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Hello everyone. I, (Student), will be giving a presentation on the analysis of data and an idea for enhancing the quality of the program. Improving the standard of treatment provided by medical institutions is the goal of a Quality Improvement (QI) project that focuses on the evaluation of data (Puri et al., 2023). Evidence through the Agency for Healthcare Research and Quality (AHRQ) standards reveals some unsettling patterns in St. Anthony’s hospice scheme, particularly in relation to family caregiver contact and the service’s reaction to changing the caregiver and patient requirements. The plan makes use of the analysis of data from the hospice services program to discover deficiencies in the present system and highlight areas that need to be improved. The plan then goes into how to address these problems and improve the experiences of patients.
It is possible to highlight any modifications in all four Agency for Healthcare Research and Quality (AHRQ) identifiable standards connected to care for hospice patients in order to examine the given hospice statistics for 2020–2021 to detect a medical issue or topic of significance.
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Description | 2020 | 2021 |
Hospice patients whose hospice care team always treated them with dignity and respect, and cared about them | 78% | 80% |
Hospice patients whose hospice care team always communicated well with their family caregivers about taking care of them | 78% | 75% |
Hospice patients who always received enough help for pain, sadness, breathing, or constipation from the hospice care team | 65% | 68% |
Hospice patients and family caregivers who always get help as soon as they need it from the hospice care team | 70% | 68% |
Hospice patients’ perception of the treatment group’s commitment to treating them with equal dignity and honor rose from 78% in 2020 to 80% in 2021. This shows that things are getting better and implies that by serving individuals with respect and decency, the hospice either sustains or raises the standard of care. The proportion of hospice patients who thought that the staff caring for them interacted successfully with their family providers on a regular basis dropped somewhat from 78% in 2020 to 75% in 2021. This trend needs to be further examined to determine the causes underlying the fall since it might cause worries regarding the efficacy of communication. Additionally, the data indicates that a higher proportion of hospice patients—68% in 2021 compared to 65% in 2020—always got enough assistance from medical professionals for pain, depression, respiration, or constipation. Even if there is an enhancement, it is crucial to think about whether this rise satisfies benchmark standards or still needs development. Last but not least, from 70% in 2020 to 68% in 2021, fewer hospice recipients and their family caregivers said that they always got assistance as quickly as they required it. This might be a cause for worry, and further research is needed to find out what’s causing this decline in prompt aid.
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