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1.
Hinyokika Kiyo ; 61(10): 383-7, 2015 Oct.
Article in Japanese | MEDLINE | ID: mdl-26563619

ABSTRACT

OBJECTIVES: We compared sexual function by the expanded prostate cancer index composite (sexual domains of EPIC), health-related quality of life (SF-8), and International Prostate Symptom Score (I-PSS) inpatients using tadalafil after prostate brachytherapy (PB). Forty-five patients who underwent PB between April 2011 and January 2014 were included in this study. Patients were divided into the tadalafil (20 mg,once/week or once/two weeks) treated and non-treated (NT) groups. Sexual function was assessed prior to PB treatment and followed up to 24 weeks after PB. SF-8, sexual domains of EPIC, IPSS and subjective symptoms were assessed pre-PB and at 4, 8, 16, and 24 weeks post-PB. Patients in the tadalafil group achieved higher sexual function scores compared to NT group at all time points. For SF8, the patients in the tadalafil group significantly improved in mental health by the eighth week, and significantly worsened in the NT group (8 w ; p = 0.04). The voiding domains of EPIC score were found to worsen significantly after 4 weeks from PB in both groups, but the score tended to improve over 24 weeks. There was no significant difference between two groups. The I-PSS total score was found to worsen significantly in both groups post-PB, but the tadalafil group had a tendency to worsen less. PB treatment of localized prostate cancer is preferred for the preservation of sexual function. Management of sexual dysfunction with tadalafil after PB does not worsen sexual functions. We concluded that tadalafil might be applicable to mental health care in the treatment of patients with a high interest in sexual function before PB.


Subject(s)
Brachytherapy/adverse effects , Prostatic Neoplasms/radiotherapy , Sexual Dysfunction, Physiological/drug therapy , Tadalafil/therapeutic use , Urination/drug effects , Humans , Male , Middle Aged , Quality of Life
2.
Hinyokika Kiyo ; 59(5): 283-5, 2013 May.
Article in Japanese | MEDLINE | ID: mdl-23719135

ABSTRACT

Between January 2005 and August 2010, transurethral lithotripsy (TUL) was performed in 117 patients with upper urinary tract stones. TUL was performed without the basket catheter ZeroTipTM in 50 patients (group A) and with ZeroTip TM in 67 patients (group B). There was no significant difference in the successful stone disintegration rate between group A (86%) and group B (90%). However, the postoperative successful stone-free rate was 76 and 88% (p=0.04) in groups A and B, respectively, and the intraoperative successful stone-free rate was 43 and 71% (p=0.002), respectively. Intraoperative ureteral stents were placed in 62 and 46% of the patients in groups A and B (p=0.004), respectively. By successfully becoming stone-free with this procedure, the need of ureteral stent placement decreased, thereby reducing the postoperative cases of irritable bladder caused by a ureteral catheter, and contributing to improvement of the patient's quality of life.


Subject(s)
Lithotripsy/instrumentation , Urinary Calculi/therapy , Adult , Aged , Aged, 80 and over , Catheters , Female , Humans , Lithotripsy/methods , Male , Middle Aged , Quality of Life , Treatment Outcome
3.
Hinyokika Kiyo ; 58(1): 7-11, 2012 Jan.
Article in Japanese | MEDLINE | ID: mdl-22343736

ABSTRACT

The prognostic factor was retrospectively analyzed in 52 castration-resistant prostate cancer treated with docetaxel (DTX) in our institutions from April, 2006 to August, 2009. The treatment outcomes were decided with prostate specific antigen (PSA) progression-free survival and overall survival. These were calculated by Kaplan-Meier methods and tested with Log-rank test. Median PSA progression-free survival was 8.8 months and median overall survival was 24.1 months. Prognostic factors on PSA progression were PSA value before DTX treatment and rate of PSA decrement after DTX treatment. Prognostic factors on overall survival were Gleason score (GS), PSA value before DTX treatment, rate of PSA decrement after DTX treatment and positive of bone metastasis in Log-rank test. Odds ratio of PSA ≧20 ng/ml before DTX treatment was 2.99 and PSA decreasing rate < 30% was 3.65. These were statistically significant (p < 0.001) risk factors in the overall survival.


Subject(s)
Antineoplastic Agents/therapeutic use , Prostatic Neoplasms/mortality , Taxoids/therapeutic use , Aged , Aged, 80 and over , Castration , Disease-Free Survival , Docetaxel , Humans , Male , Middle Aged , Prognosis , Prostate-Specific Antigen/blood , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/surgery , Retrospective Studies
4.
Clin Exp Nephrol ; 16(3): 501-4, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22186947

ABSTRACT

A differential diagnosis of common bacterial peritonitis and appendicitis is difficult in continuous ambulatory peritoneal dialysis (CAPD) patients, and thus the definite diagnosis of appendicitis is often delayed. In this case, a 60-year-old man undergoing CAPD was at first diagnosed with bacterial peritonitis but not appendicitis, and antibiotics were administered. The number of leukocytes in the peritoneal effluent decreased mildly, but the level of C-reactive protein continued to be high and the pain aggravated. When the catheter was removed, suppurative appendicitis was confirmed for the first time. Levels of matrix metalloproteinase (MMP)-2 and -9 in peritoneal effluents were markedly high. Appendicitis should be diagnosed as early as possible because MMPs directly injure the peritoneum via degradation of extracellular matrix proteins. Future studies in a greater numbers of cases of appendicitis are required.


Subject(s)
Appendicitis/diagnosis , Ascitic Fluid/chemistry , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Peritoneal Dialysis, Continuous Ambulatory/adverse effects , Appendicitis/pathology , Appendicitis/physiopathology , Bacterial Infections/complications , Female , Humans , Male , Middle Aged , Peritonitis/diagnosis
5.
Int J Urol ; 17(12): 989-95, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20946473

ABSTRACT

OBJECTIVES: Renal ischemia-reperfusion injury (IRI), leading to acute kidney injury, is a frequent complication with renal transplantation and it is associated with graft function. Its pathogenesis involves ischemia, vascular congestion and reactive oxygen metabolites. Carvedilol is an antihypertensive drug with potent anti-oxidant properties. In this study we investigated the protective effects of carvedilol in a rat renal IRI model. METHODS: Twenty-four rats were randomized into sham, untreated control and carvedilol (2 mg/kg 30 min before surgery and 12 hr after reperfusion) treatment groups and were subjected to 60 min of left renal ischemia followed by reperfusion at 24, 48, 96 and 168 hr. RESULTS: Treatment with carvedilol significantly decreased plasma creatinine levels after IRI (up to 168 hr) compared to controls (P < 0.001), suggesting an improvement in renal function. Histopathological analysis revealed decreased IRI-induced damage in kidneys from carvedilol-treated rats. A significant increase in the expression levels of Cu/Zn superoxide dismutase and reduction of 8-hydroxydeoxyguanosine and apoptosis levels (P < 0.005) suggested a protective effect after treatment with carvedilol. CONCLUSIONS: Our findings suggest that carvedilol ameliorates IRI resulting in improved renal function.


Subject(s)
Antihypertensive Agents/pharmacology , Carbazoles/pharmacology , Kidney Tubules/drug effects , Oxidative Stress/drug effects , Propanolamines/pharmacology , Renal Insufficiency/prevention & control , Reperfusion Injury/drug therapy , 8-Hydroxy-2'-Deoxyguanosine , Animals , Apoptosis/drug effects , Carvedilol , Creatinine/blood , Deoxyguanosine/analogs & derivatives , Deoxyguanosine/metabolism , Disease Models, Animal , Epithelial Cells/cytology , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Kidney Tubules/cytology , Kidney Tubules/metabolism , Male , Rats , Rats, Sprague-Dawley , Reperfusion Injury/metabolism , Reperfusion Injury/pathology , Superoxide Dismutase/metabolism
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