The current in vitro study was performed on 21 preterm infants with a gestational age of 30 - 36 weeks and 6 days (weight: 1500 - 2500 g). The babies were diagnosed with jaundice during the NICU admission. The sample size was estimated as 14 subjects using the equation of
based on the study by Nabavizadeh et al. (
13) and six other studies (the mean indirect bilirubin was 8.93 ± 1.3 in the common chicory group and 10.79 ± 2.11 in the distilled water group) and regarding α = 0.05 and β = 0.2. Considering the dropout, 21 patients were enrolled in the study.
Exclusion criteria were indications of intensive phototherapy, the presence of any clinical or laboratory signs of hemolysis or infection, any congenital anomalies of the infant, dehydration, G6PD deficiency, ABO incompatibility, positive Coombs test, history of maternal phenobarbital reception, IUGR, mechanical ventilation, and inability to use oral medication. To exclude the causes of withdrawal, examinations were conducted to determine the maternal and infant blood group, hemoglobin, CBC, reticulocyte count, peripheral blood smear, Coombs test, thyroid function tests, and G6PD for all neonates. The indication of starting phototherapy for infants was based on the criteria regarding the maximum acceptable levels of indirect serum bilirubin (mg/dL) in preterm infants.
Before enrolling the patients, the sampling method, probable side effects, and standard treatment method were explained to the legal guardians of all babies, and informed written consent was obtained. All newborns received routine treatments of neonatal jaundice to prevent the disease complications. In this study, considering the inclusion and exclusion criteria, all newborns were enrolled from 1 January 2018 until the sample size was completed.
After obtaining permission from the parents, blood samples (2 cc) were taken from 21 infants, and their baseline bilirubin levels were measured. Each sample was then divided into two parts in equal volume, and each part was added with half of its volume of chicory essence or distilled water. The bilirubin level was re-evaluated. In this way, we had 42 samples, and serum bilirubin levels were re-evaluated in these specimens. The chicory essence used was prepared from Golchekan Zamani Company with an essential oil concentration of 1.1 to 1.5 mg per 100 mL. Next, all specimens underwent phototherapy by Tosan phototherapy device with four PHILIPS fluorescence lamps for 3 hours, so that the distance between the lamps and the level of the specimens was 30 cm. Radiation was in the blue-green spectrum (wavelength of about 430 - 490 nm) with irradiance of 10 μw/cm2/nm at the center of phototherapy. The bilirubin levels were reassessed after adding distilled water/chicory essence before and after phototherapy. For all samples, direct and total bilirubin levels were checked. Then, the indirect level was obtained by subtracting the direct level from the total level. All experiments were performed at the reference laboratory of the Birjand University of Medical Sciences in accordance with the method of the Diazo of Pearlman and Lee on the Cobas Integra Autoanalyzer.
The collected data were inserted into SPSS version 21 software. Descriptive analysis was performed by mean, standard deviation, frequency, and percentage. Wilcoxon and Mann-Whitney tests were used for indirect bilirubin in the common group, and paired t-test and independent t-test for other cases. A P-value ≤ 0.05 was considered as the significance level.