Abstract
Abstract
Background
Social relationships are important health resources and may be investigated as social networks. We measured cancer patients’ social subnetworks divided into generic social networks (people known to the patients) and disease-specific social networks (the persons talked to about the cancer) during 3 years after diagnosis.
Method
Newly diagnosed patients with localized breast cancer (n = 222), lymphoma (n = 102), and prostate cancer (n = 141) completed a questionnaire on their social subnetworks at 2–5 months after diagnosis and 9, 18, and 36 months thereafter. Generic and cancer-specific numbers of persons of spouse/partner; other family; close relatives, in detail; and friends were recorded as well as cancer-specific numbers of persons in acquaintances; others with cancer; work community; healthcare professionals; and religious, hobby, and civic participation. The data was analyzed with regression models.
Results
At study entry, most patients had a spouse/partner, all had close relatives (the younger, more often parents; and the older, more often adult children with families) and most also friends. The cancer was typically discussed with them, and often with acquaintances and other patients (74–86%). Only minor usually decreasing time trends were seen. However, the numbers of distant relatives and friends were found to strongly increase by the 9-month evaluation (P < 0.001).
Conclusion
Cancer patients have multiple social relationships and usually talk to them about their cancer soon after diagnosis. Most temporal changes are due to the natural course of life cycle. The cancer widened the patients’ social networks by including other patients and healthcare professionals and by an increased number of relatives and friends.
Funder
Syöpäsäätiö
Pohjois-Suomen Terveydenhuollon Tukisäätiö
Cancer Association of Northern Finland
Signe ja Ane Gyllenbergin Säätiö
Finnish Institute for Health and Welfare
Publisher
Springer Science and Business Media LLC