10 research outputs found

    The issue is... the occupational therapist’s role in addressing the silent sequelae associated with cancer-related cognitive dysfunction among survivors of cancer

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    The National Comprehensive Cancer Network identified occupational therapy as a first line of intervention for the treatment of cancer-related cognitive dysfunction (CRCD) (National Comprehensive Cancer Network [NCCN], 2016). Thus, occupational therapists have an opportunity to develop interventions that facilitate participation in meaningful occupations for survivors of cancer living with CRCD. In this article, we argue for occupational therapists to create occupation- and evidence-based, client-centered interventions for survivors of cancer with CRCD that address the multidimensional presentation of CRCD. One survivor’s story illustrates the affect of CRCD on occupational performance and the features to consider when developing interventions to meet the unique needs of survivors of cancer with CRCD. We recommend that interventions can be provided through self-paced home programming, community settings, or delivered through modes such as tele-rehabilitation to reach the growing population of survivors of cancer

    Assessing the predictive validity of the Salzberg Scale during acute care and inpatient rehabilitation

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    Pressure ulcers (PrU) are a leading secondary medical complication in the spinal cord injury (SCI) population. With over two hundred known risk factors, PrU prevention is extremely complex but can provide an astounding difference in a patient’s recovery. Multiple risk assessment scales allow us to quantify risk across a broad range of populations, yet the literature provides little evidence that these tools are representative of PrU development in the SCI population. The Pressure Ulcer Assessment Scale for the Spinal Cord Injured (Salzberg Scale) is a risk assessment scale specific to the SCI population, composed of fifteen risk factors that divide PrU development risk into four categories. The objective of this thesis is to assess the predictive validity of the Salzberg Scale during acute care and inpatient rehabilitation following spinal cord injury. Data was extracted from a primary study on PrU outcomes for newly injured traumatic SCI patients in acute care and inpatient rehabilitation. A secondary analysis assigned subjects a raw Salzberg Scale score based on collected medical information and Salzberg Scale component definitions. The Salzberg scores were used to compute sensitivities, specificities, and accuracy of the scale with newly defined risk cut-off scores for acute hospitalization and inpatient rehabilitation. Sensitivity and specificity were calculated for the scale’s ability to predict PrU ranging from two to 22 days after administration of the Salzberg Scale risk assessment tool. The use ofthe scale in the acute care hospitalization to assess risk for PrU within 2-3 days showed the only strong predictive results with an area under the curve (AUC) of 0.8482 at the indicated cutoff score of 15. The sensitivity of 100.0% and a specificity of 75.0%, showed a more accurate prediction balance than the validation study conducted by Salzberg on a broader population sample. Overall, failure of the scale’s predictive ability to predict a pressure ulcer over a longer time period suggests further studies must be completed in order for the scale be recommended for implementation in an inpatient rehabilitation setting

    Developing a Stakeholder-Driven Cancer Rehabilitation Intervention for Older Adults with Breast Cancer

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    The number of older adult breast cancer survivors is rapidly growing. Yet with survival, this population often experiences high, persistent rates of cancer-related disability. This disability manifests in the form of activity limitations or difficulties executing daily activities that older adult breast cancer survivors need or want to do. Despite efforts to improve detection of activity limitations and referral to rehabilitation services, cancer rehabilitation remains underutilized in this population. The focus of this dissertation was threefold. First, we examined the state of the science related to nonpharmacological interventions influencing activity limitations in older breast cancer survivors. We identified that existing interventions 1) are frequently complex in nature; 2) incorporate adaptive skills training, behavioral strategies, and exercise; 3) vary in delivery features; and 4) are associated with a wide range of effect sizes. The best combination of interventions and delivery features remain unclear. Second, we conducted semi-structured interviews with older breast cancer survivors to identify preferences for cancer rehabilitation interventions. We learned that the choice to pursue cancer rehabilitation is influenced by emerging awareness of disability, coping styles, comparisons with others, provider interactions, perceptions of cancer as a lifelong project, social support, and cost of rehabilitation. Participants’ preferences for intervention content varied but included some desire for interventions that provide peer support, healthy behavior training, and symptom management. Participants preferred interventions delivered in outpatient clinics or community-based settings. Third, we compiled findings from the scoping review and stakeholder interviews for expert panel review and consensus. Using a modified Delphi process, panelists rated intervention content and delivery features according to feasibility and prioritization. Our results revealed high consensus for intervention content including physical activity and adaptive skills training as well as interventions delivered in outpatient clinics or post-treatment, through a combination of in-person and virtual visits, lasting no more than 3 months, and occurring biweekly. Overall, these findings provide important evidence-based, stakeholder-informed directions for future intervention research in cancer rehabilitation. These findings can be used to inform the development, testing, and implementation of valued and accessible interventions to address activity limitations among older breast cancer survivors

    Health system and patient-level factors associated with multidisciplinary care and patient education among hospitalized, older cancer survivors

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    Objective: The purpose of this study was to examine system- and patient-level factors associated with the number of healthcare disciplines involved in delivery of patient education among hospitalized older cancer survivors. Methods: We used electronic health record (EHR) data from a single institution documenting patient education among hospitalized older patients (≥65 years) with a history of cancer between 9/1/2018 and 10/1/2019. We used parametric ordinal logistic regression to assess the number of healthcare disciplines involved in documented education activities. Results: The sample (n = 446) was predominantly male, White, and on average 74 years old. Adjusting for patient and system-level variables, men and larger department units had higher odds of receiving education from fewer healthcare disciplines. Patients with a history of breast or prostate cancer and longer lenths of stay had lower odds of receiving patient education from fewer healthcare disciplines. Conclusion: Hospital size, severity of illness, and cancer type are associated with delivery of multidisciplinary education in this sample. Innovation: EHR provides an opportunity to identify patterns in patient education among cancer survivors. Future research should investigate provider perspectives of the findings to inform provider- and system-level strategies to improve patient education

    The influence of telehealth-based cancer rehabilitation interventions on disability: a systematic review

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    Purpose: To characterize delivery features and explore effectiveness of telehealth-based cancer rehabilitation interventions that address disability in adult cancer survivors. Methods: A systematic review of electronic databases (CINAHL Plus, Cochrane Library: Database of Systematic Reviews, Embase, National Health Service’s Health Technology Assessment, PubMed, Scopus, Web of Science) was conducted in December 2019 and updated in April 2021. Results: Searches identified 3,499 unique studies. Sixty-eight studies met inclusion criteria. There were 81 unique interventions across included studies. Interventions were primarily delivered post-treatment and lasted an average of 16.5 weeks (SD = 13.1). They were most frequently delivered using telephone calls (59%), administered delivered by nursing professionals (35%), and delivered in a one-on-one format (88%). Risk of bias of included studies was primarily moderate to high. Included studies captured 55 measures of disability. Only 54% of reported outcomes had data that allowed calculation of effect sizes ranging -3.58 to 15.66. Conclusions: The analyses suggest small effects of telehealth-based cancer interventions on disability, though the heterogeneity seen in the measurement of disability makes it hard to draw firm conclusions. Further research using more diverse samples, common measures of disability, and pragmatic study designs is needed to advance telehealth in cancer rehabilitation. Implications for Cancer Survivors: Telehealth-based cancer rehabilitation interventions have the potential to increase access to care designed to reduce disability across the cancer care continuum

    The influence of telehealth-based cancer rehabilitation interventions on disability: a systematic review

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    PURPOSE: To characterize delivery features and explore effectiveness of telehealth-based cancer rehabilitation interventions that address disability in adult cancer survivors. METHODS: A systematic review of electronic databases (CINAHL Plus, Cochrane Library: Database of Systematic Reviews, Embase, National Health Service\u27s Health Technology Assessment, PubMed, Scopus, Web of Science) was conducted in December 2019 and updated in April 2021. RESULTS: Searches identified 3,499 unique studies. Sixty-eight studies met inclusion criteria. There were 81 unique interventions across included studies. Interventions were primarily delivered post-treatment and lasted an average of 16.5 weeks (SD = 13.1). They were most frequently delivered using telephone calls (59%), administered delivered by nursing professionals (35%), and delivered in a one-on-one format (88%). Risk of bias of included studies was primarily moderate to high. Included studies captured 55 measures of disability. Only 54% of reported outcomes had data that allowed calculation of effect sizes ranging -3.58 to 15.66. CONCLUSIONS: The analyses suggest small effects of telehealth-based cancer interventions on disability, though the heterogeneity seen in the measurement of disability makes it hard to draw firm conclusions. Further research using more diverse samples, common measures of disability, and pragmatic study designs is needed to advance telehealth in cancer rehabilitation. IMPLICATIONS FOR CANCER SURVIVORS: Telehealth-based cancer rehabilitation interventions have the potential to increase access to care designed to reduce disability across the cancer care continuum
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