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A cancer experience: Relationship of patient psychosocial responses to care‐giver burden over time
Author(s) -
McCorkle Ruth,
Yost Linda Shegda,
Jepson Christopher,
Malone Dolores,
Baird Susan,
Lusk Edward
Publication year - 1993
Publication title -
psycho‐oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.41
H-Index - 137
eISSN - 1099-1611
pISSN - 1057-9249
DOI - 10.1002/pon.2960020105
Subject(s) - psychosocial , medicine , psychological intervention , schedule , family medicine , nursing care , acute care , nursing , health care , psychiatry , economics , economic growth , operating system , computer science
Cancer affects not only ill persons but also family members and close friends. An original study from which this report is derived used a longitudinal design to follow patients discharged from one of seven hospitals with one or more complex care problems requiring home care. A total of 233 patients with multiple solid tumors diagnoses and 103 care‐givers were included in the original study. Interviews were conducted at discharge and at three and six months post‐discharge. This report examined the responses of a subset of 34 subjects (17 patients and their care‐givers) for whom patient and care‐giver variables were complete on all three occasions. Findings indicate that these patients were being discharged from the hospital with acute care needs. By three and six months posthospitalization, patients' conditions stabilized or improved but their care‐givers continued to report similar levels of burden. Patient psychosocial responses were strongly correlated with care‐givers' financial impact, impact on schedule, and physical care‐giving responsibility at three and six months. Results highlight the importance of developing interventions that reduce family care‐givers' burden in providing post‐hospital nursing care for patients with complex care requirements.