فهرست مطالب

Shiraz Emedical Journal
Volume:22 Issue: 1, Jan 2021

  • تاریخ انتشار: 1399/10/16
  • تعداد عناوین: 8
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  • Zahra Anjoman Azari, Mojgan Mirghafourvand *, Ciara Hughes, Shiva Havizari Page 1

    Context:

     Constipation is a prevalent symptom of gastrointestinal disorders, which has an annoying impact on health and quality of life. On the other hand, reflexology is a popular type of complementary and alternative medicine in medical practices.

    Objectives

     The present study aimed to assess the effect of foot reflexology on constipation symptoms.

    Methods

     Nine databases were systematically searched to detect relevant Randomized Clinical Trials. The current used the Cochrane Risk of Bias tool to evaluate the methodological quality of the included articles. The primary outcome was the improvement of constipation symptoms. The Standardized Mean Difference (SMD) was measured, and random effects were reported instead of the fixed effects due to the high heterogeneity.

    Results

     Out of the 693 articles retrieved from the databases and eight additional records identified through other sources, 496 titles, 48 abstracts, and 16 full-texts were reviewed, and 11 articles were included in this study, out of which nine articles entered the meta-analysis. The findings of the meta-analysis indicated that foot reflexology had a significant effect on the constipation score (SMD: -0.82; 95% CI: -1.47 to -0.17; P value = 0.0001; I2 = 93%)

    Conclusions

     Foot reflexology can effectively improve constipation symptoms; however, clinical trials with better designs are recommended.

    Keywords: Meta-Analysis, Constipation, Systematic Review, Foot reflexology
  • Saeed Ovji, Dara Dastan, Sara Soleimani Asl, Amir Nili Ahmadabadi * Page 2
    Background

     Acetaminophen (APAP) hepatotoxicity is a highly prevalent drug used for the treatment of pain. Allium hooshidaryae is widely used as herbal medicine in western Iran.

    Objectives

     In this study, we investigated the protective effects of A. hooshidaryae methanolic extract (AhME) on liver damage induced by APAP.

    Methods

     Rats were divided into six groups. Groups 1 (negative control) and 2 (positive control) received normal saline; groups 3 received 200 mg/kg of AhME, and groups 4 - 6 received AhME at the doses of 50, 100, and 200 mg/kg once daily, by gavage, respectively. After the 14 days, except for groups 1 and 3, the other groups received 2 g/kg of APAP. After 48 hours, hepatic tissue and blood sample were taken for histopathology and biochemical experiments.

    Results

     APAP induced a notable increase in serum levels of aspartate transaminase (AST, P < 0.001), alanine transaminase (ALT, P < 0.001), alkaline phosphatase (ALP, P < 0.001), lactate dehydrogenase (LDH, P < 0.01), nitric oxide (NO, P < 0.001), and lipid peroxidation (LPO, P < 0.001) levels in hepatic tissue. It also significantly reduced the level of total antioxidant capacity (TAC), total thiol groups (TTGs) as well as glutathione contents (GSH) in hepatic tissue (For all P < 0.001). Following the use of AhME, a noteworthy improvement was observed in hepatic serum enzymes and oxidant/antioxidant parameters in liver tissue.

    Conclusions

     This study demonstrated that AhME prevents APAP-induced hepatotoxicity through improvement in the hepatic antioxidant status.

    Keywords: Oxidative Stress, Hepatotoxicity, Acetaminophen, Allium hooshidaryae
  • Ali Sharifi, Kamal Alizadeh * Page 3
    Background

     Thyroid is a gland that controls body key functions. Since thyroid hormones are responsible for controlling metabolism, the thyroid glands are one of the major organs in the body. Disruption of the glands causes thyroid disease, which is one of the most common endocrine diseases worldwide. Early diagnosis of thyroid disease is difficult since early symptoms are easily confused with those of other illnesses. In recent years, the employment of computer techniques to utilize data mining and intelligent algorithms accelerates the early diagnosis of the disease.

    Objectives

     The current study aimed at evaluating the role of the new automatic method according to a multilayer perceptron (MLP) in the diagnosis of thyroid disease.

    Methods

     The study aimed at comparing the particle swarm optimization (PSO) with the genetic algorithms (GA) as training for MLP technique used to diagnose thyroid functional disease. The data were collected for three classes: 150 cases of euthyroidism, 30 cases of hypothyroidism, and 35 cases of hyperthyroidism. MLP was used to elucidate the pattern in the data and species responsible for separating the classes. Furthermore, improved PSO and GAs were used to train the system, and the sensitivity and specificity of the model were studied in terms of accuracy, sensitivity, and specificity. All analyses were performed using MATLAB software.

    Results

     For the proposed model, the simulations results showed that the GA algorithm had a higher performance than the PSO algorithm in the diagnosis of functional thyroid disease, and the means of classification accuracy, sensitivity, and specificity were 95%, 96%, and 96%, respectively.

    Conclusions

     The results of real data indicated that the GA-MLP can be used with high diagnostic accuracy as an effective tool to clinically diagnose thyroid functional disease. The current study was a step towards prototype system development of the classification of knowledge in this area with a much lower computational cost.
     

    Keywords: Artificial Neural Networks, Multi-Layer Perceptron, Particle Swarm Optimization, Chemometrics, Thyroid Functional Disease, Genetic Algorithms
  • Arto Yuwono Soeroto *, Ining Kartika Tarmidi, Guntur Darmawan, Geraldo Laurus, Prayudi Santoso Page 4
    Background

     Pneumonia has high rates of morbidity and mortality in Indonesia. Infections caused by multidrug-resistant (MDR) pathogens are not only found in patients with nosocomial pneumonia but are also reported in patients with community-acquired pneumonia (CAP). Only a few studies have analyzed the factors associated with MDR pathogenic infections, especially in developing countries such as Indonesia. Therefore, the identification of such factors can help to predict the infections caused by MDR pathogens in CAP patients.

    Objectives

     This study aimed to determine factors associated with MDR pathogenic infections in CAP patients admitted to Hasan Sadikin General Hospital, Bandung, West Java Province, Indonesia.

    Methods

     This is an observational analytic study which compared 85 patients with MDR pneumonia and 70 patients with pneumonia caused by non-MDR pathogens from March to May 2018. Sputum of all adults patient > 18 years old with CAP who had the Murray and Washington’s criteria was collected. In vitro test was performed based on the Kirby-Bauer method with Clinical and Laboratory Standards Institute (CLSI) 2018 protocols. This study was ethically approved by the Ethics Committee of the Hasan Sadikin Hospital.

    Results

     One hundred and fifty five patients with positive sputum culture were investigated. Overall, 85 (54%) patients had MDR pathogens in their cultures. Klebsiella pneumoniae was the most common pathogen found in the CAP patients (37/155; 23.9%), while Acinetobacter baumannii accounted for the highest proportion of MDR pathogens (18/85; 21.2%). Multivariate logistic regression analysis showed that the immobilization status was the only associated factor for MDR pathogenic infections in CAP patients (adjusted prevalence ratio = 1.862 [1.432 - 2.420]; P < 0.001).

    Conclusions

     This study highlighted the need for early risk assessment of infections caused by MDR pathogens, especially immobilization status in CAP patients. Also, the local pathogen pattern should be considered to prescribed antibiotics for CAP patients. The findings showed that antibiotics against MDR pathogens should be prescribed for CAP patients with immobilization.

    Keywords: Community-Acquired Pneumonia, Multidrug-Resistant Pathogen
  • Najmeh Maharlouei, Artin Sarkarinejad, Hadi Raeisi Shahraki, Abbas Rezaianzadeh, Kamran Bagheri Lankarani * Page 5
    Background

     Children with developmental delays are at higher risk of poor health, and lower educational attainment and wellbeing than the normal ones.

    Objectives

     As previous studies had contradictory results regarding the association between socioeconomic status (SES) and child development, the current study aimed at determining this association at the age of 60 months.

    Methods

     The current prospective cohort study was conducted in Shiraz, Iran, from summer 2011 to the end of 2016. The study was conducted on 640 mothers registered in the Fars Birth Cohort study. A checklist comprised of social and economic parts was employed. The children’s communication development was also assessed using the ages and stages questionnaire for 60-month-old children. In addition, SES was determined using 25 variables. Data analysis was performed using SPSS version 19.0 and partitioning around medoid (PAM) clustering in R 3.5.0 software; P value < 0.05 was considered as the level of significance.

    Results

     The majority of the subjects (79.1%) were categorized as the moderate level of SES; 106 (16.56%) children had a delay in at least one developmental domain. The current study results showed that the education level of parents and the occupational status of mothers were significantly associated with delayed communication skills in children (P < 0.05). Delay in communication skills was significantly more prevalent among children whose parents had a low education level (P < 0.05). After controlling other confounders, the relative risk of delay in communication skills was 3.7 times higher among children in the moderate level of SES and almost 10 times higher among the ones in the low level of SES.

    Conclusions

     Children brought up in families with low SES had the highest level of delay in communication skills, followed by the ones in families with moderate SES. Considering the importance of communication skills in children socialization, more attention should be paid to SES of the families with preschool kids. It seems quite reasonable if health policymakers put more emphasis on the communication skills of preschool children.

    Keywords: Socioeconomic Status, Child Development, Educational Status, Delay
  • Saeedeh Vahedi, Sara Gholami, Hamidreza Kianifar, Tayebeh Hamzehloei * Page 6
    Background

     Alpha-1 antitrypsin (AAT) deficiency is a common genetic cause of childhood liver disorders. Its prevalence is highly variable around the world. Although this genetic deficiency is the main cause of neonatal jaundice, few studies have investigated AAT in Iran.

    Objectives

     The current study aimed to investigate the association between specific alleles of AAT with idiopathic neonatal jaundice disease in patients with idiopathic jaundice.

    Methods

     In this study, 30 neonates with a definitive diagnosis of neonatal cholestasis referred to Ghaem, and Dr. Sheikh hospitals in Mashhad (Iran) are included. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed on the extracted DNA from their blood samples. In the lack of commonly mutated alleles detected, the whole gene exons were DNA sequenced.

    Results

     In the molecular test, we found no case of PiS or PiZ allele. The mutated alleles of PiS and PiZ were not appeared in patients with neonatal jaundice using the PCR-RFLP method. DNA sequencing was performed in 30 patients. Other rare missense variations were detected in the form of heterozygous (for Glu400Asp in 8 patients and Val237Ala in 2 patients), homozygous (for Glu400Asp in 1 patient), and compound heterozygous (for Glu400Asp/Val237Ala in 3 patients and Val237Ala/Asp280Val in 1 patient).

    Conclusions

     The AAT deficiency caused by PiZ and PiS allelic variants was noted among infants with neonatal cholestasis in the Khorasan province of Iran. Other rare variants in the PiM might be caused by AAT deficiency and presenting the neonatal cholestasis. The possible functional study should be considered for the mutations identified.

    Keywords: Alpha-1-Antitrypsin, Idiopatic Jaundice, Allelic Variants
  • Niloofar Asadzadeh, Shahla Chaichian *, Mobina Ziadloo, Shahla Mirgaloy Bayat, Mehrdad Sheikhvatan Page 7
    Background

     The evolution of fertility treatment methods such as laparoscopic surgery and assisted reproductive technology (ART) leads to an increased chance for conception in women with endometriosis. However, it is still not clear which treatment is more likely to result in endometriosis recurrence.

    Objectives

     The current study aimed at assessing the recurrence rate of endometriosis and its main determinants following fertility treatment with surgery or ART.

    Methods

     The current historical cohort study was conducted on 51 consecutive women with endometriosis undergoing fertilization procedures, including laparoscopic surgery (n = 42) and ART (n = 9) in Tehran from 2006 to 2016. All patients with complete hospital records were enrolled in the study. The patients in the two groups were followed up for five years for endometriosis recurrence.

    Results

     Within the follow-up time, the rate of endometriosis recurrence in patients of the surgery and ART groups was 28.6% and 44.4%, respectively, indicating no significant difference between the groups (P = 0.436). In this regard, the 1-, 2-, and 3-year recurrence-free survival rate in the ART group was 87.5%, 50.0%, and 50.0%, and in the surgery group was 96.9%, 90.6%, and 70.5%, respectively. Using the Cox proportional hazard modeling adjusted for baseline variables, the method of fertilization (ART or surgery) could not affect the rate of long-term recurrence of endometriosis (odds ratio = 1.428, 95% confidence interval: 0.177 - 9.900, P = 0.784).

    Conclusions

     The method of fertilization treatment-e g, surgery, and ART- may not affect the rate of endometriosis recurrence in women with subfertility caused by endometriosis.

    Keywords: Recurrence, Endometriosis, ART, Subfertility
  • Parisa Derakhshan, Farin Kiany * Page 8
    Introduction

     The Wiedemann-Rautenstrauch syndrome (WRS) is a rare progeroid syndrome with an autosomal recessive pattern of inheritance. The main clinical features include severe intrauterine and postnatal growth failure, distinctive facial appearance, hydrocephaly, prominent scalp veins, absence of subcutaneous fat, sparse hair of the scalp, eyebrows, and eyelashes, generalized lipoatrophy, psychomotor delay, progressive neurological deterioration, and short life expectancy. Natal teeth and micrognathia are reported as the oral manifestations of this syndrome.

    Case Presentation

     Here is the report of a 6.5-year-old female patient with clinical signs of WRS referred to the Department of Periodontology of Shiraz School of Dentistry with the chief complaint of toothache and gingival hyperplasia. Carious teeth were extracted, and excess gingival tissue was removed through a surgical procedure under general anesthesia. The patient was the first case with a concomitant severe anterior open bite.

    Conclusions

     Therapies for WRS are symptomatic, requiring the coordinated efforts of a team of specialists. Dentists and oral surgeons can be recruited by pediatricians and family physicians to improve the quality of life of such patients.

    Keywords: The Wiedemann-Rautenstrauch Syndrome, Gingival Hyperplasia, Anterior Open Bite