Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.008
Richard M. Schulz PhD , Candace Porter MS , Marcia Lane MPH , Carol Cornman RN, PA , Len Branham PhD
Background
Community-dwelling frail elderly have an increased need for effective medication management to reside in their homes and delay or avoid admission to nursing homes.
Objective
The objective of this study was to examine the impact of a medication management system on nursing home admission within the community-dwelling frail elderly.
Methods
This prospective cohort study compared nursing home admission rates in intervention and control clients of a state Medicaid home and community-based waiver program. Groups were matched on age (±5 years), race, gender, and waiver program start date (±120 days). The medication management service consisted of 2 parts: 1) prescription medicines dispensed from the client's local pharmacy in a calendar card, and 2) a coordinating service by a health educator to address medication-related problems as they arose. The primary dependent variable was admission to a nursing home.
Results
A total of 273 clients agreed to participate, enrolled, and had at least 1 prescription dispensed. The matched control group was composed of 800 other clients. The client sample was 72 years of age, 73% (785/1073) non-white, 75% (804/1073) female, and enrolled in the waiver program approximately 50 months. The 2 groups were similar on all demographic variables examined. Six clients (2.2%) in the intervention group and 40 clients (5.0%) in the control group were admitted to a nursing home at least once during the study period. Logistic regression was used to test the model predicting at least 1 nursing home admission. Control group clients were 2.94 times more likely to be admitted to a nursing home than clients in the intervention group.
Conclusions
The medication management service implemented within this study was effective in reducing nursing home admissions in a group of frail community-dwelling elderly.
{"title":"Impact of a Medication Management System on Nursing Home Admission Rate in a Community-Dwelling Nursing Home–Eligible Medicaid Population","authors":"Richard M. Schulz PhD , Candace Porter MS , Marcia Lane MPH , Carol Cornman RN, PA , Len Branham PhD","doi":"10.1016/j.amjopharm.2011.02.008","DOIUrl":"10.1016/j.amjopharm.2011.02.008","url":null,"abstract":"<div><h3>Background</h3><p>Community-dwelling frail elderly have an increased need for effective medication management to reside in their homes and delay or avoid admission to nursing homes.</p></div><div><h3>Objective</h3><p>The objective of this study was to examine the impact of a medication management system on nursing home admission within the community-dwelling frail elderly.</p></div><div><h3>Methods</h3><p>This prospective cohort study compared nursing home admission rates in intervention and control clients of a state Medicaid home and community-based waiver program. Groups were matched on age (±5 years), race, gender, and waiver program start date (±120 days). The medication management service consisted of 2 parts: 1) prescription medicines dispensed from the client's local pharmacy in a calendar card, and 2) a coordinating service by a health educator to address medication-related problems as they arose. The primary dependent variable was admission to a nursing home.</p></div><div><h3>Results</h3><p>A total of 273 clients agreed to participate, enrolled, and had at least 1 prescription dispensed. The matched control group was composed of 800 other clients. The client sample was 72 years of age, 73% (785/1073) non-white, 75% (804/1073) female, and enrolled in the waiver program approximately 50 months. The 2 groups were similar on all demographic variables examined. Six clients (2.2%) in the intervention group and 40 clients (5.0%) in the control group were admitted to a nursing home at least once during the study period. Logistic regression was used to test the model predicting at least 1 nursing home admission. Control group clients were 2.94 times more likely to be admitted to a nursing home than clients in the intervention group.</p></div><div><h3>Conclusions</h3><p>The medication management service implemented within this study was effective in reducing nursing home admissions in a group of frail community-dwelling elderly.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 69-79"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.005
Daryl S. Schiller PharmD , Ashish Parikh MD
Background
Prostatitis is a collection of signs and symptoms that occur as a result of inflammation or swelling of the prostate gland. There are many different causes for prostatitis, including infection; occasionally no clear etiology for the inflammation is found. Effective treatment often depends on identification of the cause, but a microbiologic organism is not always detectable, especially in cases of chronic prostatitis.
Objective
The aim of this article was to review identification and treatment options for prostatitis, including pharmacologic and nonpharmacologic interventions.
Methods
Relevant information was identified through a search of MEDLINE (1966–June 2010), International Pharmaceutical Abstracts (1970–June 2010), and EMBASE (1947–June 2010). Randomized, controlled trials that examined prostate cancer, benign prostatic hypertrophy, or procedures related to the prostate (ie, biopsies) were excluded.
Results
A working classification system for prostatitis was developed in 1999, but there are few randomized controlled trials that distinguish between the various treatment options. Bacterial prostatitis can be acute or chronic but always requires some degree of antimicrobial therapy. Pharmacologic features of fluoroquinolones make them the preferred agents for most patients. These antibiotics can become trapped in a chronically inflamed prostate due to pH differences between prostatic tissue and serum. Many fluoroquinolones have penetration ratios (prostate level:serum level) of up to 4:1. A study in European men (N = 117) who received levofloxacin 500 mg/d with a diagnosis of chronic bacterial prostatitis demonstrated clinical success rates of 92% (95% CI 84.8%–96.5%), 77.4% (95% CI, 68.2–84.9%), 66.0% (95% CI, 56.2%–75.0%), and 61.9% (95% CI, 51.9%–71.2%) at 5–12 days, 1 month, 3 months, and 6 months after treatment. Additionally, there have been numerous randomized, placebo-controlled trials in patients with chronic prostatitis that have studied α-blockers, steroid inhibitors, anti-inflammatory agents, and bioflavonoids. Treatment responses to α-blockers appear to be greater with longer durations of therapy in α-blocker–naïve patients (National Institutes of Health-Chronic Prostatitis Symptom Index [NIH-CPSI] score reduction of at least 3.6 points after 6 weeks of tamsulosin therapy [P = 0.04] and up to 14.3 and 9.9 point NIH-CPSI score reductions with 14 weeks of terazosin and 24 weeks of alfuzosin therapy, respectively [P = 0.01 for both]). Combination therapy with an α-blocker, an anti-inflammatory, and a muscle relaxant does not appear to offer significant advantages over monotherapy (12.7 vs 12.4 point reduction in NIH-CPSI scores) and a stepwise approach to therapy involving antibiotics followed by bioflavonoids and then α-blockers appears to effectively reduce symptoms for up to 1 year in patients with chroni
背景:前列腺炎是由前列腺炎症或肿胀引起的一系列体征和症状。前列腺炎有许多不同的原因,包括感染;有时没有发现炎症的明确病因。有效的治疗往往取决于病因的确定,但微生物并不总是可检测的,特别是在慢性前列腺炎的情况下。目的综述前列腺炎的鉴别和治疗方法,包括药物和非药物干预。方法通过检索MEDLINE(1966 - 2010年6月)、International Pharmaceutical Abstracts(1970 - 2010年6月)和EMBASE(1947 - 2010年6月)对相关信息进行检索。检查前列腺癌、良性前列腺肥大或前列腺相关手术(即活组织检查)的随机对照试验被排除在外。结果1999年建立了前列腺炎工作分类系统,但对不同治疗方案进行区分的随机对照试验较少。细菌性前列腺炎可急性或慢性,但总是需要一定程度的抗菌治疗。氟喹诺酮类药物的药理特点使其成为大多数患者的首选药物。由于前列腺组织和血清之间的pH值差异,这些抗生素可能会被困在慢性炎症的前列腺中。许多氟喹诺酮类药物的渗透比(前列腺水平:血清水平)高达4:1。一项针对诊断为慢性细菌性前列腺炎而接受左氧氟沙星500 mg/d治疗的欧洲男性(N = 117)的研究显示,在治疗后5-12天、1个月、3个月和6个月,临床成功率分别为92% (95% CI 84.8%-96.5%)、77.4% (95% CI 68.2-84.9%)、66.0% (95% CI 56.2%-75.0%)和61.9% (95% CI 51.9%-71.2%)。此外,在慢性前列腺炎患者中进行了大量随机、安慰剂对照试验,研究了α-受体阻滞剂、类固醇抑制剂、抗炎剂和生物类黄酮。在α-blocker-naïve患者中,α-阻滞剂的治疗效果似乎随着治疗时间的延长而增加(美国国立卫生研究院慢性前列腺炎症状指数[NIH-CPSI]评分在坦舒罗新治疗6周后降低至少3.6分[P = 0.04],而在特拉唑嗪治疗14周和阿夫唑嗪治疗24周时,NIH-CPSI评分分别降低14.3和9.9分[P = 0.01])。α-受体阻滞剂、抗炎剂和肌肉松弛剂联合治疗似乎没有比单药治疗提供显著优势(NIH-CPSI评分降低12.7分vs 12.4分),而采用循序渐进的治疗方法,包括抗生素、生物类黄酮和α-受体阻滞剂,似乎可以有效减轻慢性前列腺炎患者长达1年的症状(与基线相比,NIH-CPSI平均降低9.5分,P <0.0001)。有多种治疗方案不成功的患者可以通过电磁或电针疗法直接刺激骨盆肌肉。结论前列腺炎可能与其他疾病相似,但正确的分类、了解其药理特征和治疗药物的期望有助于确定有效的治疗策略。氟喹诺酮类药物是治疗细菌性前列腺炎的首选药物,并已证明在某些尚未确定有机体的慢性前列腺炎病例中有效。然而,使用具有抗炎或抗肾上腺素能特性的药物可能需要与抗菌剂联合使用或在尝试抗菌剂后使用。
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Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.006
Lal K. Tanwani MD
Background
Most elderly patients with type 2 diabetes require, or will eventually require, insulin to achieve or maintain their glycemic goals. However, insulin therapy remains underused in this population.
Objective
The goal of this review is to evaluate the role of insulin therapy in elderly patients and identify strategies to improve its use in this patient population.
Methods
Searches of the MEDLINE and EMBASE databases were conducted to identify papers published in English between January 1990 and March 2010. The following search terms were used: diabetes mellitus, insulin, elderly, geriatric, analog, premix, pen device, and human insulin. Papers selected for review included meta-analyses, randomized controlled trials of insulin therapy, or evidence-based reviews and/or expert opinion regarding the use of insulin in elderly patients with diabetes.
Results
Insulin therapy is the most effective antidiabetic agent when appropriately dosed; however, only a minority of elderly patients with diabetes uses it. Although there are few randomized controlled studies on insulin use in the elderly, an individualized approach to insulin therapy is recommended to account for varying clinical and practical factors that affect diabetes care in this patient population. Therapy with insulin analogs offers several advantages compared with human insulin regimens, including a more physiologic pharmacologic profile, increased convenience, and a reduced risk of hypoglycemia, which may make them particularly attractive in older adults. Premixed insulin analog therapy may provide added convenience, as well as improved glycemic control. Insulin pen devices are also recommended to facilitate insulin dosing and help patients maintain their independence.
Conclusions
The improved clinical profiles of insulin analogs and the ease of use of newer insulin delivery devices may be advantageous in elderly patients with diabetes; however, additional research on the efficacy and safety of insulin regimens is urgently needed.
{"title":"Insulin Therapy in the Elderly Patient With Diabetes","authors":"Lal K. Tanwani MD","doi":"10.1016/j.amjopharm.2011.02.006","DOIUrl":"10.1016/j.amjopharm.2011.02.006","url":null,"abstract":"<div><h3>Background</h3><p>Most elderly patients with type 2 diabetes require, or will eventually require, insulin to achieve or maintain their glycemic goals. However, insulin therapy remains underused in this population.</p></div><div><h3>Objective</h3><p>The goal of this review is to evaluate the role of insulin therapy in elderly patients and identify strategies to improve its use in this patient population.</p></div><div><h3>Methods</h3><p>Searches of the MEDLINE and EMBASE databases were conducted to identify papers published in English between January 1990 and March 2010. The following search terms were used: <em>diabetes mellitus, insulin, elderly, geriatric, analog, premix, pen device</em>, and <em>human insulin</em>. Papers selected for review included meta-analyses, randomized controlled trials of insulin therapy, or evidence-based reviews and/or expert opinion regarding the use of insulin in elderly patients with diabetes.</p></div><div><h3>Results</h3><p>Insulin therapy is the most effective antidiabetic agent when appropriately dosed; however, only a minority of elderly patients with diabetes uses it. Although there are few randomized controlled studies on insulin use in the elderly, an individualized approach to insulin therapy is recommended to account for varying clinical and practical factors that affect diabetes care in this patient population. Therapy with insulin analogs offers several advantages compared with human insulin regimens, including a more physiologic pharmacologic profile, increased convenience, and a reduced risk of hypoglycemia, which may make them particularly attractive in older adults. Premixed insulin analog therapy may provide added convenience, as well as improved glycemic control. Insulin pen devices are also recommended to facilitate insulin dosing and help patients maintain their independence.</p></div><div><h3>Conclusions</h3><p>The improved clinical profiles of insulin analogs and the ease of use of newer insulin delivery devices may be advantageous in elderly patients with diabetes; however, additional research on the efficacy and safety of insulin regimens is urgently needed.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 24-36"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.001
Sherrie L. Aspinall PharmD, MSc , Xinhua Zhao MS , Chester B. Good MD, MPH , Roslyn A. Stone PhD , Joy Boresi PharmD , Sarah Cox PharmD , Chad Bartholomew PharmD , David Jansen PharmD , Sarah Guterman PharmD , Mauricio Patino PharmD , Giselle Rivera-Miranda PharmD , Mark Burlingame PharmD , Justin Frazer PharmD , Janelle Sellers PharmD , Valerie Stanard Steele PharmD , Lauri Witt PharmD , Francesca E. Cunningham PharmD
Objectives
The objectives of this study were to describe changes in glyburide prescribing in cohorts that were and were not targeted by a risk reduction project, assess factors associated with glyburide discontinuation, and evaluate changes in glycated hemoglobin (ie, HbA1c) levels and rates of serious hypoglycemia.
Methods
This historical cohort study included a targeted cohort of 4368 outpatient veterans aged ≥65 years with active prescriptions for glyburide between April 1, 2007 and June 30, 2007 and serum creatinine (SCr) ≥2 mg/dL and a nontargeted cohort of 1886 outpatients meeting these same criteria between July 1, 2007 and September 3, 2007. The intervention in the risk reduction project took place on September 4, 2007 and entailed giving regional pharmacy leaders information about the increased risk of hypoglycemia with glyburide and the list of targeted patients for follow up with providers. For each patient, the study period was the time between the date they first met the eligibility criteria and March 31, 2008. All data were obtained from Veterans Affairs (VA) administrative databases. The primary outcome was the discontinuation of glyburide. Secondary outcomes were the change in HbA1c after stopping glyburide and the rate of serious hypoglycemia after intervention.
Results
Incidence rate ratios (IRRs) for glyburide discontinuation in targeted versus nontargeted cohorts were statistically significantly elevated in September (IRR 2.1; 95% CI 1.7–2.5), October (IRR 1.3; 95% CI 1.1–1.6), and November 2007 (IRR 1.4; 95% CI 1.1–1.7). The intervention, black race, SCr, Charlson comorbidity score, new glyburide use, and VA region were independently associated with discontinuation. Among patients in the targeted cohort who discontinued glyburide, mean (SD) HbA1c at baseline and after discontinuation were 7.17% (1.35%), and 7.22% (1.34%), respectively (P = 0.36). The hypoglycemia rates/1000 person-days were 0.093 before the intervention and 0.070 afterwards (P = 0.10).
Conclusion
A one-time intervention in a risk reduction project decreased glyburide use over a 3-month period in elderly outpatients with renal insufficiency without compromising glucose control.
本研究的目的是描述格列本脲在风险降低项目和非风险降低项目目标人群中的处方变化,评估与格列本脲停药相关的因素,并评估糖化血红蛋白(即HbA1c)水平和严重低血糖发生率的变化。方法本历史队列研究纳入4368例年龄≥65岁、2007年4月1日至2007年6月30日服用格列本脲有效处方且血清肌酐(SCr)≥2 mg/dL的门诊退伍军人,以及1886例2007年7月1日至2007年9月3日符合相同标准的门诊退伍军人。降低风险项目的干预于2007年9月4日进行,包括向地区药房负责人提供格列本脲增加低血糖风险的信息,以及与供应商进行随访的目标患者名单。对于每位患者,研究期间是从他们首次符合资格标准到2008年3月31日之间的时间。所有数据均来自退伍军人事务(VA)管理数据库。主要结局是停用格列本脲。次要结局是停用格列本脲后HbA1c的变化和干预后严重低血糖的发生率。结果:9月份格列本脲停药的靶向组与非靶向组的发生率比(IRR)显著升高(IRR 2.1;95% CI 1.7-2.5), 10月(IRR 1.3;95% CI 1.1-1.6)和2007年11月(IRR 1.4;95% ci 1.1-1.7)。干预、黑人种族、SCr、Charlson合并症评分、新格列本脲的使用和VA区域与停药独立相关。在停用格列本脲的目标队列患者中,基线和停药后的平均(SD) HbA1c分别为7.17%(1.35%)和7.22% (1.34%)(P = 0.36)。干预前和干预后低血糖率分别为0.093和0.070 /1000人天(P = 0.10)。结论:降低风险项目中的一次性干预降低了老年肾功能不全门诊患者格列本脲在3个月期间的使用,且不影响血糖控制。
{"title":"Intervention to Decrease Glyburide Use in Elderly Patients With Renal Insufficiency⁎","authors":"Sherrie L. Aspinall PharmD, MSc , Xinhua Zhao MS , Chester B. Good MD, MPH , Roslyn A. Stone PhD , Joy Boresi PharmD , Sarah Cox PharmD , Chad Bartholomew PharmD , David Jansen PharmD , Sarah Guterman PharmD , Mauricio Patino PharmD , Giselle Rivera-Miranda PharmD , Mark Burlingame PharmD , Justin Frazer PharmD , Janelle Sellers PharmD , Valerie Stanard Steele PharmD , Lauri Witt PharmD , Francesca E. Cunningham PharmD","doi":"10.1016/j.amjopharm.2011.02.001","DOIUrl":"10.1016/j.amjopharm.2011.02.001","url":null,"abstract":"<div><h3>Objectives</h3><p>The objectives of this study were to describe changes in glyburide prescribing in cohorts that were and were not targeted by a risk reduction project, assess factors associated with glyburide discontinuation, and evaluate changes in glycated hemoglobin (ie, HbA<sub>1c</sub>) levels and rates of serious hypoglycemia.</p></div><div><h3>Methods</h3><p>This historical cohort study included a targeted cohort of 4368 outpatient veterans aged ≥65 years with active prescriptions for glyburide between April 1, 2007 and June 30, 2007 and serum creatinine (SCr) ≥2 mg/dL and a nontargeted cohort of 1886 outpatients meeting these same criteria between July 1, 2007 and September 3, 2007. The intervention in the risk reduction project took place on September 4, 2007 and entailed giving regional pharmacy leaders information about the increased risk of hypoglycemia with glyburide and the list of targeted patients for follow up with providers. For each patient, the study period was the time between the date they first met the eligibility criteria and March 31, 2008. All data were obtained from Veterans Affairs (VA) administrative databases. The primary outcome was the discontinuation of glyburide. Secondary outcomes were the change in HbA<sub>1c</sub> after stopping glyburide and the rate of serious hypoglycemia after intervention.</p></div><div><h3>Results</h3><p>Incidence rate ratios (IRRs) for glyburide discontinuation in targeted versus nontargeted cohorts were statistically significantly elevated in September (IRR 2.1; 95% CI 1.7–2.5), October (IRR 1.3; 95% CI 1.1–1.6), and November 2007 (IRR 1.4; 95% CI 1.1–1.7). The intervention, black race, SCr, Charlson comorbidity score, new glyburide use, and VA region were independently associated with discontinuation. Among patients in the targeted cohort who discontinued glyburide, mean (SD) HbA<sub>1c</sub> at baseline and after discontinuation were 7.17% (1.35%), and 7.22% (1.34%), respectively (<em>P</em> = 0.36). The hypoglycemia rates/1000 person-days were 0.093 before the intervention and 0.070 afterwards (<em>P</em> = 0.10).</p></div><div><h3>Conclusion</h3><p>A one-time intervention in a risk reduction project decreased glyburide use over a 3-month period in elderly outpatients with renal insufficiency without compromising glucose control.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 58-68"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.004
Walid F. Gellad MD, MPH , Jerry L. Grenard PhD , Zachary A. Marcum PharmD
Background
Medication nonadherence is a common problem among the elderly.
Objective
To conduct a systematic review of the published literature describing potential nonfinancial barriers to medication adherence among the elderly.
Methods
The PubMed and PsychINFO databases were searched for articles published in English between January 1998 and January 2010 that (1) described “predictors,” “facilitators,” or “determinants” of medication adherence or that (2) examined the “relationship” between a specific barrier and adherence for elderly patients (ie, ≥65 years of age) in the United States. A manual search of the reference lists of identified articles and the authors' files and recent review articles was conducted. The search included articles that (1) reviewed specific barriers to medication adherence and did not solely describe nonmodifiable predictors of adherence (eg, demographics, marital status), (2) were not interventions designed to address adherence, (3) defined adherence or compliance and specified its method of measurement, and (4) involved US participants only. Nonsystematic reviews were excluded, as were studies that focused specifically on people who were homeless or substance abusers, or patients with psychotic disorders, tuberculosis, or HIV infection, because of the unique circumstances that surround medication adherence for each of these populations.
Results
Nine studies met inclusion criteria for this review. Four studies used pharmacy records or claims data to assess adherence, 2 studies used pill count or electronic monitoring, and 3 studies used other methods to assess adherence. Substantial heterogeneity existed among the populations studied as well as among the measures of adherence, barriers addressed, and significant findings. Some potential barriers (ie, factors associated with nonadherence) were identified from the studies, including patient-related factors such as disease-related knowledge, health literacy, and cognitive function; drug-related factors such as adverse effects and polypharmacy; and other factors including the patient-provider relationship and various logistical barriers to obtaining medications. None of the reviewed studies examined primary nonadherence or nonpersistence.
Conclusion
Medication nonadherence in the elderly is not well described in the literature, despite being a major cause of morbidity, and thus it is difficult to draw a systematic conclusion on potential barriers based on the current literature. Future research should focus on standardizing medication adherence measurements among the elderly to gain a better understanding of this important issue.
{"title":"A Systematic Review of Barriers to Medication Adherence in the Elderly: Looking Beyond Cost and Regimen Complexity","authors":"Walid F. Gellad MD, MPH , Jerry L. Grenard PhD , Zachary A. Marcum PharmD","doi":"10.1016/j.amjopharm.2011.02.004","DOIUrl":"10.1016/j.amjopharm.2011.02.004","url":null,"abstract":"<div><h3>Background</h3><p>Medication nonadherence is a common problem among the elderly.</p></div><div><h3>Objective</h3><p>To conduct a systematic review of the published literature describing potential nonfinancial barriers to medication adherence among the elderly.</p></div><div><h3>Methods</h3><p>The PubMed and PsychINFO databases were searched for articles published in English between January 1998 and January 2010 that (1) described “predictors,” “facilitators,” or “determinants” of medication adherence or that (2) examined the “relationship” between a specific barrier and adherence for elderly patients (ie, ≥65 years of age) in the United States. A manual search of the reference lists of identified articles and the authors' files and recent review articles was conducted. The search included articles that (1) reviewed specific barriers to medication adherence and did not solely describe nonmodifiable predictors of adherence (eg, demographics, marital status), (2) were not interventions designed to address adherence, (3) defined adherence or compliance and specified its method of measurement, and (4) involved US participants only. Nonsystematic reviews were excluded, as were studies that focused specifically on people who were homeless or substance abusers, or patients with psychotic disorders, tuberculosis, or HIV infection, because of the unique circumstances that surround medication adherence for each of these populations.</p></div><div><h3>Results</h3><p>Nine studies met inclusion criteria for this review. Four studies used pharmacy records or claims data to assess adherence, 2 studies used pill count or electronic monitoring, and 3 studies used other methods to assess adherence. Substantial heterogeneity existed among the populations studied as well as among the measures of adherence, barriers addressed, and significant findings. Some potential barriers (ie, factors associated with nonadherence) were identified from the studies, including patient-related factors such as disease-related knowledge, health literacy, and cognitive function; drug-related factors such as adverse effects and polypharmacy; and other factors including the patient-provider relationship and various logistical barriers to obtaining medications. None of the reviewed studies examined primary nonadherence or nonpersistence.</p></div><div><h3>Conclusion</h3><p>Medication nonadherence in the elderly is not well described in the literature, despite being a major cause of morbidity, and thus it is difficult to draw a systematic conclusion on potential barriers based on the current literature. Future research should focus on standardizing medication adherence measurements among the elderly to gain a better understanding of this important issue.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 11-23"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Older diabetic patients are at increased risk for skin infections, often with methicillin-resistant Staphylococcus aureus (MRSA). Linezolid offers oral therapy with MRSA coverage. We present a case of linezolid-associated hypoglycemia in a 64-year-old diabetic patient with presumed MRSA cellulitis.
Case summary
A 64-year-old man with diabetes was treated for cellulitis. Linezolid was started when amoxicillin/clavulanate failed. Within 7 days, he developed frequent diaphoresis and tremulousness, with glucoses of 30 to 60 mg/dL. Hypoglycemia worsened despite decreasing insulin use, discontinuing glyburide, and increasing caloric intake. The day of admission, he awoke with a glucose level of 30 mg/dL. He took no medications, ate a large breakfast, and presented to clinic. He was symptomatic with a glucose level of 35 mg/dL. Hypoglycemia persisted despite IV dextrose. Linezolid was discontinued immediately in favor of vancomycin. Dextrose was weaned and his diabetes medications were resumed without further hypoglycemia.
Conclusions
Linezolid has monoamine oxidase (MAO) inhibitory properties, and MAO inhibitors have been reported to contribute to hypoglycemia. The use of linezolid in older diabetic patients, especially those patients already taking agents with the potential to cause hypoglycemia, represents an area of concern. Increased comorbidities and polypharmacy in geriatric patients adds to this concern.
{"title":"Linezolid-Associated Hypoglycemia in a 64-Year-Old Man With Type 2 Diabetes","authors":"Timothy Bodnar MD , Katelyn Starr PharmD , Jeffrey B. Halter MD","doi":"10.1016/j.amjopharm.2011.02.002","DOIUrl":"10.1016/j.amjopharm.2011.02.002","url":null,"abstract":"<div><h3>Background</h3><p>Older diabetic patients are at increased risk for skin infections, often with methicillin-resistant <em>Staphylococcus aureus</em><span><span> (MRSA). Linezolid offers oral therapy with MRSA coverage. We present a case of linezolid-associated hypoglycemia in a 64-year-old diabetic patient with presumed MRSA </span>cellulitis.</span></p></div><div><h3>Case summary</h3><p>A 64-year-old man with diabetes was treated for cellulitis. Linezolid was started when amoxicillin/clavulanate failed. Within 7 days, he developed frequent diaphoresis<span><span> and tremulousness, with glucoses of 30 to 60 mg/dL. Hypoglycemia worsened despite decreasing insulin use, discontinuing glyburide, and increasing </span>caloric intake<span>. The day of admission, he awoke with a glucose level of 30 mg/dL. He took no medications, ate a large breakfast, and presented to clinic. He was symptomatic with a glucose level of 35 mg/dL. Hypoglycemia persisted despite IV dextrose. Linezolid was discontinued immediately in favor of vancomycin. Dextrose was weaned and his diabetes medications were resumed without further hypoglycemia.</span></span></p></div><div><h3>Conclusions</h3><p>Linezolid has monoamine oxidase<span><span> (MAO) inhibitory properties, and MAO inhibitors have been reported to contribute to hypoglycemia. The use of linezolid in older diabetic patients, especially those patients already taking agents with the potential to cause hypoglycemia, represents an area of concern. Increased comorbidities and </span>polypharmacy<span> in geriatric patients adds to this concern.</span></span></p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 88-92"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2011-02-01DOI: 10.1016/j.amjopharm.2011.02.003
Kenneth Rockwood MD, FRCPC , Ryan Walsh MSc , Earl Martin MSc , Sultan Darvesh MD, PhD, FRCPC
Background
Older adults are susceptible to a variety of illnesses, many of which can be treated with medications that may need to be used for the long term. Considerable attention has been paid to drugs that, in addition to their intended function, may have an anticholinergic effect that results in undesirable side effects, including impairment in cognition. Cholinesterase inhibitors are used as procholinergic drugs to improve cognitive dysfunction in Alzheimer's disease. We hypothesized that some of the drugs commonly used by older adults might, in addition to their intended function, also have procholinergic effects by virtue of inhibiting cholinesterases.
Objective
To determine the potential procholinergic nature of some of the commonly used drugs by examining their cholinesterase inhibiting properties.
Methods
The Ellman spectrophotometric method was used with human acetylcholinesterase and butyrylcholinesterase, in the absence and presence of increasing concentrations of each test drug. To compare inhibition potencies, from enzyme kinetic data, we determined half maximal inhibitory concentration (IC50 values) for each cholinesterase by each drug.
Results
Of the 28 drugs examined, over half (17/28) inhibited one or both of the human cholinesterases. The inhibition potencies were often within 1 to 2 orders of magnitude of reversible cholinesterase inhibitors currently used to treat Alzheimer's disease. These included trazodone, quetiapine, risperidone, indapamide, and perindopril.
Conclusions
Many drugs used by older adults for other reasons have potentially clinically relevant procholinergic effects. The effect of cumulative cholinesterase inhibition merits clinical evaluation.
{"title":"Potentially Procholinergic Effects of Medications Commonly Used in Older Adults","authors":"Kenneth Rockwood MD, FRCPC , Ryan Walsh MSc , Earl Martin MSc , Sultan Darvesh MD, PhD, FRCPC","doi":"10.1016/j.amjopharm.2011.02.003","DOIUrl":"10.1016/j.amjopharm.2011.02.003","url":null,"abstract":"<div><h3>Background</h3><p>Older adults are susceptible to a variety of illnesses, many of which can be treated with medications that may need to be used for the long term. Considerable attention has been paid to drugs<span><span> that, in addition to their intended function, may have an anticholinergic effect that results in undesirable side effects, including impairment in cognition. </span>Cholinesterase inhibitors<span> are used as procholinergic drugs to improve cognitive dysfunction<span><span> in Alzheimer's disease. We hypothesized that some of the drugs commonly used by older adults might, in addition to their intended function, also have procholinergic effects by virtue of inhibiting </span>cholinesterases.</span></span></span></p></div><div><h3>Objective</h3><p>To determine the potential procholinergic nature of some of the commonly used drugs by examining their cholinesterase inhibiting properties.</p></div><div><h3>Methods</h3><p><span><span>The Ellman spectrophotometric method was used with human acetylcholinesterase and butyrylcholinesterase, in the absence and presence of increasing concentrations of each test drug. To compare inhibition potencies, from </span>enzyme kinetic data, we determined half maximal inhibitory concentration (IC</span><sub>50</sub> values) for each cholinesterase by each drug.</p></div><div><h3>Results</h3><p><span><span><span>Of the 28 drugs examined, over half (17/28) inhibited one or both of the human cholinesterases. The inhibition potencies were often within 1 to 2 orders of magnitude of reversible cholinesterase inhibitors currently used to treat Alzheimer's disease. These included trazodone, </span>quetiapine, </span>risperidone, </span>indapamide<span>, and perindopril.</span></p></div><div><h3>Conclusions</h3><p>Many drugs used by older adults for other reasons have potentially clinically relevant procholinergic effects. The effect of cumulative cholinesterase inhibition merits clinical evaluation.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"9 1","pages":"Pages 80-87"},"PeriodicalIF":0.0,"publicationDate":"2011-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.amjopharm.2011.02.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29788344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2010-12-01DOI: 10.1016/S1543-5946(10)80005-4
Seema D. Dedhiya PhD , Emily Hancock PharmD , Bruce A. Craig PhD , Caroline C. Doebbeling MD, MSc , Joseph Thomas III PhD
Background: Most studies of potentially inappropriate medication (PIM) use among older adults have focused on prevalence rather than incidence.
Objectives: The goals of this study were to determine the 1-year incidence of PIM use among elderly Indiana Medicaid residents of nursing homes and to examine associations between incident PIM use and hospitalization and mortality.
Methods: A retrospective analysis was conducted using Indiana Medicaid enrollment and administrative claims files. Individuals were included if they were Medicaid eligible and aged ≥65 years as of January 2003 and received nursing home services in each month of 2003 or until death in 2003. Individuals also had to receive nursing home services from October 2002 through December 2002 for inclusion in the sample. To focus analysis on incident PIM use, individuals who received any PIM prescription medication from October 2002 through December 2002 were excluded from the sample, as were those not prescribed any new medication in 2003. PIMs were identified using the 2003 Beers criteria. Associations between incident PIM use and hospitalization and mortality were assessed using logistic regression models after controlling for other risk factors. Potential selection bias was examined using bivariate probit models.
Results: The study sample consisted of 7594 individuals (mean age, 83.07 years). A majority of the sample was female (76.5%), white (89.7%), and widowed (58.8%). Most individuals received care in nursing homes located in urban areas (5306 [69.9%]) and in the central region of Indiana (2838 [37.4%]). One-year incidence of PIM use was 42.1%. Incident PIM users were more likely to be hospitalized (odds ratio [OR] = 1.27; 95% CI, 1.10–C1.46) and more likely to die (OR = 1.46; 95% CI, 1.31–C1.62) in the 12 months after first receiving a PIM than nonusers, even after adjusting for demographic and clinical risk factors.
Conclusions: Incident PIM use was high among these elderly Indiana Medicaid residents of nursing homes. Individuals who began use of a PIM were at a higher risk of hospitalization and of dying.
{"title":"Incident use and outcomes associated with potentially inappropriate medication use in older adults","authors":"Seema D. Dedhiya PhD , Emily Hancock PharmD , Bruce A. Craig PhD , Caroline C. Doebbeling MD, MSc , Joseph Thomas III PhD","doi":"10.1016/S1543-5946(10)80005-4","DOIUrl":"10.1016/S1543-5946(10)80005-4","url":null,"abstract":"<div><p><strong>Background:</strong> Most studies of potentially inappropriate medication (PIM) use among older adults have focused on prevalence rather than incidence.</p><p><strong>Objectives:</strong> The goals of this study were to determine the 1-year incidence of PIM use among elderly Indiana Medicaid residents of nursing homes and to examine associations between incident PIM use and hospitalization and mortality.</p><p><strong>Methods:</strong> A retrospective analysis was conducted using Indiana Medicaid enrollment and administrative claims files. Individuals were included if they were Medicaid eligible and aged ≥65 years as of January 2003 and received nursing home services in each month of 2003 or until death in 2003. Individuals also had to receive nursing home services from October 2002 through December 2002 for inclusion in the sample. To focus analysis on incident PIM use, individuals who received any PIM prescription medication from October 2002 through December 2002 were excluded from the sample, as were those not prescribed any new medication in 2003. PIMs were identified using the 2003 Beers criteria. Associations between incident PIM use and hospitalization and mortality were assessed using logistic regression models after controlling for other risk factors. Potential selection bias was examined using bivariate probit models.</p><p><strong>Results:</strong> The study sample consisted of 7594 individuals (mean age, 83.07 years). A majority of the sample was female (76.5%), white (89.7%), and widowed (58.8%). Most individuals received care in nursing homes located in urban areas (5306 [69.9%]) and in the central region of Indiana (2838 [37.4%]). One-year incidence of PIM use was 42.1%. Incident PIM users were more likely to be hospitalized (odds ratio [OR] = 1.27; 95% CI, 1.10–C1.46) and more likely to die (OR = 1.46; 95% CI, 1.31–C1.62) in the 12 months after first receiving a PIM than nonusers, even after adjusting for demographic and clinical risk factors.</p><p><strong>Conclusions:</strong> Incident PIM use was high among these elderly Indiana Medicaid residents of nursing homes. Individuals who began use of a PIM were at a higher risk of hospitalization and of dying.</p></div>","PeriodicalId":50811,"journal":{"name":"American Journal Geriatric Pharmacotherapy","volume":"8 6","pages":"Pages 562-570"},"PeriodicalIF":0.0,"publicationDate":"2010-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1543-5946(10)80005-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29701177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}