Pub Date : 2023-09-01DOI: 10.1080/15360288.2023.2194873
Raymond Y Wen, Kyle P Edmonds, Rabia S Atayee
Methadone is an effective analgesic with unique pharmacokinetic and pharmacodynamic variables. There is no national consensus on methadone equianalgesia tools. Our study aimed to compare methadone equianalgesic tools from various national institutions with the primary objective to summarize current practice and secondary objective to determine if a national consensus can be established. Out of 25 institutional methadone equianalgesic tools reviewed, 18 contained sufficient data and were included in this study. Fifteen (15) of the institution evaluated tools utilized a wide variety of dose-dependent modalities for methadone conversion with the hospice and palliative care (HAPC) Consensus method being the most common. Based on the variability of the equianalgesia tools evaluated in this study, we were unable to recommend a consensus methadone conversion method. Further trials exploring methadone equianalgesia beyond our study are needed.
{"title":"Comparing National Methadone Equianalgesic Tools.","authors":"Raymond Y Wen, Kyle P Edmonds, Rabia S Atayee","doi":"10.1080/15360288.2023.2194873","DOIUrl":"https://doi.org/10.1080/15360288.2023.2194873","url":null,"abstract":"<p><p>Methadone is an effective analgesic with unique pharmacokinetic and pharmacodynamic variables. There is no national consensus on methadone equianalgesia tools. Our study aimed to compare methadone equianalgesic tools from various national institutions with the primary objective to summarize current practice and secondary objective to determine if a national consensus can be established. Out of 25 institutional methadone equianalgesic tools reviewed, 18 contained sufficient data and were included in this study. Fifteen (15) of the institution evaluated tools utilized a wide variety of dose-dependent modalities for methadone conversion with the hospice and palliative care (HAPC) Consensus method being the most common. Based on the variability of the equianalgesia tools evaluated in this study, we were unable to recommend a consensus methadone conversion method. Further trials exploring methadone equianalgesia beyond our study are needed.</p>","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10139553","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 : 2023-09-01DOI: 10.1080/15360288.2023.2245738
Laura Meyer-Junco, Julie M Waldfogel, Nakia Duncan
Peer review is a collaborative process among reviewers and the journal editor to assess the validity and significance of submitted manuscripts. Constructive comments from peer reviewers improve the scientific writing of authors and ultimately readers’ confidence in the integrity of the published article (1, 2). To support the growth of peer reviewers, the Journal of Pain and Palliative Care Pharmacotherapy (JPPCP) has created a Peer Review Q&A editorial series to serve as a comprehensive guide to the peer review process (3). In this installment How? Part II, we will focus on the peer review process for particular article types: case reports, systematic reviews, narrative reviews, and opinion pieces. For general tips on thinking like a peer reviewer and reviewing research articles specifically, check out the How? Part I editorial published in the Quarter 2 issue of 2023 (4).
{"title":"Peer Review Questions & Answers: How?","authors":"Laura Meyer-Junco, Julie M Waldfogel, Nakia Duncan","doi":"10.1080/15360288.2023.2245738","DOIUrl":"https://doi.org/10.1080/15360288.2023.2245738","url":null,"abstract":"Peer review is a collaborative process among reviewers and the journal editor to assess the validity and significance of submitted manuscripts. Constructive comments from peer reviewers improve the scientific writing of authors and ultimately readers’ confidence in the integrity of the published article (1, 2). To support the growth of peer reviewers, the Journal of Pain and Palliative Care Pharmacotherapy (JPPCP) has created a Peer Review Q&A editorial series to serve as a comprehensive guide to the peer review process (3). In this installment How? Part II, we will focus on the peer review process for particular article types: case reports, systematic reviews, narrative reviews, and opinion pieces. For general tips on thinking like a peer reviewer and reviewing research articles specifically, check out the How? Part I editorial published in the Quarter 2 issue of 2023 (4).","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10129328","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 : 2023-09-01DOI: 10.1080/15360288.2023.2200412
Neil K Shah, Michael W Chandler, Anne V Cetto, Lisa L Luciani, Jacob Painter, Danielle Bailey
The objective of this study was to understand the effect buprenorphine rotations have on respiratory risk and other safety outcomes. This was a retrospective observational study evaluating Veterans who underwent an opioid rotation from full-agonist opioids to buprenorphine products or to alternative opioids. The primary endpoint was change in the Risk Index for Overdose or Serious Opioid-induced Respiratory Depression (RIOSORD) score from baseline to six months post-rotation. Median baseline RIOSORD scores were 26.0 and 18.0 in the Buprenorphine Group and the Alternative Opioid Group, respectively. There was no statistically significant difference between groups in baseline RIOSORD score. At six months post-rotation, median RIOSORD scores were 23.5 and 23.0 in the Buprenorphine Group and Alternative Opioid Group, respectively. The difference in change in RIOSORD scores between groups was not statistically significant (p = 0.23). However, based on changes in RIOSORD risk class, an 11% and 0% decrease in respiratory risk was observed in the Buprenorphine and Alternative Opioid groups, respectively. This finding may be considered clinically significant given a change in risk was observed as predicted by RIOSORD score. Further research is needed to clarify the effect that opioid rotations have on respiratory depression risk and other safety outcomes.
{"title":"Retrospective Cohort Study of Safety Outcomes Associated with Opioid Rotations to Buprenorphine.","authors":"Neil K Shah, Michael W Chandler, Anne V Cetto, Lisa L Luciani, Jacob Painter, Danielle Bailey","doi":"10.1080/15360288.2023.2200412","DOIUrl":"https://doi.org/10.1080/15360288.2023.2200412","url":null,"abstract":"<p><p>The objective of this study was to understand the effect buprenorphine rotations have on respiratory risk and other safety outcomes. This was a retrospective observational study evaluating Veterans who underwent an opioid rotation from full-agonist opioids to buprenorphine products or to alternative opioids. The primary endpoint was change in the Risk Index for Overdose or Serious Opioid-induced Respiratory Depression (RIOSORD) score from baseline to six months post-rotation. Median baseline RIOSORD scores were 26.0 and 18.0 in the Buprenorphine Group and the Alternative Opioid Group, respectively. There was no statistically significant difference between groups in baseline RIOSORD score. At six months post-rotation, median RIOSORD scores were 23.5 and 23.0 in the Buprenorphine Group and Alternative Opioid Group, respectively. The difference in change in RIOSORD scores between groups was not statistically significant (<i>p</i> = 0.23). However, based on changes in RIOSORD risk class, an 11% and 0% decrease in respiratory risk was observed in the Buprenorphine and Alternative Opioid groups, respectively. This finding may be considered clinically significant given a change in risk was observed as predicted by RIOSORD score. Further research is needed to clarify the effect that opioid rotations have on respiratory depression risk and other safety outcomes.</p>","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10139564","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 : 2023-09-01DOI: 10.1080/15360288.2023.2222021
Hollie Porras, Elizabeth Johnson, Mariya Kotova, James Chenoweth, Daniel Colby
Buprenorphine inductions traditionally require an opioid-free period due to the risk of precipitated opioid withdrawal. Hospitalized patients with opioid use disorder and concurrent acute pain may be eligible for buprenorphine therapy. However, effective buprenorphine induction strategies in this patient population have not been well established. Investigators sought to review the completion of a low dose induction protocol that does not require an opioid-free period prior to buprenorphine initiation. Hospitalized patients who completed a 7-day low dose induction protocol via buprenorphine transdermal patches October 2021 - March 2022 were examined via retrospective chart review (N = 7). All seven patients completed the induction and were discharged on sublingual buprenorphine. Low dose transdermal buprenorphine provides a reasonable strategy for hospitalized patients on full agonist opioid therapy or those who have failed conventional buprenorphine induction strategies. Reducing barriers such as opioid abstinence is key to combating opioid use disorder.
{"title":"Buprenorphine Inductions via Transdermal Patches for Opioid Use Disorder in the Inpatient Setting.","authors":"Hollie Porras, Elizabeth Johnson, Mariya Kotova, James Chenoweth, Daniel Colby","doi":"10.1080/15360288.2023.2222021","DOIUrl":"https://doi.org/10.1080/15360288.2023.2222021","url":null,"abstract":"<p><p>Buprenorphine inductions traditionally require an opioid-free period due to the risk of precipitated opioid withdrawal. Hospitalized patients with opioid use disorder and concurrent acute pain may be eligible for buprenorphine therapy. However, effective buprenorphine induction strategies in this patient population have not been well established. Investigators sought to review the completion of a low dose induction protocol that does not require an opioid-free period prior to buprenorphine initiation. Hospitalized patients who completed a 7-day low dose induction protocol via buprenorphine transdermal patches October 2021 - March 2022 were examined via retrospective chart review (N = 7). All seven patients completed the induction and were discharged on sublingual buprenorphine. Low dose transdermal buprenorphine provides a reasonable strategy for hospitalized patients on full agonist opioid therapy or those who have failed conventional buprenorphine induction strategies. Reducing barriers such as opioid abstinence is key to combating opioid use disorder.</p>","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10515231","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 : 2023-09-01Epub Date: 2023-03-30DOI: 10.1080/15360288.2023.2194870
Ronakkumar Patel, Reuben O Mogoi, Sayed K Ali
Management of malignant wounds, especially from tumor infiltration, remains challenging especially in low-middle income country where resources, such as opioids, may be limited. Management of such wounds is also compounded by the use of intravenous or oral opioids that often might improve the pain, but result in various side effects. Our pharmacy department helped prepare a topical ointment that contained fixed amounts of both morphine and lidocaine specifically for use in malignant wounds. Ninety milligrams of 2% lidocaine gel was mixed with 80 mgs of oral morphine sulfate in a pestle until the mixture was consistent. Four to eight milliliters, depending on the size of the wound, was applied to a gauze and placed over the wound every 8 hours. Table 1 highlights the use of the ointment in select patients with malignant wound and improvement in pain scores over a 2 week period. About 5–10% of patient with metastatic cancer will go on to develop fungating wound that are often associated with pain as most common symptoms (1, 2). These wound share complex pathophysiological process compounded by the an inflammatory process that is often chronic in nature with stimulation of the skin afferent receptors, compression of the wound bed tissue, erosion of the blood and nerves surrounding the wound, resulting in various symptoms including pain that can often be difficult to manage (3). Even though topical agents have been used for pain management, data on the use of such agents in resource limited settings is non-existent. Compound lidocaine creams/gels have been shown to be safe to use in malignant wound managements. Application can reduce pain caused by the inflammatory process and also during the dressing process. The vasodilatory effects of lidocaine, resulting in increased blood flow, have been shown to help with wound healing (4). Lidocaine, also works by inhibiting the transmission of pain signals by blocking the voltage-gated sodium channels in nerve cells. This prevents the initiation and propagation of pain signals, resulting in pain relief (5). Application of such gels have been shown to offer long term relief, without associated systemic side effects and can also decrease the need and use of systemic opioids (3, 4). Topical morphine application to malignant wounds has also been showing to improve pain scores and quality of life, with fewer side effects and reduced need for systemic opioid therapy (6, 7). Topical morphine is thought to act on the peripheral opioid receptors that play a role in modulation of pain (6). In addition, normal, unaffected tissues contain silent opioid receptors that are activated soon after injury to the tissue. In fact, trauma, and inflammatory processes have been shown to increase the synthesis and transport of opioid receptors from the dorsal root ganglia to the peripheral sensory nerve endings (8). Opioid receptors have been found in skins
{"title":"Topical Lidocaine and Morphine Gel Use for Malignant Wound Pain.","authors":"Ronakkumar Patel, Reuben O Mogoi, Sayed K Ali","doi":"10.1080/15360288.2023.2194870","DOIUrl":"10.1080/15360288.2023.2194870","url":null,"abstract":"Management of malignant wounds, especially from tumor infiltration, remains challenging especially in low-middle income country where resources, such as opioids, may be limited. Management of such wounds is also compounded by the use of intravenous or oral opioids that often might improve the pain, but result in various side effects. Our pharmacy department helped prepare a topical ointment that contained fixed amounts of both morphine and lidocaine specifically for use in malignant wounds. Ninety milligrams of 2% lidocaine gel was mixed with 80 mgs of oral morphine sulfate in a pestle until the mixture was consistent. Four to eight milliliters, depending on the size of the wound, was applied to a gauze and placed over the wound every 8 hours. Table 1 highlights the use of the ointment in select patients with malignant wound and improvement in pain scores over a 2 week period. About 5–10% of patient with metastatic cancer will go on to develop fungating wound that are often associated with pain as most common symptoms (1, 2). These wound share complex pathophysiological process compounded by the an inflammatory process that is often chronic in nature with stimulation of the skin afferent receptors, compression of the wound bed tissue, erosion of the blood and nerves surrounding the wound, resulting in various symptoms including pain that can often be difficult to manage (3). Even though topical agents have been used for pain management, data on the use of such agents in resource limited settings is non-existent. Compound lidocaine creams/gels have been shown to be safe to use in malignant wound managements. Application can reduce pain caused by the inflammatory process and also during the dressing process. The vasodilatory effects of lidocaine, resulting in increased blood flow, have been shown to help with wound healing (4). Lidocaine, also works by inhibiting the transmission of pain signals by blocking the voltage-gated sodium channels in nerve cells. This prevents the initiation and propagation of pain signals, resulting in pain relief (5). Application of such gels have been shown to offer long term relief, without associated systemic side effects and can also decrease the need and use of systemic opioids (3, 4). Topical morphine application to malignant wounds has also been showing to improve pain scores and quality of life, with fewer side effects and reduced need for systemic opioid therapy (6, 7). Topical morphine is thought to act on the peripheral opioid receptors that play a role in modulation of pain (6). In addition, normal, unaffected tissues contain silent opioid receptors that are activated soon after injury to the tissue. In fact, trauma, and inflammatory processes have been shown to increase the synthesis and transport of opioid receptors from the dorsal root ganglia to the peripheral sensory nerve endings (8). Opioid receptors have been found in skins","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10125119","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 : 2023-09-01DOI: 10.1080/15360288.2023.2194868
Michelle Krichbaum, Neil Miransky, Alexandra Perez
The aim of this research was to compare pain medication use trends among adults with and without type 2 diabetes in the US. This cross-sectional study used data of adults with and without (type 2) diabetes from the National Health and Nutrition Examination Survey waves 2005-2018. Use of pain medication including opioids, prescription nonsteroidal anti-inflammatory drugs, gabapentinoids, serotonin norepinephrine reuptake inhibitors, skeletal muscle relaxants, and headache treatment agents was compared by diabetes status and within select social determinants of health and clinical factors. Adults with type 2 diabetes were twice as likely to be prescribed pain medications compared to those without a diabetes diagnosis (16.2% vs 8.6%). Females and those with a history of smoking or arthritis were more likely to be on pain medications. Opioid use was the most prevalent regardless of diabetes status, and use was twice as high among those with diabetes (10.8% vs 5.5%). Patients with type 2 diabetes in the US are twice as likely to be prescribed pain medications overall as well as opioids compared with those without diabetes. Clinical guideline recommendations are necessary to find pharmacologic and nonpharmacologic nociceptive pain management specific for patients with diabetes.
这项研究的目的是比较美国有2型糖尿病和没有2型糖尿病的成年人使用止痛药的趋势。这项横断面研究使用了2005-2018年全国健康和营养检查调查中患有和不患有(2型)糖尿病的成年人的数据。使用止痛药,包括阿片类药物、处方非甾体抗炎药、加巴喷丁类药物、血清素去甲肾上腺素再摄取抑制剂、骨骼肌松弛剂和头痛治疗药物,与糖尿病状况进行比较,并选择健康和临床因素的社会决定因素。与没有糖尿病诊断的成年人相比,患有2型糖尿病的成年人服用止痛药的可能性是后者的两倍(16.2% vs 8.6%)。女性和有吸烟史或关节炎的人更有可能服用止痛药。无论糖尿病状况如何,阿片类药物的使用最为普遍,糖尿病患者的阿片类药物使用率是糖尿病患者的两倍(10.8%对5.5%)。在美国,与没有糖尿病的患者相比,2型糖尿病患者总体上服用止痛药和阿片类药物的可能性是后者的两倍。临床指南建议有必要找到针对糖尿病患者的药物和非药物伤害性疼痛管理方法。
{"title":"Trends in Pain Medication Use in Patients With Type 2 Diabetes: NHANES 2005-2018.","authors":"Michelle Krichbaum, Neil Miransky, Alexandra Perez","doi":"10.1080/15360288.2023.2194868","DOIUrl":"https://doi.org/10.1080/15360288.2023.2194868","url":null,"abstract":"<p><p>The aim of this research was to compare pain medication use trends among adults with and without type 2 diabetes in the US. This cross-sectional study used data of adults with and without (type 2) diabetes from the National Health and Nutrition Examination Survey waves 2005-2018. Use of pain medication including opioids, prescription nonsteroidal anti-inflammatory drugs, gabapentinoids, serotonin norepinephrine reuptake inhibitors, skeletal muscle relaxants, and headache treatment agents was compared by diabetes status and within select social determinants of health and clinical factors. Adults with type 2 diabetes were twice as likely to be prescribed pain medications compared to those without a diabetes diagnosis (16.2% vs 8.6%). Females and those with a history of smoking or arthritis were more likely to be on pain medications. Opioid use was the most prevalent regardless of diabetes status, and use was twice as high among those with diabetes (10.8% vs 5.5%). Patients with type 2 diabetes in the US are twice as likely to be prescribed pain medications overall as well as opioids compared with those without diabetes. Clinical guideline recommendations are necessary to find pharmacologic and nonpharmacologic nociceptive pain management specific for patients with diabetes.</p>","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10142540","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 : 2023-07-03DOI: 10.1080/15360288.2023.2234261
Emily Casey, Tanya J. Uritsky
Background: Comfort care order sets support evidence-based best practices that promote high-quality end-of-life care through mitigation of physical symptoms associated with the dying process. Pain and dyspnea are among the most common symptoms at the end of life, for which opioids are the mainstay of treatment. Sublingual (SL) formulations of opioids are often utilized in hospice care, though there are no available data comparing the efficacy of this route compared to oral or intravenous (IV) routes. Due to concern for medication shortages during the COVID-19 pandemic, the comfort care order set at our institution was modified to recommend initial opioid management with SL rather than IV medication. This study aimed to characterize opioid use by patients utilizing the comfort care order set before and after this change was made.
{"title":"Evaluations of Adaptations to a Comfort Care Order Set: A Retrospective Cohort Review","authors":"Emily Casey, Tanya J. Uritsky","doi":"10.1080/15360288.2023.2234261","DOIUrl":"https://doi.org/10.1080/15360288.2023.2234261","url":null,"abstract":"Background: Comfort care order sets support evidence-based best practices that promote high-quality end-of-life care through mitigation of physical symptoms associated with the dying process. Pain and dyspnea are among the most common symptoms at the end of life, for which opioids are the mainstay of treatment. Sublingual (SL) formulations of opioids are often utilized in hospice care, though there are no available data comparing the efficacy of this route compared to oral or intravenous (IV) routes. Due to concern for medication shortages during the COVID-19 pandemic, the comfort care order set at our institution was modified to recommend initial opioid management with SL rather than IV medication. This study aimed to characterize opioid use by patients utilizing the comfort care order set before and after this change was made.","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42691382","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 : 2023-07-03DOI: 10.1080/15360288.2023.2234259
Athena C. Triglia, Kyle Quirk
{"title":"Evaluation of Use of Intravenous Buprenorphine for Cancer Pain at a Large Academic Medical Center","authors":"Athena C. Triglia, Kyle Quirk","doi":"10.1080/15360288.2023.2234259","DOIUrl":"https://doi.org/10.1080/15360288.2023.2234259","url":null,"abstract":"","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48686941","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 : 2023-07-03DOI: 10.1080/15360288.2023.2234262
Wesley Faulkner, Sandra L DiScala, Christine M. Vartan, Belal Dakroub, Jennifer Quellhorst, Anupama Nair, M. Miller, Mythili Bharadwaj, Michael Silverman
Background: Patients receiving palliative-focused care have complex medication regimens and multi-morbidity. Risk of adverse drug reactions (ADR), fall risk, and drug-drug interactions are increased with polypharmacy. Within the Department of Veteran’s Affairs a commonly used deprescribing model is the VIONE methodology. VIONE catego-rizes medications into vital/life-saving medications, important for quality of life, optional, not indicated/treatment complete, and every medication has a diagnosis. The VIONE dashboards aids providers identify potentially inappropriate medications and prioritizes patients. This study aimed to pilot implementation of board-certified clinical pharmacist practitioners utilizing the VIONE model of deprescribing within an older adult patient-aligned care team at the West Palm Beach VAHCS. Methods: The PGY2 Pain Management and Palliative Care resident reached out via telephone to the patients for an initial medication regimen review to identify medication optimization opportunities and a 14 day follow up call. Primary outcomes were quantity of medications depre-scribed per patient, classes of medications that were deprescribed,
{"title":"Implementation of a Pilot VIONE PharmD Telephone Clinic within an Older Adult Patient-Aligned Care Team at the West Palm Beach VA Healthcare System","authors":"Wesley Faulkner, Sandra L DiScala, Christine M. Vartan, Belal Dakroub, Jennifer Quellhorst, Anupama Nair, M. Miller, Mythili Bharadwaj, Michael Silverman","doi":"10.1080/15360288.2023.2234262","DOIUrl":"https://doi.org/10.1080/15360288.2023.2234262","url":null,"abstract":"Background: Patients receiving palliative-focused care have complex medication regimens and multi-morbidity. Risk of adverse drug reactions (ADR), fall risk, and drug-drug interactions are increased with polypharmacy. Within the Department of Veteran’s Affairs a commonly used deprescribing model is the VIONE methodology. VIONE catego-rizes medications into vital/life-saving medications, important for quality of life, optional, not indicated/treatment complete, and every medication has a diagnosis. The VIONE dashboards aids providers identify potentially inappropriate medications and prioritizes patients. This study aimed to pilot implementation of board-certified clinical pharmacist practitioners utilizing the VIONE model of deprescribing within an older adult patient-aligned care team at the West Palm Beach VAHCS. Methods: The PGY2 Pain Management and Palliative Care resident reached out via telephone to the patients for an initial medication regimen review to identify medication optimization opportunities and a 14 day follow up call. Primary outcomes were quantity of medications depre-scribed per patient, classes of medications that were deprescribed,","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48085928","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 : 2023-07-03DOI: 10.1080/15360288.2023.2234264
E. Murter, Benjamin Miskle, Lori J. Fisher, M. Schmidt, J. Ray
{"title":"Development of a Screening Tool for Opioid-Induced Endocrinopathy in Adult Patients","authors":"E. Murter, Benjamin Miskle, Lori J. Fisher, M. Schmidt, J. Ray","doi":"10.1080/15360288.2023.2234264","DOIUrl":"https://doi.org/10.1080/15360288.2023.2234264","url":null,"abstract":"","PeriodicalId":16645,"journal":{"name":"Journal of Pain & Palliative Care Pharmacotherapy","volume":null,"pages":null},"PeriodicalIF":1.1,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44379934","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}