AI Article Synopsis

  • Family members are essential in the treatment and decision-making processes for ICU patients, and enhancing their comfort can improve satisfaction levels.
  • A study at King George's Medical University assessed the satisfaction of families with polytrauma patients in the ICU, involving 66 participants and using a specific satisfaction questionnaire.
  • Results indicated overall satisfaction with ICU care was good, but families expressed lower satisfaction regarding the ICU environment and their involvement in decision-making, with notable differences in response times to queries based on gender.

Article Abstract

Background: Family members play a crucial role in ICU patients' treatment and decision-making, despite the stress and uncertainty they may experience, ensuring high-quality medical care. Providing comfortable spaces with noise-reducing techniques can boost family satisfaction. Further research is needed to support families in intensive care units (ICU). This study aims to evaluate family satisfaction and decision-making in polytrauma patients in the ICU, identify improvement opportunities, and analyze demographic and socioeconomic factors influencing satisfaction.

Methods: This cross-sectional study was conducted at King George's Medical University, Lucknow, over a period of one year. A total of 66 patients, aged between 20 and 70, their family members, and those who gave written informed consent were included. Exclusion criteria included those who died within 48 hours of ICU admission or did not give consent. Patient characteristics, such as age, sex, Acute Physiology and Chronic Health Evaluation (APACHE) II score, and hospital stay length, were also collected. The family satisfaction in the intensive care unit (FS-ICU) questionnaire, consisting of 24 items with five Likert response options, was used to assess satisfaction levels in ICU care and decision-making.

Results:  A study of 66 patients which included 78.79% male and 21.21% female. The majority of the patients (66.67%) lived with their family members. The mean ICU stay was 13.03 days, with an APACHE score of 17.39. The results showed that families were very satisfied with a considerable portion of the ICU stay. The overall satisfaction score was 57.00. Families were less satisfied with the atmosphere in the ICU and involvement in the decision-making process. The satisfaction scores were comparable for both genders, except for the time taken to respond to questions, which was significantly higher for women.

Conclusion: Although families were very satisfied with the ICU stay, several areas were identified as having potential for improvement. The present study shows that the quality of treatment and communication during hospitalization is a major factor in the need for follow-up care. This underlines the need for a constant focus on communication skills in the training of nurses and doctors and in their practical training in the ICU. Participation in decision-making, especially by family members of survivors, was identified as an area for improvement. We recommend more research to be conducted in India focusing on family satisfaction with involvement in the decision-making in ICU considering the unique racial, cultural, ethnic, and linguistic differences in India.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11358507PMC
http://dx.doi.org/10.7759/cureus.65702DOI Listing

Publication Analysis

Top Keywords

family satisfaction
16
family members
16
intensive care
12
icu stay
12
families satisfied
12
icu
11
family
9
polytrauma patients
8
care unit
8
involvement decision-making
8

Similar Publications

Maternal prenatal depressive symptoms (PD symptoms) pose a risk factor for child adjustment difficulties (CAD), defined as internalizing and externalizing symptoms. This study examined the underlying mechanisms of the link between PD symptoms and CAD in a longitudinal study. Longitudinal data from pregnancy to age 3, encompassing four assessment points, were analyzed for = 582 mothers participating in the German family panel .

View Article and Find Full Text PDF

Public Health.

Alzheimers Dement

December 2024

LMI, New Freedom, PA, USA.

Background: A Medicare Voluntary Advance Directive Framework (Framework) would enable the creation, storage, and sharing of advance directive documents, ensuring end-of-life care appropriately honors the individual and their care wishes, while supporting healthcare teams and family members in making care decisions for their patients and loved ones. With Medicare enrollment reaching over 65 million beneficiaries in 2023, and Alzheimer's becoming one of the most expensive conditions - CMS policy makers have a growing responsibility to improve care quality at end-of-life.

Method: The federal government will be called upon to assist providers in navigating documents and legal variations of approved forms of directives among the different states, and in ensuring privacy standards that keep an individual's health data secure.

View Article and Find Full Text PDF

Background: Subjective cognitive complaints (SCCs) are self-reported cognitive concerns, often without objective impairment and are associated with higher risk of MCI and/or dementia. Moreover, the related subjective cognitive decline is suggested as a form of cognitive impairment, and precursor to Alzheimer's disease and related dementias (ADRD). Sleep, stress, and anxiety have been shown to explain significant portions of variance in relationships between multi-morbidity and SCCs.

View Article and Find Full Text PDF

There is need to identify evidence-based early childhood obesity prevention programs that are feasible and demonstrate cost-effectiveness for a broader health impact. This scale-out study leveraged community-engaged principles to compare the feasibility and cost-effectiveness of three delivery modes of a childhood obesity prevention family meals program (Simple Suppers) that demonstrated positive impacts on child and caregiver diet/nutritional health-related outcomes in a previous experimental trial tested among elementary-aged children. This three-arm (in-person, online, hybrid) pre-(T0) and post-(T1)-test study included families recruited from Head Start.

View Article and Find Full Text PDF

Background: The progression of dementia may be followed by decreased sexual activity for People with Alzheimer's Disease (PwAD) and their spouse-carers. We designed this study to investigate the perception of change in sexual activity and sexual satisfaction among couples whose spouses were diagnosed with Alzheimer's Disease (AD).

Method: Using a cross-sectional design, we compared 74 dyads of people with Alzheimer´s disease (PwAD) and their spouse-carers, and 21 elderly dyads control.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!