What is collaborative practice and why is it important in palliative care?

Author(s):  
Dave Roberts
2021 ◽  
pp. 787-799
Author(s):  
Nathan I. Cherny ◽  
Stein Kaasa

The division of cancer care into initial primary antitumour therapies followed by hospice or palliative care for patients who have progressive disease is anachronistic. Since the goals of medical oncology extend beyond the reduction of tumour burden and the deferral of death and incorporate a quality-of-life dimension, there is need for a continuum in patient care independent of whether the treatment intention is curative, life-prolonging, or symptomatic. Palliative care interventions should be integrated according to the clinical circumstances of the patient. This chapter outlines the oncologist’s role in the delivery of palliative care to cancer patients, emphasizing issues related to communication, interdisciplinary care, and collaborative practice with palliative medicine experts, and emphasizing principles of non-abandonment and continuity of care.


Author(s):  
Gusgus Ghraha Ramdhanie

<span class="fontstyle0">Kematian anak akibat penyakit terkait HIV/AIDS sebagai korban transmisi vertikal atau disebut<br /></span><span class="fontstyle0">Mother To Child Transmission </span><span class="fontstyle0">(MTCT) mencapai 110.000 setiap tahun. Dalam hitungan rinci terjadi<br />sekitar 400 anak terinfeksi HIV dan sekitar 290 kematian karena AIDS terjadi setiap harinya. Sebagai<br />korban transmisi infeksi vertikal, banyak anak yang kurang mendapat dukungan dari keluarga. Orang<br />tua dengan HIV/AIDS selain mempunyai masalah kesehatannya sendiri, juga dapat menjadikan anak<br />seorang “yatim piatu” sehingga anak tidak mendapatkan asuhan orang tua. Perlu kajian manajemen<br />pengelolaan asuhan, salah satunya adalah dengan penerapan perawatan paliatif pada anak. Tujuan dari<br />penulisan </span><span class="fontstyle0">literature review </span><span class="fontstyle0">ini yaitu untuk mengetahui perawatan paliatif pada anak dengan<br />HIV/AIDS sebagai korban infeksi vertikal berdasarkan pada sumber literatur jurnal penelitian ilmiah<br />terkait.<br />Metode yang digunakan dalam penulisan </span><span class="fontstyle0">literature review </span><span class="fontstyle0">ini adalah penelusuran internet dari<br />database </span><span class="fontstyle0">Google Scholar, PubMed, Proquest, Medscape</span><span class="fontstyle0">, dan EBSCO dengan menggunakan kata kunci<br /></span><span class="fontstyle0">pediatric palliative care</span><span class="fontstyle0">, </span><span class="fontstyle0">palliative care</span><span class="fontstyle0">, dan </span><span class="fontstyle0">pediatric </span><span class="fontstyle0">HIV/AIDS. Perawatan paliatif pada anak adalah<br />model terintegrasi dimana komponen layanan paliatif dilakukan setelah pasien mulai terdianosis.<br />Sebagian besar pasien anak dengan HIV/AIDS ditemukan dalam stadium klinis berat pada usia yang<br />sangat dini. Manajemen terapi farmakologis, non-farmakologis dan dukungan psikososial serta<br />spiritual diberikan dalam perawatan. Selain itu, manajemen tanda gejala dalam perawatan paliatif harus<br />dilakukan dengan tepat. Perawatan paliatif merupakan pelayanan tenaga profesional dengan<br />mengimplementasikan </span><span class="fontstyle0">interprofesional collaborative practice </span><span class="fontstyle0">yang dapat diintegrasikan dengan<br />pelayanan berbasis rumah. Perawatan paliatif pada anak dengan HIV/AIDS dapat meningkatkan<br />kualitas hidup anak.</span> <br /><br />


2014 ◽  
Vol 32 (31_suppl) ◽  
pp. 63-63
Author(s):  
Jeanne Elnadry ◽  
Tina Duarte ◽  
Gregory John C. Yang ◽  
Ambuga Badari

63 Background: In rural Yuma, AZ there are too few palliative care specialists to meet the needs of the population. This report presents a unique approach to interdisciplinary care for pain management beginning early in cancer care. To address this need a palliative care specialist collaborated with the entire clinical staff of the community cancer center, including physicians, nurses, social worker, pharmacist, and medical assistants, to initiate a new distress screening tool and develop an interdisciplinary collaborative practice model for pain management. Methods: Data was analyzed from 274 consecutive patients using a review of systems form which was modified 3/2014 to include more information regarding pain, depression/anxiety, communication about illness, spiritual needs, and educational needs, and from 55 patients admitted to home hospice. All clinical staff reviewed the data together and mapped clinical processes. A pain assessment protocol was developed for nurses and medical assistants, who gave the assessment summary to the physician seeing the patient. Further training for nurses taught an algorithm to collaborate with physicians for pain medication orders driven by the assessment findings. Results: About 1/3 of patients had significant concerns about pain. End-of-life data showed that 31% of 55 patients admitted from the cancer center to a local hospice had moderate to severe pain (pain score 4-10) at the time of hospice admission. 88% of these patients’ pain was controlled within 48 hours of admission to home hospice, with pain score 0-3. Data for 274 consecutive clinic patients showed that 30% of patients had concerns about pain, 30% about advanced care planning and communication, and 32% about anxiety, depression, and coping. Of the 162 patients who reported distress, 57% reported distress in 2 or more domains. Conclusions: Hospice data showed that nearly all cancer patients with moderate to severe pain could have pain control within 48 hours. Patients undergoing treatment should be able to have similar results, but were not. Follow-up data collection to assess effect of the collaborative practice model intervention is planned for August 2014.


2019 ◽  
Vol 28 (3) ◽  
pp. 1356-1362
Author(s):  
Laurence Tan Lean Chin ◽  
Yu Jun Lim ◽  
Wan Ling Choo

Purpose Palliative care is a philosophy of care that encompasses holistic, patient-centric care involving patients and their family members and loved ones. Palliative care patients often have complex needs. A common challenge in managing patients near their end of life is the complexity of navigating clinical decisions and finding achievable and realistic goals of care that are in line with the values and wishes of patients. This often results in differing opinions and conflicts within the multidisciplinary team. Conclusion This article describes a tool derived from the biopsychosocial model and the 4-quadrant ethical model. The authors describe the use of this tool in managing a patient who wishes to have fried chicken despite aspiration risk and how this tool was used to encourage discussions and reduce conflict and distress within the multidisciplinary team.


ASHA Leader ◽  
2013 ◽  
Vol 18 (6) ◽  
pp. 22-22

A recent ASHA survey asked members about their experience with collaborative practice.


ASHA Leader ◽  
2017 ◽  
Vol 22 (9) ◽  
Author(s):  
Brenda Arend ◽  
Kate Krival
Keyword(s):  

2010 ◽  
Vol 44 (9) ◽  
pp. 48-49
Author(s):  
M. ALEXANDER OTTO
Keyword(s):  

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