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Referral for information & support as part of routine cancer management D Hill, P Livingston, V White, D Akkerman
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Background Paradoxes: Clinicians viewed as most credible source of medical information. Time for answering questions limited. Information is the greatest reported unmet need of cancer patients. High satisfaction among Cancer Information Support Service (CISS) users. Patients must initiate contact with CISS. Lack of awareness Lack of provider referral
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Cancer Information Support Service Staffed by trained oncology nurses. Information on range of issues: cancer treatment coping strategies with cancer diagnosis referral to local health, welfare & support services
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Challenge Find a way of connecting cancer patients to a support service at appropriate times: cost-effective all patients at earliest opportunity access during stressful periods Focus on males: underutilise health services, and less research to improve health outcomes in men with cancer
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To assess whether a specialist referral and outcall program reduces psychological morbidity associated with a cancer diagnosis. Aim
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4-month telephone questionnaire 7-month telephone questionnaire 12-month telephone questionnaire PASSIVE REFERRAL Consultation with specialist (diagnosis) ACTIVE REFERRAL 1: 4 CISS outcalls Call 1: <1 week after diagnosis Call 2: 6 wks post- diagnosis Call 3: 3 mths post-diagnosis Call 4: 6 mths post-diagnosis ACTIVE REFERRAL 2: 1 CISS outcall PROSTATE & MALE COLORECTAL PATIENTS (N=1020) PRESENTING FOR CANCER DIAGNOSIS Block randomisation Recruitment Baseline questionnaire Possible patient-initiated calls to CISS: 1300 66 22 80 Recruitment
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The cancer dx Treatment management issues What to expect from surgery Communication with specialist Partner / family issues Psychological / emotional issues Understanding the language of cancer Diet and nutrition Other support services Issues covered by nurse counsellors
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Patients interviewed at 4, 7 & 12 months post-diagnosis. Psychological distress. Fear of recurrence, pain & suffering. Social support; quality of life. Patient satisfaction with referral process & outcall program. Specialists’ satisfaction with referral process. Assessment
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Total referrals Total referrals110 Total eligible Total eligible107 Ineligible3 Refused at baselinen=13 (12%) Withdrew at 4 month follow-upn=14* (13%) Participants Participants79 (74%) *1 patient was deceased at the 4 month follow-up
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Worry about cancer * *p=0.001; ** p=0.003 **
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Worry about dying * *p=0.001
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Worry about physical problems associated with surgery/treatment * *p=0.001
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Satisfaction with the Service 88% reported calls from CISS acceptable. 83% found the calls helpful. 86% of the Active Referrals said the timing of the calls was helpful.
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Satisfaction with the Service "I just thought the referral process was a matter of course, thought it was a good idea“ "Instead of asking stupid questions, now ask sensible questions - broadened my knowledge of disease" "I think probably that prostate cancer is not greatly talked about by men - so the more discussions take place, the easier it becomes to talk not only to your doctor, but to other men as well!"
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Conclusions Preliminary results indicate that the: w intervention has the potential to reduce psychological morbidity associated with a cancer diagnosis; w service acceptable to patients; and w if effective, referral for information and support could be included in the management of all patients from diagnosis.
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