In this cross-sectional study, we selected 50 patients with HAM/TSP who referred to the Urology Clinic of Imam Reza Hospital, Mashhad, during 2017 - 2018 using a non-random goal-directed sampling method. All participants consented before they took part in the study. The Ethics Committee of Mashhad University of Medical Sciences approbated the performance of this study.
The inclusion criteria were having LUTS or neurologic findings of HTLV-1 and giving informed written consent. All patients were cases of HTLV-1 whose HAM diagnosis was confirmed by laboratory and clinical findings. Patients with any of the following were excluded from the study: pregnancy and a documented history of neurologic (e.g. spinal trauma, multiple sclerosis, etc.) or urologic diseases (e.g. active urinary infection, urethral stricture, benign prostatic hyperplasia, etc.) that interfered with assessed findings.
After obtaining informed consent from all patients, a thorough medical history was taken with an emphasis on stimulatory (dysuria, frequency, urgency, and nocturia) and obstructive urinary symptoms (dribbling, hesitancy, poor stream, retention, etc.). Then, a complete physical examination, especially neurologic examination, was performed. After the prescription of prophylactic antibiotics, all patients underwent urodynamic studies under standard settings by a single expert operator. Data were collected using checklists for further extraction and analysis.
Urodynamic studies were performed in three phases of uroflowmetry, cystometry, and pressure-flow study (PFS). During uroflowmetry, maximal urinary flow (Qmax), mean urinary flow (Qave), and the shape of the urinary diagram were recorded and assessed. The inner pressure of the bladder (Pves), abdomen (Pabd), and detrusor (Pdet), as well as capacity, compliance, involuntary contractions of detrusor, and urinary leak, were assessed and recorded by cystometry. PFS was performed to investigate the urination of patients in terms of urinary obstruction and detrusor contraction force, based on Abraham-Griffith nomogram. Moreover, urodynamic urinary incontinence (UD) was recorded during urodynamic studies.
The collected data were analyzed using SPSS software (version 22 for Windows, IBM Statistics, Chicago, USA). The Kolmogorov-Smirnov test was used to assess the normal distribution of the data. The independent samples t-test, Mann-Whitney test, and chi-square test were used to compare data between groups. Descriptive statistics were used to present data.