The present study was extracted from a Master’s thesis on critical care nursing, which was approved by the Ethics Committee of the Gonabad University of Medical Sciences (Code:
IR.GMU.REC.1400.040) and registered in the Iranian Registry of Clinical Trials (No.:
IRCT20210626051716N1).
This randomized, self-controlled, single-blind two-group clinical trial was conducted among 54 eligible hemodialysis patients referred to the Nikan Farda Clinic in 2021. The subjects were selected based on the inclusion criteria using the convenience sampling method. Sampling continued as long as data saturation was reached, informed written consent was obtained from the participants. Then they were randomly assigned to rhythmic breathing and lidocaine spray groups by applying permuted block technique with four blocks. In each group, the sample size was calculated to be 24 according to the mean comparison formula and the results reported by Asgari et al. (
22), regarding the test power of 80%, a confidence level of 95%, and the mean ± SD of pain score in the two groups (3.96 ± 2.14 and 2.3 ± 1.91). Considering the 10% dropout rate, 37 patients were assigned to each group. The formula is as follows:
The inclusion criteria were willingness to participate in this study, aged 18 - 60 years, no addiction to analgesic drugs, and controlled diabetes with fasting blood sugar (FBS) and blood sugar (BS) of 70 - 150 and 120 - 250, respectively. The other criteria were the lack of known lidocaine sensitivity, passing at least three months of fistula placement in the forearm, and having an active record (treating with hemodialysis for three four-hour sessions per week). The other inclusion criteria were having no pacemaker, skin problems, speech, visual, hearing, and cognitive impairment, anesthesia, neuropathic disorders, and vascular diseases in the fistula site.
However, exclusion criteria were failure to insert the needle into the arteries of the fistula area in the first attempt, need for repeated cannulation, lidocaine sensitivity, and unconsciousness at each phase of the study. The patients who were not inclined to cooperate experienced the onset of other chronic pains affecting the assessment of the pain induced by needle insertion into the arteries and did not refer during the research phases (referral to other medical centers to continue treatment, travel, kidney transplant, death) were excluded from the study.
The data were collected using a questionnaire addressing demographic characteristics and information on the history of hemodialysis and the visual analogue scale (VAS) for pain intensity. Many studies have employed the instrument to measure the pain intensity of hemodialysis fistula cannulation (
14). VAS is a 10 cm horizontal line from 0 (no pain) to 10 (worst pain) measuring pain intensity based on the patients’ statements. Moreover, the scientific validity and reliability of the questionnaire have been evaluated by several researchers. For example, a study confirmed its reliability by applying the McGill pain questionnaire among individuals with chronic back pain in Tehran (correlation coefficient: 0.86) (
23).
Before the intervention, the two groups were examined for pain intensity during needle insertion one minute after completing the hemodialysis needle insertion and fixing the needles in the first hemodialysis session without intervention.
The intervention group was asked to do rhythmic breathing for two minutes before entering the hemodialysis vascular needles. For this purpose, the rhythmic breathing method was taught individually to the subjects in a session prior to the intervention so that they could perform this technique independently without error. In this respect, the patients laid comfortably, closed their eyes, and took a long deep breath via the nose after counting one to three. Then they held their breath in the lungs for three numbers and exhaled through their mouths slowly with three numbers. The subjects repeated this breathing type while inserting hemodialysis vascular needles into the fistula by concentrating on the exercise. Finally, they opened their eyes after one minute of insertion and needle fixation; their pain intensity during the needle insertion was evaluated by the researcher, who was not informed of the type of intervention.
As for the lidocaine group, two puffs of 10% lidocaine spray (20 mg) were sprayed to the needle insertion area from a distance of 5 cm five min before insertion. Then the pain intensity was assessed one minute after the procedure and needle fixation.
Unaware of the type of intervention, the researcher evaluated the pain intensity felt during the insertion of arteriovenous needles using VAS. The intervention was iterated in three consecutive hemodialysis sessions, and pain intensity scores were compared in two groups at pre- and post-intervention phases.
Prior to the intervention, all subjects laid in a comfortable position two minutes before inserting the needles into the fistula vessels, and the insertion site was disinfected with 70% alcohol by the department nurse.
To match the conditions as much as possible, all patients were placed in a supine position under a convenient situation before and after the intervention, the face of whom was rotated to the opposite side of the hand with a fistula, and cannulation was then performed. In all study phases, a dialysis needle (No. 16) was inserted by two skilled nurses into the fistula site from at least a five cm distance with a 30 - 40° angle when the oblique edge of the needle was upside.
Further, SPSS software version 20 was used to analyze the data. The data were analyzed at a significance level of 0.05.