جستجوی مقالات مرتبط با کلیدواژه "treatment efficacy" در نشریات گروه "پزشکی"
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To assess the impact of budesonide-formoterol on pulmonary ventilation function and prognosis in patients with mild-to-moderate acute exacerbations of bronchial asthma. A retrospective analysis was conducted on clinical data from 232 patients with acute exacerbations of bronchial asthma. These patients were divided into 2 groups based on their treatment: a control group (n=104) receiving budesonide dry powder inhalation and an observation group (n=107) receiving budesonide-formoterol dry powder inhalation. Clinical efficacy and safety indicators were compared. The results showed that the total treatment effectiveness rate in the observation group was significantly higher than that in the control group. Following treatment, the observation group exhibited significantly higher scores in the Asthma Quality of Life Questionnaire (AQLQ), as well as improved levels of forced expiratory volume in one second (FEV1), forced vital capacity (FVC), and peak expiratory flow (PEF), compared to the control group. Moreover, levels of tumor necrosis factor-alpha, interleukin-6, and C-reactive protein were significantly lower in the observation group. The incidence of adverse reactions between groups was comparable. Based on these findings, the application of budesonide-formoterol demonstrated significant effectiveness in patients with mild-to-moderate acute exacerbations of bronchial asthma. The combination therapy led to improved clinical outcomes, including enhanced pulmonary ventilation function and reduced inflammatory markers. Importantly, the safety profile of budesonide-formoterol was comparable to that of budesonide monotherapy. These results highlight the potential benefits of using budesonide-formoterol as an alternative treatment option for patients experiencing acute exacerbations of mild-to-moderate bronchial asthma.
Keywords: Acute Exacerbation, Bronchial Asthma, Budesonide, Combination Therapy, Formoterol, Pulmonary Ventilationfunction, Treatment Efficacy -
Background
Addressing the Coronavirus disease 2019 (COVID-19) pandemic remains a significant challenge for healthcare systems globally. Despite the absence of a proven cure, ivermectin has been proposed as a potentially effective agent against it.
ObjectivesThis study aimed to evaluate the therapeutic effects of ivermectin compared to a placebo group in non-critically ill confirmed COVID-19 patients.
MethodsA double-blind, randomized clinical trial was conducted on 110 patients with moderate-to-severe (non-critical) confirmed COVID-19 infection. The patients were equally divided into two groups, with one group receiving ivermectin tablets (14 mg every 12 hours for three days) and the other group receiving a placebo. The efficacy and safety of ivermectin were assessed in both groups.
ResultsA total of 110 patients, including 62 (56.4%) men and 48 (43.6%) women, with an average age of 53.36 ± 15.10 years, were enrolled in our double-blind, randomized clinical trial. The baseline characteristics of the two groups were similar. The findings demonstrated that ivermectin significantly reduced the need for Intensive Care Unit admission (32.7% vs. 5.5%; P < 0.001), hospitalization duration (six vs. four days; P < 0.001), and median time to symptom resolution period (P < 0.05) in COVID-19 patients compared to the placebo group, without any serious side effects (P > 0.05).
ConclusionsIvermectin appears to be a potentially effective and safe medication for COVID-19 patients with moderate disease.
Keywords: COVID-19, Ivermectin, Treatment Efficacy, Drug Safety, Randomized Controlled Trial -
Background
Tuberculosis (TB) causes over a million deaths annually and is still one of the most important public health problems worldwide. According to the World Health Organization estimates, the highest rates of TB in the European Region are in Tajikistan, Kazakhstan, Moldova, Kyrgyzstan, Romania, and Uzbekistan. The purpose of this study was to investigate the spectrum of nonspecific microorganisms isolated in patients with multidrug-resistant TB in Central Kazakhstan and to assess their susceptibility to antimicrobial drugs.
MethodsThe patients were divided into 2 groups: group 1 with multidrug-resistant forms of pulmonary TB (n = 107 patients); group 2 with sensitive forms of pulmonary TB (n = 122 patients). Gender, age, and social status of the patients were studied. Microorganisms were identified using the MALDI-TOF method. The statistical significance of different values for binary and nominal parameters was determined using the chi-square test. Changes in binary variables were analyzed using the McNeimer test.
ResultsDuring the study, an expectedly high proportion of tetracycline-resistant pneumococcal strains (66.7% and 60%, respectively) was isolated, which was a consequence of a long-term and practically uncontrolled use of these drugs in Kazakhstan. Fluoroquinolones showed low activity. The results showed that beta-lactam antibacterial drugs maintained their high activity against the causative agents of pneumococcal infection.
ConclusionIt was concluded that secondary microorganisms isolated in patients with multidrug-resistant TB were represented by the strains that were resistant to modern antibacterial drugs. Therefore, for appropriate antibiotic prescription, it is necessary to study materials from the respiratory system in all patients admitted for TB treatment to study the spectrum of nonspecific microorganisms and assess their susceptibility to antimicrobial drugs.
Keywords: Health care, Treatment efficacy, Non-specific microorganisms, Antibacterial drugs -
Background
A successful delivery depends on the coordinated work of all medical personnel. Compliance with the basic principles of teamwork is the key to the quality of medical care. The purpose of this study was to investigate the issues of teamwork of healthcare professionals during delivery.
MethodsThis descriptive study was conducted in 2019 in Almaty, Republic of Kazakhstan. A total of 40 doctors and 40 midwives who provide inpatient care for women during childbirth took part in the study. Based on the questionnaire, the authors conducted a standardized survey. The tools for statistical processing of the obtained data were Microsoft Excel and Software IBM SPSS Statistics 25.0. The authors used the Student's t-test to calculate the significance of differences.
ResultsThe results of the study showed that 85% of the respondents believed that the size of the team did not require changes. Approximately 2/3 of the respondents evaluated the efficacy of delivery techniques used by the team as “medium” and “low”. Compliance with the general approach based on mutually agreed principles was partial. The opinions of the doctors and midwives differed significantly regarding fair distribution of responsibilities in the team and the level of trust in the team.
ConclusionAs a result of the study, it was concluded that there is an urgent need to introduce modern team-building technologies into the daily practice of healthcare professionals of the obstetrician-gynecological service.
Keywords: Health Care, Treatment Efficacy, Non-Specific Microorganisms, Antibacterial Drugs -
Background
One of the relatively common symptoms in non-fluent aphasia is agrammatism. Agrammatism is characterized with low syntactic complexity and deficits in verb inflection, especially tense markers. Verbs as the main core of sentences in the Persian language have vital functions for people to have effective communication.
ObjectivesThe current study aimed at evaluating the effect of morphosemantic method on verb-tense inflection in Persian-speaking patients with aphasia and agrammatism.
MethodsMorphosemantic treatment was conducted in five stages in a case report study. The material was 46 black and white line-drawing pictures related to 23 verbs including 10 training, 10 expansion, and three exemplar verbs drawn in present and past tenses. In three phases, the percentage of correct verb inflection in the training and expansion verbs was measured and also the graph examination of level, slope of trend, and C statistic, 2-standard deviation band, effect size (percentage of non-overlapping data), and d statistic were used to analyze the data.
ResultsBoth participants demonstrated significant changes in training and expansion verbs during therapeutic sessions in comparison with the baseline. The effect of therapy was maintained for a three-week follow-up.
ConclusionsTherapy for verb inflection in spontaneous speech is clinically important. The current study demonstrated that morphosemantic method can be successfully used for tense marker deficits in Persian-speaking patients with aphasia and agrammatism.
Keywords: Treatment Efficacy, Case Report, Aphasia, Agrammatism -
هدفسرعت نامیدن یکی از مولفه های پردازش واجی است که در کودکان نارساخوان مورد بررسی قرار گرفته است. بسیاری از نارساخوان ها در نامیدن سریع محرکات بینایی، به خصوص محرک هایی که مستلزم دستیابی به سرعت، توالی و بازیابی برچسبهای کلامی- عددی هستند، با مشکل مواجه می-شوند. هدف از این مطالعه، بررسی اثربخشی برنامه طراحی شده، بر سرعت نامیدن حروف، در دانش آموزان نارساخوان پایه سوم ابتدایی است.روش کارپژوهش حاضر از نوع مداخله ای با طرح پیش آزمون، پس آزمون و گروه کنترل بوده است. جمعیت مورد مطالعه در این پژوهش شامل 18 دانش آموز نارساخوان پایه سوم ابتدایی است. افراد شرکت کننده در آزمون، به طور تصادفی به دو گروه آزمایش و شاهد تقسیم شدند. گروه آزمایش به مدت 10 جلسه در برنامه درمانی شرکت کردند. قبل و بعد از مداخله آزمون های سرعت نامیدن روی دو گروه اجرا شد. جهت مقایسه تاثیر درمان، داده های به-دست آمده با آزمون های تی مستقل، تی جفت شده در نرم افزارآماری19 SPSS و اندازه اثر مورد تجزیه و تحلیل قرار گرفت.یافته هاداده های به دست آمده از آزمون های آماری نشان داد که میانگین سرعت نامیدن حروف، در گروه آزمایش از 11/44 قبل از مداخله به 26 و در گروه شاهد از 11/ 49 به 77/ 44 رسیده است. بین سرعت نامیدن در دو گروه، بعد از درمان تفاوت معناداری وجود دارد (P<0.05).نتیجه گیرینتایج حاصل از تجزیه و تحلیل آماری حاکی از آن است که توانایی سرعت نامیدن حروف در دو گروه پس از مداخله درمانی تفاوت معنی داری دارند و اندازه اثر در گروه آزمایش بیشتر از گروه شاهد بوده است. بنابراین برنامه طراحی شده توانسته با نسبت بهتری منجر به بهبود مهارت سرعت نامیدن در دانش آموزان نارساخوان شود.
کلید واژگان: اثربخشی درمان, سرعت نامیدن, نارساخوانیAimRapid naming is one of the components of phonological processing that have been studied in dyslexic children. Most of the dyslexic children have difficulties in rapid naming of visual stimulus, especially stimulants which require fast access and retrieval sequence of verbal numeric labels. The purpose of this study was to evaluate the effectiveness of programs designed to increase rapid naming of letters in third grade elementary students with dyslexia.MethodsThis study was an interventional study with pretest-posttest and a control group. Eighteen third grade dyslexic students participated in this study. Before and after the intervention, rapid naming test were conducted. Participants were divided randomly into two groups. The experimental group participated in 10 sessions of therapy. To compare the clinical efficacy, the data obtained were analyzed with independent t-test, paired t in SPSS 19 and effect size.ResultsData analysis showed that rapid naming of letters increased in both groups with different effect size, such that the training group went from 44.11 before the intervention to 26 and the control group went from 49.11 to 44.77. The speed of naming between the two groups after treatment showed a significant difference (p <0.05).ConclusionThe results of statistical analysis showed that the mean rapid naming letters are significantly different in the two groups after the intervention. Given the size of the effect in the experimental group than the control group, it can be concluded that the program designed, improved speed of naming skills in dyslexic students.Keywords: Dyslexia, Naming speed, Treatment efficacy -
مقدمهکفایت دیالیز از اصلی ترین عوامل تعیین کننده میزان بقا و مرگ و میر در بیماران همودیالیزی است. لذا، مطالعه ی حاضر با هدف کلی تعیین کفایت همودیالیز در بیماران همودیالیزی مراجعه کننده به یکی از بیمارستانهای ارتش انجام گردید.روش بررسیاین مطالعه ی توصیفی-تحلیلی بر روی 44 بیمار همودیالیزی در مرکز همودیالیز بیمارستان که به روش در دسترس انتخاب شدند در آبان ماه سال 1393 انجام شد. اطلاعات جمعیت شناختی بیماران با استفاده از پرسشنامه ی محقق ساخته و کفایت دیالیز با استفاده از فرمول های SpKt/v، URR و eKt/v اندازه گیری گردید و به وسیله ی آزمون های آماری در نرم افزار SPSS نسخه ی 20 تجزیه و تحلیل گردید.یافته هامیانگین کلی شاخص های کفایت دیالیز که با فرمول های SpKt/v، URR و eKt/v محاسبه شده بود به ترتیب 30/0± 08/1، 43/9± 36/58 درصد و 12/0± 13/0 به دست آمد و حاکی از این بود که تنها 5/29% (13نفر) از بیماران از کفایت دیالیز مطلوب برخوردار بودند و 7/47% (21نفر) بیماران از کیفیت دیالیز نزدیک به میزان مطلوب و 7/22% (10نفر) بیماران کیفیت دیالیز نامطلوب داشتند. تنها 2/18% (8 نفر) بیماران دارای URR مطلوب (بیش از 65%) بودند.بحث و نتیجه گیریبا توجه به اینکه کفایت دیالیز اندازه گیری شده در این بررسی در حد خیلی مطلوبی قرار ندارد و در اکثر بیماران مورد مطالعه پایین تر از میزان استاندارد است؛ لذا، توصیه می شود ضمن ارزیابی دوره ای کفایت دیالیز در مراکز همودیالیز اقداماتی در جهت بهبود و مطالعاتی جهت بررسی علل پایین بودن آن انجام گیرد.
کلید واژگان: نارسایی مزمن کلیوی, کفایت درمان, همودیالیزEBNESINA, Volume:17 Issue: 2, 2015, PP 36 -42BackgroundDialysis adequacy is of the main determinants of survival and mortality in patients undergoing hemodialysis. Therefore, the present study was performed to determine the adequacy of hemodialysis in hemodialysis patients a military hospital.Materials And MethodsIn a cross-sectional study, 44 patients in dialysis center were selected by convenience sampling in 2014. Demographics data using a researcher-made questionnaire and the adequacy of dialysis patients using formulas Spkt/v, URR and ekt/v was measured. Data were analyzed by SPSS version 20 statistical software.ResultsThe mean hemodialysis efficacy indicators that was calculated with the formula Spkt/v, URR and ekt/v was 1.08±0.3, 58.36±9.43 and 0.13±0.12, respectively. It was indicated that only 29.5% (13 patients) had a desired dialysis adequacy, 47.7% (21 patients) had adequacy of dialysis close to the desired level, and 22.7% (10 patients) had undesirable adequacy of dialysis. Only 18.2% (8 patients) had a desired URR (upper than 65%).ConclusionThe measured dialysis adequacy in this study is not desirable and in most patients is lower than the standard rate. Therefore, it is recommended to evaluate periodically the adequacy of dialysis in dialysis centers and investigate the reasons of low efficacy of hemodialysis.Keywords: Chronic Renal Failure, Treatment Efficacy, Hemodialysis -
ObjectiveProviding a safe and efficient dental treatment for a young patient is a challenge for the dentist and the child. The purpose of this study was to investigate the effectiveness, safety and acceptability of buccal midazolam in dental pediatric patients and to compare it with oral Midazolam.MethodsEighteen uncooperative healthy children aged 2.5-6 years were randomized to each of buccal midazolam (0.3mg/kg) or oral midazolam (0.5mg/kg) at the first visit, the alternative has been used at the second visit in a cross-over manner. The study took place at pediatric dentistry clinic of Shahed University, Tehran, from November 2011 to June 2012. The patients` vital signs and behavioral scores were recorded. The patient, the operator and the observer were blinded to the applied medication. Post operatively, patients` and parents` satisfaction were assessed by Visual Analogue Score and a questionnaire respectively. The P-value was set at 0.05 for significance level.FindingsThere were no significant differences in physiologic factors in the medication groups at time 0, 10, 20, 30 minutes and discharge. There was also no significant difference between the two groups in behavioral parameters. The majority of parents rated both sedative agents as “effective” or “very effective” and their children mostly were without anxiety or with minor anxiety.ConclusionBuccal midazolam may be safely and efficiently used in sedation of pediatric dental patients.Keywords: Sedation, Midazolam, Pediatric Dentistry, Clinical Trial, Treatment Efficacy
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ObjectiveRecurrent aphthous stomatitis (RAS) is the most common and painful oral inflammatory lesion with an unknown etiology. This study aims to determine the therapeutic effects of ibuprofen, diphenhydramine and aluminum magnesium simethicone (AlMgS) syrup on reducing oral aphthous ulcer pain.Materials And MethodsThirty-one patients with RAS participated in this double-blind clinical trial. Subjects were randomly divided into two groups. The control group (n=14) received drug mixture as drug A (diphenhydramine and AlMgS) and the case group (n=17) received drug B (ibuprofen, diphenhydramine and AlMgS). Drugs were topically applied on ulcers by the patients three times a day for 3 days. Patients were re-examined for the symptoms on the fourth day following their first visits using VAS (Visual Analogue Scale) tool. Statistical analysis was performed using paired t-test, independent t-test and chi-square test.ResultsThe mean of pain reduction was 3.17±2 (P<0.001) and 3.82±1.79 (P<0.001) in the case and control group, respectively. The difference in pain reduction between both groups was not statistically significant. In addition, no significant difference was detected between the two groups regarding the duration of pain or burning sensation (P=0.57).ConclusionThe results of this study demonstrate that in comparison with diphenhydramine and AlMgS syrup, the studied mixture did not effectively reduce the level of pain, duration and burning sensation.Keywords: Stomatitis, Aphthous, Ibuprofen, Treatment Efficacy
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مقدمهآرتریت روماتویید یک بیماری مزمن التهابی با توانایی تخریب مفصلی و ایجاد ناتوانی در بیماران است. درمان های معمول تاثیر به نسبت خوبی در کنترل علایم بیماری دارند، اما گاهی با عوارضی همراه هستند.ژل رویال با اثرات ضد التهابی و آنتی اکسیدانی می تواند به درمان اضافه شود. هدف این مطالعه ارزیابی تاثیر ژل رویال بر (Clinical Disease Activity Index یا CDAI) و خشکی صبح گاهی در بیماران مبتلا به آرتریت روماتویید است.روش ها80 بیمار مبتلا به آرتریت روماتویید (بر اساس معیارهای انجمن روماتولوژی آمریکا ACR-1987) فعال (8/2 < CDAI)، به صورت تصادفی ژل رویال یا دارونما را در کنار درمان قبلی خود به مدت 3 ماه دریافت کردند. خشکی صبح گاهی، تعداد مفاصل متورم، تعداد مفاصل حساس، ارزیابی کلی بیماری توسط پزشک و ارزیابی کلی بیماری توسط بیمار بر اساس مقیاس آنالوگ بصری (Visual analogue scale یا VAS) قبل و سه ماه بعد از مداخله تعیین شد. تغییر شاخص های ذکرشده به وسیله ی نرم افزار SPSS ارزیابی شد.یافته ها65 بیمار مطالعه را تا پایان ادامه دادند (35 نفر در گروه ژل رویال و 30 نفر در گروه دارونما). سن، جنس، محل سکونت، طول مدت بیماری و داروهای دریافتی در 2 گروه تفاوت معنی داری نداشت (05/0 < P). در پایان مطالعه در گروه اول CDAI، تعداد مفاصل متورم، تعداد مفاصل حساس و خشکی صبح گاهی تغییر آماری معنی داری داشت (به ترتیب 004/0 = P، 027/0 = P و 012/0 = P) ولی تنها خشکی صبح گاهی در بین دو گروه تفاوت آماری معنی داری را نشان داد (05/0 > P).نتیجه گیریژل رویال تاثیر خوبی بر خشکی صبح گاهی دارد اما بر CDAI تاثیر قابل توجهی ندارد و می تواند به عنوان درمان کمکی به درمان های استاندارد بیمار اضافه شود. امید می رود مطالعات بیشتر نتایج بهتری را نشان دهد.
کلید واژگان: التهاب, آرتریت روماتویید, اثردرمانی, مفصلBackgroundRheumatoid arthritis (RA) is a chronic inflammatory disease which can cause articular destruction and disability in patients. Current therapies are relatively effective and sometimes harmful. Royal Jelly with anti-inflammatory and anti-oxidative properties may be used as an adjunct therapy. The aim of this study was to assess the effect of Royal Jelly on Clinical Disease Activity Index (CDAI) and morning stiffness in patients with rheumatoid arthritis.MethodsAccording to American College of Rheumatology (ACR) 1987 classification criteria، 80 patients with RA، who had active disease (CDAI > 2. 8)، were randomly assigned to receive Royal Jelly or placebo beside background treatment for 3 months. Morning stiffness، tender joint count (TJC)، swollen joint count (SJC)، evaluator global assessment (EGA) and patient’s global assessment (PGA) [based on visual analogue scale (VAS)] were determined before and after 3 months of intervention. The changes in aforementioned indexes were analyzed by SPSS software.Findings65 patients completed the study (35 in Royal Jelly and 30 in placebo group). The sex، age، residence، disease duration and drug consumption had no significant changes (P > 0. 050). In the first group، CDAI (P = 0. 012)، SJC (P = 0. 024)، TJC (P = 0. 027)، and morning stiffness (P = 0. 004) had significant statistical changes; but only changes in morning stiffness were statistically different between the two groups (P < 0. 05).ConclusionRoyal Jelly has good effect on morning stiffness but not on CDAI and may be a suitable adjunct therapy. Further studies may demonstrate more significant results.Keywords: Inflammation, Rheumatoid arthritis, Treatment efficacy, Articular -
Methamphetamine (MA) is a potent, addictive psychostimulant that has dramatic effects on the central nervous system (CNS). The onset of methamphetamine use has been linked to heightened attention, and chronic methamphetamine use has been associated with deficits in different aspects of attention that can significantly persist into abstinence. Attention deficits in chronic methamphetamine users may be associated with severity of methamphetamine use, craving, relapse, and as a result, poor treatment outcomes. This review summarizes evidence that the continuity of attention deficits, especially during abstinence, should be considered as a potential target during methamphetamine use treatment. Implementing attention rehabilitation techniques during treatment may enhance motivation for treatment in chronic methamphetamine users, and may facilitate treatment adherence, craving control and promote relapse prevention. This issue has important clinical implications for enhancing treatment efficacy and as a result, increasing treatment outcomes.Keywords: Methamphetamine, Attention Deficits, Abstinence, Treatment Efficacy
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