negar yazdani
-
Background
Subclinical hypothyroidism (SCH) is marked by elevated thyroid-stimulating hormone (TSH) levels while maintaining normal thyroxine levels. Although the link between insulin resistance (IR) and overt hypothyroidism is well-established, less is known about this relationship in children and adolescents with SCH.
ObjectivesThis study aimed to explore the association between insulin resistance and SCH in individuals aged 4 to 18 years.
MethodsIn this case-control study, 30 patients with SCH aged 4 - 18 from the Endocrinology Clinic at Imam Reza Hospital, Shiraz, Iran, were chosen as the case group through convenient sampling. Additionally, 30 healthy children and adolescents from the same clinic were randomly selected as controls. Exclusion criteria included positive Anti-TPO, goiter, previous thyroid disease, systemic diseases, chronic or acute diseases, diabetes, and a BMI ≥ 85%. Levels of TSH, insulin, fasting blood sugar (FBS), triglycerides, cholesterol, low-density lipoprotein, and high-density lipoprotein were compared between the groups. Data were analyzed using SPSS 25.
ResultsThe study found that levels of FBS, insulin, and Homeostatic Model Assessment for IR (HOMA-IR) were significantly higher in the SCH group than in the control group. There was a significant correlation between TSH levels and both insulin levels and IR in the SCH group. Subclinical hypothyroidism was found to significantly increase the risk of developing IR among pediatric patients compared to healthy controls.
ConclusionsOverall, our findings indicate a positive correlation between TSH levels and IR in children with SCH. Additionally, HOMA-IR levels were significantly higher with elevated TSH in the SCH group compared to healthy children. It is recommended that IR be evaluated and treated timely in SCH patients to prevent future complications.
Keywords: Hypothyroidism, Insulin Resistance, Child, Adolescent, Diabetes Mellitus -
BackgroundVitamin D has multifaceted effects on the mother’s health and fetus. Since its deficiency can cause numerous maternal and fetal complications, this study aimed to investigate the relationship between the maternal and umbilical cord blood vitamin D.MethodsThis cross-sectional study was conducted on 48 pregnant mothers and their 48 babies in Hafez Hospital, Shiraz, in 2021. First, 5cc the blood clot was taken from the mother and the baby's umbilical cord after delivery. Also, a checklist included the mother's age, pregnancy conditions, gender, weight, height, head circumference, age of baby teeth eruption, and the first and fifth minute Apgar score of their babies was filled. Data were analyzed using SPSS-26.ResultsThe mean of vitamin D from the umbilical cord blood (35.95±11.97), and from mothers' serum (21.85±7.3); were correlated significant (r=0.80, P<0.001). The mean vitamin D serum level of mothers who received supplements during pregnancy (23.72±6.04) was higher than mothers who did not use them during pregnancy (8.29±19.45) (P<0.05). There was a significant relationship between the mother's vitamin D and umbilical cord vitamin D with the sprouting of the first milk tooth.ConclusionIn this study, most mothers reported vitamin D deficiency, and their vitamin D levels were directly correlated to the umbilical cord vitamin D. These findings show the importance of monitoring the mother's vitamin D to indicate the vitamin D status of the fetus and encourage mothers to make effective use of sunlight and the enrichment food with vitamin D.Keywords: Pregnancy, Infant, Mothers, Umbilical Cord Blood, Vitamin D Deficiency
-
Background
There is a lack of conclusive evidence regarding thyroid function test (TFT) abnormalities in COVID-19, especially among children.
ObjectivesThis study aimed to investigate TFT abnormalities in COVID-19 pediatric patients compared to healthy children.
MethodsThis study was conducted on 37 COVID-19-positive children who were admitted to Namazi Hospital from January 21 to March 1, 2022, compared with 37 healthy children. Within 48 h of positive real-time polymerase chain reaction (PCR) results for severe acute respiratory syndrome coronavirus 2, a blood sample was taken to measure serum levels of thyroid-stimulating hormone (TSH) and total thyroxine (tT4) in the two groups. Additional tests, including free and total triiodothyronine, free T4, and thyroperoxidase antibodies, were also conducted on cases. The chi-square, Pearson correlation coefficient, and analysis of variance tests were used for data analysis.
ResultsTwenty-five patients were male, and 49 were female, with a mean age of 7.99 ± 5.02. The abnormal TFT and TSH frequency was significantly higher in the case group than in the control group. Nevertheless, there was no significant difference between the case and control groups regarding tT4 abnormalities. We could not establish an association between the mean of TSH and tT4 and age groups in the two groups and between abnormalities of TFTs and COVID-19 severity.
ConclusionsAlthough abnormalities of TFT were significantly more common among COVID-19 children, they were not associated with the disease severity. However, studies with larger sample sizes are recommended to evaluate thyroid abnormalities and their clinical course in COVID-19 children.
Keywords: COVID-19, Thyroid Gland, Pediatrics, Thyroxine, Case-Control Studies -
Background
Sepsis is a leading cause of morbidity and mortality in neonates.
ObjectivesThis study aimed to investigate the bacterial profile and antibiotic sensitivity in infants with sepsis.
MethodsThis cross-sectional study was conducted on 90 neonates with sepsis admitted to the neonatal intensive care unit of Namazi Hospital, a tertiary-level hospital, in Shiraz, Iran, from 2020 to 2021. Demographic and clinical data including gestational age, previous diseases, maternal infectious, underlying diseases, history and duration of premature rupture of the membrane and delivery, clinical symptoms (fever, reduced breastfeeding, and lethargy), laboratory results (complete blood cell and C-reactive protein), and results of blood and urine cultures were recorded and analyzed.
ResultsAmong 90 neonates with sepsis, the average age was 6.7 ± 7.6 days; 54 were male (60.0%), and 36 were female (40.0%). Fifty (55.5%) neonates had early sepsis. Gram-negative organisms were grown in 61% of positive blood cultures; the most common was Klebsiella. Among Gram-positive organisms, Staphylococcus epidermidis was the most common. Most organisms were sensitive to colistin, and most were resistant to cefotaxime. There was a significant relationship between the age of onset of sepsis symptoms and birth weight in infants with positive blood cultures (P = 0.004) (r = 0.3).
ConclusionsGram-negative bacteria are the most common causes of sepsis, mainly resistant to aminoglycosides and cefotaxime. Therefore, increasing awareness about the optimal use of antibiotics is necessary to curb the increase in resistance levels.
Keywords: Microbial Sensitivity Tests, Sepsis, Intensive Care Units, Neonatal, Anti-bacterial Agents -
Background
Congenital hypothyroidism (CH) can influence neonates’ neurodevelopment. There are controversies on the cause of infantile hypothyroidism and its relationship with maternal hypothyroidism.
ObjectivesThis study aimed to investigate the relationship between maternal hypothyroidism and the incidence of CH.
MethodsThis cross-sectional study was conducted on 712 newborns with hypothyroidism born in Fars province, Iran, between 2018 and 2020, identified through the national screening program for genetic, metabolic, and endocrine congenital diseases recruited by the census sampling method. The information on infants’ files was recorded in a researcher-made checklist. Descriptive data were reported by mean ± SD and No. (%). The independent t-test, chi-square test, Pearson correlation, and Spearman’s rank correlation coefficient were used to evaluate relationships between variables.
ResultsOf 179,448 infants screened, 712 (4 of 1,000 live births) had CH with a mean thyroid stimulating hormone (TSH) level of 22.34+24.8 mlU/L. Of these, 252 infants (35.4%) had a family history of hypothyroidism in the mother (OR = 4.951, P < 0.001). There was a significant relationship between CH and maternal hypothyroidism. Moreover, there was a significant difference in the mean TSH level between hypothyroid infants born to mothers with a history of hypothyroidism (19.10 ± 21.30 mlU/L) and those who had healthy mothers (24.23 ± 26.44 mlU/L, P = 0.027). The prevalence of CH in 2018, 2019, and 2020 were reported to be 0.34%, 0.4%, and 0.45%, respectively.
ConclusionsOur results showed a significant relationship between maternal hypothyroidism and CH. Considering the importance of the prompt diagnosis of CH, especially in high-risk groups such as infants of hypothyroid mothers, it is recommended to conduct more studies to design more precise guidelines to screen infants who are at risk of CH.
Keywords: Infant, Mother, Congenital Hypothyroidism, Prevalence, Neonatal Screening -
مقدمه
بیماری دیابت و عوارض ناشی از آن هزینه های سیستم سلامت را افزایش می دهد. لذا پیشگیری و تشخیص به موقع این بیماری نقش مهمی در کاهش هزینه ها و عوارض آن دارد. مطالعات انجام شده دراین باره بر نقش آموزش در درمان و آگاهی مردم در پیشگیری و تشخیص زودهنگام تاکید کرده اند. مطالعه حاضر با هدف بررسی آگاهی مراجعان مراکز بهداشتی شیراز در مورد بیماری دیابت انجام شد.
روش هااین مطالعه مقطعی روی 270 نفر از مراجعان مراکز بهداشتی شیراز در بازه سنی 65-12 سال در سال 1398 انجام شد. برای این پژوهش پرسشنامه 18 سوالی با زیرگروه های اطلاعات دموگرافیک، اطلاعات کلی بیماری، علت و عوامل بیماری، علایم و تشخیص، پیشگیری و درمان، و عوارض و مشکلات تکمیل شد. اطلاعاتی نیز مانند وجود فرد دیابتی در خانواده و منبع کسب آن ثبت گردید. داده ها توسط نرم افزار SPSS 21 آنالیز شد.
یافته هامیانگین سنی افراد 05/10±96/33 سال بود که 82/54% آن ها زن و 18/45% آن ها مرد بودند. بیشترین منبع آگاهی بیماری دیابت، دوستان و آشنایان بودند. میانگین نمره کل آگاهی 03/5±18/15 محاسبه شد. آزمون ها رابطه معناداری بین شغل، سطوح تحصیلی، سن و منبع آگاهی با نمره آگاهی نشان دادند (001/0>P)، اما این ارتباط با متغیرهای جنسیت (068/0=P)، وضعیت تاهل (196/0=P) و سابقه خانوادگی (060/0=P) معنادار نشد.
نتیجه گیریبه طورکلی می توان گفت که آگاهی جامعه آماری پژوهش در رابطه با بیماری دیابت در سطح متوسط بود. همچنین مردان، متاهلان، افراد مسن و با تحصیلات پایین، از آگاهی کمتری نسبت به سایرین برخوردار بودند؛ بنابراین پیشنهاد می گردد در برنامه های سیستم سلامت با اهداف آگاه سازی تمام جامعه در مورد بیماری دیابت، این موارد در نظر گرفته شود.
کلید واژگان: آگاهی، مطالعات مقطعی، دیابت ملیتوس، ایرانIntroductionDiabetes and its consequences increase the health system costs. Therefore, prevention and early diagnosis can reduce the cost and consequences. The studies have emphasized the role of education in treatment and people’s awareness of prevention and early diagnosis. Thus, the present study aimed to assess the awareness of people referring to Shiraz health centers with diabetes.
MethodsThis cross-sectional study was conducted on 270 people aged 12-65 Y/O referred to Shiraz health centers in Iran in 2019. Participants completed an 18-item questionnaire with subscales of demographic data, general information about patients, causes and factors of diabetes, symptoms and diagnosis, prevention and treatment, and consequences and problems. Furthermore, other information, such as the presence of diabetic patients in the family and sources of information, was recorded. Data were analyzed using SPSS software-21.
ResultsThe participants’ mean age was 33.96±10.05; 54.82% were female, and 45.18% were male. The main sources of information were friends and relatives. The mean score of awareness was calculated to be 15.18±5.03. Statistical tests revealed a significant relationship between job, educational levels, age, and source of information with the score of awareness (P<0.001), while this relationship with gender (P=0.068), marital status (P=0.196), and family history (P=0.060) was insignificant.
ConclusionOverall, public awareness of diabetes in Shiraz was found to be moderate. Moreover, it is observed that men, married individuals, as well as older and less educated people exhibited lower levels of awareness. Hence, it is recommended that these factors be taken into account when designing health system programs aimed at educating all communities about diabetes.
Keywords: Awareness, Cross-sectional studies, diabetes mellitus, Iran -
Background
Peripherally inserted central catheters (PICCs) are an effective method for medication and nutrition infusion in preterm neonates. The present study aimed to identify the incidence of the most common complications of PICC implantation and evaluate the risk factors of each complication.
MethodsThis historical cohort study was conducted on 2500 neonates with birth weights (BWs)≥500 g and gestational age (GA)>24 weeks who had a history of PICC inserted in three NICUs between August 2015 and August 2018. Data were collected by reviewing medical records. Demographic data and indices of catheter placement, duration of catheter placement, and common complications were recorded. Data analysis was done using SPSS-21.
ResultsThe median cubital vein had the most PICC placement (43%). The most common complication was tip malposition (48.2%). The incidence rates (95% CI) of the main complications such as malposition, edema/occlusion, and PICC migration were 0.0356 (0.0337-0.0377), 0.0134 (0.0122-0.0147), and 0.0088 (0.0079-0.0099), respectively. PICC insertion position was the strongest predictor of malposition for the cephalic vein. Besides, the incidence of malformation in the cephalic vein was about six times higher than in the median cubital vein. Independent risk factors for non-technical complications included BW (OR=0.59, 95% CI 0.44-0.79), administration of hyperosmolar medications (OR=3.43, 95% CI 2.62-4.51), position (OR=2.43, 95% CI 1.92- 3.08), and duration of catheter presence (OR=1.02, 95% CI 1.01-1.03) (P<0.001).
ConclusionThe most common complication was malposition related to catheter placement in an emergency. Moreover, BW, administration of hyperosmolar medications, and duration of catheter presence were the most critical risk factors for non-technical complications. Therefore, it is recommended to educate the PICC insertion team to reduce tip malposition and replace long-term catheters.
Keywords: Bacteremia, Catheterization, Infant, Premature birth, Risk factors -
Background
Diabetic ketoacidosis (DKA) can cause several complications. The myocardial damage in children with DKA was not evaluated clearly. This study aimed to investigate the troponin level as a biochemical marker of myocardial damage in children with DKA during the disease and after recovery.
MethodsThis cross-sectional study was conducted in the pediatric endocrinology department of Namazi Hospital, Shiraz, Iran, from May to December 2019. Fifty diabetic children aged 1 to 18 years old with DKA by census sampling method. All patients were examed, and electrocardiography (ECG) was carried out. Troponin level was measured at admission and 48 hours after recovery. Finally, data were analysed using SPSS software 20.
ResultsAt the time of admission, the mean troponin level was 11.56±5.35 ng/mL and it became 2.15±1.21 ng/mL after recovery. Although the initial troponin level during DKA in three patients was higher than the expected normal reference range, their echocardiography and ECG were normal. Moreover, there was no statistical relationship between troponin level with age, diabetes duration, and DKA severity.
ConclusionThe troponin level was remarkably different during DKA and after recovery. However, in merely 6% of DKA patients, the troponin level was higher than the expected value. We recommended that these patients be followed for future cardiovascular complications.
-
Background
Because of the high daily mortality and quarantine procedures, coronavirus disease 2019 (COVID-19) can cause several psychological problems, especially in younger people.
ObjectivesSince most studies have mainly focused on physical problems of COVID-19 and they have neglected children in their analysis, this study aimed to evaluate the frequency and severity of stress symptoms and associated factors amongst children and adolescents aged 4 - 18 years during the COVID-19 outbreak.
MethodsUsing a convenience sampling technique, this descriptive-analytic cross-sectional study was conducted in Shiraz, Iran, from March 2020 to June 2020. To collect data, the link of the online Children's Self-Reported Stress Symptoms Questionnaire was sent to eligible participants via SMS and WhatsApp. The data were analyzed using SPSS software version 21.
ResultsAccording to our results, 270, 77, and 16 cases had low, moderate, and severe stress, respectively. Age group, living with both parents, and birth rank had a significant relationship with the degree of stress. Furthermore, more than 50% of participants reported cognitive-emotional symptoms more than physical ones. There was a significant relationship between the age group and physical symptoms, the duration of quarantine with bad temper and sadness, and between no clear thoughts with mother’s workplace and father’s job.
ConclusionsGenerally, almost 25% of participants reported moderate-to-severe stress. The most common symptoms of stress in children and adolescents were worrying, anger, and weakness. Furthermore, older children, those being the first child, and children living with both parents were more exposed to stress. Therefore, these items should be included in the healthcare team's training.
Keywords: Adolescent, Child, Psychological, Disease Outbreaks, Coronavirus -
مقدمه
بیماری سلیاک از واکنش بین گلوتن، سیستم ایمنی، ژنتیک و فاکتورهای محیطی پدید می آید که با علایم بالینی مانند کاهش وزن، دفع مدفوع چرب و سوء تغذیه تشخیص داده می شود. این بیماری معمولا در کودکان دارای سوء تغذیه و نارسایی رشد مشاهده می شد، اما اخیرا در تعدادی از کودکان چاق نیز گزارش شده است. از آنجاییکه امروزه غربالگری گروه های در معرض خطر تاکید شده است، مطالعه حاضر با هدف ارزیابی فراوانی سرولوژیک بیماری سلیاک در کودکان چاق انجام شد.
روش هااین مطالعه مقطعی بر روی 104 کودک چاق مراجعه کننده به کلینیک غدد دانشگاه علوم پزشکی شیراز در سال 1395 انجام شد. داده ها با استفاده از پرسشنامه از طریق مصاحبه مستقیم جمع آوری شدند. جهت اندازه گیری Anti TTG IgA و IgA Ab total، حدود 5 میلی لیتر خون از بیمار گرفته شد. داده ها با استفاده از نرم افزار SPSS-18 تجزیه و تحلیل شدند.
یافته هامیانگینسن و BMI شرکت کنندگان در مطالعه به ترتیب 39/2±33/10 و 78/4±71/24 بود که 65 درصد آنها دختر بودند. در این مطالعه تعداد 5 نفر (9/4%) از بیماران دارای Anti TTG IgA مثبت بودند که 80% آنها علایم گوارشی مثبت گزارش کرده بودند. آزمون ها رابطه مثبت و معناداری بین علایم گوارشی و Anti TTG IgA نشان دادند.
نتیجه گیریدر مقایسه با شیوع 2 درصدی سرولوژیک TTG Anti در جامعه ما، شیوع 5% افزایش Anti TTG IgA در کودکان چاق می تواند نشان دهنده این باشد که افزایش احتمال potential celiac در کودکان چاق نسبت به جمعیت نرمال وجود دارد. لذا غربالگری دوره ایاین کودکان و در صورت تداوم بالابودن Anti TTG، اندوسکوپی و بیوپسی مجدد آنها توصیه می شود.
کلید واژگان: بیماری سلیاک، کودک، چاقی، شیوع، سرولوژیIntroductionCeliac disease results from the interaction of gluten, the immune system, and genetic and environmental factors, which is diagnosed via clinical symptomsincludingweight loss, steatorrhea, and malnutrition. It is usually presented in children who have malnutrition and failure to thrive, but it has been recently reported in some obese children. Since nowadays screening of high-risk/susceptible groups has been emphasized, this study aimed to evaluate the frequency of serologic celiac disease in obese children.
MethodsThis cross-sectional study was conducted on 104obese children who referred to the Endocrine Clinic of Shiraz University of Medical Sciences, Shiraz, Iran in 2016. Data were collected using a questionnaire through face to face interviews. To measure Anti TTG IgA and total IgA Ab, 5 ml blood sample was taken. Data analysis was done using SPSS version 18.
ResultsThe mean age and BMI of the participants were 10.33±2.39 and 24.71±4.78, respectively, 65% of whom were girls. In this study, five patients (4.9%) had positive Anti TTG IgA, 80% of whom had reported positive gastrointestinal symptoms. The statistical tests suggested a positive and significant correlation between gastrointestinal symptoms and Anti TTG IgA.
ConclusionCompared to 2% prevalence of serological TTG Anti in our community, a 5% prevalence Anti TTG IgA in obese children may indicate that there is an increased risk of potential celiac in obese children compared to the normal population. Therefore, it is recommended to screen obese children for celiac disease periodically and perform endoscopy and biopsy in the cases with persistence of anti-TTG.
Keywords: Celiac Disease, Child, Obesity, prevalence, Serology -
Background
Although selenium is one of the nutrients that has an important role in the metabolism of thyroid hormones, it has been investigated in rare studies. This study aimed to evaluate role of selenium deficiency in children and adolescents with acquired hypothyroidism.
MethodsThis case and control study was conducted on 60 acquired hypothyroidism and 60 healthy children who had been referred to the pediatrics endocrine clinic in Shiraz, Iran, from November 2018 to April 2019. Some information such as age, gender, weight, height, duration of disease, and level of plasma selenium were recorded. Plasma selenium level was measured by atomic absorption spectrophotometer. Data were analyzed using SPSS software 21.0.
ResultsThe mean of selenium level in the case and control groups were 93.77 ± 24.90 µg/dl and 85.96 ± 25.20 µg/dl, respectively. There was no significant difference between the two groups in the mean levels of selenium. Independent t‑test showed no significant difference in the mean levels of selenium in male and female samples in the case group, but this difference was significant in the control group.
ConclusionSelenium deficiency may not have significant role as a cause of acquired hypothyroidism in pediatric and adolescent age group, in south of Iran. Thus, it does not seem necessary to routinely check the level of selenium for patients with thyroid dysfunction.
Keywords: Deficiency, hashimoto disease, hypothyroidism, selenium, selenoproteins -
Background and aims
Since ventricular septal defect (VSD) is the most common congenital heart disease, this study aimed to investigate its prevalence, characteristics, and associated diseases in a referral children’s heart clinic in south of Iran.
MethodsIn this cross-sectional study that was conducted based on the databases of children with heart diseases, patients under 18 years of age referring to Imam Reza clinic were examined. All patients with at least one record of VSD in echocardiography during 2016-2017 were included. Demographic and echocardiographic characteristics including size of VSD, shunt gradient, pulmonary hypertension (PH), aortic regurgitation, and associated cyanotic and acyanotic defects were analyzed.
ResultsThe prevalence of VSD found in 7458 echocardiography records was 12%, the median age of patients was 9.3, and the male/female ratio was 1.08. The perimembranous VSDs were determined to be the most common types of VSD. The most common associated complication with VSD was detected to be PH followed by aortic regurgitation. Sub-pulmonic showed the highest association with aortic failure. Atrial septal defect and tetralogy of Fallot (TOF) were the most common acyanotic and cyanotic heart defects, respectively. Only 0.5% of the patients had Eisenmenger syndrome.
ConclusionFortunately, the prevalence of the complication of VSD was not high in south of Iran, and the number of Eisenmenger syndrome was low. The types of VSD and the number of its complications identified in study population were similar to those in other populations.
Keywords: Aortic regurgitation, Atrial septal defect, Fars, Iran, Tetralogy of Fallot, Ventricular septal defect -
مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران، سال هفتاد و هشتم شماره 12 (پیاپی 240، اسفند 1399)، صص 835 -842زمینه و هدف
زردی از مشکلات شایع نوزادان است که در موارد شدید به کرنیکتروس منجر می شود. از آنجایی که تشخیص و درمان به موقع زردی در پیشگیری از عوارض آن اهمیت دارد، ارزیابی بیلی روبین پیش از ترخیص نوزاد ضروری است. روش های تشخیصی مختلفی برای اندازه گیری سطح بیلی روبین وجود دارد. از این رو این مطالعه با هدف مقایسه روش اندازه گیری پوستی بیلی روبین با اندازه گیری بیلی روبین سرم با اسپکتروفتومتری برای غربالگری زردی نوزادان ترم پیش از ترخیص از بیمارستان انجام شد.
روش بررسیاین مطالعه مشاهده ای تحلیلی بر روی 600 نوزاد سالم، با وزن تولد حداقل g 2000 و سن حاملگی حداقل 35 هفته از مهر 1391 تا اسفند 1391 در بیمارستان حافظ شیراز انجام شد. بیلی روبین نوزادان با دو روش اسپکتروفتومتری و پوستی با دستگاه بیلی چک دارای طول موج های چندگانه اندازه گیری و مقایسه شد.
یافته ها:
آزمون آماری همبستگی معناداری را بین دو روش اسپکتروفتومتری و پوستی نشان داد (63/0r=)، (05/0P<). بین بیلی روبین اندازه گیری شده با هر یک از دو روش در گروه های مختلف جنسی (896/0=P)، وزن تولد (419/0=P) و نوع تغذیه (323/0=P) اختلاف معنادار مشاهده نشد، ولی در گروه های مختلف سن حاملگی و سن پس از تولد اختلاف معنادار شد (0001/0>P). همچنین یافته ها ارتباط معناداری را بین دو روش اسپکتروفتومتری و پوستی در متغیرهای دموگرافیک نشان داد (0001/0>P).
نتیجه گیری:
به طورکلی روش اندازه گیری پوستی، بیلی روبین را کمتر از روش سرمی تخمین می زند و این اختلاف در نوزادان با سن حامگی و سن پس از تولد کمتر، قابل توجه تر می باشد.
کلید واژگان: بیلی روبین، غربالگری نوزادن، زردی، اسپکتروفتومتری، روش پوستیBackgroundNeonatal jaundice is an almost common problem among neonates that may cause complications such as kernicterus in severe cases. Since early diagnosis and proper treatment of neonatal jaundice is vital to prevent the related complications, it is necessary to check bilirubin before discharging the neonates. There are several evaluating and diagnostic methods to measure the level of bilirubin. Thus, this study aimed to compare the transcutaneous method versus measurement of serum bilirubin, using spectrophotometry for jaundice screening of full-term neonates before discharge from hospital.
MethodsThis observational analytic study was conducted on six hundred neonates with birth weight more than 2000 grams and gestational age more than 35 weeks from September 2012 to March 2013 in Hafez hospital, Shiraz University of Medical Sciences. Parameters such as bilirubin level of neonates were measured and compared, using spectrophotometry and transcutaneous by Bili check with multi waves.
ResultsSix hundred neonates were enrolled in this study. The Pearson correlation test showed that there was a significant correlation between the two methods of the transcutaneous versus measurement of serum bilirubin, using spectrophotometry (r=0.63), (P>0.05). There was no significant difference between the mean of measured bilirubin, using each method in some demographic variables such as the different groups of gender (P=0.896), birth weight (P=0.419), and type of feeding in neonates (P=0.323), but it was significant in other demographic variables such as the different groups of gestational age and post-neonatal age (P<0.0001). Also, the results revealed that there was a significant correlation between two methods of the trans cutaneous versus measurement of serum bilirubin, using spectrophotometry based on demographic variables (P<0.0001).
ConclusionIn general, the bilirubin measurement using trans-cutaneous method may estimate bilirubin significantly less than the serum bilirubin measurement method, and this difference can be more obviously noticeable in infants with less gestational age and also less post-natal age.
Keywords: bilirubin, neonatal screening, jaundice, spectrophotometry, transcutaneous -
فصلنامه پرستاری دیابت، سال هشتم شماره 4 (پاییز 1399)، صص 1212 -1222مقدمه و هدف
از آنجاییکه دیابت نوع1 یک بیماری مزمن و بدون درمان قطعی است، یکی از اهداف مهم سیستم سلامت افزایش خودتوانمندی بیماران در کنترل قندخون و مدیریت بیماری می باشد. با توجه به انجام مطالعات محدود در این گروه سنی، مطالعه حاضر با هدف بررسی تاثیرآموزش خودمدیریتی تیمی بر کنترل قندخون کودکان و نوجوانان دیابتی نوع1 انجام شد.
مواد و روش هادر این مطالعه نیمه تجربی،32 بیمار مبتلا به دیابت نوع یک 18-6 سال وارد مطالعه شدند. در ابتدا HbA1c بیماران اندازه گیری و آموزش های خودمدیریتی توسط تیم درمان ارایه شد. از بیماران درخواست شد که علت افزایش یا کاهش قندخون و میزان قندخون را یادداشت نمایند. این برنامه به مدت 3 ماه و در 6 جلسه تداوم داشت. در نهایت سطح HbA1c، میزان نوسانات قندخون، دفعات افت قندخون و بستری بیمار و دوز انسولین روزانه قبل و بعد از مطالعه با یکدیگر مقایسه شد. داده ها توسط نرم افزار SPSS نسخه 18 آنالیز شدند.
یافته هامیانگین سن شرکت کنندگان 5/0±59/12 سال بود. میانگین سطح HbA1c قبل از برنامه mg/dl 40/96±0/10 و بعد از آن mg/dl 35/85±0/9 بود که این اختلاف میانگین معنی دار بود (0/05>P). دوز انسولین کوتاه اثر در پایان طرح به طور معنی داری کاهش (0/05>P) و دوز انسولین طولانی اثر افزایش یافت (0/05>P). تعداد دفعات بستری و ایجاد هیپوگلیسمی تفاوت معنی داری را قبل و بعد از مطالعه نشان نداد (0/05<P).
نتیجه گیریاز آنجاییکه برنامه خودمدیریتی نقش موثری در کاهش HbA1c و دوز انسولین مصرفی دارد، اجرای آن در بیماران دیابت نوع1 با هدف کنترل بهتر قندخون و کاهش نیاز به مصرف انسولین پیشنهاد می گردد.
کلید واژگان: خودمدیریتی، دیابت نوع یک، تیم مراقبت سلامت، کودک، نوجوانJournal of Diabetes Nursing, Volume:8 Issue: 4, 2021, PP 1212 -1222IntroductionSince diabetic type1 is a chronic and without definitive treatment disease, one of the main goals of health system is increasing of patients’ self-empowerment to control blood sugar and manage the disease. According to doing rare study in this age group, this study aimed to investigate the effect of team self-management training on blood sugar control in children and adolescents with type1 diabetes.
Materials and MethodsIn this quasi-experimental study, 32 patients with type1 diabetes aged 6-18 years old were included. Initially, HbA1c was measured and self-management education was delivered by treatment team. Patients were asked to record the cause of increasing and decreasing of blood sugar and its’ level. This program lasted for three months in six sessions. Finally, HbA1c level, fluctuations in blood sugar, frequency of hypoglycemia and hospitalization, and daily insulin dose were compared pre and post of the study. Data were analyzed by SPSS18.
ResultsThe mean age of participants was 12.59±0.5 years. Mean of HbA1c was 10.96±0.40 mg/dl and 9.85±0.35 mg/dl pre and post of the study, respectively that this mean difference was significant(P<0.05). After study, short-acting insulin dose had significantly decreased(P<0.05) and long-acting insulin dose had increased(P<0.05). The frequency of hospitalizations and hypoglycemia showed no significant difference between before and after the study (P>0.05).
ConclusionSince self-management program had an effective role in decreasing of HbA1c and insulin dose, it is suggested to implement it in care programs of type1 diabetic patients in order to better control blood sugar and reduce insulin requirement.
Keywords: Self-management, Type 1 Diabetes, Health Care Team, Child, Adolescent -
Background
Morbid obesity negatively affects all aspects of quality of life (QOL); therefore, the assessment of QOL can be a useful criterion to evaluate obesity outcome.
ObjectivesThe present study aimed to design a QOL questionnaire in morbid obesity and assess its validation features.
MethodsThis sequential-exploratory mixed-methods study was conducted in both qualitative and quantitative stages. The qualitative stage was carried out through 20 semi-structured interviews with morbidly obese people. Furthermore, the initial items of the questionnaire were obtained by a review of related literature. In the next stage, face, content, and construct validity were assessed. The construct validity was examined by exploratory factor analysis with 319 people. Moreover, Cronbach’s alpha and test-retest correlation coefficient were calculated to evaluate the reliability of the questionnaire. Furthermore, confirmatory factor analysis was assessed.
ResultsBased on the results of the quantitative stage, an 80-item pool was extracted. The exploratory factor analysis yielded six factors that explained 50.62% of the variance. The factors of one to six were as follows: self-dissatisfaction (15 items), functional disorders (7 items), spiro-mental experiences (11 items), perso-social isolation (7 items), physical changes (7 items), and financial pressure (3 items). The final Cronbach’s alpha coefficient of the 50-item questionnaire was calculated at 0.94. Moreover, the intra-class correlation coefficient between the test and retest scores was estimated at 0.97. All indicators of confirmatory factor analysis demonstrated that goodness of fit was acceptable for each factor. Furthermore, this questionnaire had appropriate interpretability, feasibility, and did not have any floor and ceiling effects.
ConclusionThis valid and reliable questionnaire can be used as a suitable measurement tool for assessing the QOL of morbidly obese people in Iran and other countries with similar cultural features. This questionnaire can improve the quality of future clinical research on obesity. In addition, health care providers can perform a peculiar role in the provision of efficient services to patients to prevent obesity and its associated complications.
Keywords: Morbid Obesity, Psychometrics, Quality of life, Questionnaire, Reliability, Validity -
Background
Umbilical vein catheterization is usually conducted for preterm neonates in neonatal intensive care units to administer medication, fluid and nutrition, and blood transfusion. However, catheter tip malposition can cause complications.
ObjectivesThere are different methods to detect the accuracy of catheter’s position; hence, this study aimed to compare the diagnostic accuracy of radiography vs echocardiography to determine the accurate tip position of umbilical vein catheter.
MethodsThis cross-sectional study was performed on all 104 neonates admitted to the neonatal intensive care units of hospitals affiliated to Shiraz University of Medical Sciences from March 2017 to January 2018. At first, the length of the catheter was estimated based on Dunn method. After catheterization, thoraco-abdominal radiography and echocardiography were performed by a pediatric radiologist who was blinded to the study objectives, and the data were recorded in two forms. Finally, data were analyzed by McNemar’s test, using SPSS 17 software.
ResultsThe sensitivity, specificity, positive predictive value and negative predictive value by radiography and echocardiography for the catheter tip position in the inferior vena cava-right atrium junction was calculated 100%. Moreover, catheters were located in the ductus venous, inferior vena cava, inferior vena cava-right atrium junction, right and left atrium in echocardiography were in the radiograph equal to thoracic vertebrae of T9-T11, T9, T6-T10, T5-T8, and T4-T6, respectively.
ConclusionsOur study suggests that even though echocardiography is as reliable as radiography for early detection of the catheter tip position, it can also avoid complications of catheter malposition quicker than radiography
Keywords: Catheterization, Echocardiography, Catheter Position, Radiography, Umbilical Vein -
زمینه و هدف
از آنجاییکه اطلاعات اپیدمیولوژیک در مورد بیماری دیابت نوع 1 در کودکان می تواند در کنترل آن کمک کند، این مطالعه با هدف تعیین فراوانی و ویژگی های مهم بیماران مبتلا به دیابت نوع 1 در یک دوره 11 ساله انجام شد.
مواد و روش هادر این مطالعه گذشته نگر، پرونده کلیه بیماران دیابتی 39-0 ساله بستری شده در بیمارستان نمازی بین سال های 1382 تا 1392 مورد بررسی قرار گرفتند. از آنجاییکه بیشتر موارد جدید در این بیمارستان پذیرش می شوند، داده های حاصل از بیماران این بیمارستان می تواند نماینده خوبی از داده های همه بیماران شیراز باشد. جنسیت، تاریخ تولد، سن شروع و بیماری های مرتبط با دیابت ثبت شد. داده ها با استفاده از نرم افزار SPSS نسخه 22 تجزیه و تحلیل شدند.
نتایجدر این مطالعه 546 بیمار مبتلا به دیابت در بیمارستان بستری شده که 4/52٪ آنها زن بودند. دو سن اوج مشاهده شد (9-5 و 14-10 سال). آمار مرگ دیابت 23٪ بود. در اکثر نمونه ها سابقه خانوادگی انواع مختلف دیابت وجود نداشت. 3/86 % بیماران هیچ بیماری همراه نداشتند. همچنین بین سن شروع بیماری با سابقه خانوادگی مثبت بیماری دیابت و نحوه ارایه بیماری رابطه معنی داری مشاهده شد. تعداد بیماران دیابتی در طول دوره یازده سال روند رو به رشدی داشت.
نتیجه گیریبروز بیماری های دیابت نوع 1 روند رو به رشد داشته و سن اوج بیماری مشابه اکثر مطالعات قبلی است. به هر حال درصد کتواسیدوز دیابتی بیشتر از کشورهای توسعه یافته بود. بنابراین افراد و پزشکان به کسب اطلاعات بیشتر برای تشخیص سریع تر دیابت نوع 1 و جلوگیری از عوارض آتی توصیه می شوند.
کلید واژگان: دیابت ملیتوس، نوع یک، کتواسیدوز دیابتی، اپیدمیولوژیBackground & ObjectiveSince epidemiological information on type1 diabetes in children can help to control it, this study aimed to determine the frequency and characteristics of type1 diabetes patients during an 11-year period.
Materials & MethodsIn this retrospective study, records of all 0-39 years old diabetic patients admitted to Nemazee hospital 2004-14 were reviewed. Since most new cases are admitted to this hospital, the patient’s data might be a good representative of all patients in Shiraz. Gender, date of birth, age of onset and associated diseases were recorded. Data were analyzed, using SPSS 22.0.
ResultsIn this study, 546 diabetes patients were admitted, of which 52.4% were females. Two peak age was observed (5-9 Y/O and 10-14 Y/O). The mortality rate was 23%. Most of them had no family history of diabetes. Majority of patients (86.3%( did not have any other medical condition. Moreover, there was a significant relationship between age of onset with positive family history and mode of presentation. The frequency of diabetic patients had a rising trend during this eleven-year period.
ConclusionIncidence of type1 diabetes had a growing trend and peak age of presentation was similar to most previous studies. However, the percentage of diabetic ketoacidosis was more than that of developed countries. Therefore, people and physicians are recommended to have more information on type1 diabetes for early diagnosis to prevent further complications.
Keywords: Diabetes Mellitus, Type 1, Diabetic Ketoacidosis, Epidemiology -
BACKGROUND
Morbid obesity is rising around the world. Surgery is a selective treatment intervention for it. Since most of the surgeons use weight loss for evaluating of the morbid obesity surgical outcomes and paying attention to the the quality of life (QOL) and body image evaluation are rare, this study aimed to assess the QOL and body image in pre‑ and postsurgery with other interventions.
MATERIALS AND METHODSThis case–control study was done on 200 morbidly obese patients (n = 100 in each group) who referred to the obesity clinic in Shiraz. The data were collected by Body Image Concern Inventory and 12‑item Short Form Survey. The data were analyzed by t‑test, Pearson correlation coefficient test, analysis of variance, and regression analysis. P = 0.05 was considered as significant.
RESULTSThe paired t‑test showed a significant difference in mean scores of body image (P < 0.001) and all dimensions of the QOL (P < 0.001) in the case and control groups. In the case group, there was a significant difference between the mean scores of the QOL and the different categories of body mass index (BMI) in postsurgery (P < 0.05) and the different mean scores of body image and the different categories of BMI in pre‑ and postsurgery wasn’t significant (P > 0.05). Age was a predictor variable for the QOL of morbidly obese persons after surgery (P < 0.001). After surgery, men showed better QOL than women (P < 0.001).
CONCLUSIONFinal results indicated that body image and QOL defects caused by obesity could be more improvement after surgery. This study can promote health‑care team’s knowledge about holistic supporting of all dimensions’ QOL of obese individuals. It is suggested that supporting interventions should be done as effective methods of maintenance for effects of weight loss methods such as surgery.
Keywords: Body image, morbid obesity, quality of life, surgery -
International Journal of Community Based Nursing and Midwifery, Volume:7 Issue: 2, Apr 2019, PP 138 -149BackgroundMorbid obesity (body mass index≥40 kg/m2 or >35 kg/m2 with co-morbidity) is an important factor in reducing the quality of life which is influenced by the characteristics of the individual, his social, cultural, and environmental conditions; also, each disease has unique effects on it. Although most of the studies have been conducted on obesity (25>BMI>40), how to prevent it and improve life quality, there is lack of knowledge about what morbid obese people really experience about their life quality. Thus, this qualitative study aimed to explore the viewpoints of morbid obese people about life quality.MethodsIn this conventional content analysis, data were collected using semi-structured interviews with 20 morbid obese patients who were referred to nutrition and obesity clinics of Shiraz and Ahvaz Jundishapur University of Medical Sciences. Purposeful sampling was processed from May 2016 to January 2017. The sampling continued until data saturation. Each interview was recorded by audio recorder and typed in the MAXQDA10 software. Data were analyzed after each interview. The meaning units were encoded and the codes were categorized. This trend continued until the main and sub-categories emerged.ResultsData analysis indicated 1835 codes, 76 sub-subcategories, 26 subcategories and 6 main categories including physical changes, psychological experiences, socio-personal dysfunction, negative body image, financial pressure, and change in the spirituality.ConclusionFinal results indicated that life quality had a special definition in morbid obesity and includes very different dimensions. This study can promote health care providers’ knowledge (nurses) for supporting obese people and improving their quality of life by community-based care approaches.Keywords: Morbid obesity, Iran, Qualitative study, Quality of life
-
BackgroundAdvances in medical science and success in increasing the survival rate of vulnerable infants have raised the future evolution issues of these children. Developmental and behavioral disorders are the most common problem in children after discharge from NICU. A lot of factors are involved in the occurrence of developmental disorders.ObjectivesAccording to the importance of the subject and lack of accurate regional information, this study aimed to investigate the developmental disorders and related factors in low weight infants.MethodsThis retrospective cohort study was performed on 76, 4 - 12 month-old infants with a history of hospitalization in NICU of Shiraz Hazrat Zeinab Hospital with an average weight of 1800 grams. These infants were evaluated developmentally by ASQ (Age and stage questionnaire). The data was analyzed by statistical tests.ResultsUsing ASQ, 17% of children were detected as having developmental disorders. The percentages of developmental disorders for fine and gross motor domains, problem solving ability, communication and personal-social behaviors were 14.5%, 23.7%, 19.7%, 17.6% and 14.5%, respectively. The correlation coefficient statistical test did not show any significant relationship between developmental disorder with mechanical ventilation, duration of hospitalization, surfactant and betamethasone injection, and final diagnosis of diseases (r < 1).ConclusionsAlthough improvement in respiratory therapy, monitoring system, non-invasive procedures and developmental care have decreased neonatal mortality rate and prematurity complications, but we cannot find any relationship between related risk factors and neurological outcomes. Developmental delay of low birth weight infants must be detected and rehabilitation started soon after discharge from NICUKeywords: Low Birth Weight, Developmental Disorders, Neonatal Intensive Care Unit (NICU)
-
International Journal of Community Based Nursing and Midwifery, Volume:6 Issue: 2, Apr 2018, PP 175 -184BackgroundMorbid obesity is rising around the world. It can cause unpleasant appearance and body image. Most of the studies have aimed to evaluate the psychopathology of overweight and obesity and paying attention to mental well-being in morbid obese individuals is rare. Therefore, this study aimed to assess the relationship between body image and psychological well-being in morbid obese patients.MethodsThis cross-sectional study, using simple random sampling method, was done on 124 morbid obese patients who referred to obesity clinic in Shiraz from 2016 to 2017. The data were collected by body image index and psychological well-being questionnaire. Results were analyzed using descriptive statistics, Pearson correlation coefficient test, ANOVA, and Regression analysis.ResultsThe results showed a significant relationship between body image and psychological well-being (r=0.43) (P0.05).ConclusionFinal results indicated that body image defects caused by obesity could lie in negative psychological well-being in all aspects. This study can promote health clinicians knowledge in supporting of mental status of obese individuals. It is suggested that preventing and supporting intervention should be performed as effective methods for encountering and coping with psychological effects of obesity.Keywords: Body image, Morbid obesity, Psychological
-
BackgroundSince studies have demonstrated that morbid obesity can exponentially impair quality of life, the measurement of quality of life is paramount to monitoring the effects of treatment and influences the development of clinical pathways, service provision, healthcare expenditures, and public health policy. Accordingly, clinicians, researchers, and policy makers must rely on valid instruments.
Aim: This study aimed to review and critique the psychometric properties of some specific tools by COSMIN checklist and their application among morbidly obese individuals.MethodWe searched PubMed, Web of Science, PsycINFO, Ovid, Elsevier, and ScienceDirect by using the keywords related to the Quality of Life Questionnaire, namely morbid obesity, tool, and scale, to retrieve articles published during 1989-2017. Then, the psychometric properties of the selected tools were assessed using the COSMIN checklist.ResultsMost of the tools had not reported complete and desirable psychometrics properties. Demonstration of responsiveness from independent randomized controlled trials was not available in two of the eight questionnaires. These tools also did not report proper definition of interpretability. However, the data obtained by COSMIN checklist showed that Laval questionnaire is a proper scale for measuring quality of life in obese individuals, which can be recommended to researchers.
Implications for Practice: Although Laval questionnaire was found a proper tool for measuring the quality of life among morbid obese patients, developing an instrument suitable for different societies with varied cultural and social characteristics is suggested because socio-cultural factors can influence the quality of life.Keywords: Checklist, Obesity, Morbid, Psychometric, Quality of life, Review of literature -
زمینه و هدفپیشرفت درعلم پزشکی و موفقیت در افزایش میزان بقای نوزادان آسیب پذیر، مسئله ی میزان تکامل عصبی این کودکان در آینده را مطرح کرده است. اختلالات تکاملی و رفتاری، شایع ترین مشکل در این نوزادان پس از ترخیص از بخش مراقبت ویژه نوزادان می باشد. طیف وسیعی از علل در بروز اختلالات تکاملی نقش دارند. با توجه به اهمیت موضوع و کمبود اطلاعات دقیق در خصوص عوامل خطر مربوطه، در این مقاله به بررسی عوامل مرتبط با اختلالات تکاملی نوزادان کم وزن با سابقه مراقبت در بخش مراقبت ویژه نوزادان پرداخته شد.روش کاراین مطالعه کوهورت بر روی 76 نوزاد 24-4 ماهه با سابقه بستری در بخش مراقبت های ویژه بیمارستان حضرت زینب (س) شیراز با میانگین وزنی (1800گرم) انجام شد. این نوزادان بر اساس پرسشنامهASQ ارزیابی تکاملی گردیدند. اطلاعات با استفاده از آزمون های آماری تجزیه و تحلیل شدند.یافته هادر ارزیابی با آزمون ASQ، آزمون آماری ضریب همبستگی ارتباط معنی داری را بین اختلال تکاملی با تهویه مکانیکی، مدت زمان بستری، تزریق سورفکتانت و بتامتازون، تشخیص اولیه و نهایی بیماری ها نشان نداد (1r<). آزمون T-Test تفاوت معنی داری را بین میانگین وجود زایمان پرخطر و میانگین انجام عمل احیای پیشرفته در کودکان دچار اختلال تکاملی و کودکان سالم نشان نداد (05/0p>).نتیجه گیریهرجند پیشرفت در تنفس درمانی، سیستم نظارت، روش های غیرتهاجمی، و مراقبت تکاملی، باعث کاهش مرگ و میر نوزادان نارس و کاهش عوارض درمان نارسی شده است، در این مطالعه ارتباطی بین وضعیت تکاملی کودکان 4 تا 24 ماهه نارس با مشکلات آن ها در بخش مراقبت های ویژه نوزادان دیده نشد. برای کسب نتایج تکاملی بهتر، بایستی اختلالات تکاملی را در سریع ترین زمان ممکن شناسایی کرده و توانبخشی نوزادان کم وزن را، در کوتاه ترین زمان پس از ترخیص از بخش مراقبت ویژه آغاز نماییم.کلید واژگان: نوزادان کم وزن، اختلالات تکاملی، عوامل مرتبط، بخش مراقبت های ویژه نوزادان، آزمون ASQBackgroundAdvances in medical science and success in increasing the survival rate of vulnerable infants has raised the future evolution issues of these children. Developmental and behavioral disorders are the most common problem in children after discharge from Neonatal Intensive Care Unit (NICU).An extensive range of factors involve in the occurrence of developmental disorders. According to the importance of the subject and lack of accurate information in the field of risk factors, related factors with the developmental disorders was investigated in this article, in low weight infants with history of care in NICU.MethodsThis Cohort study was performed on 76, 4-24 month-old infants with a history of hospitalization in NICU of Shiraz Hazrat Zeinab (SA) hospital with an average weight of (1800gr). The information on pregnancy, child birth and problems during hospitalization was registered. These 4-24 month-old infants were evaluated developmentally according to Age & stage questionnaire (ASQ). The data was analyzed by statistical tests.ResultsIn the conducted evaluation using ASQ, the correlation coefficient statistical test did not show any significant relationship between developmental disorder with mechanical ventilation, duration of hospitalization, surfactant and betamethasone injection, initial and final diagnosis of diseases (r 0.05).ConclusionAlthough improvement in respiratory therapy, monitoring system, non-invasive or minimal invasive procedures and developmental care were decrease neonatal mortality rate and prematurity complications, but we cannot find any relationship between NICU-related risk factors and neurologic outcome. For better outcome we must detect developmental delay as soon as possible and start early rehabilitation of low birth weight infants after discharge from NICU.Keywords: Low Birth Weight, Developmental Disorders, Related Factors, Neonatal Intensive Care Unit (NICU)
-
زمینه و هدفپژوهش حاضر مطالع های توصیفی، کاربردی و تطبیقی است که به منظور ارائه ی الگو از تکنیک دلفی سه مرحله ای استفاده کرده است. مطالعه در فاصله ی سال های 1385 - 1381 صورت گرفته و هدف اصلی، ارائه ی مدلی برای بیمه های سلامت خصوصی در ایران با توجه به تجربیات کشورهای دیگر است.روش بررسیاین مطالعه با محوریت سازمان و مدیریت، به بررسی مبنای پوشش جمعیت، مبنای محاسبه ی حق بیمه، تعهدات و کلیات سیستم م یپردازد. علاوه بر این میزان مشارکت بیماران در برخورداری از خدمات، شاخص های مهم سلامتی و سازمانی و تاریخچه ی بیمه های سلامت خصوصی همراه با رو کیردهای موجود در آینده نیز مورد بررسی و تدقیق قرار گرفته است.
کشورهای مورد مطالعه عبارتند از آمر کیا، آلمان، اسپانیا، اتریش، تر یکه، سوئد، یونان، مکز کی، ژاپن، کانادا، دانمارک و ایران، انتخاب کشورها بر مبنای تقسیم بندی نظام های سلامت و ویژگی هایی از جمله عضویت در OECD و داشتن تجربیاتی در مورد بیم ه های سلامت خصوصی بوده است.یافته هابیمه های سلامت خصوصی با هدف پرکردن شکا فهای خدمتی و هزینه ای موجود در پوشش های بیمه ای پایه، افزایش رضایت مندی مردم و ایجاد قدرت انتخاب برای افراد با توانایی مالی بهتر به وجود آمده است.
مبنای پوشش بیمه های سلامت خصوصی در اکثر کشورها مبنای سکونت و توانایی پرداخت است و اولویت با ارائه ی پوش شهای گروهی است. نقش دولت در ابتدا قانون گذاری است، علاوه بر این در شروع فعالیت شرکت های بیمه ای نقش حمایت کننده و بعد از آن نقش نظارتی پیشنهاد شده است. منبع اصلی تامین منابع مالی بیم ه های خصوصی،حق بیم ه هاست که با توجه به معیارهایی چون ریسک فردی و وضعیت سلامتی نوع بسته ی مزایا، گروهی با انفرادی بودن پوشش، سن، جنس تعیین می شود. نظارت بر بیمه های سلامت خصوصی به صورت غیر متمرکز و به وسیله ی سازمان های مستقل محلی با تر یکبی از نماینده ی مصرف کنندگان و به تعداد مساوی نماینده ی ارائه دهندگان باید به صورت غیر مستقیم صورت م یپذیرد. خدمت به سازمان های بیمه ای، نماینده ی دولت، نمایند هی قوه قضائیه و بر اساس چک لیست های استاندارد شده صورت م یپذیرد.نتیجه گیرینظارت عالی از بالاترین مرجع سیاست گذاری که در این مطالعه شورای عالی سلامت کشور پیشنهاد شده است.
کلید واژگان: بیمه ی سلامت خصوصی، مطالعات تطبیقی، شکاف خدمتی، شکاف هزینه ای، بیمه ی سلامت مکمل، تکنیک دلفیBackground And ObjectiveSome of high income countries are developing the private health insurance coverage as a complementary or supplementary coverage.MethodsWe examined the private health insurance in England U.S.A, Germany, Spain, Austria, Turkey, Sweden, Greece, Mexico, Japan, Canada, Denmark and Iran between 2002 and 2006 for studding private health insurance coverage. We used data from the OECD, European Observatory and country specific resources; also we reviewed specific regulations in certain countries, based on this comparative study we designed a model for private health insurance coverage in Iran after approving by specialist in Delphi technique. The private health insurance has been created in order to cover the cost and service gapes which excite in the current basic insurance also increase the satisfaction of insured and make the choice authority for people who have higher incomes. Premiums are the main source of financial support in the private health insurance which is entertained from individual risks and criteria within health condition. In addition Legislation is primary role of government, in addition supporting role in beginning of the work and after that supervising role were suggested. Based on specialist opinions the private health insurance in Iran private health insurance could be covered the gaps of basic health insurance as a complementary or supplementary health insurance based on residency and ability to pay.Keywords: Private health insurance, Comparative Study, Complementary Health Insurance, Voluntary Health Insurance, Financing, Benefit Package
- در این صفحه نام مورد نظر در اسامی نویسندگان مقالات جستجو میشود. ممکن است نتایج شامل مطالب نویسندگان هم نام و حتی در رشتههای مختلف باشد.
- همه مقالات ترجمه فارسی یا انگلیسی ندارند پس ممکن است مقالاتی باشند که نام نویسنده مورد نظر شما به صورت معادل فارسی یا انگلیسی آن درج شده باشد. در صفحه جستجوی پیشرفته میتوانید همزمان نام فارسی و انگلیسی نویسنده را درج نمایید.
- در صورتی که میخواهید جستجو را با شرایط متفاوت تکرار کنید به صفحه جستجوی پیشرفته مطالب نشریات مراجعه کنید.