Rini Sulistyowati, Rr Catur Leni Wulandari
Literature Review: The Effect of Lemon Aromatherapy on Emesis Gravidarum 936
patient and patient 2 were included in the study group. Patients with odd numbers were
included in the control group and patients with even numbers were included in the study
group. The study involved women aged 18-45 years with singleton pregnancies between
6-14 weeks. The week of pregnancy is determined by the date of the last menstrual
period. If there is a difference of more than 1 week between the date of the last menstrual
period and the ultrasound measurement, then the ultrasound measurement is accepted in
determining the week of gestation. The diagnosis of NVP is a diagnosis of exclusion such
as Patients with multiple pregnancies, molar pregnancies, or systemic diseases
(pancreatitis, hepatitis, cholecystitis, etc.) women with hyperemesis gravidarum were
excluded from the study. Pregnant with weight loss of >5%, findings of dehydration,
ketosis, and electrolyte abnormalities are accepted as hyperemesis.
Research journal articles researched by Dr. Arshi Anjum, Dr. Kouser Fathima
Firdose, Dr. Wajeeha Begum with the title "Effect of Sikanjabeen Lemooni in Qay'al-
Haml: An Open Observational Study" using the type of research study. An open
observation study was conducted from January 2017 to December 2017 at the Dept. OBG
National Institute of Unani Medicine hospital, Bengalurus. The sample size is calculated
using the formula, n = 2 [(Zα- Zβ) × ] 2 / (μ1 - 2) 15 around the difference in the mean
PUQE of the two estimates. The mean and SD of PUQE were taken from previous
studies. n = number of samples required, 1 = mean score before treatment, 2 = mean score
after treatment, 1-μ2 = clinically significant difference, = standard deviation. The
calculated sample size is 27.08; considering 10% dropouts, the total sample size was 30.
Pregnant women with c/o nausea and vomiting with a single intrauterine pregnancy at 7
to 14 weeks gestation were included in the study. Women with hyperemesis gravidarum,
treated with other antiemetics, with pregnancy-related medical conditions such as severe
anemia, hypertension and diabetes mellitus and with a history of other non-obstetrical
causes of vomiting such as cholecystitis and appendicitis were excluded from the study
by performing Hb%, RBS, CUE, Ultrasound-obstetrics. A total of 68 patients were
screened; 3 patients were ineligible because of HG. Of the 65 eligible patients; 22 refused
to participate and 13 were excluded; 1 patient was aborted before treatment was started, 1
had multiple pregnancies, in 2 patients each gestational age >14 weeks and Hb% <11; 3
had hypothyroidism and 4 patients had UTI. 30 patients were included in this study.
This research journal article was researched by Masoumeh Namazi; Seddigheh
Amir Ali Akbari; Faraz Mojab ; Atefe Talebi ; Hamid Alavi Majd; Sharareh Jannesari
with the title “Aromatherapy With Citrus Aurantium Oil and Anxiety During the First
Stage of Labor”. This study used the method. This randomized clinical trial was
conducted on two groups of pregnant women, who were referred to Vali-Asr Hospital
(Tuyserkan, Iran) between June and September 2013. It was registered with the Iranian
Clinical Trials Registry (IRCT ID: N6 201301306807). Considering similar studies, 95%
confidence interval, and 5% probability of error, the sample size was calculated as 63
subjects in each group. Women were first briefed on the aims and methods of the study
and then asked to provide written informed consent if they were willing to participate.
Women were only included if they were Iranian, primiparous, and aged 18-35 years, had
full-term, singleton pregnancy, cephalic presentation, spontaneous contractions, cervical
dilation 3-4 cm at delivery, good hip condition and intact amniotic sac. , had not used
analgesic drugs in the past eight hours, and had no liver, gallbladder, or respiratory
disease on their records. People with impaired smell, allergy to herbal medicines, or
complications of pregnancy (eg, preeclampsia, chorioamnionitis, placental abruption, and
abnormal fetal heart rate at the time of the study) were excluded. Data were collected
using obstetric and demographic questionnaires, examination and observation checklists
including vital signs, vaginal examination, uterine contractions, and fetal heart rate, and