This is a prospective cohort study of all consenting patients who had percutaneous nephrostomy at the Department of Radiology of Aminu Kano Teaching Hospital-Nigeria.
Approval was obtained from the Research Ethics Committee of Aminu Kano Teaching Hospital, Kano-Nigeria (AKTH/MAC/SUB/12A/P-3/V1/2220). Confidentiality and anonymity of patients were observed. Patients’ ages and sex including the clinical diagnosis were extracted from the records of the Radiology department and the individual patients’ case notes.
All fifty-five consenting patients had percutaneous nephrostomy tubes inserted under ultrasound guidance following routine pre-procedure baseline serum clotting profile (with emphasis on prothrombin time and international normalized ratio [INR]) and complete blood count. Any clothing abnormalities were corrected either by vitamin K supplements or fresh whole blood transfusion. In addition, they had pre-PCN imaging (ultrasound, abdominal computed tomography, or computed tomographic urography).
Patients were scanned in a prone position with a 3.5MHZ curvilinear transducer using NORTEK CS-50, Shenzhen China 2014 ultrasound machine, and transverse/longitudinal sections of the kidney where images were obtained to identify the degree of hydronephrosis. Afterwards, the ideal puncture site into the kidney was via a posterior calyx approach. As soon as the initial puncture site was chosen, it was cleaned and draped. Local anesthesia 5 ~ 10ml of 2% lidocaine was infiltrated subcutaneously at the puncture site.
Using the Seldinger technique under real-time ultrasound guidance, an 18G long access needle (Hakko Co. Ltd, Nagano-ken, Japan) was inserted into the target lower calyx; then a curved J tip 0.038-inch guide-wire (Cook, Bloomington, IN, USA) was passed through the needle sheath into collecting system with the help of an assistant (Fig. 1). Thereafter, the sheath was removed and the wire was retained. Further skin and fascia incision was widened, to allow for serial dilatation using plastic disposable percutaneous dilators. Over the guide wire, the drainage catheter set without inner metallic stylet was introduced into the collecting system after which the metallic trocar was removed. The drainage catheter was then advanced into the collecting system further following over the guide wire. Finally, after confirming the drainage catheter head curling in the collecting system, the guide wire was removed (Fig. 2). The safety string lock was tightened and the catheter was secured to the skin using silk 4 − 0 and connected to a drainage bag.
Urine samples were obtained and sent for Microbiological investigation and culture. All patients were placed on bed rest for two hours post-procedure before being discharged to the ward while the outpatients were usually observed/monitored for four hours before being discharged home on broad-spectrum antibiotics prophylaxis given for one day post-procedure.
We obtained pre-PCN and serial serum creatinine on day one, one week, and one month post-PCN. Furthermore, the patients were monitored for a minimum of two weeks for the presence of complications such as puncture site collections, intractable pain at the puncture site, lack of drainage of urine via PCN tubes, and Tube/catheter dislodgement or evidence of infection (urosepsis) and death were monitored and recorded. We also documented whether or not, the patient has continued to be on dialysis.
DATA ANALYSIS
The data collected was analyzed using the R programming software version 4.0. In the descriptive analyses, categorical data results were expressed as proportions and percentages.
Continuous data was assessed for normality. Those that are normally distributed were summarized using means and standard deviation. While those that are skewed were summarized using the median and interquartile range.
The student’s t-test to compare means between two groups for continuous variables was used. A confidence interval of 95% was used and a p-value of < 0.05 was considered statistically significant.