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Aims of
study
The National Overactive BLadder Evaluation (NOBLE) Program encompasses a series
of studies designed to provide information on the prevalence and impact of overactive
bladder (OAB) symptoms in the USA. OAB is a symptomatic diagnosis used to describe
the symptoms of urgency, frequency, with or without urge incontinence. The condition
is thought to be highly prevalent and heterogeneous. Estimates of prevalence
and individual and societal burden are dependent, in part, on the reliability
and validity of self-reported information. As part of the NOBLE Program, we
evaluated the test-retest reliability of reporting on OAB and related urinary
tract symptoms, coping strategies, and health-related quality of life in a community-based
sample.
Methods
A sample of 231 adults completed an interview twice with an average of 2 weeks
between interviews. Fifteen screening questions (i.e., yes/no format) were used
to test the reliability of reporting OAB symptoms of frequency, nocturia, urgency
and urge incontinence. The reliability of reporting symptoms of stress incontinence
were also assessed. Affirmative responses to screening questions were followed
by more detailed questions about related symptoms, coping strategies and psychological
and physical impact of symptoms in the 4 weeks before the interview. Reliability
of binary variables was estimated using the kappa statistic (0-1); non-parametric
variables were estimated using Spearman's correlation.
Results
The reliability of reporting the number of daytime and night-time micturitions
was high, as was reporting symptoms related to nocturia (see Table). Although
the reliability of answering 'yes' to any question about urgency was fairly
good (kappa 0.58), one question was superior to others (see Table). The reliability
of reporting incontinence symptoms was high (kappas 0.7-0.88), as was reporting
on the proportion of incontinence episodes that were due to either urge incontinence
(r=0.69) or stress incontinence (r=0.71). Reporting on specific activities associated
with incontinence (losing urine on the way to the bathroom, kappa 0.71; losing
urine with coughing, sneezing, etc, kappa 0.72) was more reliable than answering
'yes' to at least one question about incontinence (kappa 0.62). Overall, the
reliability of reporting on coping behaviors was good to moderate (kappa 0.47-0.64),
with relatively high reliability (kappas ³0.60) observed for selected coping
questions, including concerns about drinking more fluid, limiting travel, bathroom-seeking
behavior in a new place, and drinking less fluid at night. Subjects were highly
reliable (r=0.81) in reporting their levels of distress associated with the
need to use coping behaviors, the use of specific terms to characterize distress,
use of protective pads (r=0.82), and interference with activities (kappa >0.60)
including ability to travel, attending social events and exercising. Average
number of servings of fluid was also reliably reported (r=0.65). The reliability
of reporting the duration of time with specific symptoms varied considerably
from poor (incontinence) to very good (nocturia). Reliability was poor for compound
questions (e.g. Compared to six months ago, are you now waking up the same number
of nights, more nights or fewer nights?). Table. Test-retest reliability of
selected questions
|
Question |
Reliability
statistic (SE) |
|
o During
the day in the past 4 weeks, how many times on average did you go to the bathroom to urinate?
By daytime I mean the time period from when you wake up to when
you go to sleep. o On
nights that you woke up because you had to urinate, how many times on average did you have to urinate?
How many times per night? o In
the past 4 weeks, did you have such a strong urge to urinate that you had to stop what you were doing
and rush to the bathroom because you might lose urine?
|
Spearman’s 0.77 (0.01)
Spearman’s 0.83 (0.08)
Kappa 0.62 (0.08) |
Conclusions
In our survey, adults reliably reported their symptoms of overactve bladder,
the distress associated with these symptoms and the use of coping strategies.
With some exceptions, test-retest reliability of reporting symptoms over a 4-week
period was high, given that real change in the occurrence of symptoms may have
occurred in some individuals between interviews, thus diminishing the estimated
reliability. This is especially likely to happen among individuals who do not
have OAB but report incidental occurrence of symptoms. The screening questionnaire
is currently undergoing further clinical validation and testing as part of the
NOBLE Program. Supported by Pharmacia Corporation