December 4, 2013
Michelle Spicka, DPT
Objective: Comparison of questionnaires for the
evaluation of symptoms and quality of life in patients with chronic pelvic pain
syndrome (CPPS).
Study Design/Method:
Different questionnaires are
used by researchers and clinicians for the evaluation of patients with CPPS but
it is uncertain if their results are comparable.
The
questionnaires used were:
1.
McGill pain questionnaire (MPQ)
2.
National Institutes of Health-Chronic
Prostatitis Symptom Index (NIH-CPSI)
3.
Interstitial Cystitis Symptom and Problem
Questionnaire (ICSI)
4.
Pelvic Pain and Urgency/Frequency Questionnaire
(PUF)
Twenty-six CPPS patients were included and each participant
filled out all questionnaires during consultation and at the same sequence.
Outcome/Results:
1.
The interclass correlation was compared for pain
intensity, bladder complaints and quality of life.
2.
The interclass correlation for pain intensity of
the McGill pain questionnaire was moderate to good. All other questionnaires showed a bad
agreement.
3.
The NIH-CPSI/ICSI showed a very good agreement
for bladder complaints and the other questionnaires showed moderate to good
agreement.
4.
Mixed results were noted for comparing quality
of life.
1.
There is quite some difference between
questionnaires in how pain intensity is evaluated.
2.
If someone with chronic pain at the moment of
questioning does not have pain, this can include bias evaluating the chronic
pain state, depending on how the individual interprets the pain questions (pain
yesterday, now, today or in general)
a.
The biggest difference in comparing the
questionnaires is the concept of when the pain occurred
b. The moment of assessment influences the
results!
3.
The evaluated questionnaires assess a different
set of symptoms or the same “symptom complex” in a different way.
a.
They all have their specific properties and are
not always sufficient to evaluate the various aspects of CPPS.
b.
The difficulties in combing these questionnaires
indicates the need for a unified questionnaire containing all aspects with the
objective of standardization for future research and clinic applications.
4.
This study clearly indicates that results from
one questionnaire can’t be used for overall conclusions concerning pain
intensity and quality of life.
1.
What are the biggest barriers to using objective
questionnaires?
2.
Is there a better questionnaire for CPPS?
3.
More standardization is needed but can you
really standardize individual pain?
1.
Female Sexual Function Index
a.
Showed good ability to discriminate between
women with and without sexual dysfunctions in the CPPS population (Verit, et
al. J Sex Med. 2007 Nov;4(6):1635-41)
2. International
Prostate Symptom Score
a.
Found to determine similar symptomatic findings
as the NIH-CPSI (Schneider et al. World J Urol. 2003Aug;21(3):116-8)
3. Genitourinary
Pain Index
a.
Found to be a valid, reliable and responsive
instrument that can be used to assess the degree of symptoms in both men and
women with genitourinary pain complaints. (Clemens et al. Urology.
2009Nov;74(5):983-7)
4. Bladder
Pain/Interstitial Cystitis Symptom Score
a.
Found to be a reliable, valid and appropriate
questionnaire to select for bladder pain syndrome/interstitial cystic patients
for clinical trials (Humphrey et al. Eur Urol.2012 Feb;61(2):271-9)
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