Pub Date : 2025-10-30DOI: 10.1016/j.healthpol.2025.105482
Albert Prades-Colomé
Background
As populations age, understanding the health impact of long-term care systems is critical for shaping effective policy.
Objective
This study investigates the association between long-term care benefits and mortality risk among older adults in Catalonia, Spain, using comprehensive administrative data from July 2015 to December 2024.
Methods
The analysis focuses on applicants of long-term care benefits in Catalonia aged 50+, categorizing them by severity of their needs (Grades I–III) and type of benefit received: home care, residential care, a combination of both or no benefit. It applies survival analysis techniques—including Kaplan-Meier estimators and Cox proportional hazards models.
Results
Individuals with long-term care needs receiving benefits have significantly lower mortality hazards. Notably, individuals transitioning from home to residential care exhibit the most favourable hazard ratios, suggesting that responsive care pathways are associated with better survival outcomes, potentially due to a most accurate matching of care to needs. Residential care alone is associated to higher mortality risk than home care in the population with the highest grades of long-term care needs. Individuals with recognized long-term care needs who do not receive any benefits face significantly higher risks. Mortality risk also varies by sex, age, and clinical profile, with higher hazards observed among men, older individuals, and those with previous haematological, neoplastic, or respiratory conditions.
Conclusion
These findings underscore the association between formal long-term care systems and lower mortality risk and emphasize the importance of timely, adaptive care pathways in mitigating health decline among ageing populations.
{"title":"Mortality risk factors in Catalonia’s long-term care system: A population-based survival analysis","authors":"Albert Prades-Colomé","doi":"10.1016/j.healthpol.2025.105482","DOIUrl":"10.1016/j.healthpol.2025.105482","url":null,"abstract":"<div><h3>Background</h3><div>As populations age, understanding the health impact of long-term care systems is critical for shaping effective policy.</div></div><div><h3>Objective</h3><div>This study investigates the association between long-term care benefits and mortality risk among older adults in Catalonia, Spain, using comprehensive administrative data from July 2015 to December 2024.</div></div><div><h3>Methods</h3><div>The analysis focuses on applicants of long-term care benefits in Catalonia aged 50+, categorizing them by severity of their needs (Grades I–III) and type of benefit received: home care, residential care, a combination of both or no benefit. It applies survival analysis techniques—including Kaplan-Meier estimators and Cox proportional hazards models.</div></div><div><h3>Results</h3><div>Individuals with long-term care needs receiving benefits have significantly lower mortality hazards. Notably, individuals transitioning from home to residential care exhibit the most favourable hazard ratios, suggesting that responsive care pathways are associated with better survival outcomes, potentially due to a most accurate matching of care to needs. Residential care alone is associated to higher mortality risk than home care in the population with the highest grades of long-term care needs. Individuals with recognized long-term care needs who do not receive any benefits face significantly higher risks. Mortality risk also varies by sex, age, and clinical profile, with higher hazards observed among men, older individuals, and those with previous haematological, neoplastic, or respiratory conditions.</div></div><div><h3>Conclusion</h3><div>These findings underscore the association between formal long-term care systems and lower mortality risk and emphasize the importance of timely, adaptive care pathways in mitigating health decline among ageing populations.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105482"},"PeriodicalIF":3.4,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145469093","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-30DOI: 10.1016/j.healthpol.2025.105481
Pedro Atienza Montero , Luis Ángel Hierro Recio , Antonio José Garzón Gordón
Background
Outpatient pharmaceutical tenders are not a widespread measure. In Spain, the sub-central government of the Andalusian region is the only Spanish health administration to have applied them.
Objective
This work aims to evaluate the effectiveness of this measure in reducing public pharmaceutical expenditure during the period it was in force –from June 2012 to December 2020.
Methods
We use the Synthetic Control Method (SCM), which estimates a counterfactual (synthetic) value for our variable of interest (outpatient pharmaceutical expenditure per capita) based on a set of predictor variables from a combination of units from the potential control group (in this case, the rest of the regions in Spain).
Results
The results of the SCM show no evidence that the pharmaceutical tender implemented in Andalusia reduced pharmaceutical spending. Statistical tests show that the null hypothesis of no differential effect of the measure on pharmaceutical spending during the period in which it was in force cannot be rejected. These results are robust to various robustness tests.
Conclusions
Public tenders for outpatient pharmaceuticals in Andalusia did not prove effective as a mechanism for controlling public expenditure during the period it was in force and failed to lead to a reduction in expenditure when compared to the rest of the regions in Spain, which did not apply it.
{"title":"The effectiveness of pharmaceutical tenders as a cost containment mechanism: analysis through the Synthetic Control Method. The case of Andalusia (Spain)","authors":"Pedro Atienza Montero , Luis Ángel Hierro Recio , Antonio José Garzón Gordón","doi":"10.1016/j.healthpol.2025.105481","DOIUrl":"10.1016/j.healthpol.2025.105481","url":null,"abstract":"<div><h3>Background</h3><div>Outpatient pharmaceutical tenders are not a widespread measure. In Spain, the sub-central government of the Andalusian region is the only Spanish health administration to have applied them.</div></div><div><h3>Objective</h3><div>This work aims to evaluate the effectiveness of this measure in reducing public pharmaceutical expenditure during the period it was in force –from June 2012 to December 2020.</div></div><div><h3>Methods</h3><div>We use the Synthetic Control Method (SCM), which estimates a counterfactual (synthetic) value for our variable of interest (outpatient pharmaceutical expenditure per capita) based on a set of predictor variables from a combination of units from the potential control group (in this case, the rest of the regions in Spain).</div></div><div><h3>Results</h3><div>The results of the SCM show no evidence that the pharmaceutical tender implemented in Andalusia reduced pharmaceutical spending. Statistical tests show that the null hypothesis of no differential effect of the measure on pharmaceutical spending during the period in which it was in force cannot be rejected. These results are robust to various robustness tests.</div></div><div><h3>Conclusions</h3><div>Public tenders for outpatient pharmaceuticals in Andalusia did not prove effective as a mechanism for controlling public expenditure during the period it was in force and failed to lead to a reduction in expenditure when compared to the rest of the regions in Spain, which did not apply it.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105481"},"PeriodicalIF":3.4,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145432957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-28DOI: 10.1016/j.healthpol.2025.105479
So Sato , Hideo Yasunaga , Yuichiro Matsuo , Hiroki Matsui , Kiyohide Fushimi , Atsushi Miyawaki
Background
Low-value care offers little clinical benefit and contributes to inefficient healthcare utilization. Although socioeconomic disparities in healthcare access are well documented, data on low-value care among disadvantaged inpatients remain limited.
Objective
To examine the association between neighborhood-level socioeconomic status (SES) and the proportion of low-value care services in Japanese inpatient settings using the area deprivation index (ADI) as a proxy for SES.
Methods
We conducted a cross-sectional study using a nationwide inpatient database from 920 hospitals in Japan between April 2022 and March 2023. Hospitalizations of patients aged ≥18 years receiving one of 12 selected low-value care services were included. The outcome was whether a service provided during hospitalization was classified as low-value based on established algorithms. Patients from deprived areas (top 10 % ADI) were compared with those from non-deprived areas, adjusting for patient case-mix and hospital fixed effects.
Results
Among 524,705 hospitalizations (42.3 % female; mean age, 69.9 ± 15.5 years), 33,271 (6.3 %) were classified as low-value care. After adjustment, patients from deprived areas had a higher proportion of low-value care than those from non-deprived areas (6.6 % vs. 6.3 %; adjusted difference, +0.2 percentage points; 95 % CI, 0.03 to 0.5; P = 0.02). Subgroup analyses showed stronger associations among patients aged ≥65, females, and those treated in non-academic hospitals. Results remained consistent after accounting for hospital fixed effects.
Conclusions
Patients from disadvantaged areas are slightly more likely to receive low-value inpatient care than are those from non-disadvantaged areas. Older adults, women, and patients treated in non-academic hospitals appeared more affected.
背景:低价值护理提供很少的临床效益,并导致低效率的医疗保健利用。尽管在医疗保健获取方面的社会经济差异有充分的记录,但关于弱势住院患者的低价值护理的数据仍然有限。目的:以区域剥夺指数(ADI)为指标,探讨社区社会经济地位(SES)与日本住院机构低价值护理服务比例之间的关系。方法:我们在2022年4月至2023年3月期间使用日本920家医院的全国住院患者数据库进行了一项横断面研究。年龄≥18岁的住院患者接受了12种选定的低价值护理服务之一。结果是根据已建立的算法,住院期间提供的服务是否被归类为低价值。将来自贫困地区的患者(ADI前10%)与来自非贫困地区的患者进行比较,并根据患者病例组合和医院固定效果进行调整。结果:524,705例住院患者(42.3%为女性,平均年龄69.9±15.5岁)中,33,271例(6.3%)被归为低价值护理。调整后,来自贫困地区的患者接受低价值护理的比例高于来自非贫困地区的患者(6.6%对6.3%;调整后差异为+0.2个百分点;95% CI, 0.03 ~ 0.5; P = 0.02)。亚组分析显示,年龄≥65岁的患者、女性和在非学术医院治疗的患者之间存在更强的相关性。考虑到医院固定效应后,结果保持一致。结论:贫困地区患者接受低价值住院治疗的可能性略高于非贫困地区患者。老年人、女性和在非学术医院接受治疗的患者似乎更容易受到影响。
{"title":"Association between socioeconomic disadvantage and low-value care in acute care hospitals in Japan: Cross-sectional study","authors":"So Sato , Hideo Yasunaga , Yuichiro Matsuo , Hiroki Matsui , Kiyohide Fushimi , Atsushi Miyawaki","doi":"10.1016/j.healthpol.2025.105479","DOIUrl":"10.1016/j.healthpol.2025.105479","url":null,"abstract":"<div><h3>Background</h3><div>Low-value care offers little clinical benefit and contributes to inefficient healthcare utilization. Although socioeconomic disparities in healthcare access are well documented, data on low-value care among disadvantaged inpatients remain limited.</div></div><div><h3>Objective</h3><div>To examine the association between neighborhood-level socioeconomic status (SES) and the proportion of low-value care services in Japanese inpatient settings using the area deprivation index (ADI) as a proxy for SES.</div></div><div><h3>Methods</h3><div>We conducted a cross-sectional study using a nationwide inpatient database from 920 hospitals in Japan between April 2022 and March 2023. Hospitalizations of patients aged ≥18 years receiving one of 12 selected low-value care services were included. The outcome was whether a service provided during hospitalization was classified as low-value based on established algorithms. Patients from deprived areas (top 10 % ADI) were compared with those from non-deprived areas, adjusting for patient case-mix and hospital fixed effects.</div></div><div><h3>Results</h3><div>Among 524,705 hospitalizations (42.3 % female; mean age, 69.9 ± 15.5 years), 33,271 (6.3 %) were classified as low-value care. After adjustment, patients from deprived areas had a higher proportion of low-value care than those from non-deprived areas (6.6 % vs. 6.3 %; adjusted difference, +0.2 percentage points; 95 % CI, 0.03 to 0.5; <em>P</em> = 0.02). Subgroup analyses showed stronger associations among patients aged ≥65, females, and those treated in non-academic hospitals. Results remained consistent after accounting for hospital fixed effects.</div></div><div><h3>Conclusions</h3><div>Patients from disadvantaged areas are slightly more likely to receive low-value inpatient care than are those from non-disadvantaged areas. Older adults, women, and patients treated in non-academic hospitals appeared more affected.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105479"},"PeriodicalIF":3.4,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-28DOI: 10.1016/j.healthpol.2025.105478
Luigi Siciliani , Gaetan Lafortune , Marie-Clémence Canaud , Chekwube Madichie
Background
Many OECD countries suspended elective (non-emergency) care during the pandemic to divert efforts towards COVID-19 patients, which generated a backlog of patients.
Objective
This study measures the extent to which waiting times and volume changed over time before and after COVID-19 in OECD countries (between 2016-2023). We test whether COVID-19 had a different effect on the waiting time of the patients on the list versus the wait of patients treated, two common measures of waiting times. It discusses how waiting times and volume can be used as measures of health system resilience for elective care.
Methods
The study uses data on a selection of high-volume elective surgeries and OECD countries that report waiting times for patients on the list or from addition to the list to treatment. We use regression methods to quantify the extent to which waiting times increased and volumes decreased after the pandemic across OECD countries.
Results
We find that the wait on the list increased on average by 27-30% in the first three years. In contrast, the wait to treatment increased only to a small extent and the effect was not statistically significant. Volume reduced on average by 19% and 10% in the first two years. There were heterogeneous effects across countries, but these do not appear to be systematically related to health spending, physicians and acute beds.
Conclusion
Measures of health system resilience for elective care should monitor both the wait on the list and the wait to treatment, in addition to volumes.
{"title":"Backlogs, waiting times and waiting lists of elective surgeries across OECD countries","authors":"Luigi Siciliani , Gaetan Lafortune , Marie-Clémence Canaud , Chekwube Madichie","doi":"10.1016/j.healthpol.2025.105478","DOIUrl":"10.1016/j.healthpol.2025.105478","url":null,"abstract":"<div><h3>Background</h3><div>Many OECD countries suspended elective (non-emergency) care during the pandemic to divert efforts towards COVID-19 patients, which generated a backlog of patients.</div></div><div><h3>Objective</h3><div>This study measures the extent to which waiting times and volume changed over time before and after COVID-19 in OECD countries (between 2016-2023). We test whether COVID-19 had a different effect on the waiting time of the patients on the list versus the wait of patients treated, two common measures of waiting times. It discusses how waiting times and volume can be used as measures of health system resilience for elective care.</div></div><div><h3>Methods</h3><div>The study uses data on a selection of high-volume elective surgeries and OECD countries that report waiting times for patients on the list or from addition to the list to treatment. We use regression methods to quantify the extent to which waiting times increased and volumes decreased after the pandemic across OECD countries.</div></div><div><h3>Results</h3><div>We find that the wait on the list increased on average by 27-30% in the first three years. In contrast, the wait to treatment increased only to a small extent and the effect was not statistically significant. Volume reduced on average by 19% and 10% in the first two years. There were heterogeneous effects across countries, but these do not appear to be systematically related to health spending, physicians and acute beds.</div></div><div><h3>Conclusion</h3><div>Measures of health system resilience for elective care should monitor both the wait on the list and the wait to treatment, in addition to volumes.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105478"},"PeriodicalIF":3.4,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145469092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1016/j.healthpol.2025.105477
Callum Thomas , Justine Gosling , Ruth E Ashton , Rebecca Owen , Mark A Faghy
Background
As with other frontline healthcare services, the delivery of rehabilitation services has been greatly affected by the COVID-19 pandemic with many services suspended, despite WHO’s mandate that rehabilitation is an essential service.
Objective
This review aimed to provide an overview of policy responses that were taken across the WHO European Region to identify systems and processes that helped to inform and shape decisions pertaining to rehabilitation during the COVID-19 pandemic.
Methods
A scoping literature search was conducted according to PRISMA-ScR guidelines and prospectively registered on Prospero (ID: CRD42024550641). Cinahl, Cochrane, PubMed and Scopus databases were searched from inception to February 2024. Eligibility criteria for selecting publications: Published work that includes any policy documents that informed rehabilitation during the COVID-19 pandemic in any of the 53 World Health Organisation European member states. Search results were extracted using the PESTLE heading framework in Microsoft Excel.
Results
Seven publications comprising seven policy documents from Italy (N=2), England (N=2) and the United Kingdom (N=3) were included in this review. Five key areas were identified in response to COVID-19 and rehabilitation: 1) government direction, 2) funding, 3) education, 4) telerehabilitation, and 5) social distancing and isolation.
Conclusions
Our study's findings demonstrate a dearth of published government policy documentation referring to rehabilitation in response to the COVID-19 pandemic. This lack of published documents indicates that rehabilitation is not considered an essential health service during emergency response. Research should investigate the systems and processes of key decision-makers to inform future rehabilitation pandemic preparations.
{"title":"A scoping literature review of rehabilitation policy recommendations during the COVID-19 pandemic in the WHO European Region","authors":"Callum Thomas , Justine Gosling , Ruth E Ashton , Rebecca Owen , Mark A Faghy","doi":"10.1016/j.healthpol.2025.105477","DOIUrl":"10.1016/j.healthpol.2025.105477","url":null,"abstract":"<div><h3>Background</h3><div>As with other frontline healthcare services, the delivery of rehabilitation services has been greatly affected by the COVID-19 pandemic with many services suspended, despite WHO’s mandate that rehabilitation is an essential service.</div></div><div><h3>Objective</h3><div>This review aimed to provide an overview of policy responses that were taken across the WHO European Region to identify systems and processes that helped to inform and shape decisions pertaining to rehabilitation during the COVID-19 pandemic.</div></div><div><h3>Methods</h3><div>A scoping literature search was conducted according to PRISMA-ScR guidelines and prospectively registered on Prospero (ID: CRD42024550641). Cinahl, Cochrane, PubMed and Scopus databases were searched from inception to February 2024. Eligibility criteria for selecting publications: Published work that includes any policy documents that informed rehabilitation during the COVID-19 pandemic in any of the 53 World Health Organisation European member states. Search results were extracted using the PESTLE heading framework in Microsoft Excel.</div></div><div><h3>Results</h3><div>Seven publications comprising seven policy documents from Italy (N=2), England (N=2) and the United Kingdom (N=3) were included in this review. Five key areas were identified in response to COVID-19 and rehabilitation: 1) government direction, 2) funding, 3) education, 4) telerehabilitation, and 5) social distancing and isolation.</div></div><div><h3>Conclusions</h3><div>Our study's findings demonstrate a dearth of published government policy documentation referring to rehabilitation in response to the COVID-19 pandemic. This lack of published documents indicates that rehabilitation is not considered an essential health service during emergency response. Research should investigate the systems and processes of key decision-makers to inform future rehabilitation pandemic preparations.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105477"},"PeriodicalIF":3.4,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145469091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1016/j.healthpol.2025.105476
J.T. Dros , C.E. van Dijk , R.A. Verheij , I. Bos , B.R. Meijboom
Background
Bundled payments for patients with cardiovascular diseases (CVD) aim to enhance primary care utilization in the Netherlands.
Objective
This study assesses changes in healthcare utilization patterns and costs for CVD between 2014 and 2019, while investigating the potential association with bundled payment adoption.
Method
We studied patients at very high risk for CVD with routinely recorded nationwide healthcare data, using an observational study design. Multilevel logistic- and gamma regressions were conducted to assess healthcare utilizations patterns between 2014 and 2019, and the impact of bundled payments on the likelihood of receiving medical specialist care and the height of associated costs.
Results
The odds of medical specialist involvement declined over time for the 152,591 unique patients included in our study. Practices with a higher level of bundled payments had lower odds of medical specialist involvement. Medical specialist costs did also significantly decrease between 2014 and 2019, and patients in practices with the highest level of bundled payments had significantly lower medical specialist costs. When general practice costs were included however, healthcare costs per patient stayed the same, both over time and stratified by use of bundled payments.
Conclusion
Our findings suggest an association between bundled payments and specialized healthcare use, potentially facilitating the transition to primary care. While we found no evidence for costs savings, our findings do suggest that due to bundled payments more patients are actively monitored.
{"title":"Healthcare utilization and costs for cardiovascular diseases across different levels of bundled payment adoption in general practice: A data linkage study","authors":"J.T. Dros , C.E. van Dijk , R.A. Verheij , I. Bos , B.R. Meijboom","doi":"10.1016/j.healthpol.2025.105476","DOIUrl":"10.1016/j.healthpol.2025.105476","url":null,"abstract":"<div><h3>Background</h3><div>Bundled payments for patients with cardiovascular diseases (CVD) aim to enhance primary care utilization in the Netherlands.</div></div><div><h3>Objective</h3><div>This study assesses changes in healthcare utilization patterns and costs for CVD between 2014 and 2019, while investigating the potential association with bundled payment adoption.</div></div><div><h3>Method</h3><div>We studied patients at very high risk for CVD with routinely recorded nationwide healthcare data, using an observational study design. Multilevel logistic- and gamma regressions were conducted to assess healthcare utilizations patterns between 2014 and 2019, and the impact of bundled payments on the likelihood of receiving medical specialist care and the height of associated costs.</div></div><div><h3>Results</h3><div>The odds of medical specialist involvement declined over time for the 152,591 unique patients included in our study. Practices with a higher level of bundled payments had lower odds of medical specialist involvement. Medical specialist costs did also significantly decrease between 2014 and 2019, and patients in practices with the highest level of bundled payments had significantly lower medical specialist costs. When general practice costs were included however, healthcare costs per patient stayed the same, both over time and stratified by use of bundled payments.</div></div><div><h3>Conclusion</h3><div>Our findings suggest an association between bundled payments and specialized healthcare use, potentially facilitating the transition to primary care. While we found no evidence for costs savings, our findings do suggest that due to bundled payments more patients are actively monitored.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105476"},"PeriodicalIF":3.4,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1016/j.healthpol.2025.105473
Niek Kok , Myrthe van de Meulenhof , Wilson F. Abdo , Jelle L.P. van Gurp , Gert Olthuis
Background
In 2020, the Netherlands adopted an opt-out registration system for organ donation meaning that consent for donation is presumed except when someone actively objects against this. This change in organ donation default policy may change the division of roles between relatives and physicians during conversations.
Objectives
To compare role performance of relatives and physicians in organ donation conversations in the opt-in and opt-out systems.
Methods
We applied an institutional ethnographic approach to compare cases from the former opt-in system in which there was ‘no registration’ to the ‘presumed consent cases’ in the opt-out system.
Results
We audio-recorded six no registration conversations from the opt-in period, and compared these with eight presumed consent conversations from the opt-out period, and conducted sixteen interviews with physicians conducting the conversations. The data show the effect of the system transition on the role division between relatives and physicians in donation conversations. In the opt-in system, physicians and relatives together aimed for a yet to be taken decision, while in the opt-out system, the physicians started the conversation with the registered choice. Ethical deliberation about organ donation is therefore pushed to the background the role of the physician is more tilted to providing relevant factual information and implementing the patient’s choice.
Conclusions
The change to opt-out did likely alleviates the burdensome role of relatives to make morally charged donation choices for their relatives, since organ donation conversations about patients presumed to consent commence with a clear picture of what the potential donor’s wish is.
{"title":"Physician and relatives’ role change after shifting to an opt-out organ donation system in the Netherlands: A before and after ethnographic study","authors":"Niek Kok , Myrthe van de Meulenhof , Wilson F. Abdo , Jelle L.P. van Gurp , Gert Olthuis","doi":"10.1016/j.healthpol.2025.105473","DOIUrl":"10.1016/j.healthpol.2025.105473","url":null,"abstract":"<div><h3>Background</h3><div>In 2020, the Netherlands adopted an opt-out registration system for organ donation meaning that consent for donation is presumed except when someone actively objects against this. This change in organ donation default policy may change the division of roles between relatives and physicians during conversations.</div></div><div><h3>Objectives</h3><div>To compare role performance of relatives and physicians in organ donation conversations in the opt-in and opt-out systems.</div></div><div><h3>Methods</h3><div>We applied an institutional ethnographic approach to compare cases from the former opt-in system in which there was ‘no registration’ to the ‘presumed consent cases’ in the opt-out system.</div></div><div><h3>Results</h3><div>We audio-recorded six no registration conversations from the opt-in period, and compared these with eight presumed consent conversations from the opt-out period, and conducted sixteen interviews with physicians conducting the conversations. The data show the effect of the system transition on the role division between relatives and physicians in donation conversations. In the opt-in system, physicians and relatives together aimed for a yet to be taken decision, while in the opt-out system, the physicians started the conversation with the registered choice. Ethical deliberation about organ donation is therefore pushed to the background the role of the physician is more tilted to providing relevant factual information and implementing the patient’s choice.</div></div><div><h3>Conclusions</h3><div>The change to opt-out did likely alleviates the burdensome role of relatives to make morally charged donation choices for their relatives, since organ donation conversations about patients presumed to consent commence with a clear picture of what the potential donor’s wish is.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"162 ","pages":"Article 105473"},"PeriodicalIF":3.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145424747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-21DOI: 10.1016/j.healthpol.2025.105474
Andreas Nielsen Hald , Ulrika Enemark , Martin Limbikani Mwale , Viola Burau
Background
Primary healthcare (PHC) systems across Europe are under increasing pressure. In response, research has focused on how to develop and support PHC workforces. However, studies often neglect how stakeholders conceptualise the PHC workforce, even though this may influence reform processes. Denmark offers a relevant case due to the involvement of many stakeholders and longstanding tensions over workforce organisation.
Objective
To examine the literature on how stakeholders in Denmark conceptualise the PHC workforce and how conflicting narratives influence policy contestation.
Methods
We conducted a meta-narrative-inspired literature review, following RAMESES guidelines. The review included 49 sources (1980–2025), drawing on peer-reviewed articles, organisational documents, professional journals, policy texts, and political news. Documents were screened, appraised, and synthesised using an iterative narrative analysis. We identified dominant stakeholders, primary narratives, and key areas of policy contestation relevant to the PHC workforce.
Results
Across 45 years of reform and policy debate, three primary narratives have structured stakeholder perspectives: a medical narrative emerging in the mid-1960s, a health economics narrative gaining prominence during the 1990s, and a community narrative growing since the early 2010s. These narratives compete across and within stakeholder groups, most visibly in debates over governance, task-shifting, and whether recipients are framed as patients or citizens.
Conclusions
Stakeholders in Denmark conceptualise the PHC workforce differently depending on the narratives they invoke and the reform context in which they act. Reforms are more likely to gain traction when engaging these perspectives. Narrative-informed approaches can help anticipate resistance and support more effective PHC workforce development.
{"title":"Conceptualising the primary health care workforce: A meta-narrative-inspired review of stakeholder perspectives in Denmark","authors":"Andreas Nielsen Hald , Ulrika Enemark , Martin Limbikani Mwale , Viola Burau","doi":"10.1016/j.healthpol.2025.105474","DOIUrl":"10.1016/j.healthpol.2025.105474","url":null,"abstract":"<div><h3>Background</h3><div>Primary healthcare (PHC) systems across Europe are under increasing pressure. In response, research has focused on how to develop and support PHC workforces. However, studies often neglect how stakeholders conceptualise the PHC workforce, even though this may influence reform processes. Denmark offers a relevant case due to the involvement of many stakeholders and longstanding tensions over workforce organisation.</div></div><div><h3>Objective</h3><div>To examine the literature on how stakeholders in Denmark conceptualise the PHC workforce and how conflicting narratives influence policy contestation.</div></div><div><h3>Methods</h3><div>We conducted a meta-narrative-inspired literature review, following RAMESES guidelines. The review included 49 sources (1980–2025), drawing on peer-reviewed articles, organisational documents, professional journals, policy texts, and political news. Documents were screened, appraised, and synthesised using an iterative narrative analysis. We identified dominant stakeholders, primary narratives, and key areas of policy contestation relevant to the PHC workforce.</div></div><div><h3>Results</h3><div>Across 45 years of reform and policy debate, three primary narratives have structured stakeholder perspectives: a medical narrative emerging in the mid-1960s, a health economics narrative gaining prominence during the 1990s, and a community narrative growing since the early 2010s. These narratives compete across and within stakeholder groups, most visibly in debates over governance, task-shifting, and whether recipients are framed as patients or citizens.</div></div><div><h3>Conclusions</h3><div>Stakeholders in Denmark conceptualise the PHC workforce differently depending on the narratives they invoke and the reform context in which they act. Reforms are more likely to gain traction when engaging these perspectives. Narrative-informed approaches can help anticipate resistance and support more effective PHC workforce development.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"162 ","pages":"Article 105474"},"PeriodicalIF":3.4,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145363227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The global healthcare workforce is facing a substantial shortage and an uneven distribution of qualified professionals, which restricts access to essential healthcare services. This shortage may be mitigated through more effective support of healthcare workers in training. Therefore, an overview of existing economic barriers for this demographic is necessary.
Objective
To review the existing literature on financial challenges of students and early-career professionals in the healthcare sector.
Methods
Following the PRISMA-ScR guidelines, articles published between January 2008 and February 2024 were identified using PubMed and Scopus. A total of 17,268 articles were screened by reviewing their titles and abstracts followed by a detailed review of full texts with cross-validation. Themes were identified, clustered, and analyzed.
Results
This scoping review included 167 articles focusing on the themes debt (36.5%, n=61) and loans (10.2 %, n=17) and their influence on career pathways, the role of employment for career satisfaction, summarizing findings concerning salary (29.9%, n=50), finances (25.1%, n=42), funding (10.8%, n=18), and savings (10.2%, n=17), and obstacles toward a sustainable lifestyle, which included results considering career choice (34.1%, n=57), migration (7.2%, n=12), gender disparity (6.0%, n=10), and working conditions (2.4%, n=4).
Conclusions
Efforts to close the healthcare workforce gap require greater investment in training, compensation, and support for junior healthcare workers. Students and early-career professionals warrant particular attention to build a sustainable, resilient, and reliable healthcare workforce.
{"title":"Exploring financial challenges of students and early-career professionals working in the healthcare sector: A scoping review","authors":"Samin Huq , Yoonjung Choi , Paul Künzle , Mfonobong Timothy , Cornelia Santoso , Stephanie Hwang , Sherly Meilianti","doi":"10.1016/j.healthpol.2025.105475","DOIUrl":"10.1016/j.healthpol.2025.105475","url":null,"abstract":"<div><h3>Background</h3><div>The global healthcare workforce is facing a substantial shortage and an uneven distribution of qualified professionals, which restricts access to essential healthcare services. This shortage may be mitigated through more effective support of healthcare workers in training. Therefore, an overview of existing economic barriers for this demographic is necessary.</div></div><div><h3>Objective</h3><div>To review the existing literature on financial challenges of students and early-career professionals in the healthcare sector.</div></div><div><h3>Methods</h3><div>Following the PRISMA-ScR guidelines, articles published between January 2008 and February 2024 were identified using PubMed and Scopus. A total of 17,268 articles were screened by reviewing their titles and abstracts followed by a detailed review of full texts with cross-validation. Themes were identified, clustered, and analyzed.</div></div><div><h3>Results</h3><div>This scoping review included 167 articles focusing on the themes debt (36.5%, <em>n</em>=61) and loans (10.2 %, <em>n</em>=17) and their influence on career pathways, the role of employment for career satisfaction, summarizing findings concerning salary (29.9%, <em>n</em>=50), finances (25.1%, <em>n</em>=42), funding (10.8%, <em>n</em>=18), and savings (10.2%, <em>n</em>=17), and obstacles toward a sustainable lifestyle, which included results considering career choice (34.1%, <em>n</em>=57), migration (7.2%, <em>n</em>=12), gender disparity (6.0%, <em>n</em>=10), and working conditions (2.4%, <em>n</em>=4).</div></div><div><h3>Conclusions</h3><div>Efforts to close the healthcare workforce gap require greater investment in training, compensation, and support for junior healthcare workers. Students and early-career professionals warrant particular attention to build a sustainable, resilient, and reliable healthcare workforce.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105475"},"PeriodicalIF":3.4,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145520885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17DOI: 10.1016/j.healthpol.2025.105455
Annemarie De Leo , Christelle Schofield , Emily Jeffery , Emily Mountford , Elle Cotton , Joshua Lewis , Jonathan Hodgson , Mary A. Kennedy
Background
Integrating supportive cancer services into routine cancer care is challenging, especially in regional and rural settings where accessibility to healthcare is a known issue. This scoping review aimed to describe and map barriers to nutrition services from the perspectives of people living with cancer and health service providers. Exploring the applicability of Levesque’s Accessibility Framework in identifying and prioritising service gaps was a secondary aim.
Methods
Electronic database searches were conducted in Allied and Contemporary Medicine, CINAHL, Informit, Medline and SPORTDiscus between May-July 2023. Studies reporting on perceived barriers to nutrition services from the perspectives of health service providers and people living with cancer in regional and rural settings were included. We categorised these into demand or supply determinants, which were mapped across the ten dimensions of Leveque’s Accessibility Framework.
Results
Eight studies were included in this review. Thirty-seven barriers were identified and mapped across the ten dimensions described within Levesque’s Accessibility Framework. The most frequently reported barriers related to: Availability and Accommodation of regional health services, Approachability of regional health services and Ability of patients to engage.
Conclusion
This review identified the most commonly reported barriers to nutrition services for people living with cancer in regional and rural settings. Levesque’s Accessibility Framework demonstrates value in categorising barriers to accessibility, which can be used to identify service gaps and inform future policy-setting agendas.
背景:将支持性癌症服务纳入常规癌症治疗具有挑战性,特别是在地区和农村环境中,在那里获得医疗保健是一个已知的问题。这项范围审查旨在从癌症患者和卫生服务提供者的角度描述和绘制营养服务的障碍。探索Levesque的无障碍框架在识别和优先考虑服务差距方面的适用性是第二个目标。方法于2023年5 - 7月在Allied and Contemporary Medicine、CINAHL、Informit、Medline和SPORTDiscus等电子数据库进行检索。从保健服务提供者和区域和农村环境中的癌症患者的角度报告了对营养服务的感知障碍的研究。我们将这些因素分类为需求或供应决定因素,并将其映射到Leveque无障碍框架的十个维度上。结果本综述共纳入8项研究。在Levesque的无障碍框架中,我们确定了37个障碍,并在十个维度上进行了映射。最常报告的障碍涉及:区域卫生服务的可获得性和可提供性、区域卫生服务的可获得性和患者参与的能力。本综述确定了区域和农村地区癌症患者获得营养服务最常见的障碍。Levesque的无障碍框架展示了对无障碍障碍进行分类的价值,可用于识别服务差距并为未来的政策制定议程提供信息。
{"title":"Exploring barriers to nutritional support for oncology patients in regional and rural settings: A scoping review through the lens of Levesque’s accessibility framework","authors":"Annemarie De Leo , Christelle Schofield , Emily Jeffery , Emily Mountford , Elle Cotton , Joshua Lewis , Jonathan Hodgson , Mary A. Kennedy","doi":"10.1016/j.healthpol.2025.105455","DOIUrl":"10.1016/j.healthpol.2025.105455","url":null,"abstract":"<div><h3>Background</h3><div>Integrating supportive cancer services into routine cancer care is challenging, especially in regional and rural settings where accessibility to healthcare is a known issue. This scoping review aimed to describe and map barriers to nutrition services from the perspectives of people living with cancer and health service providers. Exploring the applicability of Levesque’s Accessibility Framework in identifying and prioritising service gaps was a secondary aim.</div></div><div><h3>Methods</h3><div>Electronic database searches were conducted in Allied and Contemporary Medicine, CINAHL, Informit, Medline and SPORTDiscus between May-July 2023. Studies reporting on perceived barriers to nutrition services from the perspectives of health service providers and people living with cancer in regional and rural settings were included. We categorised these into demand or supply determinants, which were mapped across the ten dimensions of Leveque’s Accessibility Framework.</div></div><div><h3>Results</h3><div>Eight studies were included in this review. Thirty-seven barriers were identified and mapped across the ten dimensions described within Levesque’s Accessibility Framework. The most frequently reported barriers related to: Availability and Accommodation of regional health services, Approachability of regional health services and Ability of patients to engage.</div></div><div><h3>Conclusion</h3><div>This review identified the most commonly reported barriers to nutrition services for people living with cancer in regional and rural settings. Levesque’s Accessibility Framework demonstrates value in categorising barriers to accessibility, which can be used to identify service gaps and inform future policy-setting agendas.</div></div>","PeriodicalId":55067,"journal":{"name":"Health Policy","volume":"163 ","pages":"Article 105455"},"PeriodicalIF":3.4,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145420205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}