Case Study Treatment of Benign Prostatic Hyperplasia
Mohammad Battikhi*
Battikhi Central Laboratory, Canada
Submission: March 22, 2017; Published: March 27, 2017
*Corresponding author: Battikhi Mohammed Nizar, 1017-1645 DeMaisonneuve O, Montreal H3H2N3 QC, Canada, Email: M_nizar11@hotmail.com
How to cite this article: Mohammad B. Case Study Treatment of Benign Prostatic Hyperplasia. Open Access J Surg. 2017; 3(2): 555607. DOI: 10.19080/OAJS.2017.03.555607
Introduction
BPH is a disease which results in the appearance of a characteristic spectrum of lower urinary tract symptoms (LUTS) which comprise ‘voiding’ symptoms directly due to the outflow obstruction such as reduced urinary flow or hesitancy during voiding and ‘storage’ symptoms due to secondary effects on the bladder which include increased day-time and night-time urinary frequency and urgency [1-3]. It is a histologic diagnosis that refers to the proliferation of smooth muscle and epithelial cells within the prostatic transition zone [4,5]. BPH also called lower urinary tract symptoms (LUTS) as characterized by lower urinary tract symptoms is a common condition in the elderly male population and very common in men age >50 years [6]. The relationship between LUTS and sexual dysfunction has been controversial [7]. Other study showed the relation between erectile dysfunction (ED) and ejaculation disorders dysfunction (EjD) are related to increasing age and the severity of LUTS [8,9-12].
LUTS are strongly associated with sexual dysfunction and spoilt sex life, more ever the prevalence of erectile dysfunction and reduced ejaculation increases with the severity of LUTS [6]. Emerging clinical evidence suggests that the ‘storage’ symptoms of BPH, particularly increased night-time frequency (nocturia) are the most bothersome to the patients and result in a greater reduction in quality of life than the ‘voiding’ symptoms. Thus a drug which relieves the ‘storage’ symptoms of BPH either alone or in combination with a drug which targets the ‘voiding’ symptoms e.g. an alpha adrenergic receptor antagonist would be expected to confer a therapeutic benefit [13]. Traditionally; the primary goal of treatment has been to alleviate bothersome LUTS that result from prostatic enlargement. More recently, treatment has additionally been focused on the alteration of disease progression and prevention of complications that can be associated with BPH/LUTS [14]. A variety of pharmacologic classes are employed including alpha-adrenergic antagonists (alpha-blockers), 5-alpha- reductase inhibitors (5-ARIs), anticholinergics and phytotherapeutics.as suggested by AUA BPH treatment guideline [15].
Although doxazosin and terazosin require dose titration and blood pressure monitoring, they are inexpensive, are dosed once daily, and appear to be equally effective to tamsulosin and alfuzosin. In addition, they have generally similar side effect profiles, except ejaculatory dysfunction which has been reported less frequently with alfuzosin. Moreover, these older agents do not appear to increase the risk of the intraoperative floppy iris syndrome (IFIS), and doxazosin has demonstrated efficacy relative to placebo over four years of follow-up. The Panel wishes to remind clinicians that these agents remain excellent choices for the management of bothersome LUTS attributed to BPH [14].
It has been documented that alfuzosin, doxazosin, tamsulosin, and terazosin are appropriate and effective treatment alternatives for patients with bothersome, moderate to severe LUTS secondary to BPH (AUA-SI score ≥8). Although there are slight differences in the adverse events profiles of these agents, all four appear to have equal clinical effectiveness. As stated in the 2003 Guideline [14,15]. A variety of pharmacologic classes are employed including alpha-adrenergic antagonists (alpha-blockers), 5-alpha- reductase inhibitors (5-ARIs), anticholinergics and phytotherapeutics [14,15]. Many studies showed treating BPH patients with either single or combined drugs illustrate that the main concern is in choosing the correct medical treatment for BPH and even so the choice of drug is truly complex and ever-changing [16,17].
Method
Case Report
We present here a case of 60 year male who was hospitalized for voiding Dysfunction catheter was implanted for eight days during that period patient was giving 4.0 mg doxazosin mesylate (Cardura) for eight days after being diagnosed as BPH patients. Catheter was removed and patient kept on 2.0 mg doxazosin mesylate for three month where after new protocol for treatment was followed by giving patient dose of alfuzosine 10.0 mg and finassteride 5.0 mg daily for 18 month afterword patient was given tamsulosin 0.4 mg once daily.
Results
Results of the three protocols treatments were as follow .Protocol number one revealed improvement of voiding dysfunction however, patient suffered from severe blood pressure drop. Meanwhile the result of protocol number two patient showed stable blood pressure however, other symptoms were developed as incidence of ED, decreased libido and abnormal ejaculation. The third protocol revealed more stable condition considering blood pressure and ED however, patient showed abnormal ejaculation.
Discussion
The primary goal of this study was to trigger out the best treatment to alleviate bothersome LUTS that result from prostatic enlargement. More recently, treatment has additionally been focused on the alteration of disease progression and prevention of complications that can be associated with BPH/ LUTS treatment [14,15]. Many studies showed that a variety of pharmacologic classes were employed for BPF treatment including alpha-adrenergic antagonists (alpha-blockers), 5-alpha- reductase inhibitors (5-ARIs), anticholinergics and phytotherapeutics [14-16]. Many studies showed that the main concern of treating BPH patients with either single or combined drugs is in choosing the correct medical treatment for BPH and even so the choice of drug is truly complex and ever-changing [17]. In this case study patient was treated with three different drugs where he started on doxazosin mesylate 4.0 mg while he was hospitalized followed by combination of alfuzosine 10.0 mg and finassteride 5.0 mg due to drop in his blood pressure for eighteen month afterward he was recommended to stay on tamsulosin 0.4mg. The effect of each drug revealed different symptoms which are in agreement with other studies [14-16] where treating BPH patients with either single or combined drugs illustrate that the main concern is in choosing the correct medical treatment for BPH and even so the choice of drug is truly complex and ever-changing [16] which is supportive with results of this case study.
Conclusion
The results obtained in this study indicated that choosing the correct drug of is complex and the main concern is in choosing the correct medical treatment.
References
- Brookes ST, Donovan JL, Peters TJ, Abrams P, Neal DE (2002) Sexual dysfunction in men after treatment for lower urinary tract symptoms: evidence from randomised controlled trial. BMJ 324(7345): 1059- 1061.
- Frankel SJ, Donovan JL, Peters TI, Abrams P, Dabhoiwala NFl, et al. (1998) Sexual dysfunction in men with lower urinary tract symptoms. J Clin Epidemiol 51(8): 677-685.
- Nickel JC (2003) The use of alpha1-adrenoceptor antagonists in lower urinary tract symptoms: beyond benign prostatic hyperplasia. Urology 62(Suppl 3A): 34-41.
- Lee C, Kozlowski J, Grayhack J (1997) Intrinsic and extrinsic factors controlling benign prostatic growth. Prostate 31(2): 131.
- Auffenberg G, Helfan B, McVary K (2009) Established medical therapy for benign prostatic hyperplasia. Urol Clin North Am 36(4): 443.
- Man-Kay Li, Lester A. Garcia Raymond Rosen (2005) Lower urinary tract symptoms and male sexual dysfunction in Asia: a survey of ageing men from five Asian countries. BJU Int 96(9): 1339-1354.
- Sasayama S, Ishii N, Ishikura F, Kamijima G, Ogawa S, et al. (2003) Men’s Health Study: epidemiology of erectile dysfunction and cardiovascular disease. Circ J 67(8): 656-659.
- Frankel SJ, Donovan JL, Peters TI, Abrams P, Dabhoiwala NF, et al. (1998) Sexual dysfunction in men with lower urinary tract symptoms. J Clin Epidemiol 51(8): 677-685
- Nicolosi A, Moreira ED, Shirai M, Bin Mohd Tambi MI, Glasser DB (2003) Epidemiology of erectile dysfunction in four countries: crossnational study of the prevalence and correlates of erectile dysfunction. Urology 61(1): 201-206.
- Macfarlane GJ, Botto H, Sagnier PP, Teillac P, Richard F, et al. (1996) The relationship between sexual life and urinary condition in the French community. J Clin Epidemiol 49(10): 1171-1176.
- Blanker MH, Bohnen AM, Groeneveld FP, Bernsen RM, Prins A, et al. (2001) Correlates for erectile and ejaculatory dysfunction in older Dutch men: a community-based study. J Am Geriatr Soc 49(4): 436- 442.
- Braun MH, Sommer F, Haupt G, Mathers MJ, Reifenrath B, et al. (2003) Lower urinary tract symptoms and erectile dysfunction: co-morbidity or typical ‘Aging Male’ symptoms? Results of the ‘Cologne Male Survey’. Eur Urol 44(5): 588-594.
- Newgreen (2005) Treatment of BPH US 20050020646 A1Patent application publication.
- Kevin T McVary, Claus G Roehrborn, Andrew L Avins, Michael J Barry, Reginald C Bruskewitz, et al. (2017) Benign Prostatic Hyperplasia American Urological Association Guideline: Management of Benign Prostatic Hyperplasia (BPH) 36.
- Kevin T McVary, Claus G Roehrborn, Andrew L Avins, Michael J Barry, Reginald C Bruskewitz, et al. (2011) Update on AUA Guideline on the Management of Benign Prostatic Hyperplasia. J Urol 185(5): 1793- 1803.
- Lowe FC (2005) Treatment of lower urinary tract symptoms suggestive of benign prostatic hyperplasia: sexual function. BJU Int 95(4): 12-18.
- Miner M, Rosenberg MT, Perelman MA (2006) Treatment of lower urinary tract symptoms in benign prostatic hyperplasia and its impact on sexual function. Clin Ther 28(1): 13-25.