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Articoli di riviste sul tema "Palliative care"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 31 luglio 2024

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1

Signer, Michaela. "Depression in Palliative Care". Therapeutische Umschau 69, n. 2 (1 febbraio 2012): 99–106. http://dx.doi.org/10.1024/0040-5930/a000259.

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Depression ist eine häufige komorbide behandlungsbedürftige Störung, diedie Lebensqualität von Patienten und ihren Angehörigen erheblich beeinträchtigt. Phänomenologisch ist in palliativen Situationen ein breites Spektrum an Störungen anzutreffen, die es voneinander abzugrenzen gilt: "normal" zu wertende Reaktionen auf eine unheilbare Erkrankung wie Trauer, Wut und Verzweiflung bis hin zu schweren depressiven Störungen. Durch häufige Symptomüberschneidungen zwischen der somatischen Grunderkrankung und einer Depression sind die gängigen ICD-10-Kriterien zur Diagnosestellung Depression in der Palliative Care nicht anwendbar. Es empfiehlt sich, alle Symptome auszuschließen, die auch Folge der Grunderkrankung sein könnten. Durch eine adäquate palliative Betreuung als eines der wenigen Evidenz-basierten Elemente in der Betreuung palliativer Patienten mit Depression kann eine maximale Prävention erreicht werden. Bei der Therapieauswahl sollte neben dem Therapieziel die zu erwartende verbleibende Lebenszeit richtungweisend sein.

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Kornblith, Alice B. "Does Palliative Care Palliate?" Journal of Clinical Oncology 19, n. 8 (15 aprile 2001): 2111–13. http://dx.doi.org/10.1200/jco.2001.19.8.2111.

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3

Carey, Peter. "Researching Palliative Care Researching Palliative Care". Nursing Standard 15, n. 41 (27 giugno 2001): 29. http://dx.doi.org/10.7748/ns2001.06.15.41.29.b126.

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4

Hertler, Caroline, e Thomas Hundsberger. "Palliative Care in der Neurologie". Praxis 110, n. 15 (novembre 2021): 897–901. http://dx.doi.org/10.1024/1661-8157/a003786.

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Zusammenfassung. In der Neurologie als Disziplin finden sich klare Überschneidungen mit der Palliative Care. Dennoch findet eine frühe Integration von palliativer Versorgung begleitend zur neurologischen Behandlung eher selten statt, und weiterhin bestehen Missverständnisse in Bezug auf den Zeitpunkt des Einbezugs von Palliative Care und deren Rolle jenseits der oft verwechselten reinen «End-of-Life Care» und Hospizpflege. Ein weiterer Ausbau und die Nutzung der Synergien sollte in den kommenden Jahren integraler Bestandteil beider Disziplinen werden und eine entsprechende Schulung insbesondere junger ärztlicher Kolleginnen und Kollegen im Fokus der Ausbildung stehen.

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5

Wadiwala, Janvi, Mausam Patel, Chenghui Li, Sanjay Maraboyina, Ahmed Safar e Thomas Kim. "Health care disparities and barriers to palliative care among metastatic renal cell carcinoma patients: An NCDB analysis." Journal of Clinical Oncology 39, n. 15_suppl (20 maggio 2021): 4545. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.4545.

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4545 Background: Palliative care improves quality of life for both patients and caregivers but may be underutilized due to socioeconomic barriers to access. An NCDB analysis was performed to analyze the effect of socioeconomics on palliative care receipt among patients with metastatic renal cell carcinoma. Methods: A retrospective hospital-based analysis was performed using the National Cancer Database to identify variables that significantly affect receipt of palliative care among patients diagnosed with metastatic renal cell carcinoma diagnosed between 2004 and 2016. Sub-cohort analysis was also performed among patients with the most severe disease. Multivariate binominal logistic regression was performed to determine the association of underlying socioeconomics with receipt of palliative care. The odds of receiving palliative care based on socioeconomic factors was reported as odds ratios (OR) with 95% CI. Results: There were 50405 patients meeting inclusion criteria with 40448 (80.2%) undergoing no palliation and 9957 (19.8%) undergoing palliative care. Both Black and Spanish/Hispanic patients had decreased odds of receiving palliative care (OR, 0.816, 95% CI, 0.753 to 0.885 and OR, 0.599, 95% CI, 0.540 to 0.665, respectively). Increasing age, papillary histology, increasing income, and increasing distance were also significantly associated with decreased odds of receiving palliation while treatment at an integrated network cancer program or comprehensive community cancer program and higher educational attainment were associated with increased odds of receiving palliative care. Similar findings were demonstrated among patients with the most severe disease. Limitations include the retrospective design and potential underlying selection biases of this study. Conclusions: Significant associations between receipt of palliative care and socioeconomic factors exist among patients with metastatic renal cell carcinoma. In this study among patients with metastatic renal cancer, we found associations between socioeconomics and palliative care access including age, race, Spanish/Hispanic origin, income, education, and other factors.

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6

Henriksen, K. "Palliative Care Symposium: Promoting Joint Palliative Care". Journal of the Royal College of Physicians of Edinburgh 41, n. 3 (19 settembre 2011): 254–55. http://dx.doi.org/10.4997/jrcpe.2011.316.

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7

Alsirafy, Samy A., Ahmad M. Abou-Alia e Hafez M. Ghanem. "Palliative Care Consultation Versus Palliative Care Unit". American Journal of Hospice and Palliative Medicine® 32, n. 3 (2 dicembre 2013): 275–79. http://dx.doi.org/10.1177/1049909113514476.

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8

Franjic, Sinisa. "Nursing in Palliative Care". Emergency and Nursing Management 1, n. 1 (21 dicembre 2022): 01–04. http://dx.doi.org/10.58489/2836-2179/001.

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Palliative care is the best example of the art of nursing that looks at the circumstances and difficulties that cause suffering and affect the quality of life of patients. Palliative care is comprehensive care aimed at providing the necessary health care to patients with incurable diseases. A palliative approach is a completely holistic approach to another person, one of whom is a health professional and the other a patient. Palliative care interventions are aimed primarily at reducing suffering and pain which improves the quality of life of patients. The nurse is responsible for planning, conducting and evaluating health care with continuous assessment, educating patients and families, and collaborating with other members of the interdisciplinary team.

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Ganapathy Sankar U., Monisha R., Christopher Amalraj Vallaba Doss e Palanivel R. M. "Evaluation of palliative care knowledge among health care students- A pilot study". International Journal of Research in Pharmaceutical Sciences 11, n. 2 (3 aprile 2020): 1433–37. http://dx.doi.org/10.26452/ijrps.v11i2.2015.

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Palliative care is given much importance in the curriculum of medical and health sciences. Before planning a new design and curriculum development, it is mandatory to test the knowledge and awareness of Occupational therapy students on palliative care. Thus it will help the expert’s panel to enhance the syllabus designing methods appropriate to the student’s knowledge. Without paying much attention to enhance knowledge on palliative care among students might lead to failure in providing quality care. To evaluate the knowledge in palliative care among undergraduate occupational therapy students. The study population included BOT 1ST Year and BOT Final year students and CRI from SRM College OF Occupational therapy, Kattankulathur. After obtaining informed consent signed from the participants, they have been instructed to fill in the questionnaire. The questionnaire has demographic data and 35 questions under nine groups, for which the students were instructed to answer (Yes, No, Don’t know). A detailed instruction was there in the questionnaire to avoid leaving any questions blank. It was found that occupational therapy students were aware of palliative care. Knowledge in palliative care was not precise among occupational therapy students related to healthcare. Hence there is an emerging need to include palliate care in the curriculum for the development of knowledge in palliative care.

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10

Bierle, Rebecca (Schuetz), Karen M. Vuckovic e Catherine J. Ryan. "Integrating Palliative Care Into Heart Failure Management". Critical Care Nurse 41, n. 3 (1 giugno 2021): e9-e18. http://dx.doi.org/10.4037/ccn2021877.

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Background The World Health Organization defines palliative care as an approach that improves the quality of life of patients and their families through the prevention and relief of suffering by assessment and treatment of physical, psychosocial, and spiritual problems. Any patient with chronic debilitating disease, including heart failure, is a candidate for interdisciplinary palliative care to manage their complex physical and psychosocial needs. Clinical Relevance The philosophy of palliative care has evolved to include a vision of holistic care extended to all individuals with serious illness and their families or caregivers that should be integrated throughout the continuum of care, including the acute phase. The critical care nurse will likely encounter patients with heart failure who are receiving or are eligible to receive palliative care at various time points during their illness. Critical care nurses therefore play a pivotal role in symptom palliation affecting the heart failure patient’s quality of life. Purpose To review the models of palliative care and the role that the critical care nurse plays in symptom palliation and preparation of the patient and their family for transition to other levels and settings of care. Content Covered This review addresses the principles and models of palliative care along with how to integrate these principles into all phases of the heart failure disease continuum. Also included are recommendations for palliation of symptoms specific to heart failure patients as well as a discussion of the role of the critical care nurse and the importance of shared decision-making.

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Horváth, Orsolya, Enikő Földesi e Katalin Hegedűs. "Mikor és hogyan integráljuk az onkológiai és a palliatív ellátást?" Orvosi Hetilap 162, n. 44 (31 ottobre 2021): 1769–75. http://dx.doi.org/10.1556/650.2021.32254.

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Összefoglaló. A palliatív ellátások korai bevonása az onkológiai betegek ellátásába előnnyel jár mind a beteg életminősége, mind a kezelés színvonala, mind a költséghatékonyság szempontjából. Szükség van egy olyan modellre, mely alapján a megfelelő időben, a megfelelő beteg a megfelelő minőségű palliatív ellátásban részesül. Ebben a közleményben a palliatív ellátás korai integrációjának előnyei, szintjei és a speciális palliatív ellátás fogalmának ismertetése után a leginkább elterjedt beutalási modellek előnyeit és hátrányait mutatjuk be a nemzetközi szakirodalom alapján. A speciális palliatív ellátást igénylő betegek kiszűrésére szolgáló, prognózisalapú modellek hátránya, hogy nincs elég kapacitás az ilyen módon beutalt nagyszámú beteg ellátására, ezért széles körben nem terjedtek el. A tüneteken alapuló modellek sokszor bonyolultak és a mindennapi klinikai gyakorlatban nem használatosak. Az új kutatások alapján egyszerű, gyakorlatias kérdéssorokat alkalmaznak, melyekkel könnyen kiemelhetők, akik profitálnak a speciális palliatív intervencióból. Ezek közül a Yale egyetemi és a PALLIA -10 modellt ismertetjük részletesen. Amennyiben az aktív onkológiai ellátást végzők a megfelelő palliatív beutalási kritériumokat ismerik és alkalmazzák, a betegek időben jutnak a megfelelő komplex kezeléshez anélkül, hogy a palliatív ellátórendszer túlterhelődne. Orv Hetil. 2021; 162(44): 1769–1775. Summary. Early integration of palliative care into the trajectory of cancer care brings advantages into the patients’ quality of life, the level of care and cost-efficiency, too. On the basis of a predefined model, the right patient may receive the right level of palliative care at the right time. Having defined the advantages, the levels of early integration of palliative care and the concept of special palliative care, we also aim to describe the advantages and disadvantages of the most common referral models on the basis of international literature in this article. The drawback of prognosis-based models to identify patients needing special palliative care is the lack of capacity to provide care for the large number of patients so recognised; therefore they have not become widespread. Needs-based models tend to be complicated and thus rarely applied in everyday clinical practice. On the basis of new researches, simple, pragmatic questionnaires are utilised through which the patients who could benefit from special palliative care interventions are easy to identify. Here we give a detailed report of the Yale University and PALLIA-10 models. On condition that appropriate palliative referral criteria are known and applied by active oncology care providers, patients may receive adequate complex care without the palliative care system being overloaded. Orv Hetil. 2021; 162(44): 1769–1775.

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Beider, Shay. "An Ethical Argument for Integrated Palliative Care". Evidence-Based Complementary and Alternative Medicine 2, n. 2 (2005): 227–31. http://dx.doi.org/10.1093/ecam/neh089.

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‘In the midst of life, we are in death’from The Book of Common PrayerThe Palliative Care, or comfort care, movement in the USA is on the rise. Currently, palliative services are not integrated in an organized way throughout healthcare. If we accept the argument that palliative care is ethically desirable and that all patients are entitled to palliative services regardless of a terminal diagnosis, it follows that it needs to be integrated across a wide range of healthcare services. Ethical questions regarding palliative care and well-known ethical frameworks are discussed and an argument is made for integrating palliative healthcare services throughout the healthcare system and not simply at the end of life. Complementary and alternative medicine (CAM) therapies are discussed as useful and necessary components of palliative care. If we as a society look beyond separating cures and palliation, we will come closer to incorporating compassionate care throughout the disease process.

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Klenk, Laurence, Nicoletta M. Iucolano, Christian Tasso Braun, Aristomenis K. Exadaktylos e Steffen Eychmüller. "Endstation Notfallstation: Perzeption und Rezeption des Begriffs «palliativer Patient» sowie Ansätze zur Verbesserung der interdisziplinären Zusammenarbeit – ein Survey unter notfallmedizinischem Personal auf einer Schweizer Notfallstation". Praxis 104, n. 1 (1 gennaio 2015): 19–25. http://dx.doi.org/10.1024/1661-8157/a001884.

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Hintergrund: Wegen sich verändernder Strukturen im Spitalbereich sowie im Bereich der Hausarztabdeckung als auch infolge zunehmenden Drucks auf das Gesundheitssystem kommen mehr Patienten auf die Notfallstationen, die aufgrund ihrer Grunderkrankung und des fortgeschrittenen Krankheitsstadiums von einem palliativen Behandlungskonzept profitieren. Eine wesentliche Herausforderung ist hierbei bereits die Definition von «Palliative Care» (PC), sowie die Klärung, was genau die palliative Versorgung beinhaltet. Häufig vermischt wird der Terminus «Palliative Care» mit «End of life care». Die vorliegende Studie ist eine Standortbestimmung im Universitären Notfallzentrum des Inselspitals Bern (UNZ), das jährlich rund 32 400 Patienten versorgt. Ziel ist es, mehr über den Wissensstand und die persönliche Einstellung der Mitarbeiter zu palliativen Fragestellungen und speziell zum Begriff «Palliative Care» zu erhalten. Methodik: Die Mitarbeiter des Universitären Notfallzentrums des Inselspitals Bern (UNZ) wurden mittels einer Online-Umfrage durch eine spitalexterne Fachinstitution interviewt. Diese Befragung basiert auf einem Instrument [1], das in einer vergleichbaren Studie auf einer Notfallstation in den USA entwickelt und validiert wurde. Resultate: Von 154 Mitarbeitenden (Pflege und Ärzte) füllten 60 Mitarbeitende die Befragung vollständig aus, entsprechend einer Antwortrate von 39%. Die Definition von Palliative Care (von n=60) war sehr heterogen und konnte in sechs Themenbereiche eingeteilt werden. Bei den Fragen nach spezifischen Leistungsangeboten äusserten die Mitarbeitenden den Wunsch nach einem erleichterten Zugang zu bestehenden Patientendaten, nach einem 24-Stunden-Palliative-Care-Konsiliardienst und nach mehr Besprechungszeit für Fragestellungen der PC im klinischen Alltag. Schlussfolgerungen: Die heterogene Begriffsdefinition von «Palliative Care» bestätigt sich. Es besteht kein klares Vorgehen, und zudem lässt sich ein Zeitmangel für ausführliche Patientengespräche in palliativen Situationen im UNZ feststellen. Der Patientenwunsch oder Patientenverfügungen mit DNR/DNI-Prozedere stehen nicht im Widerspruch zu den persönlichen Wertvorstellungen der meisten Mitarbeitenden. Die 24-Stunden-Verfügbarkeit eines spezialisierten PC-Teams, das Erarbeiten von Guidelines und vermehrtes Training für PC würde von den UNZ-Mitarbeitenden begrüsst.

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_, _. "Palliative Care". Journal of the National Comprehensive Cancer Network 4, n. 8 (settembre 2006): 776. http://dx.doi.org/10.6004/jnccn.2006.0068.

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Over the past 20 years, increasing attention has been paid to quality-of-life issues in oncology. As the hospice movement has grown in this country, palliative care has developed into an integral part (rather than the antithesis) of comprehensive cancer care. Palliative care must be integrated earlier into the continuum of cancer care, and palliative, symptom-modifying therapy should be provided simultaneously with disease-modifying therapy from diagnosis. The goal of the NCCN palliative care guidelines is to help assure that each patient with cancer experiences the best possible quality of life throughout the illness trajectory. These guidelines are intended to help oncology teams provide the best care possible for their patients with incurable cancer. For the most recent version of the guidelines, please visit NCCN.org

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Levy, Michael H., Anthony Back, Costantino Benedetti, J. Andrew Billings, Susan Block, Barry Boston, Eduardo Bruera et al. "Palliative Care". Journal of the National Comprehensive Cancer Network 7, n. 4 (aprile 2009): 436–73. http://dx.doi.org/10.6004/jnccn.2009.0031.

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Levy, Michael H., Michael D. Adolph, Anthony Back, Susan Block, Shirley N. Codada, Shalini Dalal, Teresa L. Deshields et al. "Palliative Care". Journal of the National Comprehensive Cancer Network 10, n. 10 (ottobre 2012): 1284–309. http://dx.doi.org/10.6004/jnccn.2012.0132.

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Marks, Marilyn. "Palliative care". Nursing Standard 8, n. 2 (29 settembre 1993): 21–31. http://dx.doi.org/10.7748/ns.8.2.21.s79.

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Koshy, Cherian. "Palliative care". Indian Journal of Palliative Care 13, n. 1 (2007): 22. http://dx.doi.org/10.4103/0973-1075.37189.

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Marks, Marilyn. "Palliative care". Nursing Standard 6, n. 33 (6 maggio 1992): 9–15. http://dx.doi.org/10.7748/ns.6.33.9.s51.

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Swetz, Keith M., e Arif H. Kamal. "Palliative Care". Annals of Internal Medicine 156, n. 3 (7 febbraio 2012): ITC2. http://dx.doi.org/10.7326/0003-4819-156-3-201202070-01002.

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Bruera, E. "Palliative care". CA: A Cancer Journal for Clinicians 50, n. 2 (1 marzo 2000): 68–69. http://dx.doi.org/10.3322/canjclin.50.2.68.

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Newshan, Gayle, e Deborah Witt Sherman. "PALLIATIVE CARE". Nursing Clinics of North America 34, n. 1 (marzo 1999): 131–45. http://dx.doi.org/10.1016/s0029-6465(22)02366-0.

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Malone, Angie. "Palliative Care". Critical Care Nursing Clinics of North America 34, n. 1 (marzo 2022): i. http://dx.doi.org/10.1016/s0899-5885(22)00003-x.

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Swetz, Keith M., e Arif H. Kamal. "Palliative Care". Annals of Internal Medicine 168, n. 5 (6 marzo 2018): ITC33. http://dx.doi.org/10.7326/aitc201803060.

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Nadeem, Ramsha, Samina Qamar, M. Abbas Khokhar, Maryam Abid e Remisha Zahid. "PALLIATIVE CARE". Professional Medical Journal 25, n. 12 (8 dicembre 2018): 1910–14. http://dx.doi.org/10.29309/tpmj/18.4753.

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Pain is a devastating symptom of advanced cancers. Inadequate assessment and failure in following WHO (World health organization) guidelines for pain management are barriers to pain control in cancer patients. Objectives: To determine frequency of inadequate pain assessment leading to inadequate pain control in advanced stage cancer patients receiving palliative care. Subjects and Methods: 180 patients, within age 18 to 70 years of both genders, of cancer with stage 3 and 4 disease receiving palliative treatment for pain due to primary or metastatic disease requiring opioidanalgesics presenting to inpatient department of Medical Oncology, Mayo Hospital Lahore were selected using non probability, consecutive sampling. Study Design: Cross sectional descriptive study. Setting: Department of Medical Oncology, Mayo Hospital Lahore. Period: 6 months after approval of synopsis from 01.06.2017 to 01.01.2018. The Pain scales used were Numerical Rating Scale- NRS, followed by Visual Analogue Scale-VAS. All patients were evaluated whether or not their pain was assessed by a standard pain scale, the type of malignancy, and the stage of cancer. Results: A total of 180 patients with mean age of 49.68 years, with 62.2% females and 37.8% males were selected. Out of these 124 (68.89%) patientsreceived inadequate assessment for their pain intensity as no documented pain scale was being used to assess them. Out of them 50(49.02%) were males and 52 (50.98%) were females. 56 patients (31.11%) were receiving inadequate pain assessment. 17 (30.35%) of them were assessed using VAS and 39 (69.65%) were assessed using NRS. The median pain score was 7.8/10 with the stage 4 patients mainly presenting with a score of >7/10 (69.94%) and stage 3 patients making up majority of pain with <7/10 score (58.82%). Conclusion: This study showed that pain is poorly managed in patients with advanced malignancy as majority of patients are not assessed according to standard methods for cancer pain. There is a strong need of physicians’ education, development of proper palliative care services and implementation of WHO guidelines to achieve effective pain management for oncology patients.

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Brennan, Gena. "Palliative Care". Journal of Christian Nursing 39, n. 1 (gennaio 2022): 59. http://dx.doi.org/10.1097/cnj.0000000000000904.

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Kashiwagi, Tetsuo. "Palliative Care." Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics 36, n. 12 (1999): 854–56. http://dx.doi.org/10.3143/geriatrics.36.854.

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Kaur, Simrat, e Bhivu Atwal. "Palliative Care". International Journal of Nursing Education and Research 8, n. 1 (2020): 121. http://dx.doi.org/10.5958/2454-2660.2020.00026.5.

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Watson, Max, e Nazia Hussain. "Palliative care". InnovAiT: Education and inspiration for general practice 7, n. 10 (7 gennaio 2014): 633–34. http://dx.doi.org/10.1177/1755738013504389.

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Meier, Diane E. "Palliative Care". Oncology Times 23, n. 5 (maggio 2001): 2. http://dx.doi.org/10.1097/01.cot.0000285839.62853.73.

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Riahi, Shadan, e Marjan Khajehei. "Palliative Care". Critical Care Nursing Quarterly 42, n. 3 (2019): 315–28. http://dx.doi.org/10.1097/cnq.0000000000000269.

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Twycross, Robert G. "Palliative Care". Journal of Pain & Palliative Care Pharmacotherapy 16, n. 1 (gennaio 2002): 61–79. http://dx.doi.org/10.1080/j354v16n01_05.

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Kitzes, Judith A., e Timothy Domer. "Palliative Care". Journal of Pain & Palliative Care Pharmacotherapy 17, n. 3-4 (gennaio 2004): 201–10. http://dx.doi.org/10.1080/j354v17n03_30.

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Paterson, John. "Palliative care". Medical Journal of Australia 150, n. 1 (gennaio 1989): 49. http://dx.doi.org/10.5694/j.1326-5377.1989.tb136339.x.

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Student, Johann-Christoph. "Palliative Care". CNE.fortbildung 2, n. 05 (1 novembre 2008): 1. http://dx.doi.org/10.1055/s-0033-1348382.

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Woroniecka, Karolina. "Palliative Care". Academic Medicine 90, n. 3 (marzo 2015): 364. http://dx.doi.org/10.1097/acm.0000000000000621.

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Alsirafy, Samy A., Somaia M. Mousa e Stuart M. Brown. "Palliative Care". American Journal of Hospice and Palliative Medicine® 29, n. 1 (19 aprile 2011): 7–8. http://dx.doi.org/10.1177/1049909111406708.

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Creutzfeldt, Claire J., Robert G. Holloway e J. Randall Curtis. "Palliative Care". Stroke 46, n. 9 (settembre 2015): 2714–19. http://dx.doi.org/10.1161/strokeaha.115.008224.

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Morrison, R. Sean, e Diane E. Meier. "Palliative Care". New England Journal of Medicine 350, n. 25 (17 giugno 2004): 2582–90. http://dx.doi.org/10.1056/nejmcp035232.

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Castro, Maria. "Palliative Care". AJN, American Journal of Nursing 115, n. 4 (aprile 2015): 13. http://dx.doi.org/10.1097/01.naj.0000463007.19518.84.

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41

Estle, Karen. "Palliative Care". Journal of Palliative Medicine 8, n. 5 (ottobre 2005): 1059. http://dx.doi.org/10.1089/jpm.2005.8.1059.

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42

Koshy, Cherian. "Palliative Care". Journal of Palliative Medicine 11, n. 4 (maggio 2008): 636–37. http://dx.doi.org/10.1089/jpm.2007.9920.

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43

Greer, Steven, e Marie Joseph. "Palliative Care". Integrative Cancer Therapies 15, n. 1 (dicembre 2015): 5–9. http://dx.doi.org/10.1177/1534735415617015.

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44

Weinstein, Barbara E. "Palliative Care". Hearing Journal 68, n. 1 (gennaio 2015): 23. http://dx.doi.org/10.1097/01.hj.0000459740.48510.d0.

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45

Irwin, Scott A. "Palliative Care". FOCUS 11, n. 1 (gennaio 2013): 48–51. http://dx.doi.org/10.1176/appi.focus.11.1.48.

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46

Ballantyne, Jane C. "Palliative Care". Clinical Journal oF Pain 28, n. 5 (giugno 2012): 463. http://dx.doi.org/10.1097/ajp.0b013e31823984cb.

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47

Jindal, SurinderK. "Palliative care". Lung India 24, n. 2 (2007): 43. http://dx.doi.org/10.4103/0970-2113.44208.

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48

Clarke, Pamela N. "Palliative Care". Nursing Science Quarterly 23, n. 3 (17 giugno 2010): 220. http://dx.doi.org/10.1177/0894318410371843.

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49

Spaulding, Aaron, Debra A. Harrison e Jeffrey P. Harrison. "Palliative Care". Health Care Manager 35, n. 3 (2016): 189–98. http://dx.doi.org/10.1097/hcm.0000000000000115.

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&NA;. "Palliative Care". Oncology Times 23, n. 7 (luglio 2001): 4. http://dx.doi.org/10.1097/01.cot.0000313784.46586.27.

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