This paper highlights my experience during the practicum, evidence-based practices, state policies, and ethics affecting my nursing practice. During the second part of the practicum, I met various individuals with diverse hypertension management methods. These included nurse practitioners, dieticians, physicians, patients and their families, healthcare technology professionals, care coordinators, and community resource providers. I collected information regarding the patient’s or the patient’s family members’ experiences with the signs, symptoms, and effects of hypertension and their management of the illness. I learned the tools used to monitor and manage the condition from healthcare technology professionals, including blood pressure cuffs, pulse oximeters, and glucose monitors. I then discovered some apps for tablets and smartphones that can manage the illness.
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I heard about the numerous types of care—including home care, physical therapy, dialysis, and other forms of care—that can be utilized to address the condition of hypertension from the care coordinators. I also gained knowledge about the various types of assistance that may be obtained through support groups, places of worship, and other non-medical forms of care. I learned about the many modes of transportation and other services that can facilitate access to care and other services from community resource providers. Finally, from the medical professionals, I learned about the recommended therapies and precautions and the impacts that hypertension can have on the standard of care and patient safety.
The websites and publications I evaluated for this assessment on evidence-based practice (EBP) were mainly concerned with the effects of community resources, care coordination, and healthcare technology on hypertension. They provided a comprehensive understanding of the evidence available about the advancements in managing hypertension. I learned more about the long-term impact of this condition on the standard of care, patient safety, and expenses to the system and the individual through these websites. I learned about the potential contributions that community resources, care coordination, and healthcare technology can make to the fight against hypertension. I learned specifically about the advancements in managing hypertension, including the use of devices to monitor and manage the condition. I also learned about the possible obstacles to using technology, care coordination, and local resources, such as costs.
I could better comprehend the long-term effects of hypertension by examining the effect of the condition on the standard of care, patient safety, and costs to the system and individual. I learned specifically about the likelihood of poor outcomes if the ailment is not treated and the higher expenses connected with the use of technology, care coordination, and community resources. Furthermore, I understood how timely and efficient management of the ailment can lead to favorable outcomes and lower expenses.
I used three stages to investigate the impact of hypertension on patient safety, healthcare quality, and system and individual costs. The patient’s present health and medical needs must first be evaluated. The patient’s lifestyle, medications, and degree of physical activity should all be evaluated, along with their health history and any present issues. The second step is to create a care plan that uses community resources, care coordination, and healthcare technology. Finally, it is essential to continuously assess how the treatment plan affects the client’s health, the standard of care, patient security, and system and personal costs.
My strategy for resolving the problem was changed because of my experiences. I learned more about the intricacy of the issue and the supportive components necessary to address it successfully through my interactions with the members I met. With the help of the available technology, care coordination techniques, and community resources, I created a plan of care that better fulfilled the patient’s medical needs as a result of this knowledge.
The extent of the patient’s support and resources, which came from various sources, including healthcare professionals, religious organizations, support groups, and community resources, astonished me the most. This is particularly intriguing because it sheds light on the intricate healthcare system that may be used to offer individuals with c