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Pro-inflammatory cytokine (IL-6) and total count lymphocyte profiles in COVID-19 patients with different severity levels 不同严重程度COVID-19患者的促炎细胞因子(IL-6)和淋巴细胞总数
Pub Date : 2021-07-01 DOI: 10.19106/jmedsci005303202101
S. Sari, Wening Tri Mawanti, Dewi Martalena, E. Listiyaningsih, Rizkyana Avissa, Rini Latifah, W. Sukarya
COVID-19 is caused by the SARS-CoV-2 infection that attacked the human respiratory system. In severe conditions it causes pneumonia, kidney failure, acute respiratory distress syndrome (ARDS) and even death. The SARS-CoV-2 infection triggers the immune cells to secrete an excess of pro-inflammatory cytokines that lead to cytokine storm. It is believed to become one of the mechanisms that cause the ARDS condition. The level of pro-inflammatory cytokines will differ with each case severity. This study aimed to evaluate the profile of pro-inflammatory cytokines in COVID-19 patients with different severity. Therefore, it could be used as a therapeutic approach for cytokine storm conditions. It was a cross sectional study using plasma samples of COVID-19 patients from Jakarta Islamic Hospital Pondok Kopi and Dr. M. Goenawan Partowidigdo Hospital Cisarua Indonesia. The COVID-19 patients with severe (n=20) and mild to moderate (n=25) severity were involved in this study. As a negative control plasma sample from healthy subjects (n=13) was used. Plasma IL-6 levels were measured using the ELISA technique and plasma lymphocyte levels were measured using a hematology analyzer. The results showed that no significant difference between severity and gender was observed (p=0.256). Meanwhile there is a significant difference in IL-6 level between negative control mild-moderate and severe categories (p=0.015). The average IL-6 level in severe categories was higher than mild-moderate and negative control categories with values 105.375 59.75 and 64.577 pg/mL respectively. This result becomes supporting evidence that there is a cytokine storm condition in severe COVID-19 patients. Furthermore, the lymphocyte level in the severe group is significantly lower than the mild to moderate group. This result may indicate lymphocytopenia in the severe group.
COVID-19是由攻击人类呼吸系统的SARS-CoV-2感染引起的。在严重的情况下,它会导致肺炎、肾衰竭、急性呼吸窘迫综合征(ARDS)甚至死亡。SARS-CoV-2感染触发免疫细胞分泌过量的促炎细胞因子,导致细胞因子风暴。这被认为是导致ARDS的机制之一。促炎细胞因子的水平会随着病情的严重程度而有所不同。本研究旨在评估不同严重程度COVID-19患者的促炎细胞因子特征。因此,它可以作为一种治疗细胞因子风暴的方法。这是一项横断面研究,使用了来自印度尼西亚雅加达伊斯兰医院Pondok Kopi和Dr. M. Goenawan Partowidigdo医院的COVID-19患者的血浆样本。本研究纳入重症(n=20)和轻中度(n=25)的COVID-19患者。阴性对照采用健康受试者(n=13)的血浆样本。采用ELISA技术测定血浆IL-6水平,采用血液学分析仪测定血浆淋巴细胞水平。结果显示,严重程度与性别无显著差异(p=0.256)。阴性对照轻、中度、重度组患者IL-6水平差异有统计学意义(p=0.015)。重度组平均IL-6水平高于轻、中度组和阴性对照组,分别为105.375、59.75和64.577 pg/mL。这一结果成为支持COVID-19重症患者存在细胞因子风暴条件的证据。重度组淋巴细胞水平明显低于轻、中度组。此结果可能提示重症组淋巴细胞减少。
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引用次数: 2
Innovative approach of nanoformula moisturizer applications in atopic dermatitis: a review 纳米配方保湿剂在特应性皮炎中的应用:综述
Pub Date : 2021-06-14 DOI: 10.19106/jmedsci005302202112
Nyoman Suryawati, Made Wardhana
The skin barrier defect is the first step in the development of atopic dermatitis (AD). Various therapeutic guidelines recommend using moisturizers to maintain the skin barrier and the prevention of AD. The use of a moisturizer in the form of barrier cream is considered to improve the skin barrier. However, this dosage form is occlusion and has an oily texture, resulting in patient noncompliance with therapy. Various techniques were developed to improve patient compliance in applying topical preparations, one of which is by developing nanotechnology. Recent studies aim to develop nanoformula preparations because they can help deliver drug molecules to specific targets with minimize side effects. The application of nanoformula moisturizer is promising in the management of AD because of its ability to reduce water loss and prevent irritation and produce formulations with a thinner texture to increase therapeutic compliance in AD patients.
皮肤屏障缺损是发展为特应性皮炎(AD)的第一步。各种治疗指南建议使用润肤霜来维持皮肤屏障和预防AD。使用屏障霜形式的保湿霜被认为可以改善皮肤屏障。然而,这种剂型是闭塞的,具有油性质地,导致患者不遵守治疗。开发了各种技术来提高患者在应用局部制剂时的依从性,其中之一是开发纳米技术。最近的研究旨在开发纳米配方制剂,因为它们可以帮助将药物分子运送到特定的目标,同时将副作用降到最低。纳米配方润肤霜的应用在阿尔茨海默病的治疗中很有前景,因为它能够减少水分流失和防止刺激,并产生更薄的质地配方,以增加阿尔茨海默病患者的治疗依从性。
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引用次数: 0
The predictor factor of final visual acuity (VA) of acute retrobulbar neuritis patients receiving optic neuritis treatment trial (ONTT) regiment 视神经炎治疗试验(ONTT)组急性球后神经炎患者最终视力(VA)的预测因素
Pub Date : 2021-06-09 DOI: 10.19106/jmedsci005302202104
Tatang Talka Gani, Melvina Nidya Sandra, I. Mahayana, Datu Respatika, H. Hartono
The study aimed to investigate the efficacy of intravenous optic neuritis treatment trial (ONTT) regiment on the treatment ofpatients with acute retrobulbar neuritis.This was a cross sectional studyusing medical records data of patients diagnosed with unilateral or bilateral retrobulbar neuritis by normal funduscopic findings and typical optic neuritis perimetry results within 14 days of onset fromtheNeuro-ophthalmology Clinic, Department of Ophthalmology, Dr. Sardjito General Hospital, Yogyakarta from January to December 2015. Medical records data of patients who received 1000 mg methylprednisolone IV per day for 3 days followed by 11 days 1 mg/kg body weight oral prednisolone were reviewed. Visual acuity (VA) at onset, final VA at time of follow up, delta VA improvement and time of follow up were included in the analyses.Twenty data of patients aged 33.95±8.07 years with VA at onset of 1.96±0.81 (~ 1 mCF) were analyzed in this study. Significantly improvement in final VAafter treatment to be 1.39±1.12 (~5mCF) was reported (p=0.001). The VA at onsetwas a predictive factor for final VA (p 0.05). In conclusion, there is VA improvement after the treatment of ONTT regiment. The VA at onset is a predictive factorof final VA on patients with acute retrobulbar neuritis. ABSTRAK Penelitian ini bertujuan mengkaji efektivitas regimen optic neuritis treatment trial (ONTT) intravena pada pengobatan pasien dengan neuritis retrobulbar faseakut. Penelitian potong lintang ini menggunakan rekam medis pasien yang didiagnosis neuritis retrobulbar unilateral atau bilateral dengan temuan funduskopi normal dan hasil perimetri neuritis optik yang khas dalam waktu 14 haris etelah onset dari Klinik Neuro-optamalmologi, Departemen Oftalmologi, Rumah Sakit Umum Pusat Dr. Sardjito, Yogyakarta dari Januari-Desember 2015. Data rekam medis pasien yang menerima1000 mg metilprednisolon IV per haris elama 3 hari diikuti oleh prednisolon oral selama 11 hari dengan dosis 1 mg/kg berat badan dianalisis. Ketajaman visual (VA) saat onset, VA akhir saat tindaklanjut, peningkatan VA, dan waktu tindak lanjut dianalisis. Sebanyak 20 data pasien berumur 33,95 ±8,07 tahun dengan VA saat onset 1,96 ±0,81 (~ 1 mCF) dianalisis dalam penelitian ini. Perbaikan VA akhir menjadi 1,39±1,12 (~5mCF) dilaporkan (p=0,001). Ketajaman visual saat onset merupakan factor predictor VA akhir (p 0,05). Dapat disimpulkan, terdapat peningkatan VA pasien setelah pengobatan regimen ONTT. Ketajaman visual saat onset merupakan factor prediktor VA akhir pada pasien dengan neuritis retrobulbar akut.
本研究旨在探讨静脉视神经炎治疗试验(ONTT)团治疗急性球后神经炎的疗效。这是一项横断面研究,使用了2015年1月至12月在日惹Dr. Sardjito总医院眼科欧洲眼科诊所就诊的14天内通过正常眼底检查结果和典型视神经炎周边检查结果诊断为单侧或双侧球后神经炎的患者病历数据。对每日1000mg IV甲基强的松龙治疗3天,随后11天口服1mg /kg体重的强的松龙患者的病历资料进行回顾。分析发病时的视敏度(VA)、随访时的终视敏度(VA)、视敏度(delta VA)改善情况和随访时间。本文分析了20例年龄为33.95±8.07岁的VA患者的资料,发病时为1.96±0.81 (~ 1 mCF)。治疗后的终值为1.39±1.12 (~5mCF),差异有统计学意义(p=0.001)。发病时VA是最终VA的预测因素(p < 0.05)。综上所述,ONTT组治疗后VA有改善。急性球后神经炎患者发病时VA是最终VA的预测因素。摘要/ abstract摘要:Penelitian inibertujuan mengkaji有效治疗方案视神经炎治疗试验(ONTT):静脉注射Penelitian bertujuan mengkaji有效治疗方案视神经炎。Penelitian potong lintang ini menggunakan rekam medis pasien yang诊断神经炎球后单侧atau双侧dengan teman funduskopi正常danhasil周围神经炎optik yang khas dalam waktu 14 hari etelah发作dari Klinik神经系统疾病,神经内科,Rumah Sakit Umum Pusat博士,日惹2015年1月至12月。数据分析:每日口服甲替尼松龙1 mg/kg;每日口服甲替尼松龙1 mg/kg;每日口服甲替尼松龙3 mg/kg;每日口服甲替尼松龙1 mg/kg;Ketajaman visual (VA) at onset, VA akhir saat tindaklanjut, peningkatan VA, dan waktu tindaklanjut dianalt。Sebanyak 20例数据显示:1、96±0.81 (~ 1 mCF)的起始值为33,95±8,07。Perbaikan VA akhir menjadi 1,39±1,12 (~5mCF) (p=0,001)。Ketajaman视力障碍的发作与merupakan因子预测因子的相关性(p < 0.05)。Dapat disimpulse, terdapat peningkatan VA pasien setelah pengobatan养生法ONTT。ktajaman视炎发作的merupakan因子预测因子VA的研究进展。
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引用次数: 0
Prevalence and risk factors of intestinal protozoan infection among child students with disabilities in Bantul District, Yogyakarta Special Region, Indonesia 印尼日惹特区班图尔区残疾学生肠道原生动物感染流行及危险因素
Pub Date : 2021-06-09 DOI: 10.19106/jmedsci005302202109
Fahriana Azmi, E. H. Murhandarwati, M. A. Wijayanti
Children with disabilities are excluded from many aspects of life. Unfortunately, they have an increased risk of infection from many kinds of pathogens including intestinal protozoan. This study aimed to determine the prevalence of intestinal protozoan infections and to evaluate the associated factors among children with disabilities in Bantul District, Yogyakarta Special Region, Indonesia. A cross-sectional study was conducted at school with special needs between June-December, 2019. A total of 150 participants were recruited through simple random sampling. Stool samples were examined microscopically by formalin-ether concentration and Ziehl-Neelsen staining technique. Age was analyzed using the Mann-Whitney tests, while the other variables used chi-square tests. Multivariable logistic regression was conducted to identify factors associated with intestinal protozoan infections. The adjusted prevalence ratio with a 95% confidence interval at a 5% level of significance was used to measure the strength of association. Overall, there were 15 children infected by intestinal protozoan among 130 subjects with mean age of participants of 9.83 ± 3.1 years. The intestinal protozoan species were Entamoeba histolytica 7 (5.38%), Giardia lamblia 4 (3.08%), Blastocystis hominis 7 (5.38%) and Iodamoeba butschlii 1 (0.77%). Prevalence of intestinal protozoan infection among children with disabilities in Bantul District, Yogyakarta, Special Region was 11.54%. There were no significant correlations between the risk factors and intestinal protozoan infection among children with disabilities (p>0.05).
残疾儿童被排除在生活的许多方面之外。不幸的是,它们受到包括肠道原生动物在内的多种病原体感染的风险增加。本研究旨在确定印度尼西亚日惹特区班图尔区残疾儿童肠道原生动物感染的流行情况,并评估相关因素。2019年6月至12月期间,在有特殊需求的学校进行了一项横断面研究。通过简单随机抽样,共招募了150名参与者。采用福尔马林-乙醚浓度和Ziehl-Neelsen染色技术对粪便样品进行显微镜检查。年龄采用Mann-Whitney检验,其他变量采用卡方检验。采用多变量logistic回归来确定与肠道原虫感染相关的因素。采用95%置信区间在5%显著性水平上的校正患病率来衡量关联强度。总体而言,130名受试者中有15名儿童感染肠道原虫,平均年龄为9.83±3.1岁。肠道原虫种类为溶组织内阿米巴7(5.38%)、贾第鞭毛虫4(3.08%)、人芽囊虫7(5.38%)和布氏碘达摩巴1(0.77%)。日惹特区班图尔区残疾儿童肠道原虫感染率为11.54%。危险因素与残疾儿童肠道原虫感染无显著相关性(p>0.05)。
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引用次数: 0
Epidermophyton floccosum as apossible aethiological agent of tinea capitis: a case report 絮体表皮植物可能是头癣的病原学因子1例
Pub Date : 2021-06-04 DOI: 10.19106/jmedsci005302202110
R. Chandra, N. Z. Lubis
Tinea capitis is a superficial fungal infection of scalp that affects particularly school-aged children. It is usually caused by dermatophytes, although Epidermophyton floccosum can cause the tinea capitis. Tinea capitis caused by the E. floccosum is quite interesting because it can confirm the sporadic occurrence of hair parasitism by this dermatophyte. In this article, it was reported tinea capitis caused by E. floccosum. A 15-year-old girl, presented with itchy scaly alopecia on scalp since 1 week ago. The patient denied any contact with cat or dog, and there was not any family history. On physical examinations, lymphadenopathies were found at both lateral neck and alopecia with scales and crusts, lenticular to nummular sizes, at scalp. Hair-pull test was positive. The trichoscopy examination found comma hairs, broken hairs, and black dots. The fungal culture examination discovered the growth of E. floccosum. The patient was diagnosed with tinea capitis and treated with 500 mg of griseofulvin orally, 10 mg of cetirizine orally, and 2% of ketoconazole shampoo. Epidermophyton floccosum is an anthropophilic dermatophyte that frequently causes tinea cruris, tinea pedis, tinea corporis and onychomycosis, but not tinea capitis. Several reports have showed the capability of E. floccosum in perforating hairs and causing tinea capitis. In conclusion, E. floccosum is a possible aethiological agent of tinea capitis through its ability to perforate hairs.
头癣是一种浅表头皮真菌感染,尤其影响学龄儿童。它通常是由皮肤癣菌引起的,虽然絮状表皮癣菌可以引起头癣。由絮状绦虫引起的头癣是非常有趣的,因为它可以证实这种皮肤真菌的头发寄生的散发发生。本文报道了由絮状绦虫引起的头癣。一名15岁女孩,自1周前出现头皮发痒鳞状脱发。患者否认与猫、狗有过接触,无家族史。在体格检查中,在颈部外侧发现淋巴结病变,头皮有鳞片和结痂,透镜状到数字状大小。拔毛试验呈阳性。毛镜检查发现了逗号毛、断毛和黑点。真菌培养检查发现菌体生长。患者诊断为头癣,口服灰黄霉素500 mg,口服西替利嗪10 mg, 2%酮康唑洗发水治疗。絮状表皮植物是一种嗜人的皮肤植物,经常引起头癣、足癣、体癣和甲癣,但不会引起头癣。有几篇报道表明,絮状绦虫有穿孔毛发和引起头癣的能力。综上所述,通过其刺穿毛发的能力,绒球菌可能是头癣的病原学因子。
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引用次数: 1
Comparison of diagnostic accuracy between clinical examination and magnetic resonance imaging (MRI) in diagnosing anterior cruciate ligament (ACL) rupture on Indonesian population 临床检查与磁共振成像(MRI)诊断印尼人群前交叉韧带(ACL)断裂的准确性比较
Pub Date : 2021-05-25 DOI: 10.19106/jmedsci005302202107
Luthfi Hidayat, A. F. R. Triangga, Muhamad Afrizal Farkhan, B. F. P. Rahayu, R. Magetsari
Anterior cruciate ligament (ACL) injury is the most common knee ligament injured. Anterior drawer and Lachman tests are the most common physical examinations for helping diagnose ACL injuries, while magnetic resonance imaging (MRI) is the first choice of supporting examination for evaluating any internal abnormality of the knee. However, studies concerning the accuracy of those examinations in the Indonesian population are limited. This study aimed to compare the accuracy between the anterior drawer test, Lachman test, and MRI in diagnosing ACL injury in Javanese patients. This retrospective study used medical records data of patients who underwent knee arthroscopy in the Department of Orthopaedics and Traumatology, Dr. Sardjito General Hospital, Yogyakarta in 2018. The MRI and the clinical examination results were compared to the arthroscopy results as the gold standard. The study showed the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy for the anterior drawer test were 86.67% (95%CI: 69.28-96.24%), 80% (CI: 44.39-97.48%), 92.86% (CI: 78.88-97.84), 66.67% (CI: 43.28-83.98%), and 85% (CI: 70.16-94.29%), respectively. Lachman test had 96.67% (CI: 82.78-99.92%) sensitivity, 90% (CI: 55.50-99.75%) specificity, 96.67% (CI: 81.86-99.47%) PPV, 90% (CI: 56.44-98.43%) NPV, and 95% (CI: 83.08-99.39%) accuracy. The diagnostic parameters of MRI were 83.33% (CI: 65.28-94.36%) for sensitivity, 60% (CI: 26.24-87.84%) for specificity, 86.21% (CI: 74.21-93.14%) for PPV, 54.55% (CI: 31.77-75.57%) for NPV, and 77.50% (CI: 61.55-89.16%) for accuracy. In conclusion, the Lachman test has better accuracy than the anterior drawer test. Both the anterior drawer and Lachman tests had higher accuracy compared to the MRI.
前交叉韧带(ACL)损伤是膝关节最常见的韧带损伤。前抽屉试验和拉赫曼试验是帮助诊断前交叉韧带损伤最常用的体格检查,而磁共振成像(MRI)是评估任何膝关节内部异常的首选辅助检查。但是,关于这些检查在印度尼西亚人口中的准确性的研究是有限的。本研究旨在比较爪哇患者前抽屉试验、拉赫曼试验和MRI诊断前交叉韧带损伤的准确性。这项回顾性研究使用了2018年在日惹Sardjito综合医院骨科和创伤科接受膝关节镜检查的患者的医疗记录数据。将MRI和临床检查结果与关节镜检查结果作为金标准进行比较。研究显示,前抽屉试验的敏感性、特异性、阳性预测值(PPV)、阴性预测值(NPV)和准确性分别为86.67% (95%CI: 69.28 ~ 96.24%)、80% (CI: 44.39 ~ 97.48%)、92.86% (CI: 78.88 ~ 97.84)、66.67% (CI: 43.28 ~ 83.98%)和85% (CI: 70.16 ~ 94.29%)。Lachman试验灵敏度96.67% (CI: 82.78 ~ 99.92%),特异性90% (CI: 55.50 ~ 99.75%), PPV 96.67% (CI: 81.86 ~ 99.47%), NPV 90% (CI: 56.44 ~ 98.43%),准确率95% (CI: 83.8 ~ 99.39%)。MRI诊断参数敏感性为83.33% (CI: 65.28 ~ 94.36%),特异性为60% (CI: 26.24 ~ 87.84%), PPV为86.21% (CI: 74.21 ~ 93.14%), NPV为54.55% (CI: 31.77 ~ 75.57%),准确性为77.50% (CI: 61.55 ~ 89.16%)。综上所述,Lachman试验比前抽屉试验具有更好的准确性。与MRI相比,前抽屉和拉赫曼测试都具有更高的准确性。
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引用次数: 0
Distribution and clinical characteristic of malaria patients in Weoe Public Health Center, Malaka District, East Nusa Tenggara in 2019 2019年东努沙登加拉马拉卡区威伊公共卫生中心疟疾患者分布及临床特征分析
Pub Date : 2021-05-25 DOI: 10.19106/jmedsci005302202108
Maria Seraphine Agusta, N. Ariani, C. Setiawan
Malaria remains a health problem in Indonesia including in East Nusa Tenggara (ENT) Province where its incidence is high. Weoe Public Health Center located in Malaka District, ENT Province has an important role as the front-line in the malaria control. The high number of malaria cases in this area may induce an economic burden due to unproductiveness at workplaces even death. This study aimed to overview the distribution and clinical characteristics of malaria patients in Weoe Public Public Health Center, Malaka District. This was a descriptive cross sectional study with saturated sampling method using secondary data of patient’s medical record from January-December 2019. Malaria patients treated at the Weoe Public Health Center from eight villages were selected in this study. The data of the time of ill, patient’s residence, gender, age, complaints, temperature, type of malaria, therapy, treatment results, and follow up blood smear tests result were collected. Among 815 patients suspected malaria, 198 (24.3%) were confirmed malaria positive caused by Plasmodium falciparum (41.4%) and P. vivax (58.6%). The highest cases occurred in February which reached 36.4% of the total cases. The highest incidence of malaria was found in Weoe Village (2.33%), dominated by male patients (57.6%), and mostly occurred at age 6-12 years (29.3%). Patients presented with fever (100%) followed by non-classical malaria complaints such as nausea and vomiting (46%), headache (33%), chills (30.8%), and flu symptoms (14.1%). All malaria patients were treated with combination of dihydroartemisinin-piperaquine (DHP) and primaquine (PQ) with a 100% cure rate and follow up blood smear test are negative from malaria parasite.
疟疾在印度尼西亚仍然是一个健康问题,包括在其发病率高的东努沙登加拉省。位于耳鼻喉省马六甲区的Weoe公共卫生中心作为防治疟疾的第一线发挥着重要作用。这一地区疟疾病例数量众多,可能由于工作场所生产力低下而造成经济负担,甚至死亡。本研究旨在了解马拉卡区Weoe公共卫生中心疟疾患者的分布和临床特征。这是一项描述性横断面研究,采用饱和抽样方法,使用2019年1月至12月患者病历的二次数据。本研究选择来自八个村庄的在Weoe公共卫生中心接受治疗的疟疾患者。收集患者发病时间、居住地、性别、年龄、主诉、体温、疟疾类型、治疗方法、治疗结果及随访血液涂片检查结果等资料。815例疑似疟疾患者中,恶性疟原虫(41.4%)和间日疟原虫(58.6%)引起的确诊疟疾阳性198例(24.3%)。2月份病例最多,占总病例的36.4%。疟疾发病率最高的地区为威乌村(2.33%),以男性为主(57.6%),以6 ~ 12岁年龄组为主(29.3%)。患者表现为发热(100%),其次是非典型疟疾主诉,如恶心和呕吐(46%)、头痛(33%)、发冷(30.8%)和流感症状(14.1%)。所有疟疾患者均采用双氢青蒿素-哌喹(DHP)和伯氨喹(PQ)联合治疗,治愈率100%,随访血液涂片检查均为疟原虫阴性。
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引用次数: 0
Effects of valsartan compared with telmisartan in reducing insulin resistance on type 2 diabetes mellitus (T2DM) patients with hypertension 缬沙坦与替米沙坦降低2型糖尿病合并高血压患者胰岛素抵抗的效果比较
Pub Date : 2021-05-24 DOI: 10.19106/jmedsci005302202102
Hemi Sinorita, L. B. Purnomo, R. B. Pramono
Insulin resistance is a major risk factor for patients with type 2 diabetes mellitus (T2DM). Telmisartan and valsartan are angiotensin II type I receptor blockers (ARBs) that are often used in patients with metabolic syndrome and T2DM. This study aimed to compare the effect of valsartan and telmisartan in reducing insulin resistance on T2DM with hypertension. Patients of T2DM were open-label screened at the Endocrinology Policlinic, Department of Internal Medicine, Dr. Sardjito General Hospital, Yogyakarta, and then randomized into two groups. The first group received valsartan 80 mg per day up to 160 mg per day, the second group received telmisartan 40 mg per day up to 80 mg per day in addition with life-style modifying and diabetes therapy. Homeostasis model assessment of insulin resistance (HOMA-IR), triglyceride and HDL cholesterol levels of patients were measured before and after receiving telmisartan and valsartan for 12 weeks. A total of forty-nine outpatients were involved in this study comprised of 25 female patients (51%) and 24 male patients (49%) with 27 patients (55.1%) received telmisartan and 22 patients (44.9%) received valsartan as the hypertension therapy. No significantl difference were observed between telmisartan group compared with valsartan group in HOMA-IR (14.01 ± 16.39 vs. 5.31 ± 3.51; p=0.053), triglyceride levels (165.71 ± 94.70 vs 144.41 ± 48.33 mg/dL; p=0.620), HDL-C level (48.57 ± 9.78 vs 49.24 vs 49.24 ± 12.56 mg/dL; p=0.999). In conclusion, telmisartan demonstrated no difference compared to valsartan in reducing insulin resistance on T2DM patients with hypertension.
胰岛素抵抗是2型糖尿病(T2DM)患者的主要危险因素。替米沙坦和缬沙坦是血管紧张素II型受体阻滞剂(arb),常用于代谢综合征和T2DM患者。本研究旨在比较缬沙坦和替米沙坦降低T2DM合并高血压患者胰岛素抵抗的效果。2型糖尿病患者在日惹Sardjito总医院内科内分泌科进行开放标签筛查,然后随机分为两组。第一组接受缬沙坦80毫克/天至160毫克/天,第二组接受替米沙坦40毫克/天至80毫克/天,此外还有生活方式改变和糖尿病治疗。在替米沙坦和缬沙坦治疗12周前后,测量患者胰岛素抵抗(HOMA-IR)、甘油三酯和高密度脂蛋白胆固醇水平的稳态模型评估。本研究共纳入49例门诊患者,其中女性25例(51%),男性24例(49%),其中27例(55.1%)患者接受替米沙坦治疗,22例(44.9%)患者接受缬沙坦治疗。替米沙坦组与缬沙坦组HOMA-IR无显著差异(14.01±16.39∶5.31±3.51;p=0.053),甘油三酯水平(165.71±94.70 vs 144.41±48.33 mg/dL;p=0.620), HDL-C水平(48.57±9.78 vs 49.24 vs 49.24±12.56 mg/dL;p = 0.999)。总之,替米沙坦与缬沙坦在降低T2DM合并高血压患者胰岛素抵抗方面无差异。
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引用次数: 0
Correlation between vascular endothelial growth factor (VEGF) expression with histopathological findings in osteosarcoma 血管内皮生长因子(VEGF)表达与骨肉瘤组织病理学表现的相关性
Pub Date : 2021-05-24 DOI: 10.19106/jmedsci005302202101
Fikar Arsyad Hakim, Y. Putro, Y. M. Sakti, R. Magetsari, I. Widodo, E. Dwianingsih
Vascular endothelial growth factor (VEGF) expression is associated with malignancy progression, metastasis, and poor prognosis in many malignancies, including osteosarcoma. However, studies concerning correlations between VEGF expression and histopathological prognostic factors ofosteosarcoma are limited. This study aimed to evaluate the correlations between VEGF expression and histopathological findings in osteosarcoma’spatients.This was a cross-sectional study using formalin-fixed paraffin embedded (FFPE) samples of 32 osteosarcoma’s patients from Dr. Sardjito General Hospital, Yogyakarta. Histopathological findings of specimens were re-evaluated by two independent observers, recorded for the subtypes, invasiveness, grading, mitotic counts, and tumor infiltrating lymphocytes (TIL). Expression of VEGF was determined based on immunostaining and evaluated using immunoreactivity score (IRS).Chi-square and Spearman correlation test were used to analyze the association between variables. Range of VEGF expression score was 0 to 11, with mean 5.09. Significant negative correlation between the VEGF expression and TIL was observed (p=0.046). However, there was no significant correlations between the VEGF expression and osteosarcomas subtypes, invasion, grading or mitotic counts (p> 0.05). In conclusion, the VEGF expression is associated with TIL. Further study is needed to evaluate the roles of VEGF and lymphocytes in osteosarcoma development dan progression in order to better understand of the role of VEGF in immunotherapy of osteosarcoma.
血管内皮生长因子(VEGF)的表达与包括骨肉瘤在内的许多恶性肿瘤的恶性进展、转移和不良预后相关。然而,关于VEGF表达与骨肉瘤组织病理学预后因素之间相关性的研究是有限的。本研究旨在评估骨肉瘤患者VEGF表达与组织病理学结果的相关性。这是一项横断面研究,使用福尔马林固定石蜡包埋(FFPE)样本,来自日惹Dr. Sardjito总医院的32例骨肉瘤患者。由两名独立观察员重新评估标本的组织病理学结果,记录亚型、侵袭性、分级、有丝分裂计数和肿瘤浸润淋巴细胞(TIL)。免疫染色法检测VEGF表达,免疫反应性评分法(IRS)评价VEGF表达。采用卡方检验和Spearman相关检验分析变量间的相关性。VEGF表达评分范围为0 ~ 11分,平均5.09分。VEGF表达与TIL呈显著负相关(p=0.046)。然而,VEGF表达与骨肉瘤亚型、侵袭、分级或有丝分裂计数无显著相关性(p < 0.05)。综上所述,VEGF表达与TIL相关。为了更好地了解VEGF在骨肉瘤免疫治疗中的作用,需要进一步研究VEGF和淋巴细胞在骨肉瘤发生和进展中的作用。
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引用次数: 0
Hirschsprung’s disease: epidemiology, diagnosis, and treatment in a retrospective hospital-based study 巨结肠病:一项回顾性医院研究的流行病学、诊断和治疗
Pub Date : 2021-04-23 DOI: 10.19106/jmedsci005302202103
Andi Sinapati Palissei, Ahmadwirawan Ahmadwirawan, M. Faruk
Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized by the absence of ganglion cells in the myenteric (Auerbach’s) and submucosal (Meissner’s) plexuses of the intestine, causing maximum obstruction in neonates. The purpose of this study was to investigate patient characteristics, clinical presentation, investigations, surgical treatment, and outcome. This study is a retrospective study of HD cases. Data obtained from medical records at the institution. Of the 109 with a positive rectal biopsy diagnosis, 91 were patients with this disease. There were more cases in boys than girls with a ratio of 1.37: 1. The patients were grouped into 4 age groups: neonates 29 cases (26.61%); infants/toddlers/young children 55 cases (50.46%); children over 5 years16 cases (14.69%); and teenagers 9 cases (8.24%). The neonates generally presented with abdominal distension, green vomiting, and a history of delayed meconium release, while the toddler, child, and adolescent groups experienced constipation and abdominal distension. Furthermore, from 37 patients (33.94%) that got barium enema examination, the most common transition zone was observed in the rectosigmoid (17 patients, or 45.9%). In addition, The Duhamel procedure was the most frequent pull-through procedure found in our cohort which was performed in 40 patients (36.70%). In conclusion, HD is mostly found in male infants/toddlers/young children with abdominal distention and chronic constipation as common symptoms. The barium enema shows the rectosigmoid as the most common transition zone, while the Duhamel pull-through procedure is the primary definitive operative action performed.
先天性巨结肠病(先天性巨结肠)是一种以肠肌丛(奥尔巴赫氏)和粘膜下(迈斯纳氏)神经丛中神经节细胞缺失为特征的疾病,可引起新生儿最大程度的梗阻。本研究的目的是探讨患者的特征、临床表现、调查、手术治疗和结果。本研究是对HD病例的回顾性研究。从该机构的医疗记录中获得的数据。在109例直肠活检阳性诊断中,91例为本病患者。男孩比女孩多,比例为1.37:1。患者分为4个年龄组:新生儿29例(26.61%);婴幼儿55例(50.46%);5岁以上儿童16例(14.69%);青少年9例(8.24%)。新生儿一般表现为腹胀、绿色呕吐和胎便释放延迟,而幼儿、儿童和青少年组则出现便秘和腹胀。此外,在37例(33.94%)行钡灌肠检查的患者中,最常见的过渡区位于直肠乙状结肠(17例,45.9%)。此外,在我们的队列中,Duhamel手术是最常见的拉通手术,有40例患者(36.70%)接受了该手术。总之,HD多见于男性婴幼儿,以腹胀和慢性便秘为常见症状。钡灌肠显示直肠乙状结肠是最常见的过渡区,而Duhamel拉通手术是主要的确定手术操作。
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引用次数: 0
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Journal of thee Medical Sciences (Berkala Ilmu Kedokteran)
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