2015
DOI: 10.1016/j.pmn.2014.07.001
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Effect of Hospice Nonprofessional Caregiver Barriers to Pain Management on Adherence to Analgesic Administration Recommendations and Patient Outcomes

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Cited by 23 publications
(17 citation statements)
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References 30 publications
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“…Our findings support the need also to include caregivers in the educational process, especially since another researcher found that misunderstandings about pain management affected their caregiving activities related to medication adherence. 9 Optimally, this education should occur early after the cancer diagnosis as part of cancer survivorship programs 32 so that pain control is an expectation across the cancer trajectory, and the focus of end-of-life care does not need to include this type of education unless patients are diagnosed with advanced cancer and have a rapid decline toward death.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Our findings support the need also to include caregivers in the educational process, especially since another researcher found that misunderstandings about pain management affected their caregiving activities related to medication adherence. 9 Optimally, this education should occur early after the cancer diagnosis as part of cancer survivorship programs 32 so that pain control is an expectation across the cancer trajectory, and the focus of end-of-life care does not need to include this type of education unless patients are diagnosed with advanced cancer and have a rapid decline toward death.…”
Section: Discussionmentioning
confidence: 99%
“…[11][12][13] In a recent study of 46 hospice lay caregivers, investigators combined item scores in unique subscales, but those similar to prior scales had scores also similar to the dyad studies. 9 From the publications we identified, caregivers generally report BQ scores that are higher for concerns about addiction, medication tolerance, disease progression, and side effects of pain medications than the other areas of concern. However, the evidence about patient-caregiver dyads is from research conducted 1.5 to 2 decades ago and may or may not represent current beliefs about pain management or their relationships with pain intensity experienced by hospice patients with cancer.…”
Section: Introductionmentioning
confidence: 99%
“…A large study of 4707 cancer survivors revealed that two‐thirds reported at least 1 barrier to cancer pain management, with the most vulnerable groups—those who were nonwhite, less educated, older, or having more comorbidities—being most adversely affected . Numerous studies have examined specific barriers expressed by patients and family/caregivers regarding pain and pain management, with fears of addiction consistently being cited as a substantial concern . Physician barriers to cancer pain management include inadequate assessments and a reluctance to administer and prescribe opioids .…”
Section: Introductionmentioning
confidence: 99%
“…1 Analgesic medication errors are more likely when understanding is limited, 3 and family caregivers less effectively make decisions about analgesic regimens. 4 In our prior work we found that the majority of medical words used during care planning discussions are medication names, most of which are never explained. 5 Communication between team members and caregivers averaged fourth-grade level and reading ease was associated with caregiver understanding of and comfort with symptom management; 6 however, as grade level talk between caregivers and team members increased so did caregiver anxiety, and higher anxiety was associated with greater difficulty in understanding medication and symptom management.…”
Section: Introductionmentioning
confidence: 99%