Family physicians' roles in cancer care. Survey of patients on a provincial cancer registry.

نویسندگان

  • Jeffrey J Sisler
  • Judith Belle Brown
  • Moira Stewart
چکیده

OBJECTIVE To describe cancer patients' experience of the role of family physicians (FPs) in their care. DESIGN Mail survey of a random sample of patients from the Manitoba Cancer Registry. SETTING Manitoba. PARTICIPANTS Two hundred two adults, 6 to 12 months after diagnosis. MAIN OUTCOME MEASURES Proportion needing different kinds of help from FPs and their rating of FPs' response; FACT-G quality-of-life score. RESULTS Response rate was 56.6%; two thirds of the sample were in the follow-up phase. Most (91%) had an FP involved in their care, but FP involvement decreased after diagnosis. The most frequently needed kinds of help (with general medical problems, quick referrals, taking extra time, and quick office appointments) were well provided by FPs, but family support was not. Higher quality-of-life scores were associated with more help with general medical problems, more provision of cancer-related information, and more emotional support of patients and their families. CONCLUSION Family physicians respond well to the most common needs of cancer patients and should be proactive in offering their support to both patients and families.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Non-oncology physician visits after diagnosis of cancer in children

BACKGROUND Children diagnosed with cancer often require extensive care for medical, psychosocial and educational problems during and after therapy. Part of this care is provided by family physicians and non-cancer specialists, but their involvement in the first years after diagnosis has barely been studied. Studying non-oncology physician visits may provide insight into the roles of different h...

متن کامل

نظام ثبت سرطان بیمارستانی در ایران و مقایسه آن با آمریکا

Introduction: Cancer research is one of the essential activities for its control and treatment. Hospital based cancer registry system is an information system designed to collect, organize and analyze data on cancer. The objective of the present study was to compare hospital based cancer registry system in Iran with that in the USA. Methods: This research was a comparative study. Studied popul...

متن کامل

Care needs of patients with cancer: A scoping review study

Aims: cancer patients have to face with the disease, invasive treatments and adverse effects of the disease and treatments in a long term period. These people have various needs in long term process of diagnosis, treatments and recovery that often remain unknown and unmet. The present research aimed at evaluating the care needs of cancer patients in various aspects of life. Materials and Metho...

متن کامل

Provincial primary care and cancer engagement strategy.

PROBLEM ADDRESSED To improve integration of cancer care, Cancer Care Ontario-a provincial agency responsible for planning, advising on, implementing, and monitoring initiatives to improve cancer outcomes-proposed a primary care and cancer engagement strategy in its Ontario Cancer Plan 2008-2011. OBJECTIVE OF PROGRAM The strategy was designed to focus initially on improving screening for color...

متن کامل

Recruiting regional primary care leads for cancer care ontario.

Cancer Care Ontario (CCO) is a provincial agency responsible for improving cancer outcomes in Ontario. With funding from the Ministry of Health and Long-Term Care, CCO plans and delivers cancer programs in partnership with 13 Regional Cancer Programs across the province. Over the past decade, CCO’s Clinical Programs group has worked with clinicians in the Regional Cancer Programs to improve the...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Canadian family physician Medecin de famille canadien

دوره 50  شماره 

صفحات  -

تاریخ انتشار 2004