Our research was approved by the Science Council and Medical Ethics Council of Can Tho University of Medicine and Pharmacy. This non-controlled clinical intervention included all patients presenting with the symptoms of lower urinary tract disorders admitted to the urology clinic and treated at the Urology Center-HIFU of Can Tho University of Medicine and Pharmacy Hospital from 5/2021 to 5/2022.
Biopsy taking was considered in patients with a solid or nodular mass in the rectal examination of the prostate (i.e., clinical presentation), serum PSA levels above 10 ng/mL (i.e., subclinical presentation), or suspicious ultrasound, CT, or MRI images (muffler drive, unbalanced prostate, breakage of the prostate capsule, etc.). The procedure was conducted when there were no contraindications (blood clotting disorders, immunodeficiencies, acute prostatitis, unstable clinical condition, complicated prostatic hyperplasia (e.g., bladder stones, urinary tract infections, and kidney failure), and anorectal diseases (hemorrhoids, anal infections, perineum, anal stenosis), or when the patient refused to undergo prostate biopsy.
3.1. Selection of Patients Eligible for Prostate Biopsy
All patients were surveyed using a questionnaire to conduct history taking, recording presenting complaints, and past medical and surgical history. The patients also underwent clinical examination and the tests required to identify patients meeting pre-specified eligibility criteria.
All the data were recorded in a questionnaire and presented using descriptive statistics (mean ± standard deviation for continuous variables and rates and percentages for categorical variables). The data were analyzed using Statistical Package for the Social Sciences version 20.0 (SPSS Inc).
The data included the patient’s medical history, administrative information, reason for admission, history of other diseases, clinical examination findings, and the international prostate syndrome score (IPSS) and quality of life (QoL) indices.
3.2. Rectal Examination
A rectal examination was performed after obtaining a blood sample from the patient. The patient was lying in the obstetrical position (lying on the back, bending and spreading out legs to the sides). The doctor stood to the right of the patient. If the patient was lying on the left side, the lower leg was extended; the upper leg was bent, and the doctor stood behind the patient’s back in an inferior position to the patient’s buttocks.
The urologist wore gloves and applied the lubricant before inserting his index finger slowly and gently into the anus. The finger must be rotated so that the entire circumference of the rectal ball can be examined. The superior surface of the rectum was touched to determine the groove between the prostate and the 2 lateral lobes and to assess the surface and density of the prostate.
3.3. Paraclinical Testing
The patient's blood sample was taken to measure the total PSA serum level before rectal examination. Abdominal ultrasound was conducted when the patient was urinating to estimate prostate size and other features. Then the patient underwent an ultrasound of the bladder to determine the residual urine volume. Based on the results of these tests, the patients indicated for prostate biopsy were identified.
3.4. Research Materials
Research tools included a data collection checklist, Siemens ultrasound system, hematology and biochemistry auto-analyzers, and a prostate biopsy system [including a color ultrasound system with 7.5 MHz rectal transducers and a synchronous integrated biopsy canal, a biopsy gun compatible with the biopsy needle (18 G, length: 200 mm, cores length: 22 mm)].
3.5. Procedures
The transrectal biopsy of the prostate gland was performed under ultrasound guidance. Patient preparation steps before biopsy included antibiotic treatment (bicefzidim 1 g daily by slow intravenous injections twice a day, each time one vial, metronidazole 0.25 g, orally two times per day, two tablets each time). The patients were instructed to eat soft easy-to-digest food and remain completely fasted before the procedure. For colon preparation, fleet enema (2 tubes of anal pump 3 - 4 hours before biopsy) was administered. The patients were explained about the biopsy procedure and its possible peri- and post-complications to help the patient prepare psychologically and cooperate well with the physician. The patient’s vital signs were recorded before biopsy taking. The patient would lay on the left side; the thigh was perpendicular to the body, and the leg was perpendicular to the thigh. The tools required were disinfectants, the ultrasound device and probes, a biopsy gun, a biopsy needle, lidocaine 2%, and sample vials containing a fixative for biopsy specimens (formalin) numbered in order from 1 to 12.
Treatment steps included disinfection of the perineum, anus, and rectum via sterile towels, inserting the ultrasound probe into the rectum, moving the probe to observe and evaluate the prostate, injecting anesthetics around the prostate, targeting the biopsy site, inserting the biopsy gun into the biopsy canal, obtaining needle biopsy samples, place specimens into labeled fixative-containing vials, proceeding toward next positions.
The biopsy was performed at 12 cores, 6 cores per lobe (left, right), according to prostate location (top, center, base of prostate). After completing the procedure, vital signs were checked, and if they were stable, the patient was released and returned to rest in the ward. The samples (12 biopsies) were sent for pathological examination at the Pathology Department of Can Tho University of Medicine and Pharmacy Hospital. The patients in the ward were followed up for post-biopsy complications, including pain, anal bleeding, urinary status, infections, etc.