In this cross-sectional study, all patients hospitalized with OP poisoning at Sina Hospital - the Northwest Poisoning Center of Iran - during 2016 and 2017 were included as the study sample. The inclusion criteria encompassed patients admitted to the poisoning wards, with an initial diagnosis made by a medical toxicologist based on the symptoms reported by the patient and findings from the physical examination. Additionally, a serum cholinesterase test confirmed the diagnosis in cases where the type of poisoning was uncertain or when confirmation was deemed necessary. Patients who met any of the exclusion criteria were not included in the study. The exclusion criteria were as follows:
(1) Individuals with pre-existing conditions such as diabetes, cardiovascular diseases, respiratory diseases, kidney failure, and liver failure.
(2) Patients who had undergone surgery within one month prior to the poisoning incident.
(3) Individuals who had ingested other drugs or poisons concurrently with the OP poisoning.
(4) Patients who showed adequate response to the coma cocktail (comprising dextrose, naloxone, and thiamine) upon admission due to a decreased level of consciousness.
(5) Patients who had received medical interventions like gastrointestinal decontamination, atropine, pralidoxime, intubation, and ventilation at other centers before being referred to the Sina Poisoning Center.
(6) Patients presenting with electrolyte disorders, including hypo- or hypernatremia, hypo- or hyperkalemia, hypo- or hypercalcemia, and hypo- or hypermagnesemia.
(7) Patients whose medical records and clinical examination did not reveal symptoms indicative of OP poisoning.
(8) Patients who tested positive for other poisons or drugs in urine screenings.
In this study, correlation analyses were conducted among the QTc interval (measured in milliseconds), blood glucose (measured in milligrams per deciliter), and plasma acetylcholinesterase levels exclusively within a group of patients poisoned by OP, designating the study as a descriptive cross-sectional type.
The sample size was determined using data from a pilot study. The pilot study indicated an average deviation in QTc interval size of 76 (msec²) and a correlation coefficient of 80% among the patients studied. We assumed a maximum estimation error of not more than 20 msec². With a 95% confidence level (accounting for a 5% type I error and a 20% type II error), a minimum of 58 samples was estimated to be necessary. Considering the opinions and experiences of the study designers about the need to increase the sample size, and after applying the inclusion and exclusion criteria of the study, a total of 104 cases were eventually included in the study.
To gather patient information, researchers reviewed and extracted relevant data from the medical records and files of the selected patients in the Medical Documentation Unit of Sina Hospital. The collected data were analyzed using SPSS software version 25. Descriptive data were presented as frequency, percentage, and quantitative data as mean ± standard deviation for normally distributed data. Statistical tests such as the chi-square, t-test, and regression were employed, setting the significance level for decision-making regarding the proposed hypotheses at P < 0.05.
For this study, the normal range for serum cholinesterase enzyme levels for both genders was considered to be between 5000 and 12000 units per liter. Additionally, the normal range for the QTc interval, calculated using the Bazett formula, was established as between 360 and 440 milliseconds for both genders. The normal range for random blood glucose levels was set between 70 and 200 milligrams per deciliter.
No diagnostic, therapeutic, or pharmaceutical interventions were conducted on the patients as part of this study. Instead, the only information available in the medical records, such as diagnoses, medical histories, examinations, and laboratory tests, was used for research purposes. These records represent routine paraclinical procedures at the Poisoning Center. Ethical approval for the study was granted by the Regional Ethics Committee, with the first approval received on March 12, 2018, under the code IR.TBZMED.REC.1396.1300 is used to investigate the association between blood glucose levels in these patients. The second approval was obtained on July 23, 2018, under the code IR.TBZMED.REC.1397.378, for researching the association with the QTc interval in these patients.