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iSIMPATHY: a multinational pre-post non-randomised intervention study transforming medication review

Por: Mair · A. · Kirke · C. · Scott · M. G. · Micheal · N. · Law · S. · Kanan · Y. · Scullin · C. · Brown · J. · Fleming · G. · Skinner · N. H. · Kyle · D.
Background

Taking multiple medicines can be appropriate but has the potential to be problematic. The Implementing Stimulating Innovation in the Management of Polypharmacy and Adherence THrough the Years (iSIMPATHY) project used the 7-Steps person-centred approach for medication reviews, supporting patients and clinicians to define and achieve realistic goals for drug treatment, and helping enable patients to lead healthy and active lives.

Objective

To assess the impact of pharmacist-led comprehensive person-centred medication reviews using the 7-Steps methodology.

Method

iSIMPATHY sought to transform the approach to optimisation of medicinces through the delivery of person-centred medication reviews for people taking multiple medicines in primary care, hospital and outpatient clinics. The reviews were conducted by embedding a single approach for polypharmacy management, building on key recommendations from SIMPATHY.

Results

Interventions made were graded, with 82% being classified as clinically significant and 4% potentially preventing major organ failure, adverse drug reactions or incidents of similar clinical importance. The average number of medications reduced from 12 to 11, with 92% of the reviews resulting in more appropriate medication use, thereby decreasing the likelihood of medication-related harm. Inappropriate medicines were stopped, reduced or altered to improve appropriateness. There were significant healthcare resource utilisation benefits as indicated by a positive return on investment for both medication and healthcare costs with a quality-adjusted life year gain of 7.4 per 100 patients.

Conclusion

Pharmacist-led, person-centred medication review using the 7-Steps approach was delivered across jurisdictions and healthcare settings, with positive impacts on the number and appropriateness of medicines, clinical interventions and cost savings outweighing expenditure on the service. The approach is scalable by means of the tools and resources developed over the duration of the project.

Cohort profile: baseline characteristics and design of the McMaster Monitoring My Mobility (MacM3) study - a prospective digital mobility cohort of community-dwelling older Canadians from Southern Ontario

Por: Beauchamp · M. · Kirkwood · R. · Cooper · C. · McIlroy · W. E. · Van Ooteghem · K. · Beyer · K. B. · Richardson · J. · Kuspinar · A. · McNicholas · P. D. · Newbold · B. · Scott · D. · Raina · P. · Fang · Q. · Gardner · P. · Zargoush · M. · Ma · J. · OHoski · S. · Rafiq · T. · MacM3 Investi
Purpose

The McMaster Monitoring My Mobility (MacM3) study aims to understand trajectories of mobility decline in later life using multisensor wearable technology. To our knowledge, MacM3 is the first major cohort to combine accelerometry and a Global Positioning System (GPS) to track real-world mobility in community-dwelling older adults.

Participants

Between May 2022 and May 2024, MacM3 recruited 1555 community-dwelling older adults (mean age 73.9 years, SD=5.5) from Hamilton and Toronto, Ontario. Of the cohort, 68.4% were female, 62.4% married/partnered, 75.3% had post-secondary education and 62.9% had≥3 comorbidities. Most were Canadian born (69.4%) and white/Caucasian (88.0%), with greater ethnocultural diversity observed at the Toronto site.

Findings to date

At baseline, 56.7% of participants reported no mobility limitations, 15.9% had preclinical limitations and 27.4% had minor mobility limitations. Mean gait speed for the total sample was 1.23 m/s, with a mean Timed Up and Go time of 9.4 s and a 5x sit-to-stand time of 13.0 s. A total of 1301 participants had valid wrist-worn device data, and 1008 participants who agreed to wear the thigh-worn device had valid data (≥7 days with ≥10 hours of wear per day). Step count data (n=1008) revealed a mean of 8437 steps per day (SD=2943), with 5073 steps in the lowest quartile and 12 303 steps in the highest.

Future plans

Ongoing work aims to develop predictive models of mobility decline by integrating wearable, clinical and environmental data. Pipeline enhancements will enable GPS/inertial measurement unit fusion to explore mobility-environment interactions and support ageing-in-place tools.

Young-onset type 2 diabetes and associations with high disability rate, low educational level and immigrant background: a study from Norwegian general practice

Por: Tibballs · K. L. B. · Kirkeboen · L. · Jenum · A. K. · Straand · J. · Berg · T. J. · Buhl · E. S.
Introduction

Young-onset type 2 diabetes (YOD), diagnosed before 40 years of age, entails a high disease burden and potential for early dependence on disability benefits. The risk of type 2 diabetes (T2D) varies with socio-economic status and ethnic background, yet the relationship between these factors and age at diagnosis is insufficiently explored. We aimed to study associations between YOD and living on disability benefits, educational level and country background.

Research design and methods

Cross-sectional data on 8640 individuals with T2D, linked to data on educational level and country background, were compared with population data from the same residential areas. Similar comparisons were made for data on disability benefits among 3854 individuals of working age (

Results

The risk of being dependent on disability benefits was three times higher in YOD (adjusted incidence rate ratio, aIRR (95% CI) 3.1 (2.7 to 3.5)) and twice as high in later-onset T2D (1.9 (1.8 to 2.1)) as in the general population. People of Norwegian background with low educational levels had threefold higher YOD risk (3.3 (2.4 to 4.4)) than those with a tertiary degree, while people of non-Western backgrounds with low educational levels had a smaller increase in YOD risk (1.5 (1.1 to 2.1)). People of non-Western backgrounds had higher YOD risk than those of Norwegian background (4.2 (3.5 to 5.0)), while people of south Asian background had an even greater relative YOD risk (9.0 (7.3 to 11.0)), threefold higher than for later-onset T2D (3.2 (2.8 to 3.7)).

Conclusions

Lifetime risk of being dependent on disability benefits was substantially higher for individuals with YOD than in later onset T2D. Non-Western and particularly south Asian backgrounds were associated with increased YOD risk. Low education was an important YOD risk factor only for people with Norwegian background.

Epidemiology and healthcare access inequities in diabetic foot disease: a retrospective study in Central Queensland, Australia

Por: Soonarane · Y. K. · Kirk · M. · Khandaker · G. · Varrall · R.
Objectives

Diabetic foot disease (DFD) requires proactive healthcare management to minimise the risk of complications. Healthcare delivery has been shown to present significant challenges in rural and regional settings with Central Queensland being a large geographic area with limited local healthcare resources. Our objectives are to describe the distribution of DFD in a regional setting and assess the impact of remoteness on healthcare accessibility for this cohort.

Design

A retrospective analysis of hospital admissions for DFD data between January 2017 and December 2023.

Setting, Participants

All recorded episodes of care for DFD patients provided by Central Queensland Hospital and Health Service (CQHHS) were included.

Primary and secondary outcome measures

Primary outcome was the number of DFD episodes. Secondary outcomes included the number of hospital bed days used by DFD cases, the number of lower extremity amputations and the number of interhospital transfers (IHTs) for DFD cases.

Results

1597 DFD episodes, 15 528 bed days, 340 lower extremity amputations and 452 IHTs were recorded. Population-adjusted outcomes showed 1054 DFD episodes per 100 000 males compared with 383 per 100 000 females (incidence rate ratio (IRR) 2.75, 95% CI: 2.46 to 3.07), and 1384 per 100 000 Indigenous Australians compared with 669 per 100 000 non-Indigenous Australians (IRR 2.07, 95% CI: 1.80 to 2.38). Remoteness was associated with lower DFD treatment completion rates at local hospitals, with only 9.3% of patients from the most remote regions completing treatment locally, compared with 76.3% from the least remote regions (p

Conclusions

Males and Indigenous Australians were disproportionately affected by DFD in Central Queensland. Remoteness poses a significant risk factor to completing treatment for DFD at a local facility. Further research into key drivers leading to the disproportionate outcomes demonstrated in this study between specific cohorts of people with DFD is suggested to help design future interventions to improve accessibility and outcomes.

Nurses' Insights on the Braden Scale and Their Vision for Artificial Intelligence Innovations: A Mixed Methods Study

ABSTRACT

Aims

This study aimed to explore nurses' experiences with the Braden Scale, assess their readiness for artificial intelligence (AI) technologies, and understand the innovations they envision for clinical practice.

Design

Explanatory sequential mixed design.

Methods

The study included 118 nurses in the quantitative data and 42 in focus groups. Quantitative data were collected using the MAIRS-MS. Qualitative data were analysed using phenomenological approaches and MAXQDA.

Results

The average age was 33.38 ± 7.42 years and 88.1% were women. The average length of professional experience is 11.66 ± 8.22 years. The average time to administer the Braden Scale was 5.02 ± 4.36 min. While 55.1% of the participants found the Braden Scale inadequate, 55.9% stated that a more comprehensive risk assessment scale was needed and the MAIRS-MS score was 78.48 ± 16.66. The sub-themes were identified: Simple and quick applicability, early risk identification, validity and reliability issues, neglecting other risk factors, making it more comprehensive and specific, developing of a new risk assessment scale, technological improvements, patient data treasure chest, creating avatars and converting speech-to-text.

Conclusions

This study highlights critical gaps in the Braden Scale's effectiveness. Nurses identified significant shortcomings, including non-specificity and the neglect of key risk factors, which undermine its utility in clinical settings. They emphasised that stronger risk predictions and personalised care plans can be achieved by AI technology.

Implications for Professional Care

This study emphasises the need to revise the Braden Scale or develop a new one due to its limitations in risk assessment, providing crucial information to improve patient care and offering new perspectives on AI integration in PI risk assessment for nursing practice.

Impact

This study highlights nurses' experiences and suggestions for improving the Braden Scale in clinical practice, emphasising their expectations for AI technology and its potential to revolutionise patient care.

Reporting Method

The study report was prepared following the Good Reporting of A Mixed Methods Study (GRAMMS) checklist.

Patient or Public Contribution

No patient or public contribution.

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