14 results on '"Jansen, Jesse"'
Search Results
2. Harm and Medication-Type Impact Agreement with Hypothetical Deprescribing Recommendations: a Vignette-Based Experiment with Older Adults Across Four Countries
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Vordenberg, Sarah E., Weir, Kristie Rebecca, Jansen, Jesse, Todd, Adam, Schoenborn, Nancy, and Scherer, Aaron M.
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- 2023
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3. The role of older patients’ goals in GP decision-making about medicines: a qualitative study
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Weir, Kristie Rebecca, Naganathan, Vasi, Carter, Stacy M., Tam, Chun Wah Michael, McCaffery, Kirsten, Bonner, Carissa, Rigby, Debbie, McLachlan, Andrew J., and Jansen, Jesse
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- 2021
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4. Exploring Different Contexts of Statin Deprescribing: A Vignette-Based Experiment with Older Adults Across Four Countries.
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Weir, Kristie Rebecca, Vordenberg, Sarah E., Scherer, Aaron M., Jansen, Jesse, Schoenborn, Nancy, and Todd, Adam
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DEPRESCRIBING ,OLDER people ,STATINS (Cardiovascular agents) ,INAPPROPRIATE prescribing (Medicine) - Abstract
This article explores the impact of contextual factors on older adults' agreement with a recommendation to stop taking statins, a medication commonly prescribed to prevent cardiovascular events. The study conducted a vignette-based online experiment with older people from Australia, the Netherlands, United Kingdom, and the United States. The results showed that contextual factors such as the statin being prescribed by a cardiologist, the patient's spouse having a stroke after stopping the statin, and viewing an image of a stroke decreased participants' agreement with the deprescribing recommendation. The study suggests that clinicians should consider these contextual factors when engaging in deprescribing conversations with patients. [Extracted from the article]
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- 2024
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5. The Patient Typology about deprescribing and medication‐related decisions: A quantitative exploration.
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Weir, Kristie Rebecca, Scherer, Aaron M., Vordenberg, Sarah E., Streit, Sven, Jansen, Jesse, and Jungo, Katharina Tabea
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DEPRESCRIBING ,OLDER people ,LOGISTIC regression analysis ,SECONDARY analysis ,POLYPHARMACY - Abstract
This study aimed to test the adequacy of a quantitative measure of our qualitatively developed Patient Typology—categories of older adults' attitudes towards medicines and medicine decision‐making—and identify characteristics associated with each Typology. We conducted secondary data analyses of a subset of survey item measures of adults (≥65 years) who were members of online survey panels in Australia, the United Kingdom, the United States and the Netherlands (n = 4688). Multinomial logistic regression analyses assessed associations between demographic, psychosocial and medication‐related measures. Mean age was 71.5 (5), and 47.5% of participants were female. Factors associated with an increased likelihood of identifying with Typology 1 'Attached to medicines' over Typology 2 'Open to deprescribing' were higher positive attitude towards polypharmacy (RRR = 1.12, p = <0.001) and higher need for certainty (RRR = 1.11, p = 0.039). Factors associated with an increased likelihood of identifying with Typology 3 'Defers (medication decision‐making) to others' over Typology 2 were older age (RRR = 1.47 per 10‐year age increase, p = <0.001) and a decreased likelihood of prior deprescribing experience (RRR = 0.73, p = 0.033). This study provides validation of the Typology with large samples from four countries, with the quantitatively‐measured typologies generally aligning with the qualitatively derived categories. Our Patient Typology measure provides a succinct way researchers can assess attitudes towards deprescribing. [ABSTRACT FROM AUTHOR]
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- 2024
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6. A systematic review of interventions to deprescribe benzodiazepines and other hypnotics among older people
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Reeve, Emily, Ong, Magdalene, Wu, Angela, Jansen, Jesse, Petrovic, Mirko, and Gnjidic, Danijela
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- 2017
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7. The deprescribing rainbow: a conceptual framework highlighting the importance of patient context when stopping medication in older people
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Todd, Adam, Jansen, Jesse, Colvin, Jim, and McLachlan, Andrew J.
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- 2018
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8. Supporting conversations about medicines and deprescribing: GPs' perspectives on a Medicines Conversation Guide.
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Weir, Kristie Rebecca, Bonner, Carissa, Naganathan, Vasi, Tam, Chun Wah Michael, Rigby, Debbie, McLachlan, Andrew J, and Jansen, Jesse
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Objectives: To explore GP perspectives on a Medicines Conversation Guide to support deprescribing communication. Methods: Semistructured interviews with GPs from Australia (n = 32). Participants were purposively sampled with varying experiences and locations. Transcribed audio recordings of interviews were coded using framework analysis. Key findings: Most GPs stated they would use the Guide in consultation with an older patient to discuss medications. The strengths of the Guide included empowering the patient voice on an important topic. Limitations included time and complex concepts. Conclusions: Overall, the Medicines Conversation Guide was perceived by GPs to be a useful communication tool to support discussions about deprescribing with patients. [ABSTRACT FROM AUTHOR]
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- 2023
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9. Opioid deprescribing: Qualitative perspectives from those with chronic non-cancer pain.
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Hamilton, Melanie, Gnjidic, Danijela, Christine Lin, Chung-Wei, Jansen, Jesse, Weir, Kristie Rebecca, Shaheed, Christina Abdel, Blyth, Fiona, and Mathieson, Stephanie
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Aim: Deprescribing is the systematic process of discontinuing medications when the harms outweigh the benefits. This study aimed to identify barriers and facilitators in people with chronic non-cancer pain when deprescribing opioid analgesics, and their views on resources that assist with deprescribing.Methods: A purposive sampling strategy was used to recruit 19 adults with chronic non-cancer pain from the community who were, or had been, on long-term opioid therapy. Recruitment continued until thematic saturation was achieved. Semi-structured telephone interviews were conducted. A five-step framework and thematic analysis method identified themes for each study aim.Results: Themes identifying barriers to opioid deprescribing raised challenges of a lack of available alternatives, managing opioid dependency and withdrawal symptoms or inability to function without opioids when in extreme pain. Facilitating themes described the value of support networks, including a trusting doctor-patient relationship and finding individual coping strategies to address deprescribing barriers. We explored a variety of resources from electronic forms such as websites and apps to paper-based or face to face. Participants expressed that whatever the form, resources need to be educational but also simple and engaging.Conclusions: Most people suffering from chronic non-cancer pain expressed dissatisfaction with being on opioids but most were still unwilling to deprescribe due to insufficient alternatives, a lack of support from their doctors and lack of information about the deprescribing process. Deprescribing can be facilitated by improving supportive networks and strategies and providing simple and positive educational resources. [ABSTRACT FROM AUTHOR]- Published
- 2022
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10. Deprescribing Opioids in Chronic Non-cancer Pain: Systematic Review of Randomised Trials.
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Mathieson, Stephanie, Maher, Christopher G., Ferreira, Giovanni E., Hamilton, Melanie, Jansen, Jesse, McLachlan, Andrew J., Underwood, Martin, and Lin, Chung-Wei Christine
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DRUG side effects ,ANALGESICS ,CHRONIC pain ,MEDICAL prescriptions ,NARCOTICS ,RISK assessment ,PAIN management ,SYSTEMATIC reviews ,CLINICAL trial registries ,DEPRESCRIBING - Abstract
Background: Deprescribing, the process of reducing or discontinuing unnecessary or harmful medicines is an essential part of clinical practice. Objective: To evaluate the efficacy of interventions designed to deprescribe opioid analgesics for pain relief in patients with chronic non-cancer pain. Methods: We searched electronic databases, including clinical trial registries, from database inception to 13th January 2020 without restrictions, and conducted citation tracking. Our systematic review included randomised controlled trials (RCTs) evaluating interventions reducing the prescription, or use of opioid analgesics in patients with chronic pain versus control. Inventions could be aimed at the patient, clinician, or both. We excluded trials enrolling patients with cancer or illicit drug use. Two authors independently screened and extracted data. Outcome follow-up timepoints were short (≤ 3 months), intermediate (> 3 but < 12 months) or long (≥ 12 months) term. Primary outcome was the reduction in opioid dose [morphine milligram equivalent (MME) mg/day]. Methodological quality was assessed using the Cochrane Risk of Bias Tool. Results: We included ten patient-focused RCT interventions (n = 835; median 37 participants) and 2 testing clinician-focused interventions (n = 291 clinicians); none at low risk of bias. Patient-focused interventions did not reduce opioid dose in the intermediate term [e.g. dose reduction protocol, mean difference (MD) − 19.9 MME, 95% CI − 107.5 to 67.7], nor did they increase the number of participants who ceased their dose, or increase the risk of serious adverse events or adverse events. One clinician intervention of education plus decision tools versus decision tools alone reduced the number of opioid prescriptions (risk difference (RD) − 0.1, 95% CI − 0.2 to − 0.1), dose (MD − 5.3 MME, 95% CI − 6.2 to − 4.5) and use (RD − 0.1, 95% CI − 0.1 to − 0.0) in the long term. Limitations: Study heterogeneity prevented meta-analysis. Conclusion: The small number of studies and heterogeneity prevented firm conclusions to recommend any one opioid-analgesic-deprescribing strategy in patients with chronic pain. Systematic review registration number: PROSPERO CRD42017068422. [ABSTRACT FROM AUTHOR]
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- 2020
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11. Availability and readability of patient education materials for deprescribing: An environmental scan.
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Fajardo, Michael Anthony, Weir, Kristie Rebecca, Bonner, Carissa, Gnjidic, Danijela, and Jansen, Jesse
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PATIENT education ,DRUG side effects ,HEALTH literacy ,OLDER people ,DRUG withdrawal symptoms - Abstract
Aims: To identify and evaluate content and readability of freely available online deprescribing patient education materials (PEMs). Methods: Systematic review of PEMs using MEDLINE, Embase, CINAHL, PsycINFO and The Cochrane Library of Systematic Reviews from inception to 25 September 2017 to identify PEMs. Additionally, deprescribing researchers and health professionals were surveyed to identify additional materials. Known repositories of materials were searched followed by a systematic Google search (22–28 January 2018). Materials were evaluated using an approach informed by the Patient Education Material Assessment Tool and the International Patient Decision Aids Standards Inventory. Readability of text‐based materials was assessed using the US‐based Gunning–Fog Index and Flesch–Kincaid Grade level. Results: Forty‐eight PEMs were identified. PEMs addressing deprescribing of medications for symptom control (81%) were most common. Preventative medications were rarely addressed and material (39%) focused on older people. Only 37% of PEMs provided information about both potential benefits (e.g. reducing risk of side effects) and harms (e.g. withdrawal symptoms, increased risk of disease) of deprescribing, while 40% focussed on benefits only. Readability indices indicated an average minimum reading level of Grade 12. Option Grids and Decision Aids (mean reading level below Grade 10) were most suitable for people with average literacy levels. Conclusions: Over 1/3 of deprescribing PEMs present potential benefits and harms of deprescribing indicating most of the freely available materials are not balanced. Most PEMs are pitched above average reading levels making them inaccessible for low health literacy populations. [ABSTRACT FROM AUTHOR]
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- 2019
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12. Barriers, facilitators, and resources to opioid deprescribing in primary care: experiences of general practitioners in Australia.
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Hamilton, Melanie, Mathieson, Stephanie, Gnjidic, Danijela, Jansen, Jesse, Weir, Kristie, Shaheed, Christina A., Blyth, Fiona, and Lin, Chung-Wei C.
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DEPRESCRIBING , *PRIMARY care , *GENERAL practitioners , *PAIN management , *OPIOID analgesics , *SEMI-structured interviews , *CHRONIC pain , *ATTITUDES of medical personnel , *PRIMARY health care - Abstract
Abstract: Deprescribing is the systematic process of discontinuing drugs when harms outweigh the benefits. We conducted semistructured telephone interviews with 22 general practitioners (GPs) who had prescribed or deprescribed opioids in patients with chronic noncancer pain within the past 6 months to investigate the barriers and facilitators to deprescribing opioid analgesics in patients with chronic noncancer pain. We also explored GPs' perspectives on the available resources to assist them with opioid deprescribing. Interviews were audio-recorded, transcribed verbatim, and then coded using an iterative process until data saturation reached. The thematic analysis process identified themes, first as concepts, and then refined to overarching themes after the merging of similar subthemes. Themes exploring barriers to deprescribing highlighted the difficulties GPs face while considering patient factors and varying prescribing practices within the confines of the health system. Patient motivation and doctor-patient rapport were central factors to facilitate deprescribing and GPs considered the most important deprescribing resource to be a multidisciplinary network of clinicians to support themselves and their patients. Therefore, although GPs emphasised the importance of deprescribing opioid analgesics, they also expressed many barriers relating to managing complex pain conditions, patient factors, and varying prescribing practices between clinicians. Some of these barriers could be mitigated by GPs having time and resources to educate and build rapport with their patients. This suggests the need for further development of multimodal resources and improved support through the public health system to enable GPs to prioritise patient-centred care. [ABSTRACT FROM AUTHOR]- Published
- 2022
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13. A systematic review of interventions to deprescribe benzodiazepines and other hypnotics among older people
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Emily Reeve, Mirko Petrovic, Magdalene Ong, Angela Wu, Jesse Jansen, Danijela Gnjidic, Reeve, Emily, Ong, Magdalene, Wu, Angela, Jansen, Jesse, Petrovic, Mirko, and Gnjidic, Danijela
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medicine.medical_specialty ,medicine.drug_class ,Psychological intervention ,law.invention ,03 medical and health sciences ,Benzodiazepines ,0302 clinical medicine ,Deprescriptions ,deprescribing ,Randomized controlled trial ,Quality of life ,law ,Sleep Initiation and Maintenance Disorders ,medicine ,Insomnia ,Humans ,Hypnotics and Sedatives ,Pharmacology (medical) ,030212 general & internal medicine ,benzodiazepines ,Psychiatry ,older adults ,Aged ,Pharmacology ,Benzodiazepine ,business.industry ,General Medicine ,Discontinuation ,Z-drugs ,Anxiety ,Deprescribing ,medicine.symptom ,business ,030217 neurology & neurosurgery - Abstract
Purpose: Benzodiazepines are effective medicines for insomnia and anxiety but are commonly used beyond recommended treatment time frames, which may lead to adverse drug events. The aim of this systematic review was to critically evaluate the success of interventions used to reduce benzodiazepines and ‘Z-drug’ use, and the impact of these interventions on clinical outcomes in older adults. Methods: A search was conducted in PubMed, Embase, Informit, International Pharmaceutical Abstracts, Scopus, PsychINFO, Cochrane Central Register of Controlled Trials (CENTRAL) and CINAHL. Studies conducted in older adults (≥65 years) and published between January 1995 and July 2015 were included. Two authors independently reviewed all articles for eligibility and extracted the data. Results: Seven studies of benzodiazepines and Z-drug withdrawal were identified. Benzodiazepine discontinuation rates were 64.3% in one study that employed pharmacological substitution with melatonin and 65.0% in a study that employed general practitioner-targeted intervention. Mixed interventions including patient education and tapering (n = 2), pharmacological substitution with psychological support (n = 1) and tapering with psychological support (n = 1) yielded discontinuation rates between 27.0 and 80.0%. Five studies measured clinical outcomes following benzodiazepine discontinuation. Most (n = 4) observed no difference in prevalence of withdrawal symptoms or sleep quality, while one study reported decline in quality of life in those who continued taking benzodiazepine vs. those who discontinued over 8 months. Conclusions: Current evidence shows that benzodiazepine withdrawal is feasible in the older population, but withdrawal rates vary according to the type of intervention. As the benefits and sustainability of these interventions are unclear, further studies should be conducted to assess this. Refereed/Peer-reviewed
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- 2016
14. Reducing Inappropriate Polypharmacy
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Debbie Rigby, Emily Reeve, Amy Page, David G. Le Couteur, Sarah N. Hilmer, Danijela Gnjidic, Elizabeth E. Roughead, Jennifer H. Martin, Kathleen N. Potter, Ian A Scott, Chris Del Mar, Jesse Jansen, Scott, Ian A, Hilmer, Sarah N, Reeve, Emily, Potter, Kathleen, Le Couteur, David, Rigby, Deborah, Gnjidic, Danijela, Del Mar, Christopher B, Roughead, Libby, Page, Amy, Jansen, Jesse, and Martin, Jennifer H
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Deprescriptions ,medicine.medical_specialty ,Drug-Related Side Effects and Adverse Reactions ,Beers Criteria ,Inappropriate Prescribing ,prescription drug ,Risk Assessment ,law.invention ,Randomized controlled trial ,law ,Internal Medicine ,Humans ,Medicine ,prevention and control ,Drug Interactions ,human ,Practice Patterns, Physicians' ,Medical prescription ,health service ,Intensive care medicine ,Adverse effect ,Polypharmacy ,Health Services Needs and Demand ,business.industry ,Communication Barriers ,medicine.disease ,non prescription drug ,Discontinuation ,risk factor ,Withholding Treatment ,Clinical Pharmacy Information Systems ,Medical emergency ,Deprescribing ,business ,Algorithms - Abstract
Inappropriate polypharmacy, especially in older people, imposes a substantial burden of adverse drug events, ill health, disability, hospitalization, and even death. The single most important predictor of inappropriate prescribing and risk of adverse drug events in older patients is the number of prescribed drugs. Deprescribing is the process of tapering or stopping drugs, aimed at minimizing polypharmacy and improving patient outcomes. Evidence of efficacy for deprescribing is emerging from randomized trials and observational studies. A deprescribing protocol is proposed comprising 5 steps: (1) ascertain all drugs the patient is currently taking and the reasons for each one; (2) consider overall risk of drug-induced harm in individual patients in determining the required intensity of deprescribing intervention; (3) assess each drug in regard to its current or future benefit potential compared with current or future harm or burden potential; (4) prioritize drugs for discontinuation that have the lowest benefit-harm ratio and lowest likelihood of adverse withdrawal reactions or disease rebound syndromes; and (5) implement a discontinuation regimen and monitor patients closely for improvement in outcomes or onset of adverse effects. Whereas patient and prescriber barriers to deprescribing exist, resources and strategies are available that facilitate deliberate yet judicious deprescribing and deserve wider application. Refereed/Peer-reviewed
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- 2015
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