Pub Date : 2026-01-12DOI: 10.1186/s12875-025-03161-w
Adam Fleischmann, Ruth Lavergne, Myles Leslie
Background: As the COVID-19 pandemic accelerated the uptake of virtual primary care (VPC) in Canada, debates over how it ought to be encouraged or discouraged, governed and paid for have intensified. Within these debates there has been little attention paid to the details of which technologies are being deployed to deliver VPC and how those technologies interact with non-technical factors to ensure efficiency and effectiveness.
Methods: The aims of the study included drawing out pragmatic considerations for policy makers by identifying the various constellations of VPC technology that are being deployed; characterizing how key informants see them working and to what purpose; and describing how those technologies are interacting with non-technical factors to shape success. 29 qualitative interviews were conducted with mid-level VPC experts from the provinces of Alberta, Nova Scotia, and Ontario.
Results: Key informants saw a broad range of VPC technologies as improving access to primary care by increasing efficiency and coordination. They deployed VPC to improve the accessibility, availability, and accommodativeness of care. They described VPC technologies interacting with and relying on: human efforts, funding models, and the institutional contexts for their success.
Conclusions: Policy-makers seeking to optimize VPC will want to consider ways to support not just purchases of technology, but: the human effort required to choose and manage technology; the funding mechanisms that incentivize the efficient use technology; and the institutional contexts and cultures that underpin access improvements through technology.
{"title":"Virtual care as deployed to improve access to primary health care in three Canadian provinces: a policy focused qualitative study.","authors":"Adam Fleischmann, Ruth Lavergne, Myles Leslie","doi":"10.1186/s12875-025-03161-w","DOIUrl":"https://doi.org/10.1186/s12875-025-03161-w","url":null,"abstract":"<p><strong>Background: </strong>As the COVID-19 pandemic accelerated the uptake of virtual primary care (VPC) in Canada, debates over how it ought to be encouraged or discouraged, governed and paid for have intensified. Within these debates there has been little attention paid to the details of which technologies are being deployed to deliver VPC and how those technologies interact with non-technical factors to ensure efficiency and effectiveness.</p><p><strong>Methods: </strong>The aims of the study included drawing out pragmatic considerations for policy makers by identifying the various constellations of VPC technology that are being deployed; characterizing how key informants see them working and to what purpose; and describing how those technologies are interacting with non-technical factors to shape success. 29 qualitative interviews were conducted with mid-level VPC experts from the provinces of Alberta, Nova Scotia, and Ontario.</p><p><strong>Results: </strong>Key informants saw a broad range of VPC technologies as improving access to primary care by increasing efficiency and coordination. They deployed VPC to improve the accessibility, availability, and accommodativeness of care. They described VPC technologies interacting with and relying on: human efforts, funding models, and the institutional contexts for their success.</p><p><strong>Conclusions: </strong>Policy-makers seeking to optimize VPC will want to consider ways to support not just purchases of technology, but: the human effort required to choose and manage technology; the funding mechanisms that incentivize the efficient use technology; and the institutional contexts and cultures that underpin access improvements through technology.</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145960863","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 : 2026-01-10DOI: 10.1186/s12875-025-03159-4
Gina R Kruse, Jordan Neil, Yuchiao Chang, Reid Anctil, Catherine S Nagawa, Ruosi Shao, Ivan Flores, Natalie Durieux, Bingjing Mao, Elyse R Park
Background: Less than one in five eligible adults has received lung cancer screening (LCS) with low dose computed tomography in the U.S. We aimed to determine factors associated with intentions to undergo LCS.
Methods: Cross-sectional survey of LCS-eligible English and Spanish speaking adults in two primary care systems in Massachusetts and Oklahoma from 02/2023-05/2024. Surveys assessed smoking, lung cancer and LCS history, attitudes, beliefs, and psychological factors. Associations between these factors and screening intentions were assessed with multivariable logistic regression using bootstrap sampling to select model variables, and latent class analysis plus chi-square tests to measure associations between classes and intentions.
Results: Of 292 LCS eligible survey respondents, most were currently smoking (n = 174, 59.6%), some had previously undergone LCS (n = 115, 39.5%), and 29.5% (n = 86) were 'extremely likely' to screen in the next 12 months. In regression models, having a healthcare provider recommend LCS (odds ratio [OR]: 4.22, 95% confidence interval (CL) 2.40-7.44), being 'somewhat' or 'extremely worried' about getting lung cancer (OR 2.45, 95%CI 1.40-4.32), and speaking English at home (OR 3.54, 95% CI 1.74-7.17) were associated with intention to screen. Four latent classes emerged that varied by age, race, ethnicity, smoking status, screening self-efficacy, perceived risks, and cancer worry. Classes were significantly associated with screening intentions (p < .0001).
Conclusions: Factors associated with LCS intentions highlight opportunities to expand screening. Attending to content for Hispanic adults, increasing discussions of LCS by health care providers, and tailoring communications to incorporate cancer worry could increase use of this life-saving intervention.
{"title":"Predictors and latent class associations with lung cancer screening intentions.","authors":"Gina R Kruse, Jordan Neil, Yuchiao Chang, Reid Anctil, Catherine S Nagawa, Ruosi Shao, Ivan Flores, Natalie Durieux, Bingjing Mao, Elyse R Park","doi":"10.1186/s12875-025-03159-4","DOIUrl":"https://doi.org/10.1186/s12875-025-03159-4","url":null,"abstract":"<p><strong>Background: </strong>Less than one in five eligible adults has received lung cancer screening (LCS) with low dose computed tomography in the U.S. We aimed to determine factors associated with intentions to undergo LCS.</p><p><strong>Methods: </strong>Cross-sectional survey of LCS-eligible English and Spanish speaking adults in two primary care systems in Massachusetts and Oklahoma from 02/2023-05/2024. Surveys assessed smoking, lung cancer and LCS history, attitudes, beliefs, and psychological factors. Associations between these factors and screening intentions were assessed with multivariable logistic regression using bootstrap sampling to select model variables, and latent class analysis plus chi-square tests to measure associations between classes and intentions.</p><p><strong>Results: </strong>Of 292 LCS eligible survey respondents, most were currently smoking (n = 174, 59.6%), some had previously undergone LCS (n = 115, 39.5%), and 29.5% (n = 86) were 'extremely likely' to screen in the next 12 months. In regression models, having a healthcare provider recommend LCS (odds ratio [OR]: 4.22, 95% confidence interval (CL) 2.40-7.44), being 'somewhat' or 'extremely worried' about getting lung cancer (OR 2.45, 95%CI 1.40-4.32), and speaking English at home (OR 3.54, 95% CI 1.74-7.17) were associated with intention to screen. Four latent classes emerged that varied by age, race, ethnicity, smoking status, screening self-efficacy, perceived risks, and cancer worry. Classes were significantly associated with screening intentions (p < .0001).</p><p><strong>Conclusions: </strong>Factors associated with LCS intentions highlight opportunities to expand screening. Attending to content for Hispanic adults, increasing discussions of LCS by health care providers, and tailoring communications to incorporate cancer worry could increase use of this life-saving intervention.</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145949511","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}
Background: Changes in healthcare governance and the rise of evidence-based medicine (EBM) have over the last decades contributed to an increase in guideline-driven management of general practice. There is a lack of recent studies investigating how this continuous development affects the practice of Swedish general practitioners (GPs) from a broad perspective. Thus, this study aims to explore how Swedish GPs relate to management control through guidelines, how it affects their daily practice and work environment, and how they reflect on its consequences.
Methods: We conducted semi-structured, face-to-face interviews during 2024 with 11 GPs from all across Sweden. The transcribed interview data were analysed using thematic analysis.
Results: We constructed three themes, each representing a field of tension created by guidelines: (1) Torn between high ambitions and their resulting negative side effects, (2) Guidelines promote measurable over unmeasurable knowledge, and (3) Although autonomy in relation to guidelines is highly valued, there are compelling reasons to submit. The first theme reflects a broad agreement on the benefits of guidelines and support of the growing ambitions they reflect. However, guidelines also result in increasing work-load and reduce flexibility in healthcare collaboration. The second theme highlights that because guidelines tend to prioritise measurable over non-measurable knowledge, other aspects of GPs' professional skills risk being underused and underdeveloped. The third theme captures how GPs exercise a high degree of autonomy in relation to guidelines, yet occasionally relinquish their clinical discretion. These tensions may result in side-effects such as a deteriorating work environment, crowding-out effects, fragmented healthcare, and potentially reduced quality in areas of general practice that are difficult to measure.
Conclusions: While management control through guidelines entails many benefits, the participants in this study also reported several adverse effects on both the quality of care and the work environment. Promoting quality by organizing healthcare through increasingly complex guidelines may seem like a natural approach in a system that focuses strongly on measuring outcomes, but it is also important for healthcare decisionmakers and guideline developers to acknowledge its potential side effects.
{"title":"General practitioners and management control through guidelines: a qualitative study of its effects on their practice.","authors":"Jens Lundegård, Åsa Grauman, Niklas Juth, Linus Johnsson","doi":"10.1186/s12875-025-03171-8","DOIUrl":"https://doi.org/10.1186/s12875-025-03171-8","url":null,"abstract":"<p><strong>Background: </strong>Changes in healthcare governance and the rise of evidence-based medicine (EBM) have over the last decades contributed to an increase in guideline-driven management of general practice. There is a lack of recent studies investigating how this continuous development affects the practice of Swedish general practitioners (GPs) from a broad perspective. Thus, this study aims to explore how Swedish GPs relate to management control through guidelines, how it affects their daily practice and work environment, and how they reflect on its consequences.</p><p><strong>Methods: </strong>We conducted semi-structured, face-to-face interviews during 2024 with 11 GPs from all across Sweden. The transcribed interview data were analysed using thematic analysis.</p><p><strong>Results: </strong>We constructed three themes, each representing a field of tension created by guidelines: (1) Torn between high ambitions and their resulting negative side effects, (2) Guidelines promote measurable over unmeasurable knowledge, and (3) Although autonomy in relation to guidelines is highly valued, there are compelling reasons to submit. The first theme reflects a broad agreement on the benefits of guidelines and support of the growing ambitions they reflect. However, guidelines also result in increasing work-load and reduce flexibility in healthcare collaboration. The second theme highlights that because guidelines tend to prioritise measurable over non-measurable knowledge, other aspects of GPs' professional skills risk being underused and underdeveloped. The third theme captures how GPs exercise a high degree of autonomy in relation to guidelines, yet occasionally relinquish their clinical discretion. These tensions may result in side-effects such as a deteriorating work environment, crowding-out effects, fragmented healthcare, and potentially reduced quality in areas of general practice that are difficult to measure.</p><p><strong>Conclusions: </strong>While management control through guidelines entails many benefits, the participants in this study also reported several adverse effects on both the quality of care and the work environment. Promoting quality by organizing healthcare through increasingly complex guidelines may seem like a natural approach in a system that focuses strongly on measuring outcomes, but it is also important for healthcare decisionmakers and guideline developers to acknowledge its potential side effects.</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145949530","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 : 2026-01-09DOI: 10.1186/s12875-025-03168-3
Romain Guignard, Daisy Luangphinith, Alice Escande, Anysia Nguyen, Justine Avenel, Olivier Smadja, Anne Pasquereau, Viêt Nguyen-Thanh
Background: Although support for tobacco smoking cessation provided by general practitioners (GP) has proven effective, such an approach remains quite rare. We designed a behavioural science-based intervention to improve GP support for patients to quit smoking. The present study aimed to evaluate the effectiveness of this in-office paper-based intervention by comparing it with a no-intervention control group.
Methods: We conducted an online randomised controlled trial between January and May 2024 among GPs in France. The intervention consisted in sending a kit containing an information sheet for GPs outlining the main stages of brief advice for smoking cessation, questionnaires for patients asking them about their smoking status and, for those who smoked, their motivation to quit, as well as a poster to be displayed in each GP's waiting room to encourage people who smoke tobacco to complete the questionnaire. The primary outcome was the proportion of people who smoke with whom GPs had discussed smoking cessation on their last full working day five weeks after the kit had been sent out. The secondary outcome was the likelihood that GPs provided cessation support (e.g., prescribed nicotine replacement therapy (NRT), proposed a follow-up consultation, and/or referred patients to other professionals) on the same day.
Results: Of the 800 GPs recruited, 641 fully completed the final survey (333 in the intervention group and 308 in the control group). The proportion of people who smoke with whom GPs had discussed cessation was significantly higher in the intervention group (59.0% vs. 52.3%, p < 0.05). The likelihood of a follow-up consultation being offered to patients who smoke was also significantly higher in the intervention group (73.8% vs. 60.3%, p < 0.05). The likelihood of NRT prescription or referral were not significantly different between groups (82.4% vs. 77.9%, and 23.3% vs. 21.5%, respectively).
Conclusions: Providing simple paper-based tools was associated with a greater likelihood of GPs discussing smoking cessation with their patients. This kind of intervention could usefully complement other primary care interventions, for example training, remuneration and financial incentives or care pathway reorganisation, with a view to significantly decreasing smoking prevalence.
Trial registration: The study was retrospectively registered on 25 November 2024 (ISRCTN10207960).
背景:尽管全科医生(GP)提供的戒烟支持已被证明是有效的,但这种方法仍然相当罕见。我们设计了一种基于行为科学的干预措施,以提高全科医生对患者戒烟的支持。本研究旨在通过与无干预对照组进行比较来评估这种基于办公室纸张的干预的有效性。方法:我们于2024年1月至5月在法国的全科医生中进行了一项在线随机对照试验。干预措施包括向全科医生发送一个工具包,其中包含一份信息表,概述了戒烟简要建议的主要阶段,向患者提供问卷调查,询问他们的吸烟状况,对那些吸烟的人,询问他们戒烟的动机,以及在每个全科医生的候诊室张贴一张海报,鼓励吸烟的人完成问卷。研究的主要结果是,在工具包发出五周后的最后一个完整工作日,与全科医生讨论戒烟问题的吸烟者的比例。次要结果是全科医生在同一天提供戒烟支持的可能性(例如,处方尼古丁替代疗法(NRT),建议随访咨询,和/或将患者转介给其他专业人员)。结果:在招募的800名全科医生中,641人完全完成了最终调查(干预组333人,对照组308人)。在干预组中,与全科医生讨论过戒烟的吸烟者比例明显更高(59.0% vs. 52.3%)。结论:提供简单的纸质工具与全科医生与患者讨论戒烟的可能性更大相关。这种干预措施可以有效地补充其他初级保健干预措施,例如培训、薪酬和财政激励或护理途径重组,以期显著降低吸烟率。试验注册:该研究于2024年11月25日回顾性注册(ISRCTN10207960)。
{"title":"Effectiveness of an in-office intervention to improve general practitioners' support for tobacco smoking cessation: results from a randomised controlled trial (TABAC-PRO).","authors":"Romain Guignard, Daisy Luangphinith, Alice Escande, Anysia Nguyen, Justine Avenel, Olivier Smadja, Anne Pasquereau, Viêt Nguyen-Thanh","doi":"10.1186/s12875-025-03168-3","DOIUrl":"https://doi.org/10.1186/s12875-025-03168-3","url":null,"abstract":"<p><strong>Background: </strong>Although support for tobacco smoking cessation provided by general practitioners (GP) has proven effective, such an approach remains quite rare. We designed a behavioural science-based intervention to improve GP support for patients to quit smoking. The present study aimed to evaluate the effectiveness of this in-office paper-based intervention by comparing it with a no-intervention control group.</p><p><strong>Methods: </strong>We conducted an online randomised controlled trial between January and May 2024 among GPs in France. The intervention consisted in sending a kit containing an information sheet for GPs outlining the main stages of brief advice for smoking cessation, questionnaires for patients asking them about their smoking status and, for those who smoked, their motivation to quit, as well as a poster to be displayed in each GP's waiting room to encourage people who smoke tobacco to complete the questionnaire. The primary outcome was the proportion of people who smoke with whom GPs had discussed smoking cessation on their last full working day five weeks after the kit had been sent out. The secondary outcome was the likelihood that GPs provided cessation support (e.g., prescribed nicotine replacement therapy (NRT), proposed a follow-up consultation, and/or referred patients to other professionals) on the same day.</p><p><strong>Results: </strong>Of the 800 GPs recruited, 641 fully completed the final survey (333 in the intervention group and 308 in the control group). The proportion of people who smoke with whom GPs had discussed cessation was significantly higher in the intervention group (59.0% vs. 52.3%, p < 0.05). The likelihood of a follow-up consultation being offered to patients who smoke was also significantly higher in the intervention group (73.8% vs. 60.3%, p < 0.05). The likelihood of NRT prescription or referral were not significantly different between groups (82.4% vs. 77.9%, and 23.3% vs. 21.5%, respectively).</p><p><strong>Conclusions: </strong>Providing simple paper-based tools was associated with a greater likelihood of GPs discussing smoking cessation with their patients. This kind of intervention could usefully complement other primary care interventions, for example training, remuneration and financial incentives or care pathway reorganisation, with a view to significantly decreasing smoking prevalence.</p><p><strong>Trial registration: </strong>The study was retrospectively registered on 25 November 2024 (ISRCTN10207960).</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145946652","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 : 2026-01-08DOI: 10.1186/s12875-026-03173-0
Keiichiro Narumoto, Misaki Fukue, Moriya Iwaizumi, Michael D Fetters, Benjamin F Crabtree, Machiko Inoue
Background: Primary care physicians face multiple challenges in integrating clinical cancer genetics into routine care. Most studies of genomic medicine come from countries with well-developed primary healthcare systems, while research on the integration of clinical genetics in primary care remains limited in Japan and Asia. In Japan, where family medicine is still emerging as a specialty, no prior studies have examined Japanese family physicians' engagement with clinical cancer genetics, including genetic counseling and referral. This study investigates Japanese family physicians' knowledge, attitudes and practices regarding hereditary cancer syndromes.
Methods: This is mixed methods research employing an explanatory sequential design with survey data collection followed by qualitative interviews. First, a quantitative survey assessed Japanese family physicians' knowledge, attitudes, and practices regarding genetic counseling and referrals for hereditary cancer syndromes. We then explored their practices and perspectives in relation to the quantitative findings through semi-structured individual interviews with a subset of the family physicians. Finally, we integrated both findings in a joint display table and generated conclusions or metainferences.
Results: A total of 149 family physicians completed a survey (response rate: 26.7%), with 11 who did not have experience in genetic counseling or referrals participating in follow-up qualitative interviews. Survey responses found that only 6% of respondents provided genetic counseling, and 5% referred patients to genetic professionals. Most family physicians (64-73%) demonstrated limited knowledge of hereditary cancer syndrome, leading to difficulty interpreting family history and assessing cancer risk in clinical practice. While many family physicians (71-94%) conceptually acknowledged the benefits of clinical genetics in the survey, interviews highlighted concerns about the potential harm of genetic testing. Interviews helped explain the reasons for low engagement rates. Family physicians were uncertain about the clinical utility of genetic interventions and about the psychological impact discussing cancer genetics might have on patients. Further, the term "heredity" carries negative connotations, which made family physicians hesitant to initiate such conversations.
Conclusion: Japanese family physicians encounter challenges in applying clinical cancer genetics. Further research is needed to explore effective approaches that support family physicians in addressing these challenges while enhancing their role in clinical cancer genetics.
{"title":"Knowledge, attitudes and practices of cancer genetics in family medicine in Japan: a mixed methods study.","authors":"Keiichiro Narumoto, Misaki Fukue, Moriya Iwaizumi, Michael D Fetters, Benjamin F Crabtree, Machiko Inoue","doi":"10.1186/s12875-026-03173-0","DOIUrl":"https://doi.org/10.1186/s12875-026-03173-0","url":null,"abstract":"<p><strong>Background: </strong>Primary care physicians face multiple challenges in integrating clinical cancer genetics into routine care. Most studies of genomic medicine come from countries with well-developed primary healthcare systems, while research on the integration of clinical genetics in primary care remains limited in Japan and Asia. In Japan, where family medicine is still emerging as a specialty, no prior studies have examined Japanese family physicians' engagement with clinical cancer genetics, including genetic counseling and referral. This study investigates Japanese family physicians' knowledge, attitudes and practices regarding hereditary cancer syndromes.</p><p><strong>Methods: </strong>This is mixed methods research employing an explanatory sequential design with survey data collection followed by qualitative interviews. First, a quantitative survey assessed Japanese family physicians' knowledge, attitudes, and practices regarding genetic counseling and referrals for hereditary cancer syndromes. We then explored their practices and perspectives in relation to the quantitative findings through semi-structured individual interviews with a subset of the family physicians. Finally, we integrated both findings in a joint display table and generated conclusions or metainferences.</p><p><strong>Results: </strong>A total of 149 family physicians completed a survey (response rate: 26.7%), with 11 who did not have experience in genetic counseling or referrals participating in follow-up qualitative interviews. Survey responses found that only 6% of respondents provided genetic counseling, and 5% referred patients to genetic professionals. Most family physicians (64-73%) demonstrated limited knowledge of hereditary cancer syndrome, leading to difficulty interpreting family history and assessing cancer risk in clinical practice. While many family physicians (71-94%) conceptually acknowledged the benefits of clinical genetics in the survey, interviews highlighted concerns about the potential harm of genetic testing. Interviews helped explain the reasons for low engagement rates. Family physicians were uncertain about the clinical utility of genetic interventions and about the psychological impact discussing cancer genetics might have on patients. Further, the term \"heredity\" carries negative connotations, which made family physicians hesitant to initiate such conversations.</p><p><strong>Conclusion: </strong>Japanese family physicians encounter challenges in applying clinical cancer genetics. Further research is needed to explore effective approaches that support family physicians in addressing these challenges while enhancing their role in clinical cancer genetics.</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145936241","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 : 2026-01-08DOI: 10.1186/s12875-025-03136-x
Sarah Opie-Martin, Freya Tracey, Emma Whitfield, Melissa Co, Jake Beech, Luisa M Pettigrew, Jonathan M Clarke, Therese Lloyd
{"title":"Evaluating the impact of capitation funding top-up payments in primary care.","authors":"Sarah Opie-Martin, Freya Tracey, Emma Whitfield, Melissa Co, Jake Beech, Luisa M Pettigrew, Jonathan M Clarke, Therese Lloyd","doi":"10.1186/s12875-025-03136-x","DOIUrl":"https://doi.org/10.1186/s12875-025-03136-x","url":null,"abstract":"","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145936604","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 : 2026-01-08DOI: 10.1186/s12875-025-03144-x
Masroor Salauddin, Umme Salma Anee, Deepa Barua, Joseph Hicks, Khaleda Islam, Helen Elsey, Rumana Huque
<p><strong>Background: </strong>In urban Bangladesh, rapid urbanisation is increasing the prevalence of hypertension (HTN) and type 2 diabetes (T2D). The plurality of providers, often with minimal public provision, adds complexity. We aimed to evaluate how well two categories of primary health care (PHC) facilities for poor urban residents - NGO-run clinics under the Ministry of Local Government, Rural Development and Cooperation and Urban Dispensaries (UDs) under the Ministry of Health and Family Welfare - are prepared to manage these two conditions.</p><p><strong>Methods: </strong>We performed a cross-sectional survey of all 19 UDs and 32 NGO clinics in Dhaka between 1st July, 2022 and 25th February, 2023. We developed a bespoke tool to assess how prepared facilities were to manage patients with HTN and T2D based on the essential requirements in Bangladesh's National Protocol for Management of Diabetes and Hypertension (2019, 2nd edition). Trained researchers observed practices in facilities and consulted facility staff to complete the checklist to assess whether the components in the checklist were adequately in place or not. The components were grouped into domains covering training, guidelines, equipment, diagnostic tests, and drugs. We also developed a separate tool to assess facility preparedness in relation to information systems. We then created an overall preparedness outcome based on the total number of components adequately in place across all domains (excluding the information system tool) and outcomes looking at whether each separate component (including those from the information systems tool) was adequately in place or not. We analysed data using generalised linear models and marginal effects approaches to estimate percentage preparedness levels within facility and disease groups and percentage point differences in preparedness levels between facility and disease groups, along with associated 95% confidence intervals.</p><p><strong>Results: </strong>Overall levels of preparedness were lacking for both HTN and T2D conditions in both facility types. For HTN management, overall preparedness was 46.8% (95% CI: 41.6%, 52%) for UDs and 32.5% (95% CI: 30.5%, 34.5%) for NGO clinics. For diabetes management, overall preparedness was 31.6% (95% CI: 27.5%, 35.6%) for UDs and 34.9% (95% CI: 33.2%, 36.6%) for NGO clinics. Training and guidelines were absent for NGO clinics for both conditions, with varying levels of preparedness related to diagnostics and drugs in both facility types for the two conditions, although basic equipment levels were high across facility types for both conditions. Only UDs recorded diagnosis and prescriptions that can be recognised and retrieved, and neither had digital records or a designated person for data management. Patient feedback mechanisms were absent for UDs but present at a high level in NGO clinics.</p><p><strong>Conclusion: </strong>Urban PHC facilities in Dhaka have considerable gaps in preparedness to
{"title":"How prepared are urban primary care facilities to manage hypertension and type 2 diabetes in Dhaka, Bangladesh? A cross-sectional descriptive study of government urban dispensaries and NGO clinics.","authors":"Masroor Salauddin, Umme Salma Anee, Deepa Barua, Joseph Hicks, Khaleda Islam, Helen Elsey, Rumana Huque","doi":"10.1186/s12875-025-03144-x","DOIUrl":"https://doi.org/10.1186/s12875-025-03144-x","url":null,"abstract":"<p><strong>Background: </strong>In urban Bangladesh, rapid urbanisation is increasing the prevalence of hypertension (HTN) and type 2 diabetes (T2D). The plurality of providers, often with minimal public provision, adds complexity. We aimed to evaluate how well two categories of primary health care (PHC) facilities for poor urban residents - NGO-run clinics under the Ministry of Local Government, Rural Development and Cooperation and Urban Dispensaries (UDs) under the Ministry of Health and Family Welfare - are prepared to manage these two conditions.</p><p><strong>Methods: </strong>We performed a cross-sectional survey of all 19 UDs and 32 NGO clinics in Dhaka between 1st July, 2022 and 25th February, 2023. We developed a bespoke tool to assess how prepared facilities were to manage patients with HTN and T2D based on the essential requirements in Bangladesh's National Protocol for Management of Diabetes and Hypertension (2019, 2nd edition). Trained researchers observed practices in facilities and consulted facility staff to complete the checklist to assess whether the components in the checklist were adequately in place or not. The components were grouped into domains covering training, guidelines, equipment, diagnostic tests, and drugs. We also developed a separate tool to assess facility preparedness in relation to information systems. We then created an overall preparedness outcome based on the total number of components adequately in place across all domains (excluding the information system tool) and outcomes looking at whether each separate component (including those from the information systems tool) was adequately in place or not. We analysed data using generalised linear models and marginal effects approaches to estimate percentage preparedness levels within facility and disease groups and percentage point differences in preparedness levels between facility and disease groups, along with associated 95% confidence intervals.</p><p><strong>Results: </strong>Overall levels of preparedness were lacking for both HTN and T2D conditions in both facility types. For HTN management, overall preparedness was 46.8% (95% CI: 41.6%, 52%) for UDs and 32.5% (95% CI: 30.5%, 34.5%) for NGO clinics. For diabetes management, overall preparedness was 31.6% (95% CI: 27.5%, 35.6%) for UDs and 34.9% (95% CI: 33.2%, 36.6%) for NGO clinics. Training and guidelines were absent for NGO clinics for both conditions, with varying levels of preparedness related to diagnostics and drugs in both facility types for the two conditions, although basic equipment levels were high across facility types for both conditions. Only UDs recorded diagnosis and prescriptions that can be recognised and retrieved, and neither had digital records or a designated person for data management. Patient feedback mechanisms were absent for UDs but present at a high level in NGO clinics.</p><p><strong>Conclusion: </strong>Urban PHC facilities in Dhaka have considerable gaps in preparedness to ","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145919381","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 : 2026-01-08DOI: 10.1186/s12875-025-03169-2
Lars Christian Kvalbein-Olsen, Eivind Aakhus, Ole Rikard Haavet, Erik L Werner
Background: Depression in older adults is common in general practice, but the optimal approach for identification and treatment is not entirely clear.
Aim: To explore physicians' experiences with a structured collaborative model involving joint consultations between patients, general practitioners (GPs), and geriatric psychiatrists for managing depression in adults aged 65 years and older.
Methods: Three focus group discussions were conducted with 13 physicians (10 GPs and 3 psychiatrists) who had participated in a structured collaboration model as part of a recent cluster randomized intervention study. Data were analyzed using Systematic Text Condensation.
Results: Five themes emerged: (1) diagnostic challenges; (2) perceived advantages; (3) feasibility; (4) concerns about overdiagnosis and overtreatment; and (5) suggested adjustments to the model. Somatic presentations often overshadowed depressive symptoms, particularly under GPs time constraints. Joint consultations strengthened the GP-patient relationship and enabled mutual learning. The presence of the GP was viewed as essential for patient engagement. The model addressed a treatment gap for GPs and was considered by psychiatrists to be highly cost-effective. All participants supported broader implementation in clinical practice.
Conclusion: The GPs' enthusiasm for this collaborative approach indicates an unmet need in the treatment of older patients with depression. By strengthening both the doctor-patient relationship and interdisciplinary collaboration between GPs and psychiatrists in a cost-effective manner, the use of such joint consultations should be further investigated.
{"title":"Joint consultations with general practitioners and geriatric psychiatrists for older adults with depression: a focus group study.","authors":"Lars Christian Kvalbein-Olsen, Eivind Aakhus, Ole Rikard Haavet, Erik L Werner","doi":"10.1186/s12875-025-03169-2","DOIUrl":"https://doi.org/10.1186/s12875-025-03169-2","url":null,"abstract":"<p><strong>Background: </strong>Depression in older adults is common in general practice, but the optimal approach for identification and treatment is not entirely clear.</p><p><strong>Aim: </strong>To explore physicians' experiences with a structured collaborative model involving joint consultations between patients, general practitioners (GPs), and geriatric psychiatrists for managing depression in adults aged 65 years and older.</p><p><strong>Methods: </strong>Three focus group discussions were conducted with 13 physicians (10 GPs and 3 psychiatrists) who had participated in a structured collaboration model as part of a recent cluster randomized intervention study. Data were analyzed using Systematic Text Condensation.</p><p><strong>Results: </strong>Five themes emerged: (1) diagnostic challenges; (2) perceived advantages; (3) feasibility; (4) concerns about overdiagnosis and overtreatment; and (5) suggested adjustments to the model. Somatic presentations often overshadowed depressive symptoms, particularly under GPs time constraints. Joint consultations strengthened the GP-patient relationship and enabled mutual learning. The presence of the GP was viewed as essential for patient engagement. The model addressed a treatment gap for GPs and was considered by psychiatrists to be highly cost-effective. All participants supported broader implementation in clinical practice.</p><p><strong>Conclusion: </strong>The GPs' enthusiasm for this collaborative approach indicates an unmet need in the treatment of older patients with depression. By strengthening both the doctor-patient relationship and interdisciplinary collaboration between GPs and psychiatrists in a cost-effective manner, the use of such joint consultations should be further investigated.</p>","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935919","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 : 2026-01-08DOI: 10.1186/s12875-025-03167-4
Muhammad Maaz, Muhammad Yasir, Anosha Siddique, Bilal Qammar, Noorul Hadi
{"title":"Type 2 diabetes care: knowledge and clinical practice among medical practitioners at Medical Teaching Institute Mardan, Pakistan - a cross-sectional study.","authors":"Muhammad Maaz, Muhammad Yasir, Anosha Siddique, Bilal Qammar, Noorul Hadi","doi":"10.1186/s12875-025-03167-4","DOIUrl":"https://doi.org/10.1186/s12875-025-03167-4","url":null,"abstract":"","PeriodicalId":72428,"journal":{"name":"BMC primary care","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145936205","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}