Impact of Chronic Graft Versus Host Disease (cGVHD) on the Health Status of Hematopoietic Cell Transplantation (HCT) Survivors: A Report from the Bone Marrow Transplant Survivor Study.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 702-702
Author(s):  
Christopher Fraser ◽  
Smita Bhatia ◽  
Kirsten Ness ◽  
Andrea Carter ◽  
Liton Francisco ◽  
...  

Abstract Chronic GVHD is a common complication following allogeneic HCT. The aim of this study was to better understand the impact of cGVHD on the overall health status of HCT survivors. Methods: We assessed 6 health status domains: general health, mental health, functional status, activity limitation, pain and disease related anxiety in HCT survivors with and without cGVHD. Eligible subjects underwent allogeneic HCT at either City of Hope or the University of Minnesota between 1974 and 2000, were 18 years or older at the time of the interview and had survived 2 or more years after HCT. Data was analyzed from 584 HCT survivors who were enrolled in this retrospective cohort study. All patients had completed a 289 item questionnaire. Information regarding diagnosis of cGVHD was abstracted from medical records and presence of active GVHD in the preceding year was self-reported. Outcome measures were chosen to facilitate a global assessment of health status. Questions assessing general health, functional impairment (needing help with personal cares, household tasks, inability to attend school or work) and activity limitation (inability to climb up stairs or walk one block) were adapted from the National Health Interview Survey, the Brief Symptom Inventory (BSI) was used to assess the mental health domain and patients were asked if they had pain or anxiety as a result of their primary disease or its treatment with HCT. Results: Median age at time of HCT was 30.8 years (range: 0.4–62) and the median length of time since transplant was 8.1 years (range: 2–27.7). The prevalence of cGVHD in participants was 54%. Of those with cGVHD 46% reported GVHD within the previous year. In a model adjusted for gender, age, time since transplant, donor type and conditioning regimen, subjects with cGVHD were more likely to report adverse general health, functional impairments, activity limitation, pain and to score in the lowest 10% of population norms on the BSI compared to those with no history of cGVHD. These adverse health outcomes were most marked for those with active cGVHD. In fact, health status did not differ between those with resolved cGVHD and those who never had cGVHD (Table 1). At least one adverse health outcome was reported in 59% of subjects with cGVHD. Conclusions: Active cGVHD has a significant impact on many aspects of the overall health status of HCT survivors. The impact was most marked in the domains of functional impairment, activity limitation and pain. Those successfully treated for cGVHD do not appear to have long-term impairments. Clinicians should be aware of the global impact of cGHVD and the need to provide ongoing care with appropriate interventions such as physical and occupational therapy and mental health support. Table 1 cGVHD General Health Mental Health Functional Impairment Activity Limitation Pain Anxiety Odds Ratios (95% confidence intervals) compared to those never diagnosed with cGVHD Ever had 1.8 (0.7–4.5) 2.4 (1.1–5.7) 5.5 (2.7–14.5) 4.5 (1.9–11.1) 4.2 (1.6–11.3) 0.7 (0.3–2.2) Active 2.5 (1.5–4.1) 2.5 (1.5–4.2) 5.3 (3.1–9.0) 4.7 (2.8–7.7) 3.9 (2.3–6.7) 1.3 (0.7–2.5) Resolved 0.7 (0.4–1.3) 0.9 (0.6–1.6) 1.1 (0.6–1.9) 1.0 (0.6–1.6) 1.1 (0.6–1.9) 0.5 (0.3–1.1)

Blood ◽  
2006 ◽  
Vol 108 (8) ◽  
pp. 2867-2873 ◽  
Author(s):  
Christopher J. Fraser ◽  
Smita Bhatia ◽  
Kirsten Ness ◽  
Andrea Carter ◽  
Liton Francisco ◽  
...  

AbstractThe aim of this study was to understand the impact of chronic graft-versus-host disease (cGVHD) on the overall health status of hematopoietic cell transplantation (HCT) survivors. Subjects included 584 individuals who had undergone allogeneic HCT between 1976 and 1999, survived 2 or more years, and completed a 255-item health questionnaire. Global assessment of health status was facilitated by measurement of 6 health status domains: general health, mental health, functional impairment, activity limitation, pain, and anxiety/fear. Information regarding diagnosis of cGVHD was abstracted from medical records, and presence of active cGVHD in the preceding 12 months was self-reported. The incidence of cGVHD in participants was 54%, of whom 46% reported active cGVHD. In multivariable analyses, subjects with active cGVHD were more likely to report adverse general health, mental health, functional impairments, activity limitation, and pain than were those with no history of cGVHD. However, health status did not differ between those with resolved cGVHD and those who never had cGVHD. We conclude that active cGVHD has a significant impact on many aspects of the overall health status of HCT survivors and that, most importantly, those successfully treated for cGVHD do not appear to have long-term impairments.


Author(s):  
John D. Fisk ◽  
Amanda Pontefract ◽  
Paul G. Ritvo ◽  
Catherine J. Archibald ◽  
T.J. Murray

ABSTRACT:Although fatigue is recognized as a symptom of MS, there have been insufficient methods for evaluating this symptom. We administered the Fatigue Impact Scale to 85 MS patients and 20 hypertensive patients. Neurologic impairment, mental health, and general health status were also assessed. MS patients reported significantly higher fatigue impact than hypertensive patients. Most MS patients reported fatigue as either their worst (14%), or one of their worst (55%) symptoms. Disease classification and neurologic impairment had little bearing on Fatigue Impact Scale scores in the MS sample. The best predictive models for mental health and general health status in the MS sample both included the Fatigue Impact Scale as a significant factor. This study demonstrates that: 1) fatigue is a very prevalent and severe problem in MS, 2) fatigue impact cannot be predicted by clinical measures of neurologic impairment, 3) fatigue has a significant effect on the mental health and general health status of MS patients.


2015 ◽  
Vol 33 (5) ◽  
pp. 479-491 ◽  
Author(s):  
Melissa M. Hudson ◽  
Kevin C. Oeffinger ◽  
Kendra Jones ◽  
Tara M. Brinkman ◽  
Kevin R. Krull ◽  
...  

Purpose To compare age-dependent changes in health status among childhood cancer survivors and a sibling cohort. Methods Adult survivors of childhood cancer and siblings, all participants of the Childhood Cancer Survivor Study, completed three surveys assessing health status. At each of three time points, participants were classified as having poor outcomes in general health, mental health, function, or daily activities if they indicated moderate to extreme impairment. Generalized linear mixed models were used to compare survivors with siblings for each outcome as a function of age and to identify host- and treatment-related factors associated with age-dependent worsening health status. Results Adverse health status outcomes were more frequent among survivors than siblings, with evidence of a steeper trajectory of age-dependent change among female survivors with impairment in at least one health status domain (P = .01). In adjusted models, survivors were more likely than siblings to report poor general health (prevalence ratio [PR], 2.37; 95% CI, 2.09 to 2.68), adverse mental health (PR, 1.66; 95% CI, 1.52 to 1.80), functional impairment (PR, 4.53; 95% CI, 3.91 to 5.24), activity limitations (PR, 2.38; 95% CI, 2.12 to 2.67), and an adverse health status outcome in any domain (PR, 2.10; 95% CI, 1.97 to 2.23). Cancer treatment and health behaviors influence the magnitude of differences by age groups. Chronic conditions were associated with adverse health status outcomes across organ systems. Conclusion The prevalence of poor health status is higher among survivors than siblings, increases rapidly with age, particularly among female participants, and is related to an increasing burden of chronic health conditions.


2007 ◽  
Vol 28 (1) ◽  
pp. 75-79 ◽  
Author(s):  
Ning-Hung Chen ◽  
Pa-Chun Wang ◽  
Meng-Jer Hsieh ◽  
Chung-Chi Huang ◽  
Kuo-Chin Kao ◽  
...  

Background.The impact of the outbreak of severe acute respiratory syndrome (SARS) was enormous, but few studies have focused on the infectious and general health status of healthcare workers (HCWs) who treated patients with SARS.Design.We prospectively evaluated the general health status of HCWs during the SARS epidemic.The Medical Outcome Study Short-Form 36 Survey was given to all HCWs immediately after caring for patients with SARS and 4 weeks after self-quarantine and off-duty shifts. Tests for detection of SARS Coronavirus antibody were performed for HCWs at these 2 time points and for control subjects during the SARS epidemic.Setting.Tertiary care referral center in Taipei, Taiwan.Subjects.Ninety SARS-care task force members (SARS HCWs) and 82 control subjects.Results.All serum specimens tested negative for SARS antibody. Survey scores for SARS HCWs immediately after care were significantly lower than those for the control group (P < .05 by the t test) in 6 categories. Vitality, social functioning, and mental health immediately after care and vitality and mental health after self-quarantine and off-duty shifts were among the worst subscales. The social functioning, role emotional, and role physical subscales significantly improved after self-quarantine and off-duty shifts (P < .05, by paired t test). The length of contact time (mean number of contact-hours per day) with patients with SARS was associated with some subscales (role emotional, role physical, and mental health) to a mild extent. The total number of contact-hours with symptomatic patients with SARS was a borderline predictor (adjusted R2 = 0.069; P = .038) of mental health score.Conclusions.The impact of the SARS outbreak on SARS HCWs was significant in many dimensions of general health. The vitality and mental health status of SARS HCWs 1 month after self-quarantine and off-duty shifts remained inferior to those of the control group.


2016 ◽  
Vol 91 ◽  
pp. 161-167 ◽  
Author(s):  
Payam Dadvand ◽  
Xavier Bartoll ◽  
Xavier Basagaña ◽  
Albert Dalmau-Bueno ◽  
David Martinez ◽  
...  

2002 ◽  
Vol 36 (3) ◽  
pp. 375-379 ◽  
Author(s):  
Jennifer M Ellis ◽  
Prabashni Reddy

OBJECTIVE: To assess the time-dependent effects of Panax ginseng on health-related quality of life (HRQOL) by use of a general health status questionnaire. METHODS: Subjects were randomized in a double-blind manner to P. ginseng 200 mg/d (n = 15) or placebo (n = 15) for 8 weeks. The Short Form-36 Health Survey version 2 (SF-36v2), a validated general health status questionnaire, was used to assess HRQOL at baseline and at 4 and 8 weeks. HRQOL between the groups was compared by use of repeated-measures analysis of covariance. A p value <0.05 was considered statistically significant. RESULTS: There were no significant differences in baseline demographics and SF-36v2 scores between the groups. After 4 weeks of therapy, higher scores in social functioning ( P. ginseng 54.9 ± 4.6 vs. placebo 49.2 ± 6.5; p = 0.014), mental health ( P. ginseng 52.2 ± 7.7 vs. placebo 47.2 ± 7.3; p = 0.075), and the mental component summary ( P. ginseng 51.3 ± 7.4 vs. placebo 44.3 ± 8.3; p = 0.019) scales were observed in patients randomized to P. ginseng; these differences did not persist to the 8-week time point. The incidence of adverse effects was 33% in the P. ginseng group compared with 17% in the placebo group (p = 0.40). Subjects given P. ginseng (58%) were more likely to state that they received active therapy than subjects given placebo (17%; p < 0.05). CONCLUSIONS: P. ginseng improves aspects of mental health and social functioning after 4 weeks of therapy, although these differences attenuate with continued use.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 3786-3786
Author(s):  
Zahra Pakbaz ◽  
Marsha Treadwell ◽  
Robert Yamashita2 ◽  
Drucilla Foote ◽  
Elliott Vichinsky

Abstract Introduction: Thalassemia patients have experienced a dramatic increase in lifespan secondary to improved and more complicated therapy. The impact of the disease and its treatment on quality of life is largely unknown. Determining the degree of health impairment as perceived by the patient is essential information needed to recommend suitable therapy. Factors that affect the quality of life of thalassemia major patients may differ from thalassemia intermedia patients. Identifying the specific causes for negative patient assessment of overall health status can result in successful intervention. The objective of this study is to determine the factors that affect quality of life in both transfused and non-transfused thalassemia patients. Methods: The Dartmouth Care Cooperative Chart System (COOP) questionnaire is a standardized, validated, visual screening tool that screens the major domains affecting quality of life. Patients rate quality of life from excellent (1) to poor (5). Scores of 1 and 2 are normal. A Score of 3 are mild to moderate impairment, and 4 and 5 are severe abnormalities. 50 patients were randomly selected during a comprehensive visit to complete a COOP questionnaire. These results were augmented by a brief medical history and chart review. Results: Forty-eight thalassemia patients, including 25 transfusion dependent (Tx) and 23 non-transfused (Non-Tx) patients (50% female) were randomly selected and completed the COOP questionnaire. The mean age of the total population was 19 years (0.9–37.9 yrs) and was similar in both groups. Half of both groups had scores of 3 or less indicating no severe impairment. However, 56% of patients had ratings of 3 indicating mild to moderate impairment of major domains. Four patients (2 Tx, 2 Non-Tx) had repeated 4–5 ratings in multiple domains indicating severe impairment of quality of life. The most commonly reported affected domains were feelings, such as anxiety, depression, and concern of overall health status or indications of recent deterioration in health. Conclusion: At least 50% of transfusion and non-transfusion dependent thalassemia patients demonstrate some impairment in quality of life. Forty-four percent of the population had a severe impairment in at least one domain. In particular, mental health issues are widespread. In contrast to previous beliefs, non-transfusion dependent patients also suffer serious impairment in quality of life. This data suggests all patients should undergo quality of life assessments and intervention, which focuses on affected domains. Studies to determine if quality of life affects patients’ adherence to chelation therapy are needed.


2020 ◽  
Vol 32 (2) ◽  
pp. 37-39
Author(s):  
Kazi Mahbubul Haque ◽  
Md Shafiqul Islam ◽  
Saida Sharmin

Mental health status is often ignored in our country. Even many health care professionals commonly ignore the impact of mental illness on both daily and professional lives, which may lead to dire consequences. The purpose of this study was to find the mental health status of physicians working in medical college hospitals of Dhaka city. A cross sectional study was conducted from January to December 2015 for this purpose among 215 number of respondents selected conveniently. Data were collected from 210 physicians by face-to face interview using a semi structured questionnaire containing 4DSQ (Four-Dimensional Symptom Questionnaire), socio economic and other variables. The prevalence of mental illness was calculated according to the scoring system of the scale. Mental illness prevalence was as follows: distress 20%, Anxiety 15.7%, Depression 15.2% and Somatization 8.6%. Majority of the respondents were interns and below 30 years of age. However, in light of current pandemic situation, regular assessment of health personnel’s mental health is needed more than ever. Bang J Psychiatry 2018;32(2): 37-39


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