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Volumn 12, Issue 5, 2017, Pages 788-798

Qualitative interviews exploring palliative care perspectives of Latinos on dialysis

Author keywords

Advance Care Planning; Advance Directives; Chronic Disease; Communication Barriers; End stage renal disease; Ethnicity; Fear; Health Literacy; Hemodialysis; Hispanic Americans; Hospice Care; Hospices; Humans; Kidney Failure, Chronic; Linguistics; Palliative Care; Patient Preference; Patient Centered Care; Punishment; Qualitative Research; Quality of life; Renal dialysis

Indexed keywords

ADULT; ADVANCE CARE PLANNING; AGED; ARTICLE; CHRONIC DISEASE; CLINICAL ARTICLE; COMMUNICATION DISORDER; DECISION MAKING; DIALYSIS; DIET RESTRICTION; END STAGE RENAL DISEASE; FEMALE; HEALTH LITERACY; HEMODIALYSIS; HISPANIC; HUMAN; INFORMATION PROCESSING; INTERVIEW; LANGUAGE ABILITY; MALE; MORTALITY; PALLIATIVE THERAPY; PHYSICAL WELL-BEING; PRACTICE GUIDELINE; PROTOCOL COMPLIANCE; QUALITATIVE RESEARCH; SELF EVALUATION; SOCIOECONOMICS; TRADITIONAL MEDICINE; ATTITUDE TO HEALTH; CHRONIC KIDNEY FAILURE; COLORADO; CULTURAL FACTOR; ETHNOLOGY; FAMILY RELATION; FEAR; HEALTH BEHAVIOR; HEALTH CARE DISPARITY; MIDDLE AGED; PATIENT PREFERENCE; PSYCHOLOGY; QUALITY OF LIFE; RELIGION; RISK ASSESSMENT; RISK FACTOR; TRANSCULTURAL CARE;

EID: 85021709996     PISSN: 15559041     EISSN: 1555905X     Source Type: Journal    
DOI: 10.2215/CJN.10260916     Document Type: Article
Times cited : (54)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.