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1.
Complement Ther Med ; 42: 312-321, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30670260

ABSTRACT

OBJECTIVE: To evaluate the effect of functional-task training on activities of daily living (ADL) in people with Parkinson`s Disease. METHODS: We searched five databases (Cinahl, Embase, Medline, Pedro and CENTRAL). The included studies were assessed on therapeutic validity and risk of bias. We classified the quality of evidence according to the principles of the GRADE approach. All assessments were executed independently by two researchers. The results of included studies were pooled in a meta-analyses and heterogeneity was explored by meta-regression analysis. RESULTS: Out of 2546 identified studies, 69 full texts articles were checked for eligibility, of which ten were included in the systematic review. Moderate quality of evidence indicated that exercise interventions containing functional-task training had a positive effect on ADL performance scores on the Unified Parkinson's Disease Rating Scale (UPDRS) in people with Parkinson (pwp) directly after intervention (UPDRS=-2.62(-5.34;0.10)). This effect improved, in favor of functional-task interventions, at the first follow-up (UPDRS=-4.0(-7.56;-0.4)). A post-hoc meta-regression analysis yielded a significant relationship between intensity rate (minutes/week) and the size of the (average) effect on ADL score. CONCLUSION: Exercise interventions containing functional-task training have a clinically important positive effect on ADL performance in pwp directly after intervention and at first follow-up, compared to no intervention or placebo. The intensity rate of the functional-task training should be as intense as possible, within the capabilities of the person with PD. Future research is necessary to determine the exact amount of effect that can be contributed to functional-task training.


Subject(s)
Activities of Daily Living , Exercise , Parkinson Disease/therapy , Physical Therapy Modalities , Quality of Life , Humans
2.
Neurourol Urodyn ; 23(3): 229-36, 2004.
Article in English | MEDLINE | ID: mdl-15098218

ABSTRACT

AIMS: To develop a condition specific quality of life measure for males and females with urinary storage symptoms of urgency, frequency, nocturia and incontinence. MATERIALS AND METHODS: A sample of community dwelling males and females aged 40 years or more who were taking part in an epidemiological study provided data for development and validation of the scale. Questions were developed from literature review and discussions with clinicians and patients. Inclusion of items was dependent on levels of missing data and principal components analysis. Validity was assessed by comparison with the Hospital Anxiety and Depression Scale, the Bradburn Negative Affect Scale and single questions concerning the problematic nature of symptoms. Construct validity was assessed by comparing cases and non-cases, and patients with different symptom patterns. Test-retest and inter-rater reliability statistics were calculated for individual items. Responsiveness to change was measured in subjects taking part in a randomised controlled trial of a nursing intervention. RESULTS: The scale showed high levels of internal consistency and measures of construct validity were as hypothesised. Test-retest and inter-rater reliability was moderate to excellent. The distribution of scores was skewed with low levels of impact but the questionnaire was responsive to conservative treatments in patients receiving a nursing intervention. CONCLUSIONS: The questionnaire proved to be a valid and reliable interviewer administered instrument for measuring impact of urinary symptoms.


Subject(s)
Quality of Life , Urologic Diseases/classification , Urologic Diseases/psychology , Aged , Female , Humans , Male , Middle Aged , Principal Component Analysis , Psychiatric Status Rating Scales , Psychometrics , Reproducibility of Results , Surveys and Questionnaires , United Kingdom/epidemiology , Urologic Diseases/epidemiology
3.
BJU Int ; 91(7): 631-6, 2003 May.
Article in English | MEDLINE | ID: mdl-12699474

ABSTRACT

OBJECTIVE: To investigate nonresponse bias in a postal survey on urinary symptoms in people aged >or= 40 years. SUBJECTS AND METHODS: Nonresponders to a postal survey on incontinence and other urinary symptoms were studied. A random sample of 1050 nonresponders (stratified for age and sex) was traced by a team of interviewers. Eligible nonresponders were asked several questions from the postal questionnaire, and their reason for not participating in the postal survey. RESULTS: Only 1% of those not responding were not traced in person or accounted for, and 12% were identified as not eligible to be in the survey sample (moved from address, deceased, residential home). Half of the eligible nonresponders (51%) did not answer the interviewer's questions, the main reason being general unwillingness or disinterest. The number in whom poor health was the reason increased with age. Comparing nonresponders who answered the interviewer's questions with a random sample of responders from the postal survey showed little difference in the reporting of urinary symptoms, although there were differences in general health and long-term health problems. Separate analyses by age showed greater reporting of some urinary symptoms and of poorer general health in the older nonresponders (>or= 70 years). CONCLUSION: Overall, for people aged >or= 40 years there was no evidence of a nonresponse bias in the reporting of urinary symptoms, providing confidence in such prevalence rates. However, poorer general health and greater reporting of some urinary symptoms by the older nonresponders (>or= 70 years) suggests prevalence rates in this age group may be underestimated.


Subject(s)
Health Surveys , Urologic Diseases/epidemiology , Adult , Age Distribution , Aged , Aged, 80 and over , Bias , England/epidemiology , Female , Humans , Male , Middle Aged , Postal Service , Sex Distribution , Surveys and Questionnaires , Urinary Incontinence/epidemiology
4.
BJU Int ; 90(3): 205-15, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12133054

ABSTRACT

OBJECTIVE: To develop a valid and reliable interviewer-administered questionnaire to measure the presence and severity of storage abnormality symptoms of incontinence, urgency, frequency and nocturia. SUBJECTS AND METHODS: Subjects were 930 men and women aged >/=40 years, taking part in a randomized controlled trial of a continence nurse practitioner (CNP) service. Criterion validity was tested by comparing questionnaire responses to 24-h pad test and 3-day urinary diary. Responsiveness was assessed by comparing questionnaire responses before and after treatment. Questions about urgency were investigated for construct validity in patients taking part in the trial who underwent urodynamic investigation (243). Test-retest and inter-rater reliability was measured at approximately 6 days in subjects recruited to an associated epidemiological study (104 and 102, respectively). RESULTS: The questionnaire responses showed significant associations with pad-test and diary measures. Questions about the severity of daytime incontinence performed better than those measuring night-time incontinence. The response categories of soaked, wet, damp and almost dry had better associations with the pad test than other measures of the severity of incontinence. Test-retest and inter-rater reliability was good for all questions, and all were responsive to change in symptoms, showing significant differences before and after treatment. CONCLUSION: There is a clear need for standardization of measurement using well-validated instruments. This interviewer-administered questionnaire is valid, reliable and sensitive to change in a wide range of severity of symptoms, and in both men and women aged >/=40 years. The questionnaire provides a useful assessment tool for primary and secondary care in research and clinical settings.


Subject(s)
Surveys and Questionnaires/standards , Urination Disorders/diagnosis , Aged , Female , Humans , Incontinence Pads/statistics & numerical data , Male , Medical Records , Middle Aged , Quality of Life , Reproducibility of Results , Severity of Illness Index , Urinary Incontinence/diagnosis , Urinary Incontinence/physiopathology , Urination/physiology , Urination Disorders/physiopathology
5.
Stroke ; 31(4): 886-91, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10753993

ABSTRACT

BACKGROUND AND PURPOSE: To establish prevalence of urinary symptoms among community-dwelling stroke survivors and how these symptoms affected lives of these survivors compared with a nonstroke population. METHODS: The present study was a community-based postal survey in Leicestershire community, UK (that excluded institutional settings), that was designed to track stroke, urinary, and bowel symptoms and the effect of such symptoms on relationships, social life, daily activities, and overall quality of life. Subjects included 14 600 people who were living in the community and

Subject(s)
Sickness Impact Profile , Stroke/complications , Urologic Diseases/epidemiology , Urologic Diseases/physiopathology , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Prevalence , Quality of Life , United Kingdom , Urologic Diseases/etiology
7.
J Exp Biol ; 128: 235-53, 1987 Mar.
Article in English | MEDLINE | ID: mdl-3559464

ABSTRACT

Rainbow trout were infused continuously for 24 h with epinephrine in order to elevate circulating levels of this hormone to those measured during periods of acute extracellular acidosis (approximately 5 X 10(-8) mol l-1). Concomitant effects on selected blood respiratory acid-base and ionic variables were evaluated. Infusion of epinephrine caused a transient respiratory acidosis as a result of hypoventilation and/or inhibition of red blood cell (RBC) bicarbonate dehydration. The acidosis was regulated by gradual accumulation of plasma bicarbonate. Even though whole blood pH (pHe) was depressed by 0.16 units, RBC pH (pHi) remained constant, thereby causing the transmembrane pH gradient (pHe-pHi) to decrease. A similar effect of epinephrine on RBC pH was observed in vitro, although the response required a higher concentration of epinephrine (2.0 X 10(-7) mol l-1). We speculate that the release of epinephrine during periods of depressed blood pH is important for preventing excessive shifts in RBC pH and for initiating a series of responses leading to plasma HCO3- accumulation and eventual restoration of blood acid-base status.


Subject(s)
Acid-Base Equilibrium/drug effects , Epinephrine/pharmacology , Erythrocytes/metabolism , Oxygen Consumption/drug effects , Salmonidae/blood , Trout/blood , Animals , Electrolytes/blood , Epinephrine/administration & dosage , Epinephrine/blood , Hydrogen-Ion Concentration , Infusions, Intra-Arterial , Kinetics , Norepinephrine/blood
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