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فهرست مطالب نویسنده:

mitra zandi

  • Mohammadhossein Akbarpour, Mitra Zandi*, Ladan Sedighi, Mojtaba Ghanbari Ghalesar
    Background

    Olfactory dysfunction, a prominent complication of COVID-19, significantly impacts patients' quality of life, persisting for months after infection. Exploring diverse methodologies to address this issue necessitates scholarly investigation. Therefore, our primary objective was to assess the impact of olfactory training on enhancing olfaction sense among COVID-19 patients.

    Methods

    This randomized controlled trial employed a pretest-posttest design to assess COVID-19 patients experiencing olfactory dysfunction at the Babol Health Center in northern Iran. Patients were allocated to either the control or intervention group using closed envelopes. Both groups, consisting of 50 patients each, completed the Olfactory Disorders - Negative Statements (QOD-NS) questionnaire before the intervention. Over a six-week period, participants in the intervention group were exposed to Phenylethyl alcohol, Eucalyptus, Citronol, and Eugenol twice daily, rotating each scent for 20 seconds with ten-second breaks in between, while the control group received no intervention. Independent and paired t-tests were utilized to analyze the relationship between the groups before and after the intervention, with analysis conducted using SPSS 16. The significance level was set at less than 0.05.

    Results

    The mean score of olfactory disorder among patients before the intervention in both the intervention and control groups was 24.32 ± 6.60 and 22.85 ± 8.04, respectively, showing no significant difference (P = 0.33). However, following the intervention, the scores decreased to 19.60 ± 5.74 and 22.52 ± 7.39 in the intervention and control groups, respectively, with a statistically significant difference observed (P = 0.034).

    Conclusion

    Olfactory training demonstrated effectiveness in enhancing olfaction sense among patients with COVID-19 experiencing olfactory disorders. Consequently, it is recommended that nurses be trained to administer this program to COVID-19 patients with olfactory disorders upon discharge, facilitating their recovery process.

    Keywords: Olfaction Disorders, COVID-19, Olfactory Training, Aromatherapy
  • سارا دستور، میترا زندی*، معصومه کریمیان
    مقدمه

    پرسنل اورژانس به دلیل ماهیت فعالیتشان ممکن است که در معرض خشونت در محیط کار قرار گیرند و استرس شغلی در آنها ‏افزایش یابد. این پژوهش با هدف بررسی تاثیر آموزش مجازی خودمدیریتی مهارت های ارتباطی بر استرس شغلی و میزان خشونت ‏علیه کارکنان اورژانس بیمارستان های وابسته به دانشگاه علوم پزشکی شهید بهشتی انجام شد.‏

    روش کار

    در این مطالعه نیمه تجربی، 60 نفر از کارکنان اورژانس به صورت نمونه گیری دردسترس انتخاب و با تخصیص تصادفی، به 30 نفر ‏در گروه آزمون و 30 نفر در گروه کنترل تقسیم شدند و در دو مرحله پرسشنامه های اطلاعات جمعیت شناختی و زمینه ای، استرس ‏شغلی بیمارستانی و خشونت محل کار در بخش سلامت را تکمیل کردند. بعد از تکمیل پرسشنامه ها در مرحله اول، مداخله به مدت ‏‏6 هفته و هر هفته یک سرفصل به گروه آزمون داده شد. داده ها نرم افزار SPSS نسخه 21 با آزمون های کای اسکور، کروسکال ‏والیس و ویلکاکسون تجزیه وتحلیل گردید.‏  

    یافته ها

    نتایج نشان داد که میانگین استرس شغلی قبل از مداخله در بین دو گروه مداخله و کنترل اختلاف معناداری نداشتند (117/0= ‏p‏)؛ ‏اما در بعد از مداخله، میانگین نمره استرس شغلی در بین دو گروه مداخله و کنترل اختلاف معناداری داشتند (034/0= ‏p‏)؛ در گروه ‏مداخله فراوانی تجربه خشونت فیزیکی، خشونت روانی (لفظی) در بعد از مداخله نسبت به قبل از مداخله بیشتر از گروه کنترل ‏کاهش یافته بود. همچنین فراوانی تجربه خشونت جنسی و نژادی در گروه کنترل بیشتر از گروه مداخله کاهش یافته بود؛ اما از نظر ‏آماری معنی دار نبود.‏

    نتیجه گیری

    بر اساس نتایج پژوهش حاضر، آموزش مجازی خودمدیریتی مهارت های ارتباطی توانسته است بر استرس شغلی تاثیر بگذارد اما بر ‏میزان خشونت علیه کارکنان اورژانس تاثیر نداشته است؛ بنابراین تهیه برنامه آموزشی جامع عوامل موثر بر خشونت علیه کارکنان ‏اورژانس، در کنار مهارت های ارتباطی و انجام مداخلات آموزشی در مدت زمان طولانی تر پیشنهاد می شود.‏

    کلید واژگان: اورژانس, آموزش مجازی, استرس شغلی, مهارت های ارتباطی, خشونت
    Sara Dastur, Mitra Zandi*, Masoumeh Karimian
    Introduction

    Emergency technicians face workplace violence and increasing occupational stress. The purpose of this study was to investigate the impact of a virtual self-management training in communication skills on occupational stress and the degree of aggression among emergency technicians.

    Material and Methods

    This study involved 60 emergency technicians randomly assigned to either the intervention or control group. They completed surveys on workplace violence and occupational stress. The intervention group received six weeks of a virtual self-management training in communication skills. Data was collected after two months and analyzed using SPSS software.

    Results

    The findings showed that there was no statistically significant difference between the control group (110.08±11.92) and the two intervention groups (114.39±11.25) in terms of the average occupational stress before the intervention; The average job stress score between the intervention (94.0±12,70) and control (98.81± 20,81) groups significantly differed following the intervention (p=0.034); After the intervention, the intervention group had lower verbal and physical abuse frequencies compared to the control group.

    Conclusion

    The virtual self-management communication training demonstrated the potential to reduce occupational stress but did not significantly decrease the violence towards the emergency technicians. A comprehensive training program addressing violence factors and communication techniques, implemented over a longer period, is recommended.

    Keywords: Emergency, Virtual Education, Occupational Stress, Communication Skills, Violence
  • Mitra Zandi, Sahar Dabaghi, Atefe Salimi Akinabadi, Narges Bagheri Lankarani, Reza Omani Samani, Mostafa Abdolmaleki
    Background

    The efficacy of Assisted Reproductive Techniques (ARTs) or technologies used to treat infertile couples has been approved. One such technique is embryo donation. However, there is insufficient knowledge of the experiences of mothers receiving donated embryos. Thus, the present study was conducted with the aim to determine the experiences of mothers receiving donated embryos.

    Materials and Methods

    This qualitative conventional content analysis study was conducted in 2018 for 8 months (from February to September). The research setting was Royan Institute. Mothers receiving donated embryos were selected from among those who were pregnant or were at the postpartum stage using the purposive sampling method. A total of 15 interviews were performed with 13 participants. The qualitative data were collected using deep unstructured interviews and analyzed using the Graneheim and Lundman (2004) method in (version 10; VERBI GmbH, Berlin, Germany) software.

    Results

    Data analysis resulted in 412 open codes that were then categorized into 7 main categories and their subcategories. The main categories were as follows: sociocultural constraint, feeling of insecurity in personal and family identity, protection of personal and family identity, confounded support, pressure and hardship, and achieving relative tranquility.

    Conclusions

    The results of this study showed that the mothers who underwent embryo donation experienced feelings of insecurity regarding both individual and family identities, were confronted with sociocultural difficulties, and faced various pressures. It is suggested that future care plans be focused on the identity crisis of these families and the children resulting from these methods, and that future plans balance the socioeconomic pressures resulting from the use of these methods.

    Keywords: Assisted reproductive techniques, embryo transfer, infertility, qualitative study
  • Sahar Dabaghi, Mitra Zandi, Abbas Abbaszadeh, Abbas Ebadi
    Introduction

    Patient safety is a key indicator and element in securing quality healthcare and this goal is multi-step, systemic, and multidisciplinary. The aim of the study was to investigate the meanings and definitions of “feeling of safety” in patient’s view and experiences during their hospital stay and to identify the antecedents and consequences of the concept.

    Methods

    This qualitative systematic review was carried out based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2009. Six databases (PubMed, Web of Science, Scopus, ProQuest, Embase, Cochrane) were searched up to 2019 with no time and language limit. Two authors individually evaluated the study quality using Joanna Briggs Institute Qualitative Assessment and Review Instrument (JBI-QARI). Data from studies meeting the inclusion criteria were analyzed with concept analysis using of Walker and Avant approach (2011).

    Results

    Twenty-five papers were included in this study. Data analysis resulted finally in eleven main categories: “receiving safe care”, “appropriate physical environment”, “resorting to spirituality”, “having previous negative experiences”, and “presence of family and friends”, “Feeling of Protection in a Safe Place”, “Emotional Enrichment and Confidence”, “Comfort and Tranquility”, “Feeling of Control on the Situation”, “Optimism towards Life” and “Coping”.

    Conclusions

    Safe care is one of the fundamental needs in creating feeling of safety in patients. Focusing on this type of patient-centered care may promote quality care and improve the treatments provided in the hospital setting.

    Keywords: Systematic Review, Qualitative Research, Safety, Patients, Patient Safety Hospitalization, Perception
  • سعید رستمی*، کیانوش نیرومند زندی، مهناز ایلخانی، میترا زندی
    مقدمه

    یوگا یکی از برنامه های بازتوانی می باشد که ذهن و بدن را برای پیامدهای مثبت سلامت درگیر می کند و نقش مهمی در پیشگیری از بیماری های قلبی عروقی دارد. این مطالعه با هدف تعیین تاثیر تمرینات تنفسی و آرام سازی یوگا بر تنش، افسردگی و اضطراب در بیماران تحت عمل جراحی پیوند عروق کرونر انجام شد.

    روش کار

    این مطالعه تجربی مداخله ای، در سال 1395 در شهر کرمانشاه انجام شد. در این پژوهش، تعداد100 بیمار آماده جراحی پیوند عروق کرونر به صورت تصادفی به گروه آزمون (تعداد 50 بیمار) و گروه شاهد (تعداد 50 بیمار) در بیمارستان های منتخب تقسیم شدند. تمرینات تنفسی و آرام سازی یوگا به مدت سه روز قبل و سه روز بعد از برداشتن لوله تراشه در گروه آزمون انجام شد. داده ها توسط پرسش نامه dass21 قبل و بعد از پایان مداخله جمع آوری شدند. سپس با استفاده از نرم افزار SPSS و آزمون های آماری تی مستقل، تی زوجی، اسپیرمن و من ویتنی مورد تجزیه و تحلیل قرار گرفتند.

    یافته ها

    مطابق با یافته ها ارتباط معنی داری بین توزیع فراوانی جنسیت، وضعیت تاهل، تحصیلات، وضعیت شغلی و سن بیماران در دو گروه مورد و شاهد یافت نشد(0.05 < P-Value). بین میانگین امتیازات تنش، اضطراب و افسردگی نمونه های پژوهش قبل و بعداز مداخله در گروه مورد تفاوت معنی داری وجود داشت(0.05P-Value<). در حالی که این تفاوت در گروه شاهد معنی دار نبود. همچنین تفاوت معنی داری بین میانگین متغیرهای تنش، اضطراب و افسردگی در دو گروه مورد و شاهد بعد از انجام مداخله وجود داشت(0.05P-Value<).

    نتیجه گیری

    با انجام تمرینات کم هزینه و ساده تنفسی و ارامسازی یوگا در بیماران تحت جراحی پیوند عروق کرونر می توان در راستای بهبودی و پیشگیری از مشکلات روانشناختی به خصوص اضطراب، تنش و افسردگی گام برداشت.

    کلید واژگان: تمرینات تنفسی, یوگا, تنش, اضطراب, افسردگی, جراحی عروق کرونر
    Saeid Rostami*, Kianoush Niroumand Zandi, Mahnaz Ilkhani, Mitra Zandi
    Introduction

    Yoga is one of the rehabilitation programs that engage the mind and body for positive health outcomes and it plays an essential role in the prevention of cardiovascular disease. The aim of this study was to determine the effect of breathing exercises and yoga relaxation on tension, depression and anxiety in patients undergoing coronary artery bypass graft surgery.

    Methods

    This experimental- intervention study was done in Kermanshah city in 2016. In this study, 100 patients with coronary artery bypass graft surgery were randomly divided into test group (50 patients) and control group (50 patients) in selected hospitals. Breathing exercises and yoga relaxation were performed for three days before and three days after removing the endotracheal tube in the case group. Data collection tool was dass21 questionnaire which was measured before and after the intervention. Then, the findings were analyzed using SPSS software and independent t-test, paired t-test, Spearman and Mann-Whitney test.

    Results

    According to the findings, no significant relationship was found between the frequency distribution of gender, marital status, education, employment status and age of patients in the case and control groups (P-Value > 0.05). There was a significant difference between the mean scores of tension, anxiety and depression before and after the intervention in the case group (P-Value < 0.05). While this difference was not significant in the control group. There was also a significant difference between the mean of tension, anxiety and depression in case and control groups after the intervention (P-Value < 0.05).

    Conclusion

    By performing low-cost and simple breathing exercises and relaxing yoga in patients undergoing coronary artery bypass graft surgery, can act to improve and prevent psychological problems, especially anxiety, tension and depression.

    Keywords: breathing exercises, yoga, tension, anxiety, depression, coronary artery surgery
  • Sorour Khari, Mitra Zandi*, Mahmoud Yousefifard
    Introduction

    There is no consensus on the performance of decision rules in predicting the prognosis of traumapatients. Therefore, the present study aimed to compare the value of Glasgow coma scale (GCS) and physiologicscoring systems in predicting mortality and poor outcome of trauma patients.

    Methods

    This diagnostic accu-racy study was conducted on multiple trauma patients admitted to the intensive care units of two hospitals inTehran, Iran, from 21 November 2020 to 22 May 2021. The patients’ demographic characteristics, length of stayin the intensive care unit (ICU), the vital signs, and the GCS on admission were recorded. Finally, the mortal-ity, disability, and complete recovery of patients at the time of discharge were evaluated and receiver operatingcharacteristics (ROC) curve analysis was used to compare the performance of physiologic scoring systems withGCS.

    Results

    200 trauma patients with the mean age of 43.53±19.84 years were evaluated (74% male). The areaunder the ROC curve for New Trauma Score (NTS), Revised Trauma Score (RTS), Worthing Physiological Scor-ing System (WPSS), Rapid Acute Physiology Score (RAPS), Rapid Emergency Medicine Score (REMS), ModifiedEarly Warning Score (MEWS), National Early Warning Score (NEWS), Glasgow Coma Scale, Age, and SystolicBlood Pressure score (GAPS) ,Glasgow coma scale (GCS) in prediction of mortality were 0.95, 0.95, 0.83, 0.89,0.91, 0.84, 0.77, 0.97, and 0.98 respectively. The performance of GCS was statistically superior to RTS (P=0.005),WPSS (P=0.0001), RAPS (P=0.0002), REMS (P=0.002), MEWS (P<0.0001), and NEWS (P<0.0001). However, theperformance of GCS, NTS (P=0.146), and GAPS (P=0.513) were not significantly different. Also, in predictionof poor outcomes, the AUC of GCS (0.98) was significantly higher than RTS (0.95), RAPS (0.85), REMS (0.85),MEWS (0.84), NEWS (0.77), and WPSS (0.75).

    Conclusion

    The GCS score seems to be a better instrument topredict mortality and poor outcome in trauma patients compared to other tools due to its high accuracy, wideapplication, and easy calculation.

    Keywords: Wounds, Injuries, Clinical Decision Rules, Patient outcome assessment, Glasgow coma scale, Intensive careunits
  • سلیمه اکبرزاده، میترا زندی*، سپیده حاجیان، لیلا نظری، ملیحه نصیری
    مقدمه

    توجه به نیازهای زوجین نابارور و مشارکت دادن آنها در برنامه درمان، به آنها این اجازه را می دهد تا به صورت موثرتری به مقابله با این مشکل بپردازند. مراقبت بیمار محور بر این اصل استوار است که کل منابع و فعالیت های سازمان باید حول محور بیمار سازماندهی شود. مطالعه حاضر با هدفبررسی کیفیت ارایه مراقبت بیمار محور از دیدگاه مددجویان نابارور انجام شد.

    روش کار

    این مطالعه توصیفی در سال 1398 بر روی 200 مددجوی نابارور مراجعه کننده به مراکز کمک باروری بیمارستان های منتخب شهید بهشتی انجام شد. گردآوری داده ها با استفاده از پرسشنامه بیمار محوری در مددجویان ناباروری انجام شد. این پرسشنامه مشتمل بر 50 سوال در 8 حیطه شامل: حیطه دسترسی، اطلاعات، ارتباطات، مشارکت بیمار، احترام به ارزش های بیمار، تداوم و حمایت از بیمار، صلاحیت کارکنان و حیطه سازمان مراقبت است که حداقل نمره در هر حیطه صفر و حداکثر 3 می باشد. تجزیه و تحلیل داده ها با استفاده از نرم افزار آماری SPSS (نسخه 18) و آزمون های توصیفی و رگرسیون انجام شد.

    یافته ها

    بیشترین عامل ناباروری مربوط به زنان با 132 نفر (0/66%) و سپس عامل مشترک مردانه و زنانه با 62 مورد (0/31%) بیان شده بود. میانگین طول مدت ناباروری 67/3±35/5 سال به دست آمد. نتایج این پژوهش نشان داد که در بازه امتیازی بین 3-0، میانگین محوریت بیماران در درمان ناباروری 50/1 بود. پایین ترین میزان بیمار محوری مربوط به حیطه دسترسی (37/0 از 3) و بالاترین آن مربوط به حیطه سازمان مراقبت (40/2 از 3) بود.

    نتیجه گیری

    کیفیت مراقبت بیمار محور سطح متوسط (5/1) از سطح مطلوب (3) به دست آمد، لذا ضروری است که زیرساخت های نظام سلامت کشور اصلاح شده و رویکرد بیمار محور به طور گسترده در کشور آموزش و اجرا شود. در جهت عملیاتی شدن این مهم باید همچنین عوامل تاثیرگزار بر مراقبت بیمار محور را شناسایی نمود.

    کلید واژگان: پرستاری بیمار محور, مراقبت بیمار محور, ناباروری
    Salimeh Akbarzadeh, Mitra Zandi *, Sepideh Hajian, Leila Nazari, Malihe Nasiri
    Introduction

    Paying attention to the needs of infertile couples and involving them in the treatment program allows them to deal with this problem more effectively. The patient-centered care is based on the principle that all resources and activities of the organization should be organized around the patient. This study was performed with aim to evaluate the quality of patient-centered care from the viewpoints of infertile clients.

    Methods

    This descriptive study was performed in 2019 on 200 infertile clients referring to the assisted reproductive centers of Shahid Beheshti selected hospitals. Data were collected using a patient-centered questionnaire in infertile clients. This questionnaire consists of 50 questions in 8 areas including: access, information, communication, patient participation, respect for patient values, patient's continuity and support, staff's competence and care organization area; the minimum score in each area is zero and maximum is 3. Data were analyzed using SPSS software (version 18) and descriptive and regression tests.

    Results

    According to the results, the most infertility factor was related to female factor with 132 cases (66.0%) and then the common factor of male and female with 62 cases (31.0%). The mean duration of infertility was 5.35±3.67 years. The results of this study showed that in the score range between 0 and 3, the mean focus of patients in infertility treatment was 1.50. The lowest patient-centered score was related to access area (0.37 from 3) and the highest was related to care organization area (2.40 from 3).

    Conclusion

    According to the results of the study, the quality of patient-centered care has been obtained moderate-level (1.5) from the desired level (3). It is necessary to reform the infrastructure of the country's health system and the patient-centered approach be widely trained and implemented in the country. In order to make this important, we should identify the influencing factors on patient-centered care.

    Keywords: Infertility, Patient-centered care, Patient-Centered Nursing
  • Zahra Kolahi, Mitra Zandi*, Roghayeh Esmaeili, Mehdi KhabazKhoob
    Introduction

    Cerebrovascular angiography is a method of diagnosing cerebrovascular disorders. Invasive procedures induce anxiety in patients. Poor management of anxiety may be life-threatening for patients. It is the duty of nurses to reduce anxiety. Given the prevalence of anxiety in patients awaiting cerebrovascular angiography and its detrimental complications and also the criticalrole of nurses in the psychosomatic support of patients and their struggle to reduce anxiety, the use of different methods of patient education such as familiarizing them with diagnostic and therapeutic processes is of utmost significance. This study investigated the effect of orientation tour on anxiety in candidates of cerebrovascular angiography.

    Methods

    In this experimental study, 114 patients awaiting cerebrovascular angiography presenting to Imam Hussein Hospital and Shohadaye Tajrish Hospital in Tehran, capital of Iran, were selected with a convenient sampling method and assigned randomly to either case or control groups. The controlgroup just received routine education in the ward. In contrast,the case group received routine education in the ward and instructions on performing angiography and its pre-, peri-, and post-operative care. Demographics questionnaire and the Depression Anxiety Stress Scale (DASS-21) were used to collect data. Patients'anxiety was measured twice with this instrument at hospitalization and after the intervention. The gleaned data were analyzed with SPSS21 using independent t-test, Chi-square test, and ANOVA.

    Results

    Distribution of age was the same in both groups (P<0.11). Independent t-test showed a significant difference in the mean score of anxiety before intervention in the control group (9.2) and case group (7.2) (P=0.02). This test also indicated a significant difference in the mean score of patients'anxiety after intervention in both the control group (9.7) and case group (6.7) (P=0.001). However, using data collected before the orientation tour as the covariate, repeated measures ANOVA showed a significantly more significantreduction of anxiety in the case group.

    Conclusions

    According to our findings, participation in the angiography room orientation tour leads to reduced anxiety in patients awaiting cerebrovascular angiography. The use of this method is advisable for patients before diagnostic and therapeutic processes.

    Keywords: Anxiety, Cerebrovascular, Angiography, Orientation Tour
  • Azam Eshaghian Dorcheh, Mitra Zandi *, Maryam Rasouli, Mamak Tahmasebi, Fatemeh Esmaielzadeh

    Background:

     Due to the increased survival of children with chronic and complex diseases, transferring a part of care provision to home and harnessing the family’s potential with the aim of shortening the length of stay and returning the child to the safe and familiar atmosphere of the family can affect the health system and the family. This study aimed to evaluate the cost-effectiveness of home-based palliative care for children with complex health care needs based on the literature review.

    Materials and Methods

    After selecting the keywords related to the research question, by examining MeSH, EMTREE and the experts’ opinions mentioned in articles, searching the databases PubMed/Medline, EMBASE, Scopus and Web of Science was done through a combination of them.

    Results

    Finally, 11 studies met the inclusion criteria, which were investigated in three groups of methodological features, economic outcomes and indirect outcomes. The reviewed studies were of medium to high quality. Eight were cohort studies, one pre-post study, and 2 economic evaluation studies. Studiesshowed that the decrease in the costs of home-based palliative care for the children in need of special health care, although little, was the result of either reduced hospital stay or the decreased number of hospitalizations. 

    Conclusion:

     In order to set up pediatric palliative care services in Iran, considering the cultural atmosphere and the limited resources of the health system, attention should be paid to the cost effectiveness of care settings and the provided services, and measures should be taken in order to improve the situation of the children with special care needs, based on social conditions.

    Keywords: Children, chronic disease, Cost effectiveness, Home Care Services
  • Sahar Dabaghi, Mitra Zandi *, Abbas Aabaszadeh, Abbas Ebadi
    Background

    Patients are meticulous supervisors of their self-care. Their perceptions and experiences play a significant role in their awareness of the overt and covert problems in the healthcare settings. However, few studies have focused on the exact details of the nature of safety experienced only by the patients.

    Aim

    This study aimed to carry out the conventional content analysis of patients’ feelings of safety during hospitalization.

    Method

    This qualitative study was conducted on a total of 31 patients hospitalized in various wards of hospitals affiliated to Shahid Beheshti University of Medical Sciences in Tehran, Iran, using purposive sampling in 2019. The data, obtained through semi-structured interviews, were analyzed by conventional content analysis using Graneheim and Lundman’s approach (2004) with MAXQDA software (version 2010).

    Results

    Finally, data analysis resulted in the establishment of three main categories, namely feeling of insecurity, insolvency, and seeking safety and security.

    Implications for Practice

    The obtained results of the present study can be helpful in designing a patient-based care program focusing on patient safety. The healthcare team can improve patient care through the consideration of factors contributing to the feeling of safety in patients.

    Keywords: feeling safe, Hospitalization, Patients, Perception, Qualitative research
  • Maryam Esmaeili, Mitra Zandi*
    Background

    Liver cancer is one of the common cancers. Despite many advances in medical sciences, it continues to be one of the main problems in the care systems. Diagnosis of the disease and its treatments result in many problems for affected patients. The purpose of this study was to assess the consequences of transcatheter arterial chemoembolization.

    Method

     The study was performed on 84 patients at Imam Khomeini Hospital in Tehran, using available sampling methods. Questionnaires on cancer treatments, Fatigue Severity Scales, Hospital Anxiety and Depression Scales, Edmonton Symptoms Scales, and demographic characteristics were filled before and after treatment. Data were analyzed using SPSS software version 21. Descriptive statistics, t test, and correlation test were used as appropriated.

    Result

    The study showed many consequences such as anxiety, pain, and fatigue. Mean physical and psychological outcomes after treatment showed a significant increase (P˂0.05), which led to a significant decrease in FACT??.

    Conclusion

    Consequences have an inverse and significant relationship with patients’ performances and their quality of life. Due to the direct effects of consequences on life, they should be reduced or eliminated.

    Keywords: Liver cancer, FACT, HRQOL, TACE, Outcomes
  • مریم اسمعیلی، میترا زندی*
    مقدمه و هدف

    پیامدهای جسمی و روان شناختی از مهم ترین مشکلات بیماران مبتلا به سرطان کبد است که با تاثیر بر توانایی و کیفیت زندگی بیماران بحران های تازه ای در آن ها ایجاد می نماید. با توجه به ضرورت کاهش و رفع این پیامد ها، مطالعه با هدف بررسی پیامدهای ناشی از روش جراحی در بیماران مبتلا به سرطان کبد انجام شد.

    مواد و روش ها

    این مطالعه توصیفی بر روی 53 بیمار مبتلا به سرطان کبد مراجعه کننده به مجتمع بیمارستانی امام خمینی(ره) شهر تهران از آبان ماه 1397 لغایت خرداد ماه 1398 به روش نمونه گیری در دسترس، با استفاده از پرسشنامه عملکردی درمان سرطان، مقیاس های اضطراب و افسردگی بیمارستانی، شدت خستگی، بررسی علایم ادمونتون و ویژگی های دموگرافیک در دو مرحله (قبل و یک ماه بعد از درمان) انجام شد. جهت روایی ابزار ها به مطالعات قبلی استناد و پایایی آن ها نیز با استفاده از آزمون مجدد بررسی قرار گرفت. تجزیه و تحلیل داده ها با استفاده از SPSS نسخه 21، آمار های توصیفی، آزمون همبستگی و تی زوجی انجام شد.

    یافته ها

     شدت خستگی، بی اشتهایی، درد، اضطراب، اختلالات خواب و سایر مشکلات بعد از درمان در مقایسه با قبل از درمان افزایش چشمگیری داشتند (0/05˂p). رابط معنی داری میان این پیامد ها با وضعیت عملکردی بیماران (0/001˂p) بود.

    نتیجه گیری

     بیماران مبتلا به سرطان کبد پیامدهای جسمی و روان شناختی را در حد متوسط تا شدید تجربه کرده اند. با توجه به تاثیر این پیامد ها بر زندگی و میزان بقاء بیماران، یکی از وظایف مهم و کلیدی در بخش های سرطان، پیشگیری، شناسایی و کنترل عوارض ناشی از درمان سرطان کبد است.

    کلید واژگان: سرطان کبد, پیامدها, اضطراب, افسردگی, جراحی, کیفیت زندگی وابسته به سلامت
    Maryam Esmaeili, Mitra Zandi*
    Background and Aim

    Physical and psychological outcomes are one of the most important problems in patients with liver cancer, which can affect new patients' ability and their quality of life. Regarding the necessity of reducing and eliminating these consequences, the study was conducted to investigate the consequences of surgery in patients with liver cancer.

    Materials and Methods

    This descriptive study was performed on 53 patients with liver cancer referred to Imam Khomeini Hospital Complex in Tehran using the available sampling method from November 2019 to June 2020. During the study, Functional Cancer Questionnaire, Hospital Anxiety, and Depression Scale, Fatigue Severity, Edmonton Symptom Evaluation, and Demographic Characteristics were used in two stages (before and one month after the treatment). Data were analyzed using SPSS 21, descriptive statistics, Pair T-test, and correlation.

    Results

    Fatigue, loss of appetite, pain, anxiety, sleep disturbances, and other problems were significantly increased in comparison with the pre-treatment period (p˂0.05). There was a significant relationship between these outcomes and the quality of life of the patients (p˂0.001).

    Conclusion

    Patients with cancer have experienced moderate to severe physical, and psychological consequences. Considering the impact of these outcomes on the survival and quality of life, one of the important tasks in the cancer department is, to prevent, identify, and control the complications of liver cancer treatment.

    Keywords: Liver cancer, Consequences, Anxiety, Depression, Surgery, Health-related quality of life
  • Maryam Esmaeili, Mitra Zandi*, Hossein Ghanaati
    Background

    Primary liver cancer is one of the most malignant and deadly cancers, which reduces the quality of life. Health-related quality of life (HRQOL) is an important criterion for evaluating the health care, controlling diseases, outcomes, benefits, and disadvantages of treatments, quality of medical treatment and nursing care, and screening individuals at risk for physical and psychological problems. The aim of this study was to investigate the predictive factors of HRQOL in patients with liver cancer. The results of this study can improve the quality of life of the patients and the level of health care.

    Materials and Methods

    This study was performed on 272 patients referred to Imam Khomeini Hospital in Tehran (2018-2019), by using convenience sampling method. For assessing patients, we used Function Assessment Cancer Therapy, Hospital Anxiety and Depression Scale, Fatigue Severity Scale, Edmonton Symptoms Assessment Scale, and Characteristics Demographic. Data were collected in two stages (before and one month after treatment). In order to validate these tools, previous studies were cited and their reliability was assessed by test-retest. Data were analyzed by using SPSS software version 21. Descriptive statistics, correlation test, paired t test, and linear regression were used as appropriated.

    Results

    The mean HRQOL score in patients with liver cancer was 58.11 (±17.31). Effective factors in HRQOL was the type of treatment, physical and psychological consequences, and some demographic characteristics.

    Conclusion

    The present study showed that many factors can predict HRQOL in patient with liver cancer. Also, awareness of these factors provides the basis for developing effective care plans to promote HRQOL and increase life expectancy in affected patients. These factors are very important because based on them HRQOL of patient with liver cancer can be estimated with 59/8% accuracy.

    Keywords: Factors Predictive, life of quality related-Health, cancer Liver
  • Fahime Hasanbeigi, Mitra Zandi *, Anoshirvan Kazamnejad, Atefe Salimi Akin Abadi

    Advancements in assisted reproductive technology (ART) has increased the nurses' contribution to the provision of ART services. The present descriptive cross-sectional study aimed to determine essential care skills for nurses working at the selected infertility clinics in Tehran, Iran, based on their perspectives within 2016-2017. A total of 59 nurses were selected via a convenience sampling method and the data were collected using a researcher-made questionnaire. Data analysis was performed using SPSS software (version 21). Furthermore, the results of the Spearman’s rank correlation coefficient highlighted items associated with three domains of knowledge, attitudes, and practices required for nurses from their perspectives (94.9%). Given that nurses have constant contact with clients in infertility clinics and considering the lack of studies on essential care skills for nurses working at such centers, the results of this study would help to define job descriptions and determine the necessary care skills for the nurses.

    Keywords: nurse, Assisted reproductive technology, skill, Care
  • Azam Eshaghian, dorcheh, Mitra Zandi *, Maryam Rassouli, Mamak Tahmasebi
     
    Background
    The growing prevalence of chronic diseases in children has increased their need for palliative care. We aimed to compare pediatric palliative care and home care training in Iran and in the selected countries.
    Materials and Methods
    This comparative study was conducted based on the classifications of palliative care for children and using databases such as Scopus, Science Direct, Ovid, ProQuest and Medline, websites affiliated with communities and associated with palliative care and home care services and according to the framework of World Health Organization’s Public Health Road Map. The selected countries consist of England, Canada, Australia and South Africa, where home care services are provided for children in addition to palliative care.
    Results
    There is a pediatric palliative care training program for doctors in the selected countries. Home care is part of these programs in these countries. Despite the lack of an independent nursing course in postgraduate education in England, Canada, and Australia, community health nurses are responsible for providing care responsible to provide care for children with life-threatening diseases in the community and at home. In South Africa, a home-based palliative care training and support package for children was designed for community care workers. In Iran, pediatric palliative care is in the early stages and home care is evolving as a need.
    Conclusion
    Education is the most important factor for integrating home care and pediatric palliative care into the health system. In countries with advanced pediatric palliative care, the knowledge and skills of care providers have been considered. In Iran, revising medical and nursing curriculums and the integration of palliative care and home care programs into the curriculum are essential.
    Keywords: Education, Home care, Pediatric, Palliative care
  • Azita Pourshirvani*, Jila Abed Saieedi, Niloofar Nekozad, Mitra Zandi
    Background and Aim
    Interventions to support stroke care givers by providing education and Training in skills essential for the day to day management of disabled stroke survivors have shown a little impact in reducing the burden of care but there are many recommended to use a more effective skill. We evaluated the effectiveness of caregiver training by Continuous Care Model to increasing patient’s functional squeal and improving patient and caregiver outcomes.
    Materials and Methods
    This research was a quazi-experimental study. A total number of 90 cases were equally divided into two groups. Continuous Care Model training was applied to the caregiver in the experimental group until ten weeks after discharge. In the same time, the control group was treated based on routine protocol. Main outcome was measured for patients, by Functional Independence Measure, which measures patient’s functional status. Recovery was quantified by the changes in the Functional Independence Measure total scores. Caregiver demographic and care home checklist for Caregiver, was completed by the researcher too.
    Finding
    Although Wilcoxon test showed significant differences in the mean scores of Functional Independence Measure (p<0/001) in each group, We used the Mann-Whitney test to compare differences in mean of changes Functional Independence Measure between two groups after intervention and it showed changes in experimental group (P<0/001) was more than control group.
    Conclusion
    Training care givers by Continuous Care Model can improve functional recovery, and activities of daily living of stroke patients.Keywords:Home care; Caregivers, Activities of Daily Living; Stroke; Patients
    Keywords: Home care, Caregivers, Activities of Daily Living, Stroke, Patients
  • Seyedeh Narjes Mousavizadeh, Tahereh Ashktorab, Fazlollah Ahmadi, Mitra Zandi
    Background
    Poor adherence of patients with type 2 diabetes to treatment is one of the most complex and important clinical concerns. It is the main issue of the present decade and acknowledged as a challenge to control and treat diabetes. This study was carried out to explore and understand how adherence to treatment process occurs among Iranian patients with type 2 diabetes.
    Methods
    The present study is qualitative with grounded theory approach. The data were collected from December 2015 to July 2016 in Tehran (Iran) through individual semi-structured in-depth interviews, field notes, and memos from 21 patients with type 2 diabetes; combined with two members of their families and a healthcare professional. The data were analyzed based on Corbin and Strauss constant comparative analysis (2008).
    Results
    Adherence to treatment is a transitional, interactive, and continuous process. For patients with diabetes, this process includes unperceived threat in diagnosis time (poor knowledge and skills, bottleneck of dependencies, superficial understanding of the new situation), bitter belief (downhill quality of life, physical and emotional treatment feedbacks), and adaptation to treatment (self-care dominance, regimen integration in daily activities). The process of adherence to treatment was influenced by knowledge and skill, social support, beliefs and values, psychological characteristics of people, and the nature of diabetes.
    Conclusion
    Adherence to treatment in Iranian people with diabetes depends on the family and social context, which is challenging for the patient and leads to the negligence of health behaviors. It is vital for healthcare providers to identify these factors to encourage patients to adhere and commit to treatment in order to prevent irreversible complications of diabetes.
    Keywords: Adherence, Patient, Diabetes mellitus, Grounded theory
  • Atefe Salimi Akin Abadi, Mitra Zandi *, Marzieh Shiva, Azita Pourshirvani, Anoshirvan Kazemnejad
    Background
    Primiparous mothers are likely to lose their sense of value in the absence of maternal skills, and mothers with a history of infertility may suffer from more anxiety and decreased self-esteem than their normal peers do.
    Aim: The aim of this study was to determine the effect of a maternal role preparation program on self-esteem of pregnant mothers undergoing in-vitro fertilization (IVF).
    Method
    This randomized clinical trial was performed at Royan Institute in 2016. Sixty mothers undergoing IVF were assigned to intervention and control groups. The research instrument was a version of Maternal Self-Report Inventory. Before implementing the preparation program, the questionnaires were completed by both groups; then, the given preparation program was held in four sessions for mothers in the intervention group. Immediately after the completion of the program and one month later, both groups took the test again. To analyze the data, t-test, Chi-squared test, and repeated measures analysis of variance (ANOVA) were run in SPSS, version 21.
    Results
    The mean ages of the intervention and control groups were 32.8±4.3 and 31.4±3.9 years, respectively. Repeated measures ANOVA showed no significant intergroup difference in the mean score of maternal self-esteem before the intervention; however, a significant difference was observed one month post-intervention between the intervention and control groups (PImplications for Practice: The maternal preparation program could enhance maternal self-esteem. Thus, implementing such programs along with providing other infertility care services could contribute to preparation for assuming maternal role.
    Keywords: Infertility, In-vitro fertilization, Maternal self-esteem, Preparation program
  • Fahimeh Hasanbeigi, Mitra Zandi, Zohreh Vanaki, Anoushirvan Kazemnejad
    Background
    The provision of optimal care is the most important goal in nursing, the fulfillment of which requires the identification of clients’ problems and needs. However, based on the review of the literature, no review study has investigated the problems and needs of the infertile patients in Iran.
    Aim: The purpose of the present study was to investigate the problems and needs of the infertile patients referring to the assisted reproduction centers.
    Method
    This review study was based on the traditional review procedure developed by Cronin et al., which entails five steps including: 1) choosing the topic of the review, 2) searching the manuscripts, 3) collecting, reading, and analyzing the texts, 4) writing the review, and 5) providing references. The articles published within 2003-2017 were searched in such valid databases as Google Scholar, Pub Med, Science Direct, Ovid, and Cochran. The inclusion criteria in this study were articles in Persian and English with the keywords referring to problems and needs of clients. Out of the 350 original articles, 31 cases were finally selected for this review study.
    Results
    In general, the infertile patients’ problems were placed under four domains of mental-psychological, social, marital, and financial factors. The needs of the infertile individuals were grouped into six domains of physical, care, informational, financial, mental-psychological, and spiritual factors.
    Implications for Practice: The identification of the patients’ problems and needs can lead to the conceptualization of strategic points targeted toward the delivery of effective interventions facilitating the provision of patient-centered infertility care. This can enhance the quality of life and lower the levels of stress during the course of treatment.
    Keywords: Assisted reproductive technology, infertility, Nursing, Patient-centered care
  • Mahboubeh Ahmadpour, Ali Darvishpoor Kakhki*, Mitra Zandi, Ramin Nourbakhsh
    Introduction
    Osteoarthritis is one of the leading causes of disability and reduction of functional independence in older people. The present study was conducted to investigate the factors related to functional independence in daily activities of older people with osteoarthritis in Mashhad, Iran.
    Methods
    In this descriptive-correlational study, 300 older people with osteoarthritis who had referred to rheumatology clinics of Mashhad University of Medical Sciences Hospitals in Mashhad in 2016 were selected and entered in the study by available sampling method. Data collection tools in this study included demographic information questionnaire and scale of activities of daily living, the validity and reliability of which were measured. SPSS-21 software was used for data analysis.
    Results
    The age average of the study subjects was 70.75 (± 7.27). The older people with higher education levels, male gender, married and who lived with a spouse or spouse and children, lower in age, economically independent (higher income and working), lower body mass index, the ones with less duration of osteoarthritis, ones who did not need to use assistive devices, did not suffer from the lack of joint mobility, and did not have hip osteoarthritis, had more independence in activities of daily living (P value < 0.05).
    Conclusions
    According to the obtained results and related factors from this study, it is necessary that more accurate planning be considered to prevent, control and manage factors leading to the dependence of older people.
    Keywords: Osteoarthritis, Older People, Activities of Daily Living, Independent Living
  • Narges Bagheri, Lankarani, Faezeh Zarei, Mitra Zandi*, Reza Omani Samani, Morteza Karimi
    Background
    There has been a dramatic increase over the past few decades in the use of modern fertility technologies and the demand by infertile couples for using these techniques have increased as well. Studies exploring the experiences of women fertilized with egg donation technique in their treatment process have been rare.
    Aim: This study aimed to explore and explain the treatment experiences of women fertilized with egg donation.
    Method
    This is a Qualitative study. Data were analyzed simultaneously as they were being collected and according to the conventional content analysis method. The study began in July 2013 and continued until September 2014. Fourteen unstructured, in-depth interviews were carried out with 12 infertile women who had been fertilized or had given birth to children through egg donation. One of Tehran’s referral centers for infertility was used as the study setting. All participants submitted their written consent prior to the start of the study.
    Results
    Analysis of the findings showed "difficult and stressful treatment" as the final theme with 6 subthemes, including: 1) religious barriers, 2) treatment difficulties, 3) treatment frustration (including the following subcategories: fatigue and despair, and the experience of frequent failures), 4) dissatisfaction with the services provided, 5) confusions in treatment, and 6) Perception of relative peace.
    Implications for Practice: Exposure to various assisted reproductive technologies, including egg donation, is a stressful process, and providing emotional support to patients is one of the most essential care services they require from treatment centers. The results of the present study can assist in planning future strategies for meeting the specific needs of these distinguished patients.
    Keywords: Assisted Reproductive Techniques, Experiences, Infertility, Nursing care, Oocyte Donation, Qualitative
  • Mitra Zandi, Zohreh Vanaki, Marziyeh Shiva, Eesa Mohammadi, Narges Bagheri Lankarani, Morteza Karimi
    Background and
    Purpose
    Surrogacy is a new assisted reproductive technology requiring to be perceived based on the real experiences of surrogacy patients regarding its legal issues so that legislators are able to enact appropriate laws for such patients'' safety. This study pursues the goal to examine the experiences of commissioning mothers and surrogates confronting legal issues.
    Methods
    This paper is part of the findings of a larger study conducted over 20 months from October 2011 to June 2013 using the grounded theory approach to explain the process of becoming a mother in commissioning mothers. The experiences of mothers using gestational surrogacy have been analyzed through the conventional content analysis method and then reported in terms of the legal issues of surrogacy. Overall there have been 20 participants including 11 commissioning mothers and 4 surrogates. For incorporating the resources, 5 fertility clinic personnel have also been interviewed. Totally 25 unstructured in-depth interviews have eventually been performed. Data have been collected via purposive sampling method within Royan Institute, and then due to the inadequate number of samples, sampling continued in other surrogacy treatment centers.
    Results
    Commissioning mothers and surrogates suffer a great amount of stress at the time of childbirth, and lack of legal support imposes plenty of problems on them. Participants’ experiences revealed a common theme of “legal constraints” with three dimensions as “inefficiency of current laws”, “receiving inadequate educational support services” and “stress and frustration”.
    Conclusion
    Results indicate disagreeable legal settings for surrogacy leading to a high level of stress imposed on the clients using these technologies. The treatment team should inform the families about the entire process ahead of them before they make their final decision so as to enable them to enter the process fully aware.
    Keywords: Assisted reproductive technologies, Infertility, Surrogate mother, Legislation, jurisprudence, Commissioning mother
  • آزیتا گشتاسبی، میترا زندی، ژیلا صدیقی، کتایون جهانگیری
    اندومتریوز یکی از شایعترین بیماری های زنان در سنین باروری است که آثار منفی بسیاری بر سلامت روان، سلامت جسم و کارآیی شغلی و اجتماعی بیماران دارد. تاثیر بیماری آندومتریوز بر سلامت جنسی زنان کمتر مورد توجه بوده و مطالعات بیشتر بر تاثیر درمان های مختلف بر دو شکایت شایع این بیماران یعنی نشانگان درد و ناباروری و به طور خاص، بر یکی از جنبه های اختلال عملکرد جنسی یعنی دیسپارونیا متمرکز بوده است. هدف این مطالعه ارزیابی جامع مطالعات موجود در زمینه بررسی تاثیر بیماری و درمان های آن بر سلامت جنسی مبتلایان و ارائه ی نمایی کلی از موضوع است تا توجه محققان و ارائه دهندگان خدمات بهداشتی را بر جنبه های مشکل آفرین و کمتر دیده شده بیماری آندومتریوز یعنی سلامت جنسی این بیماران جلب نماید. در یک مرور نظام مند با استفاده از اصول پریزما مقالات کامل منتشر شده در سالهای 1975-2013 در زمینه آندومتریوز و درمانهای آن استخراج شده و پس از ارزیابی معیارهای ورود و خرو ج و در مرحله بعد بررسی از نظر معیارهای شایستگی 37 مقاله (32 مقاله کمی و 5 مقاله کیفی) انتخاب و مرور شدند. نتایج نشان داد که در اکثر موارد دیسپارونی به عنوان یکی از نشانگان درد و نه به عنوان یک شکایت جنسی گزارش شده است و سلامت جنسی بیماران تنها در سالهای اخیر مورد توجه محققان و ارائه دهندگان خدمت قرار گرفته است. درد، تواتر رابطه جنسی، عملکرد جنسی، ارگاسم، رضایت جنسی و رضایت شریک جنسی بیشترین موارد اشاره شده در مقالات بودند. زندگی جنسی و اهمیت آن در حفظ رابطه زناشویی و کیفیت زندگی بیماران در کنار متغیرهای زیست شناختی و بالینی باید مورد توجه محققان و پزشکان قرار گیرد.
    کلید واژگان: آندومتریوز, سلامت جنسی, مرور نظام مند, دیسپارونی, ارگاسم, رضایت جنسی
    Azita Goshtasebi, Mitra Zandi, Jila Sadighi, Katayoun Jahangiri
    Objective (s): of patients has received less attention and most studies focused primarily on infertility، pain، and dyspareunia as main complaints of patients. The aim of this paper was to review the existing body of information on the impact of endometriosis and its medical and surgical treatments on sexual health of patients، providing new insight into the issue، and call attention to this overlooked aspects of women’s life.
    Methods
    Using the PRISMA guideline، papers published between 1975 and 2013 on the topic of endometriosis، and its treatments retrieved and with a critical narrative synthesis the effect of disease or its treatments on sexual health of patients were reviewed.
    Results
    In total، 37 papers were found relevant. Of these 32 papers used quantitative methods and 5were qualitative studies. The results showed that dyspareunia was the most common symptom as part of a pain syndrome and not a sexual problem. Sexual well being of patients has been included in the treatment outcomes only in recent years. Pain، frequency of sexual intercourse، sexual function، and satisfaction، and orgasm were the most accounted outcomes.
    Conclusion
    Endometriosis strongly affects sexual and marital relationships and quality of life in women. Therefore، these aspects of patients’ life as well as biological and clinical indicators should be integrated into the health care and the future research.
    Keywords: endometriosis, sexual health, systematic review, dyspareunia, orgasm, sexual satisfaction
  • Mitra Zandi, Zohreh Vanaki, Marziyeh Shiva, Eesa Mohammadi
    Background
    There are a few studies about commissioning mothers’ understanding from the surrogacy during 9 months of waiting for delivery in Iran and other countries. This study was conducted with an aim to explore and explain the nature of concerns (experiences) of commissioning mothers.
    Materials And Methods
    A qualitative design with a conventional content analysis approach was used to gather and analyze the experiences of commissioning mothers. They were selected from Royan Research Centre and other infertility centers in Iran. After purposive sampling for the selection of the participants, unstructured interviews were held for data collection. Twenty-four unstructured interviews were conducted with 12 commissioning mothers, 2 surrogate mothers, and 2 infertility center social workers who directly and continuously dealt with these mothers.
    Results
    Two main themes emerged from the data analysis: 1. cultural dilemma (consisting of three subthemes: Social taboo, concerns about disclosure to others and the child, concerns about altering maternal and child’s identity, and 2. uncertain waiting (consisting of three subthemes: Concerns about health of fetus and surrogate, concerns about an unfamiliar surrogate, and concerns about lack of preparation for maternal role).
    Conclusions
    The study reveals the importance of maternal emotional care in this group and introduces a new arena for nurses’ activity. These findings help the mothers by nurses’ activities in health care clinics and anywhere they deliver nursing care.
    Keywords: Iran, nursing, reproductive techniques, surrogacy
  • میترا زندی، زهره ونکی، مرضیه شیوا، عیسی محمدی
    مقدمه
    حمل جایگزین (رحم جایگزین) یکی از تکنولوژی های جدید کمک باروری است که تاکنون پیامدهای عمیقی در اخلاق، حقوق، مذهب و جامعه به دنبال داشته است. جمع آوری اطلاعات در این زمینه نه تنها به منظور آگاه ساختن موسسان این تکنولوژی و قانون گذاران از مسائل موجود، بلکه به منظور تنظیم قوانین مناسب و ایمن برای زوج نابارور، مادر جایگزین و کودک ضروری است. مطالعه حاضر با هدف درک و تبیین تجارب مددجویان حمل جایگزین (مادران استفاده کننده از حمل جایگزین و دهندگان رحم) از معضلات قانونی حمل جایگزین و بررسی نحوه برخورد آنان با این شرایط انجام شده است.
    روش کار
    در این مطالعه کیفی که در سال 1390 بر روی 20 نفر صورت گرفت. 11 نفر از مادران استفاده کننده از حمل جایگزین و 4 نفر از دهندگان رحم به روش نمونه گیری هدفمند از پژوهشگاه رویان و سایر مراکز ناباروری کشور انتخاب شدند. همچنین جهت تلفیق منابع با 5 نفر از پرسنل مراکز ناباروری نیز مصاحبه شد. به منظور گردآوری داده ها 25 مصاحبه بدون ساختار و عمیق انجام شد. برای سازماندهی بهتر داده ها از نرم افزار MaxQDA 2007 استفاده شد. تحلیل داده ها همزمان با گردآوری آنها و به روش آنالیز محتوای کیفی قراردادی انجام شد. این مطالعه مورد تایید کمیته اخلاق دانشگاه تربیت مدرس و پژوهشگاه رویان قرار گرفته است. اطلاعات پس از جمع آوری به روش تحلیل محتوای متعارف مورد تحلیل قرار گرفت.
    یافته ها
    تجارب مشارکت کنندگان نشان می دهد که مادران استفاده کننده از حمل جایگزین و دهندگان رحم در هنگام تولد کودک، تنش های فراوانی را متحمل شده و فقدان حمایت قانونی، معضلات فراوانی را برای آنان به دنبال داشته است. تجارب مشارکت کنندگان، مضمون مشترک «تنگنای قانونی» را آشکار کرد که دارای سه بعد «ناکارآمدی قوانین موجود»، «عدم دریافت خدمات حمایتی آموزشی مکفی» و «استرس و استیصال» می باشد.
    نتیجه گیری
    تجارب مشارکت کنندگان نشان دهنده بستر نامناسب قانونی و تحمیل تنش های فراوان ناشی از آن به مشتریان این تکنولوژی های جدید کمک باروری است. به منظور پیشگیری از تحمیل استرس های روحی روانی و مالی مضاعف، برخوردی جدی تر و تنظیم قوانینی مشخص و مورد توافق ضروری به نظر می رسد. همچنین کادر درمان، پیش از تصمیم گیری خانواده ها باید آنان را در جریان کامل روند پیش رو قرار داده و با آگاهی کامل وارد این فرآیند نمایند.
    کلید واژگان: تکنولوژی های کمک باروری, رحم جایگزین, معضلات قانونی
    Mitra Zandi, Zohreh Vanaki, Marzieh Shiva, Isa Mohammadi
    Introduction
    Surrogacy is a new reproductive technology that yet has deep ethical، legal، religious and social consequences. Collected data in this regard is necessary not only to inform the founders of this technology and legislators but also in order to set appropriate and safe rules for infertile couples، surrogate mother and the child. The purpose of this study was to explain the legal implications of surrogacy to surrogate mothers and evaluate how they encounter these situations.
    Methods
    This qualitative research was done in 2011on 20 participants and 11 commissioning mothers، 4 surrogates were selected by using targeted sampling from Royan institute and other infertility centers in Iran. In order to integrate the sources، 5 staff of infertility centers was also interviewed. Data were collected by using 25 deep unstructured interviews. For better organization of data، MaxQDA 2007 software was used. While gathering data، they were analyzed by using conventional content analysis method. This study was approved by the Ethics Committee of the Tarbiat Modares University and Royan Institute. ِData collected and analysis was performed based on conventional content.
    Results
    Results have shown that surrogate clients experience high stress during and after surrogacy and because of lack of legal supports، they experience so many problems. Participants'' experiences، the common theme of «legally bound» revealed three dimensions: «inadequacy of existing laws»، «lack of adequate educational support services» and «stress and frustration».
    Conclusion
    Participants'' experiences indicated the inadequate legal framework and great stresses to customers of this new method. Serious encounters، determined and approved rules seems necessary in order to prevent mental and financial stresses. Also، medical staff needed to make clients fully aware of ethical and legal implications when they are applied to assisted reproduction.
    Keywords: Assisted reproductive technology, Legal implications, Surrogacy
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