LONG-TERM COMBINED α –BLOCKERS AND 5- α · PDF fileand require BPH-related...
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Transcript of LONG-TERM COMBINED α –BLOCKERS AND 5- α · PDF fileand require BPH-related...
Benign prostatic hyperplasia (BPH) is a progressive
disease commonly associated with bothersome lower
urinary tract symptoms (LUTS). It may result in
complications, such as acute urinary retention (AUR),
and require BPH-related surgery [1-3]. Combination
therapy with α-blockers and 5ARIs has been proven
effective in reducing LUTS, decreasing TPV, and
reducing the risk of disease progression compared to
treatment with a single medication or placebo [4-5].
Introduction
BPH patients with lower urinary tract symptoms
(LUTS) under combination therapy were
retrospectively analyzed from 1 to 12 years span. The
therapeutics effects were assessed by International
Prostatic Symptoms Score (IPSS) and quality of life
index (QoL-I), total prostatic volume (TPV), maximum
flow rate (Qmax), voided volume (VoL), prostatic
specific antigen (PSA) at baseline and annually. The
reason and predictors of discontinued combination
therapy were also investigated. Conclusion
Methods
Results
References
A total of 625 patients, aged 40-97 (mean, 73) years,
with 1-12 years of follow-up (mean, 3 years) were
retrospectively enrolled. All measured parameters
showed significant improvement after combination
therapy. Three hundred and sixty-nine (59%) patients
discontinued combination therapy with mean
treatment duration of 2.2 years. The most common
reason for discontinuation of combination therapy was
conversion to single medication (19.8%). Age and QoL-
1 did not influence the adherence rate, but the larger
Qmax and larger TPV lead to better adherence to
combination therapy.
Results (Continued)
LONG-TERM COMBINED α –BLOCKERS AND 5- α –REDUCTASE INHIBITOR IN BPH-THERAPEUTIC EFFECTS, ADHERENCE, AND
PREDICTORS FOR WITHDRAWAL OF MEDICATION
Hueih-Ling Ong1, Chun-Hou Liao2, Hann-Chorng Kuo1
Department of Urology1, Buddhist Tzu Chi General Hospital and Tzu Chi University, Hualien, Taiwan Department of Urology2, Cardinal Tien Hospital and Fu-Jen Catholic University, New Taipei, Taiwan
1. Jacobsen SJ, Girman CJ, Lieber MM. Natural history of
benign prostatic hyperplasia. Urology 2001;58:5-16.
2. Emberton M, Fitzpratick JM, Garcia-Losa M, Qizilbash N,
Djavan B. Progression of benign prostatic hyperplasia:
systemic review of the placebo arms of clinical trials.
BJU Int 2008;102:981-6.
3. Emberton M, Cornel EB, Bassi PF, Fourcade RO, Gómez
JM, Castro R. Benign prostatic hyperplasia as a
progressive disease: a guide to the risk factors and
options for medical management. Int J Clin Pract. 2008
Jul;62(7):1076-86.
4. McConnell JD, Roehrborn CG, Bautista OM, et al. The
long-term effect of doxazosin, finasteride, and
combination therapy on the clinical progression of
benign prostatic hyperplasia. Medical Therapy of
Prostatic Symptoms (MTOPS) Research Group. N Engl J
Med. 2003;18:2387-2398.
5. Roehrborn CG, Siami P, Barkin J, et al. CombAT Study
Group. The effects of combination therapy with
dutasteride and tamsulosin on clinical outcomes in men
with symptomatic benign prostatic hyperplasia: 4-year
results from the CombAT study. Eur Urol. 2010;57:123-
131.
Patients receiving combination therapy showed
significant improvement in all measured
parameters. The most common cause of
discontinuation of combination therapy was
conversion to single medication. The larger Qmax
and larger TPV after treatment predicted patient
adherence to combination therapy.
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