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1.
Int J Tuberc Lung Dis ; 15(1): 125-30, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21276308

ABSTRACT

SETTING: The deterioration of immunity in cancer patients may be associated with a higher incidence of tuberculosis (TB). OBJECTIVE: Despite several previous studies on cancer and TB, no population-based investigation has been published. We performed a nationwide population-based study to investigate the incidence of active TB among cancer patients, and the cancer-type specific risk factors related to TB. DESIGNS: This nationwide population-based retrospective cohort study was based on data obtained from the Taiwan National Health Insurance Database. A total of 16,487 cancer patients and 65,948 controls matched for age and sex were recruited. RESULTS: The incidence of TB per 100,000 person-years was 339 in the cancer patients and 202 in the controls, which gives a crude incidence rate ratio of 1.68 (95%CI 1.42-1.98). The hazard ratio (HR) was 1.67 (95%CI 1.42-1.96) after adjusting for age, sex and comorbidity. Cox regression showed that cancers of the aerodigestive tract, including oral, nasopharyngeal and oesophageal and lung cancer (HR 3.09, 95%CI 2.42-3.94) and haematological cancers, including non-Hodgkin's lymphoma and leukaemia (HR 3.22, 95%CI 1.98-5.22), were significant risk factors for TB. CONCLUSION: Cancer patients have a higher incidence of TB than controls. Patients with aerodigestive tract, lung and haematological cancers are especially vulnerable to TB.


Subject(s)
Digestive System Neoplasms/epidemiology , Hematologic Neoplasms/epidemiology , Lung Neoplasms/epidemiology , Tuberculosis/epidemiology , Aged , Case-Control Studies , Female , Humans , Incidence , Male , Middle Aged , Proportional Hazards Models , Retrospective Studies , Risk Assessment , Risk Factors , Taiwan/epidemiology , Time Factors
2.
J Intellect Disabil Res ; 54(12): 1031-44, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20977514

ABSTRACT

BACKGROUND: This survey study aims to examine the prevalence and factors associated with depressive symptoms among primary older female family carers of adults with intellectual disabilities (ID). METHOD: In total, 350 female family carers aged 55 and older took part and completed the interview in their homes. The survey package contained standardised scales to assess carer self-reported depressive symptoms, social support, caregiving burden and disease and health, as well as adult and carer sociodemographic information. Multiple linear regressions were used to identify the factors associated with high depressive symptoms in carers. RESULTS: Between 64% and 72% of these carers were classified as having high depressive symptoms. The factors associated with carer self-reported depressive symptoms were carer physical health, social support and caregiving burden; overall, the carer self-reported physical health was a stronger factor associated with depressive symptoms than their physical disease status. The level of the adult with ID's behavioural functioning and the carer age, marital status, employment status, education level and the family income level were not significantly associated with carer depressive symptoms. CONCLUSIONS: The factors identified in this study as correlating with self-reported depressive symptoms suggest that researchers and mental health professionals should collaborate to help improve the physical health and social support networks of the most vulnerable older female family carers. This should reduce depressive symptoms directly among this high-risk group.


Subject(s)
Caregivers/psychology , Cost of Illness , Depression/diagnosis , Depressive Disorder/diagnosis , Intellectual Disability/nursing , Adult , Aged , Disabled Persons , Female , Humans , Mental Disorders/nursing , Middle Aged , Prevalence , Self-Assessment , Taiwan
3.
J Intellect Disabil Res ; 53(7): 654-64, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19490349

ABSTRACT

BACKGROUND: Little account has been taken of quality of life (QoL) among family carers of adults with an intellectual disability (ID) and family carers of adults with a mental illness (MI), particularly the female ageing carers' perceived stigma. We explore whether there are differences in the significant predictors of female ageing family carers' QoL between family carers of adults with ID and family carers of adults with MI and aim to examine the effect of these differences in stigma on carer QoL between the two groups. METHODS: A structural survey interview was administered to 350 female family carers supporting persons with ID and 66 female carers supporting persons with MI; the carers were aged 55 years and older, and the interviews were carried between July 2006 and April 2007 at the carers' homes in a county in Taiwan. The survey package contained standardised scales to measure the carer's stigma, social support, QoL and health as well as adult and carer socio-demographic data. RESULTS: The results highlight that in both groups the ageing female family carers' health and social support were strongly associated with the level of their QoL even though there was also a strong effect of carers' perceived stigma on their QoL. Contrary to previous findings, ageing female family carers of adults with MI had a higher level of QoL compared with the carers of adults with ID. Hierarchical regressions show a stronger effect of perceived stigma on the carer QoL among the family carers of adults with MI than among the carers of adults with ID. CONCLUSIONS: This study suggests that attempts to improve these female older family carers' health and social support must include their lifelong unmet needs in terms of how to cope with the perceived stigma associated with their position.


Subject(s)
Caregivers/psychology , Cost of Illness , Intellectual Disability/psychology , Mental Disorders/psychology , Prejudice , Quality of Life/psychology , Activities of Daily Living/psychology , Adult , Aged , Aged, 80 and over , Disability Evaluation , Female , Humans , Intellectual Disability/therapy , Male , Marital Status , Mental Disorders/therapy , Middle Aged , Social Support , Socioeconomic Factors , Taiwan
4.
Eur J Cancer Care (Engl) ; 17(4): 340-9, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18537814

ABSTRACT

This paper investigates the determinants of traditional Chinese medicine (TCM) and acupuncture utilization for cancer patients who are simultaneously having conventional Western medical treatments. This study used five leading cancers in Taiwan, namely cervical, breast, lung, liver and colorectal cancers. A total of 2499 cancer patients were interviewed, of which 2034 had full information and were analysed. Logistic regressions were used for both TCM and acupuncture. The results showed that type of cancer and cancer duration determine the utilization for alternative treatments. While socio-economic factors also affect choice of alternative medicine, the magnitude differs by types of alternative treatment and cancer. Compared with men and older patients, women and younger patients tend to prefer alternative medicine, and patients from south have higher preference for alternative medicine, which could be a reflection of local culture. Our results are useful for the government to determine higher users of TCM and acupuncture among cancer patients, and make policies to suit these patients' needs.


Subject(s)
Acupuncture Therapy/psychology , Medicine, Chinese Traditional/psychology , Neoplasms/therapy , Attitude to Health/ethnology , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Neoplasms/drug therapy , Surveys and Questionnaires , Taiwan
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