in English from 1980 to November 2009. Additional citations were obtained from the grey literature and conference proceedings and through stakeholder feedback. Two reviewers independently selected the studies, extracted the data and assessed risk of bias. Key outcomes of interest were hemoglobin A1c, body weight, hypoglycemia, patients' satisfaction with treatment, quality of life, long-term diabetes-related complications, withdrawals due to adverse events, serious adverse events and mortality. Mixed-treatment comparison meta-analyses were conducted to calculate mean differences between drug classes for changes in hemoglobin A1c and body weight. When appropriate, pairwise meta-analyses were used to estimate differences for other outcomes.</p><p><strong>Results: </strong>We identified 33 randomized controlled trials meeting the inclusion criteria. The methodologic quality of the studies was generally poor. Insulins (basal, biphasic, bolus), dipeptidyl peptidase-4 (DPP-4) inhibitors, glucagon-like peptide-1 (GLP-1) analogues and thiazolidinediones (TZDs) all produced statistically significant reductions in hemoglobin A1c in combination with metformin and a sulphonylurea (-0.89% to -1.17%), whereas meglitinides and alpha-glucosidase inhibitors did not. Biphasic insulin, bolus insulin, and TZDs were associated with weight gain (1.85-5.00 kg), whereas DPP-4 inhibitors and alpha-glucosidase inhibitors were weight-neutral, and GLP-1 analogues were associated with modest weight loss. Treatment regimens containing insulin were associated with increased hypoglycemia relative to comparators, but severe hypoglycemia was rare across all treatments.</p><p><strong>Interpretation: </strong>Third-line agents for the treatment of type 2 diabetes are similar in terms of glycemic control but differ in their propensity to cause weight gain and hypoglycemia. Longer-term studies with larger sample sizes are required to determine if any of the drug classes are superior with regard to reducing diabetes-related complications.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 2","pages":"e62-74"},"PeriodicalIF":0.0,"publicationDate":"2012-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cf/9b/OpenMed-06-e62.PMC3659216.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31449876","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}
Claire Kendall, Anita Palepu, Kapil Khatter, Sally Murray, John Willinsky, Lucy Turner, Anne Marie Todkill
{"title":"Open Medicine at five years.","authors":"Claire Kendall, Anita Palepu, Kapil Khatter, Sally Murray, John Willinsky, Lucy Turner, Anne Marie Todkill","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 2","pages":"e59-61"},"PeriodicalIF":0.0,"publicationDate":"2012-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/01/de/OpenMed-06-e59.PMC3659215.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31448828","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}
Paul E Ronksley, Claudia Sanmartin, Hude Quan, Pietro Ravani, Marcello Tonelli, Braden Manns, Brenda R Hemmelgarn
Background: Although effective treatments exist, many Canadians with chronic medical conditions do not receive the full care they require, possibly as a consequence of limited accessibility or availability. A commonly used indicator of inadequate access to or availability of care is the perception of unmet health care needs. The objective of this study was therefore to determine the association between chronic conditions and perceived unmet health care needs.
Methods: We extracted data for adult respondents from the combined 2001, 2003 and 2005 cross-sectional cycles of the Canadian Community Health Survey. Multivariate logistic regression was used to estimate the association between 7 high-prevalence and high-impact chronic conditions (arthritis, chronic obstructive pulmonary disease/emphysema, diabetes, heart disease, hypertension, mood disorder and stroke) and perceived unmet health care needs in the prior 12 months, adjusting for sociodemographic variables, health behaviours, health status and survey cycle.
Results: Of the 360 105 adult respondents, 12.2% reported an unmet health care need. Compared with those without chronic conditions, respondents with at least one condition were more likely to report an unmet need (adjusted odds ratio [OR] 1.51, 95% confidence interval [CI] 1.45-1.59). Those with mood disorders were almost twice as likely to report an unmet need (OR 1.94, 95% CI 1.78-2.12), while those with diabetes or hypertension were less likely to report an unmet need (diabetes OR 0.85, 95% CI 0.76-0.94; hypertension OR 0.96, 95% CI 0.89-1.04). Furthermore, the likelihood of an unmet need increased with the number of chronic conditions (OR 1.71, 95% CI 1.56-1.88 for 3 or more conditions). Respondents with chronic conditions were more likely than those without to report an unmet need related to resource availability (OR 1.14, 95% CI 1.06-1.22).
Interpretation: Adults with chronic medical conditions are more likely to report an unmet health care need, and the likelihood increases with an increasing number of conditions. Whether these unmet needs are associated with worse outcomes, and whether interventions targeted to address these needs may improve outcomes for Canadians with chronic disease, remain to be determined.
背景:虽然存在有效的治疗方法,但许多患有慢性疾病的加拿大人没有得到他们所需的充分护理,可能是由于可获得性或可获得性有限。获得或提供保健服务不足的一个常用指标是认为保健需求未得到满足。因此,本研究的目的是确定慢性病与未满足的卫生保健需求之间的关系。方法:我们从2001年、2003年和2005年加拿大社区健康调查的综合横截面周期中提取了成年受访者的数据。采用多变量logistic回归来估计7种高患病率和高影响慢性病(关节炎、慢性阻塞性肺疾病/肺气肿、糖尿病、心脏病、高血压、情绪障碍和中风)与感知到的未满足的医疗保健需求在过去12个月内的相关性,调整了社会人口统计学变量、健康行为、健康状况和调查周期。结果:在360105名成人受访者中,12.2%的人报告有未满足的卫生保健需求。与那些没有慢性疾病的人相比,至少有一种疾病的受访者更有可能报告未满足的需求(调整优势比[OR] 1.51, 95%置信区间[CI] 1.45-1.59)。情绪障碍患者报告未满足需求的可能性几乎是其两倍(OR 1.94, 95% CI 1.78-2.12),而糖尿病或高血压患者报告未满足需求的可能性较小(糖尿病OR 0.85, 95% CI 0.76-0.94;OR 0.96, 95% CI 0.89-1.04)。此外,未满足需求的可能性随着慢性病数量的增加而增加(OR为1.71,3种或3种以上的95% CI为1.56-1.88)。患有慢性病的受访者比没有慢性病的受访者更有可能报告与资源可用性相关的未满足需求(OR 1.14, 95% CI 1.06-1.22)。解释:患有慢性疾病的成年人更有可能报告未满足的医疗保健需求,并且随着疾病数量的增加,这种可能性也会增加。这些未满足的需求是否与较差的结果有关,以及针对这些需求的干预措施是否可以改善加拿大慢性病患者的结果,仍有待确定。
{"title":"Association between chronic conditions and perceived unmet health care needs.","authors":"Paul E Ronksley, Claudia Sanmartin, Hude Quan, Pietro Ravani, Marcello Tonelli, Braden Manns, Brenda R Hemmelgarn","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Although effective treatments exist, many Canadians with chronic medical conditions do not receive the full care they require, possibly as a consequence of limited accessibility or availability. A commonly used indicator of inadequate access to or availability of care is the perception of unmet health care needs. The objective of this study was therefore to determine the association between chronic conditions and perceived unmet health care needs.</p><p><strong>Methods: </strong>We extracted data for adult respondents from the combined 2001, 2003 and 2005 cross-sectional cycles of the Canadian Community Health Survey. Multivariate logistic regression was used to estimate the association between 7 high-prevalence and high-impact chronic conditions (arthritis, chronic obstructive pulmonary disease/emphysema, diabetes, heart disease, hypertension, mood disorder and stroke) and perceived unmet health care needs in the prior 12 months, adjusting for sociodemographic variables, health behaviours, health status and survey cycle.</p><p><strong>Results: </strong>Of the 360 105 adult respondents, 12.2% reported an unmet health care need. Compared with those without chronic conditions, respondents with at least one condition were more likely to report an unmet need (adjusted odds ratio [OR] 1.51, 95% confidence interval [CI] 1.45-1.59). Those with mood disorders were almost twice as likely to report an unmet need (OR 1.94, 95% CI 1.78-2.12), while those with diabetes or hypertension were less likely to report an unmet need (diabetes OR 0.85, 95% CI 0.76-0.94; hypertension OR 0.96, 95% CI 0.89-1.04). Furthermore, the likelihood of an unmet need increased with the number of chronic conditions (OR 1.71, 95% CI 1.56-1.88 for 3 or more conditions). Respondents with chronic conditions were more likely than those without to report an unmet need related to resource availability (OR 1.14, 95% CI 1.06-1.22).</p><p><strong>Interpretation: </strong>Adults with chronic medical conditions are more likely to report an unmet health care need, and the likelihood increases with an increasing number of conditions. Whether these unmet needs are associated with worse outcomes, and whether interventions targeted to address these needs may improve outcomes for Canadians with chronic disease, remain to be determined.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 2","pages":"e48-58"},"PeriodicalIF":0.0,"publicationDate":"2012-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a2/97/OpenMed-06-e48.PMC3659214.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31448827","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: Little information has been published on opioid prescribing practices in the United States as a whole for any year since 2005, despite increased use and increased overdoses. The objective of this study was to describe trends in prescribing rates and prescription sizes for commonly used opioids over the past decade.
Methods: We used 2 data systems. Vector One: National (VONA; data obtained for the period 2000-2009) is a service that can estimate the number of prescriptions dispensed by retail pharmacies. The Automation of Reports and Consolidated Orders System (ARCOS; data obtained for the period 2000-2010) is a mandatory reporting system that allows the US Drug Enforcement Administration to monitor certain controlled substances from the point of manufacture to the point of sale. ARCOS data represent the amount of controlled substances legitimately distributed at the retail level. We calculated crude prescription rates of various opioids from VONA data, total drug amounts distributed (as milligrams per 100 persons) from ARCOS data and morphine milligram equivalents (MME) per prescription by combining data from these 2 sources.
Results: The number of opioid prescriptions per 100 persons increased by 35.2%, from 61.9 to 83.7, during the period 2000-2009. The distribution of opioids to US pharmacies, in milligrams per 100 persons, increased by at least 100% for all selected opioids during the period 2000-2010. The average size of an oxycodone prescription increased by 69.7% (from 923 MME to 1566 MME) during the same period, while the average size of a hydrocodone prescription increased by 69.4% (from 170 MME to 288 MME). The increase for fentanyl was smaller (20.9%) (from 4804 MME to 5809 MME).
Interpretation: The rate of opioid prescribing, the amount of opioids distributed and the average prescription size all increased markedly in the United States over the past decade. Rates of death from opioid overdose also have increased steadily through 2008 and have likely continued to increase in subsequent years. Effective measures to prevent prescription drug overdoses have yet to be identified and employed.
{"title":"Trends in prescriptions for oxycodone and other commonly used opioids in the United States, 2000-2010.","authors":"Kristen Kenan, Karin Mack, Leonard Paulozzi","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Little information has been published on opioid prescribing practices in the United States as a whole for any year since 2005, despite increased use and increased overdoses. The objective of this study was to describe trends in prescribing rates and prescription sizes for commonly used opioids over the past decade.</p><p><strong>Methods: </strong>We used 2 data systems. Vector One: National (VONA; data obtained for the period 2000-2009) is a service that can estimate the number of prescriptions dispensed by retail pharmacies. The Automation of Reports and Consolidated Orders System (ARCOS; data obtained for the period 2000-2010) is a mandatory reporting system that allows the US Drug Enforcement Administration to monitor certain controlled substances from the point of manufacture to the point of sale. ARCOS data represent the amount of controlled substances legitimately distributed at the retail level. We calculated crude prescription rates of various opioids from VONA data, total drug amounts distributed (as milligrams per 100 persons) from ARCOS data and morphine milligram equivalents (MME) per prescription by combining data from these 2 sources.</p><p><strong>Results: </strong>The number of opioid prescriptions per 100 persons increased by 35.2%, from 61.9 to 83.7, during the period 2000-2009. The distribution of opioids to US pharmacies, in milligrams per 100 persons, increased by at least 100% for all selected opioids during the period 2000-2010. The average size of an oxycodone prescription increased by 69.7% (from 923 MME to 1566 MME) during the same period, while the average size of a hydrocodone prescription increased by 69.4% (from 170 MME to 288 MME). The increase for fentanyl was smaller (20.9%) (from 4804 MME to 5809 MME).</p><p><strong>Interpretation: </strong>The rate of opioid prescribing, the amount of opioids distributed and the average prescription size all increased markedly in the United States over the past decade. Rates of death from opioid overdose also have increased steadily through 2008 and have likely continued to increase in subsequent years. Effective measures to prevent prescription drug overdoses have yet to be identified and employed.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 2","pages":"e41-7"},"PeriodicalIF":0.0,"publicationDate":"2012-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/50/a3/OpenMed-06-e41.PMC3659213.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31448826","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: Although specialist physicians comprise nearly half of the physician workforce in Newfoundland and Labrador (NL), relatively little is known about their retention patterns. We compared 2 cohorts of physicians who were initially licensed to practise in NL between 1993 and 1997 and between 2000 and 2004, to examine whether retention had changed over time. Additionally, we examined the retention of 4 groups of physicians in each cohort: (1) fully licensed medical graduates of Memorial University, (2) fully licensed medical graduates of other Canadian universities, (3) provisionally licensed international medical graduates (IMGs) and (4) fully licensed IMGs. Provisional licences allow physicians who have not received Canadian certification to practise while obtaining credentials. We hypothesized that fully licensed physicians (largely physicians who are locally trained) would remain in NL longer than provisionally licensed physicians (largely IMGs).
Methods: Using data from the provincial medical registrar and Memorial University's office of postgraduate medical education, we used survival analysis (Cox regression) to compare the retention of the 2 cohorts and the 4 groups of physicians within each cohort.
Results: After 48 months, roughly 60% of the physicians in the 2000-04 cohort and 45% of the physicians in the 1993-97 cohort remained in NL. Medical graduates of Memorial University comprised 61/180 (33.9%) of the 2000-04 cohort and 38/211 (18.0%) of the 1993-97 cohort.Physicians in the 2000-04 cohort were 1.6 (95% confidence interval [CI] 1.23-2.08) times less likely to leave NL than physicians in the 1993-97 cohort. In the 2000-04 cohort, medical graduates of Canadian universities, provisionally licensed IMGs and fully licensed IMGs were 3.19 (95% CI 1.47-6.89), 1.85 (95% CI 1.09-3.17) and 4.39 (95% CI 1.91-10.10) times more likely to leave NL than medical graduates of Memorial University. In the 1993-97 cohort, IMGs with provisional licences were 2.16 (95% CI 1.37-3.42) times more likely to leave NL than medical graduates of Memorial University. There was no significant difference in retention between medical graduates of Memorial University and other Canadian universities or IMGs with full licences in the 1993-97 cohort.
Interpretation: The improvement in the retention of specialist physicians in NL since the 1990s may be attributable to the increase in the relative proportion of medical graduates of Memorial University. Although provisional licensing enables IMGs to begin practice in NL, it does not lead to long-term retention.
背景:虽然在纽芬兰和拉布拉多(NL),专科医生占医生劳动力的近一半,但对他们的保留模式知之甚少。我们比较了1993年至1997年和2000年至2004年期间最初在NL执业的两组医生,以检查保留是否随着时间的推移而改变。此外,我们在每个队列中检查了四组医生的保留情况:(1)纪念大学的完全许可医学毕业生,(2)加拿大其他大学的完全许可医学毕业生,(3)临时许可的国际医学毕业生(IMGs)和(4)完全许可的IMGs。临时执照允许没有获得加拿大认证的医生在获得证书的同时执业。我们假设完全许可的医生(主要是在当地接受培训的医生)会比临时许可的医生(主要是img)留在NL的时间更长。方法:使用省医疗注册局和纪念大学研究生医学教育办公室的数据,采用生存分析(Cox回归)比较两个队列和每个队列内4组医生的保留情况。结果:48个月后,2000-04队列中大约60%的医生和1993-97队列中45%的医生仍然留在NL。纪念大学的医科毕业生占2000-04年度毕业生总数的61/180(33.9%)和1993-97年度毕业生总数的38/211(18.0%)。2000- 2004年队列中的医生离开NL的可能性比1993- 1997年队列中的医生低1.6倍(95%可信区间[CI] 1.23-2.08)。在2000- 2004年的队列中,加拿大大学的医学毕业生、临时许可的img和完全许可的img离开NL的可能性是纪念大学医学毕业生的3.19 (95% CI 1.47-6.89)、1.85 (95% CI 1.09-3.17)和4.39 (95% CI 1.91-10.10)倍。在1993- 1997年的队列中,持有临时执照的img离开NL的可能性是纪念大学医学院毕业生的2.16倍(95% CI 1.37-3.42)。在1993- 1997年的队列中,纪念大学的医学毕业生与其他加拿大大学或持有正式执照的img的医学毕业生在留任方面没有显著差异。解释:自20世纪90年代以来,NL专科医生保留率的提高可能归因于纪念大学医学毕业生的相对比例的增加。虽然临时许可证使img能够在NL开始实践,但它不会导致长期保留。
{"title":"Retention of specialist physicians in Newfoundland and Labrador.","authors":"Patrick Fleming, Maria Mathews","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Although specialist physicians comprise nearly half of the physician workforce in Newfoundland and Labrador (NL), relatively little is known about their retention patterns. We compared 2 cohorts of physicians who were initially licensed to practise in NL between 1993 and 1997 and between 2000 and 2004, to examine whether retention had changed over time. Additionally, we examined the retention of 4 groups of physicians in each cohort: (1) fully licensed medical graduates of Memorial University, (2) fully licensed medical graduates of other Canadian universities, (3) provisionally licensed international medical graduates (IMGs) and (4) fully licensed IMGs. Provisional licences allow physicians who have not received Canadian certification to practise while obtaining credentials. We hypothesized that fully licensed physicians (largely physicians who are locally trained) would remain in NL longer than provisionally licensed physicians (largely IMGs).</p><p><strong>Methods: </strong>Using data from the provincial medical registrar and Memorial University's office of postgraduate medical education, we used survival analysis (Cox regression) to compare the retention of the 2 cohorts and the 4 groups of physicians within each cohort.</p><p><strong>Results: </strong>After 48 months, roughly 60% of the physicians in the 2000-04 cohort and 45% of the physicians in the 1993-97 cohort remained in NL. Medical graduates of Memorial University comprised 61/180 (33.9%) of the 2000-04 cohort and 38/211 (18.0%) of the 1993-97 cohort.Physicians in the 2000-04 cohort were 1.6 (95% confidence interval [CI] 1.23-2.08) times less likely to leave NL than physicians in the 1993-97 cohort. In the 2000-04 cohort, medical graduates of Canadian universities, provisionally licensed IMGs and fully licensed IMGs were 3.19 (95% CI 1.47-6.89), 1.85 (95% CI 1.09-3.17) and 4.39 (95% CI 1.91-10.10) times more likely to leave NL than medical graduates of Memorial University. In the 1993-97 cohort, IMGs with provisional licences were 2.16 (95% CI 1.37-3.42) times more likely to leave NL than medical graduates of Memorial University. There was no significant difference in retention between medical graduates of Memorial University and other Canadian universities or IMGs with full licences in the 1993-97 cohort.</p><p><strong>Interpretation: </strong>The improvement in the retention of specialist physicians in NL since the 1990s may be attributable to the increase in the relative proportion of medical graduates of Memorial University. Although provisional licensing enables IMGs to begin practice in NL, it does not lead to long-term retention.</p>","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 1","pages":"e1-9"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/da/4a/OpenMed-06-e1.PMC3329069.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30603139","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}
Kristin J Konnyu, Edmund Kwok, Becky Skidmore, David Moher
{"title":"The effectiveness and safety of emergency department short stay units: a rapid review.","authors":"Kristin J Konnyu, Edmund Kwok, Becky Skidmore, David Moher","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 1","pages":"e10-6"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8d/9b/OpenMed-06-e10.PMC3329070.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30603140","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":"Reviewing the medical literature: five notable articles in general internal medicine from 2010 and 2011.","authors":"Alexander A Leung, Carl van Walraven","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":88624,"journal":{"name":"Open medicine : a peer-reviewed, independent, open-access journal","volume":"6 1","pages":"e17-23"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e5/87/OpenMed-06-e17.PMC3330744.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30643443","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}