Patient‐reported outcomes in men with lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH) treated with intraprostatic OnabotulinumtoxinA: 3‐month results of a prospective single‐armed cohort study
Study Type – Therapy (prospective cohort) Level of Evidence 3a What's known on the subject? and What does the study add? Several short‐term studies have shown that intraprostatic injection of botulinum toxin (BTX) improves lower urinary tract symptoms and flow parameters in patients with BPH, b...
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Veröffentlicht in: | BJU international 2012-12, Vol.110 (11c), p.E837-E844 |
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Sprache: | eng |
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Zusammenfassung: | Study Type – Therapy (prospective cohort)
Level of Evidence 3a
What's known on the subject? and What does the study add?
Several short‐term studies have shown that intraprostatic injection of botulinum toxin (BTX) improves lower urinary tract symptoms and flow parameters in patients with BPH, but information on patient‐reported outcomes is lacking.
The present study provides useful data on patient‐perceived level of improvement and effectiveness of intraprostatic injection of BTX, as well as on patient's satisfaction with this therapy. Short‐term results are promising and comparable with those reported with standard pharmacological therapy.
OBJECTIVE
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To evaluate patient‐reported and objective outcomes after intraprostatic injection of OnabotulinumtoxinA (BTX‐A) in men with lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH).
PATIENTS AND METHODS
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A prospective single‐armed cohort study was designed.
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Patients diagnosed with LUTS due to BPH and unsatisfactory response to medical therapy, were recruited between November 2010 and July 2011.
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Patients received transperineal injection of 200 U BTX‐A in the transition zone, under transrectal ultrasonographic guidance.
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The outcome assessment was performed at 3 months and included a patient‐reported outcomes (PROs) questionnaire with questions on patient global impression of improvement (PGI‐I, 0–6 point scale), of satisfaction (PGI‐S, 0–5 point scale), and of efficacy (PGI‐E, 0–5 point scale).
RESULTS
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Of 75 screened patients, 64 with a mean (sd) age of 63 (9.3) years were available for the outcome assessment.
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Patients reported a mean reduction of 49% in International Prostate Symptom Score (IPSS), which decreased from 19.7 (7.7) to 10 (7.1) (P < 0.001), and a mean reduction of 44% in IPSS‐health‐related quality of life item score, from 4.17 (1.2) to 2.3 (1.6) (P < 0.001).
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There was a 33% increase in maximum urinary flow rate (P < 0.001) and an 80% reduction in postvoid residual urine volume (P < 0.001).
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In all, 36 (56%) patients had a subjective improvement in LUTS (PGI‐I ≥ 4), 43 (67%) reported satisfaction with the treatment (PGI‐S ≥ 3), and 44 (68%) judged the treatment as effective (PGI‐E ≥ 3). In all, 50 (79%) patients would repeat the same treatment under the same circumstances, while 54 (84%) would recommend the treatment to another person with the same diagnosis.
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There was a statistically significant positive correlation between patients' satisfaction a |
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ISSN: | 1464-4096 1464-410X |
DOI: | 10.1111/j.1464-410X.2012.11288.x |