Research article
Home Health Nurses’ Perceptions of Safety
Kiernan RileyORCID
, Kalei Crimi, Michael M. Evans , [...]
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Abstract
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To address the risks associated with potentially inappropriate prescribing (PIP) in older adults, this study aimed to determine the prevalence of PIP in home health care patients in the Taif Health Cluster, Saudi Arabia. Using the Beers, STOPP, and START criteria, a retrospective analysis was conducted on 400 older adults aged 65 and over who received home health care between February and October 2023. Results indicated that 38.5% of patients had at least one PIP incident, with polypharmacy present in 80.6% of PIP cases. PIP was more prevalent among females and those aged 75 and older. Potentially inappropriate medications (PIMs) were noted in 80.6% of cases, while potentially inappropriate omissions (PIOs) were recorded in 26.5%. The most frequent cause of PIMs was a lack of a clear indication, affecting 23.3% of total prescriptions. Angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II receptor antagonists (AIIRAs) were commonly omitted in diabetic patients with renal disease. Findings highlight the need for regular prescription reviews to reduce PIP and improve patient outcomes.
Globalization has hastened change, leading to an aging society. Elderly-living issues have become more prevalent alongside globalization, with health, relationships, education, socioeconomics, and psychology being important factors associated with enhancing the Quality of Life (QoL). The popularity of residential care for the elderly is growing, yet there is limited knowledge regarding its quality of life. The researchers aimed to explore the QoL and inform the factors affecting the QoL among the elderly who live in various residential types and related factors that can affect their QoL.
This cross-sectional cohort study recruited elderly people, 60 years old and over, who lived in the community of Chiang Mai province between May and October 2023. We measured the QoL of the participants using a translated and validated WHOQOL-OLD questionnaire. Multivariable logistic regression was performed to explore factors related to QoL.
Out of 117 participants, those living in their own homes had a significantly higher QoL score (91.0 [79.5–99.0] compared to 99.0 [90.0–110.0] for residential care). The self-own houses group showed significantly higher scores in the “sensory abilities” and “autonomy” domains.
The study showed associations between elderly demographics, living conditions, and QoL. The total participants’ average QoL was “good”. The residential care group exhibited lower scores in all six QoL dimensions, particularly in areas related to sensory abilities and autonomy. We can improve the well-being and quality of life of elderly residential care residents by focusing on sensory stimulation and autonomy.
After hospitalizations, many older adults experience a rapid functional decline and rely on home health (HH) care services to regain physical function. Understanding rehabilitation treatment elements that improve physical function is important for optimizing care. Two randomized controlled trials demonstrated similar physical function improvement in older adults (≥65 years, ≥3 comorbidities) receiving either high intensity (n=133) or standardized usual care (n=140) HH approaches in the 60 days following hospitalization. This secondary analysis examined the relationship between patient characteristics, treatment elements, and physical function improvements measured by the Short Physical Performance Battery (SPPB). In the high intensity group, lower baseline SPPB performance was associated with greater improvements (β=-0.23, p<0.01). Completing an additional exercise component per session further increased SPPB scores by 0.65-points (β = 3.94, p<0.01). For every two visits completed, there was an associated with a 0.58-point increase in SPPB (β=0.29, p<0.01), exceeding the small meaningful changes threshold (0.5 points). In contrast, four visits in usual care were associated with a 0.56-point change in SPPB (β=0.14, p<0.05). Neither approach demonstrated an association between environmental challenge exercises and functional improvement, potentially due to lower session frequency and shorter duration. These findings suggest that consistent attendance and full participation in high intensity HH components are critical for maximizing recovery. HH therapists should educate patients to prioritize attending 12 sessions and completing all prescribed treatment components to optimize physical function recovery in the 60 days after hospitalization.[AQ3]
The aim of the study is to examine the effect of Wellness Recovery Action Plan (WRAP) based psychoeducation program on health of caregivers of Alzheimer’s Disease (AD) patients. This is a quasi-experimental study of pre- and posttest, control group design. WRAP based psychoeducation was applied to the intervention group and compared with the standard caregiver education group and the control group. A total of 60 caregiver for AD patients constituted the sample. The data were collected with the perception of health, caregiver burden, and quality of life scales. It was found that there were no differences between the mean pre- and posttest scores of all group participants on the perception of health and caregiving burden scales (
Mobile vaccination units administered COVID-19 vaccines to homebound populations in Greece. This study explores the perspectives of public healthcare providers involved in the COVID-19 home vaccination program, aiming to identify challenges and propose improvements in the delivery of healthcare services at home. This study employed a cross-sectional mixed-methods design and was conducted within public Primary Health Care (PHC) facilities. It utilized a questionnaire consisting of both closed- and open-ended questions. The study population included healthcare professionals and administrative staff involved in vaccination units. Data were collected from April to July 2022 and analyzed using descriptive statistics for quantitative data and thematic analysis for qualitative data. The integration of both data types enhanced the depth and reliability of the findings. Ethical approval for the study was granted by the Bioethics Committee of the Aristotle University of Thessaloniki. Twelve hundred participants from 168 facilities across six Health Districts responded. The majority were nurses (34.1%) and general practitioners (24.7%). Participants overwhelmingly praised the concept of home-based care, aligning it with PHC, and expressed readiness for future involvement, despite time constraints. Four main themes emerged from the thematic analysis of 1,072 text responses. Challenges in providing such services included difficulties in balancing home care with existing workload, addressing understaffing, and achieving effective time management to prevent staff burnout and service disruptions. Participants’ experiences in the national COVID-19 home vaccination project highlight their positive attitudes toward home care while also underscoring several potential challenges in organizing similar home-based services.
Spouse caregivers play a vital role in the long-term care of chronically ill and dependent partners. They frequently experience caregiver burden with negative health outcomes. Caregiver burden is associated with poor mental health outcomes such as depression and anxiety among spouse caregivers. A caregiver’s mental health is essential to the well-being of the caregiver and care recipient; thus, it needs to be accounted for in patient management and in caregiver studies.
The purpose of this integrative review was to examine studies that explored relationships between caregiver burden and spouse caregivers’ mental health.
Searches in PubMed, Scopus, and CINAHL identified 18 studies that met the inclusion criteria. Twelve of the studies focused on spouse caregivers alone while six included family caregivers with spouse caregivers making up 50% or more of the sample.
Anxiety and depression were common among spouse caregivers but were often not measured or discussed. Most samples lacked racial and ethnic diversity. Mediating factors such as socioeconomic/income status which can influence mental health outcomes were rarely analyzed or reported. Functional and cognitive decline were the most common mediators of anxiety and depression. The heterogeneity of the methods and measures used in the studies could limit the generalization of findings.
More studies are needed that include historically underrepresented spouse caregivers. Accounting for confounders such as level of education, income status, and elements of social determinants of health is essential in caregiver studies because of their strong influence on health and mental outcomes.
Patients with cystic fibrosis (CF) experience multiple episodes of acute pulmonary exacerbation (APE) throughout their lifetime. Intravenous antibiotic therapy (IVAB) is the current standard of treatment. Home administration of IVABs is generally considered a safe alternative to hospital treatment which reduces disruption to the lives of patients with CF. This scoping review aimed to identify the characteristics and components of home IVAB treatments or protocols that have been reported for treatment of APE in patients with CF.
A scoping review was conducted to examine original research on home IVAB treatment for APE in patients with CF. Studies that included only pediatric patients or antibiotic administration for prevention of APE were excluded. Medline and CINAHL were searched. Study selection and data extraction was performed independently by 2 reviewers.
Eleven studies, published from 1997 to 2022, were included. Overall, there was minimal information reported among the studies about criteria for eligibility to receive IVABs at home. Some studies excluded patients requiring supplemental oxygen, intravenous nutrition, transplant recipients, and those requiring a combination of antibiotics. Few studies required a formal assessment of antibiotic administration competency. Additionally, there were insufficient descriptions of the types of antibiotics administered in the home, and no formal protocols were evident among the research for the treatment of patients with CF experiencing APE.
This review highlighted a need for standardized protocol for home IVAB for APE, with potential to improve CF management for patients and practitioners, with impacts on outcomes such as lung function, symptom severity, and quality of life.

