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Comparative analysis of clinical efficacy of stereotactic robot-guided puncture hematoma drainage and conventional puncture hematoma drainage in the treatment of intracerebral hemorrhage. 立体定向机器人引导穿刺血肿引流术与传统穿刺血肿引流术治疗脑出血的临床疗效对比分析。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-09-01 DOI: 10.12669/pjms.40.8.8833
Xin Gong, Hai-Qing Dong, Xin Li, Zhen-Jie Liu

Objective: To compare and analyze the clinical effectiveness of conventional puncture hematoma drainage and stereotactic robot-guided puncture hematoma drainage in managing intracerebral hemorrhage.

Methods: This is clinical comparative research. One hundred and twenty patients with the intracerebral hemorrhage who underwent puncture hematoma drainage in Baoding No.1 Central Hospital from March 2020 to May 2023 were included and were assigned into the control groups(n=60) and experimental groups(n=60) according to different treatment methods. The experimental group underwent stereotactic robot-guided puncture hematoma drainage, while the control group underwent conventional puncture hematoma drainage treatment. The duration and situation of surgery, levels of inflammatory factors, as well as preoperative and 1-week postoperative GCS scores and NIHSS scores were compared and analyzed between the two groups.

Results: In comparison with the control group, the experimental group exhibited considerably less surgical duration(p=0.00), higher amount of intraoperative blood drainage and hematoma clearance rate(p=0.00). The experimental group possessed a substantially more reduced incidence of complications(10%) in comparison with the control group(25%), with a statistically substantial distinction(p=0.03). After therapy, CRP, TNF-a, and IL-6 degrees were considerably more decreased (p=0.00) in the experimental group in comparison with the control group, while GCS grades were considerably more prominent and NIHSS grades were considerably more reduced (p=0.00).

Conclusion: Stereotactic robot-guided puncture hematoma drainage is a dependable and safe operative method to treat patients who had intracerebral hemorrhage, resulting in various benefits such as short length of operation, less injury, less inflammatory reaction, high hematoma clear efficiency and satisfactory recovery of neurological function.

目的比较分析传统穿刺血肿引流术和立体定向机器人引导穿刺血肿引流术在治疗脑出血中的临床效果:方法:本研究为临床对比研究。纳入2020年3月-2023年5月在保定市第一中心医院接受穿刺血肿引流术的120例脑出血患者,根据治疗方法的不同分为对照组(n=60)和实验组(n=60)。实验组行立体定向机器人引导下穿刺血肿引流术,对照组行常规穿刺血肿引流术。对比分析了两组患者的手术时间、手术情况、炎症因子水平以及术前和术后一周的 GCS 评分和 NIHSS 评分:结果:与对照组相比,实验组手术时间大大缩短(P=0.00),术中引流血量和血肿清除率更高(P=0.00)。实验组并发症发生率(10%)较对照组(25%)大幅降低,差异有统计学意义(P=0.03)。治疗后,实验组与对照组相比,CRP、TNF-a和IL-6的含量显著降低(P=0.00),而GCS分级显著提高,NIHSS分级显著降低(P=0.00):立体定向机器人引导下穿刺血肿引流术是治疗脑出血患者可靠、安全的手术方法,具有手术时间短、损伤小、炎症反应轻、血肿清除率高、神经功能恢复满意等优点。
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引用次数: 0
A rare cause of erectile dysfunction: Bilateral thrombosed internal iliac artery aneurysms. 勃起功能障碍的罕见病因:双侧髂内动脉瘤血栓形成。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-09-01 DOI: 10.12669/pjms.40.8.9005
Ibrahim Untan, Ahmed Said Cil

Internal iliac artery aneurysms are a relatively uncommon condition that can have serious consequences if left untreated. This paper presents a case of erectile dysfunction caused by thrombosis of the internal iliac artery aneurysms in a 52-years-old male patient with common iliac and internal iliac artery aneurysms. Following the intracavernous self-injection treatment, the patient's complaints about erectile dysfunction ceased. Aneurysms were monitored closely. To the best of our knowledge, this represents the first case of erectile dysfunction being presented as a consequence of thrombosed iliac artery aneurysms. Erectile dysfunction itself is not a life-threatening condition. However, it should be highlighted that erectile dysfunction can be a sign of life-threatening iliac artery diseases, as in this case. Therefore, it is crucial to recognize the potential seriousness of this condition and to investigate it thoroughly.

髂内动脉瘤是一种比较少见的疾病,如果不及时治疗可能会造成严重后果。本文介绍了一例因髂内动脉瘤血栓形成而导致勃起功能障碍的病例,患者男性,52 岁,患有髂总动脉和髂内动脉瘤。在进行椎管内自我注射治疗后,患者关于勃起功能障碍的主诉不再出现。动脉瘤得到了密切监测。据我们所知,这是首例因髂动脉瘤血栓形成而导致勃起功能障碍的病例。勃起功能障碍本身不会危及生命。但需要强调的是,勃起功能障碍可能是危及生命的髂动脉疾病的征兆,本病例就是如此。因此,认识到这种情况的潜在严重性并进行彻底检查至关重要。
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引用次数: 0
Cairo Consensus Statement on Research Integrity of Randomised Clinical Trials. 关于随机临床试验研究诚信的开罗共识声明》。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-09-01 DOI: 10.12669/pjms.40.8.9779
Patrick Fw Chien, Khalid S Khan, Mohamed Fawzy, Yacoub Khalaf
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引用次数: 0
An analysis of clinical application effects of 3d-printed act titanium trabecular intervertebral fusion cage in posterior lumbar interbody fusion (PLIF). 3d打印钛小梁椎体间融合笼在腰椎后路椎体间融合术(PLIF)中的临床应用效果分析。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-09-01 DOI: 10.12669/pjms.40.8.8759
Zhijun Li, Hong Wang, Zhaoqi Wang, Zhiming Qi, Qi Yao

Objective: To compare the clinical effects of applying a 3D-printed ACT titanium trabecular intervertebral fusion cage and a Polyetheretherketone (PEEK) cage in posterior lumbar interbody fusion (PLIF).

Methods: This was a clinical comparative study. Forty patients with degenerative lumbar diseases admitted at The Second People's Hospital of Dalian from January 2020 to December 2021 were selected and divided into an observation group (3D cage) and a control group (PEEK cage) using the random number table method, with each group of 20 cases. The visual analogue scale (VAS) scores, Japanese Orthopaedic Association (JOA) scores, Cobb angles at fusion segments, intervertebral height and intervertebral fusion situations of the patients between the groups were compared.

Results: No significant differences were found in their operation time, intraoperative blood losses and operation related complications(p>0.05). In terms of postoperative VAS and JOA scores in both groups, they are all significantly improved compared with those before the operation, and their differences are also statistically significant(p<0.05). However, no statistical significance exists in inter-group differences(p>0.05). Postoperative Cobb angles and intervertebral height of patients in both groups are considerably bettered compared with those before the operation. Their differences show statistical significance(p<0.05), while inter-group differences are proved to be not statistically significant(p>0.05).

Conclusions: Applying a 3D-printed ACT titanium trabecular intervertebral fusion cage or PEEK cage in PLIF has the potential to improve clinical symptoms of patients with degenerative lumbar diseases, and restore the Cobb angle and intervertebral height. 3D-printed ACT titanium trabecular intervertebral fusion cage can accelerate intervertebral fusion without increasing operation related complications.

目的比较在腰椎后路椎体间融合术(PLIF)中应用 3D 打印 ACT 钛小梁椎体间融合笼和聚醚醚酮(PEEK)椎体间融合笼的临床效果:这是一项临床对比研究。选取 2020 年 1 月至 2021 年 12 月大连市第二人民医院收治的 40 例腰椎退行性疾病患者,采用随机数字表法分为观察组(3D 椎间融合笼)和对照组(PEEK 椎间融合笼),每组 20 例。比较两组患者的视觉模拟量表(VAS)评分、日本骨科协会(JOA)评分、融合节段的 Cobb 角、椎间高度和椎间融合情况:结果:两组患者的手术时间、术中失血量和手术相关并发症无明显差异(P>0.05)。两组患者术后 VAS 评分和 JOA 评分均较术前明显改善,差异有统计学意义(P0.05)。但组间差异无统计学意义(P>0.05)。两组患者术后的 Cobb 角和椎间高度与术前相比均有明显改善。两组患者术后的 Cobb 角和椎间高度与术前相比均有明显改善,差异有统计学意义(P0.05),而组间差异无统计学意义(P>0.05):结论:在PLIF中应用3D打印ACT钛小梁椎体间融合笼或PEEK椎体间融合笼具有改善腰椎退行性疾病患者临床症状、恢复Cobb角和椎间高度的潜力。三维打印的 ACT 钛小梁椎体间融合保持架可加速椎体间融合,同时不会增加手术相关并发症。
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引用次数: 0
Right-sided infective endocarditis with ventricular septal defect. 右侧感染性心内膜炎伴室间隔缺损。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.8219
Fatina Munawar, Ikram Ahmed

Infective endocarditis (IE) affects the endothelium of the heart, with the heart valves most commonly involved. It has been documented that the annual incidence of infective endocarditis is 3-10 per 100,000 patient-years1. However, it can be underestimated since the incidence in developing countries cannot be determined accurately. Here, we present a case of a 37-year-old male who was referred from a local health facility with shortness of breath on presentation; the patient was anuric for one day and initial laboratory investigations showed metabolic acidosis, hyperkalemia, sepsis, and deranged renal function tests. The patient had received a three-week course of intravenous (IV) piperacillin-tazobactam at the previous health facility, being diagnosed as a case of infective endocarditis. An initial transthoracic echocardiogram (TTE) showed vegetation on the pulmonary valve; however, the patient was neither an IV drug abuser nor did he have any history of implantation of intracardiac devices or central venous catheters. There was no recent or remote history of dental or surgical procedures. Due to the acute kidney injury, hemodialysis sessions and IV imipenem were started. As the patient's hemodynamic profile improved by the fifth day of admission, TTE was repeated, revealing a small ventricular septal defect (VSD). This case report highlights the importance of even small VSD that could potentially lead to right-sided IE. Surgical correction of VSD could prevent such a life-threatening condition.

感染性心内膜炎(IE)影响心脏内皮,最常累及的是心脏瓣膜。有资料显示,感染性心内膜炎的年发病率为每 10 万患者年 3-10 例1 。然而,由于发展中国家的发病率无法准确确定,因此可能会被低估。在这里,我们介绍了一例 37 岁男性患者的病例,他因呼吸急促从当地一家医疗机构转诊而来;患者无尿一天,初步实验室检查显示代谢性酸中毒、高钾血症、败血症和肾功能检查异常。患者在之前的医疗机构接受了为期三周的哌拉西林-他唑巴坦静脉注射,被诊断为感染性心内膜炎。最初的经胸超声心动图(TTE)显示肺动脉瓣上有植被,但患者既不是静脉注射药物滥用者,也没有植入心内装置或中心静脉导管的病史。近期或远期没有牙科或外科手术史。由于急性肾损伤,患者开始接受血液透析治疗和亚胺培南静脉注射。入院第五天,患者的血液动力学状况有所改善,于是再次进行了 TTE 检查,结果发现了一个小的室间隔缺损 (VSD)。本病例报告强调了即使是小的室间隔缺损也有可能导致右侧 IE 的重要性。手术矫正 VSD 可以避免这种危及生命的情况。
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引用次数: 0
Clinical Efficacy of a Novel Titania Nanoparticle-Reinforced Bonding Agent in Reducing Post-Restorative Sensitivity: A randomized clinical trial. 新型二氧化钛纳米粒子强化粘接剂在降低修复后敏感性方面的临床疗效:随机临床试验。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.8779
Nehal Amir, Afsheen Mansoor, Nouman Noor, Khadim Hussain

Objective: To evaluate the clinical efficacy of novel titania-nanoparticle reinforced bonding agent on post-restorative sensitivity in patients.

Methods: This triple-blinded, randomized clinical trial included participants (n = 60) having Class- I and II cavitations with a minimum cavity depth of 3mm at Department of Operative Dentistry & Endodontics, School of Dentistry, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad from January 5, 2023, to June 20, 2023. They were randomly assigned into two groups A and B (n = 30). After informed consent, restorative intervention was accomplished using an etch-and-rinse adhesive strategy. In Group-A, titania-nanoparticle-incorporated bonding agent was used for composite restoration, while in Group-B, bonding agent without nanoparticles was used. The primary outcome was assessed using Visual Analogue Scale mean score. Participants were instructed to rate their sensitivity status at follow-ups: 24 hours, one week, and one month. Mann-Whitney U test was employed to compare sensitivity between the two groups.

Results: According to results of this trial, a significant difference was observed between two groups after 24 hours (p = 0.004) and one week (p = 0.002). However, no discernible difference was observed after one month (p = 0.643).

Conclusion: Post-restorative sensitivity in patients with composite restorations was reduced using titania-reinforced bonding agents as compared to bonding agents without nanoparticles. This shows that inclusion of titania nanoparticles into adhesive dentistry could be beneficial in resolving post-restorative sensitivity occurring with composite restorations.

目的评估新型二氧化钛纳米粒子强化粘接剂对患者修复后敏感性的临床疗效:该三重盲法随机临床试验的参与者(n = 60)均为伊斯兰堡沙希德-佐勒菲卡尔-阿里-布托医科大学牙科学院牙科手术与牙髓病学系的 I 级和 II 级龋洞患者,龋洞深度最小为 3 毫米,试验时间为 2023 年 1 月 5 日至 2023 年 6 月 20 日。他们被随机分配到 A 和 B 两组(n = 30)。在获得知情同意后,采用蚀刻-冲洗粘接策略进行修复干预。在 A 组中,复合树脂修复使用的是二氧化钛-纳米颗粒结合剂,而在 B 组中,使用的是不含纳米颗粒的结合剂。主要结果采用视觉模拟量表平均分进行评估。要求参与者在随访时对其敏感度进行评分:24小时、一周和一个月。采用 Mann-Whitney U 检验比较两组的敏感性:试验结果显示,24 小时后(P = 0.004)和一周后(P = 0.002),两组之间存在显著差异。然而,一个月后未观察到明显差异(p = 0.643):结论:与不含纳米颗粒的粘接剂相比,使用二氧化钛增强型粘接剂可降低复合树脂修复体患者修复后的敏感性。这表明,在牙科粘接剂中加入纳米二氧化钛颗粒有利于解决复合树脂修复体出现的修复后敏感问题。
{"title":"Clinical Efficacy of a Novel Titania Nanoparticle-Reinforced Bonding Agent in Reducing Post-Restorative Sensitivity: A randomized clinical trial.","authors":"Nehal Amir, Afsheen Mansoor, Nouman Noor, Khadim Hussain","doi":"10.12669/pjms.40.7.8779","DOIUrl":"10.12669/pjms.40.7.8779","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the clinical efficacy of novel titania-nanoparticle reinforced bonding agent on post-restorative sensitivity in patients.</p><p><strong>Methods: </strong>This triple-blinded, randomized clinical trial included participants (n = 60) having Class- I and II cavitations with a minimum cavity depth of 3mm at Department of Operative Dentistry & Endodontics, School of Dentistry, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad from January 5, 2023, to June 20, 2023. They were randomly assigned into two groups A and B (n = 30). After informed consent, restorative intervention was accomplished using an etch-and-rinse adhesive strategy. In Group-A, titania-nanoparticle-incorporated bonding agent was used for composite restoration, while in Group-B, bonding agent without nanoparticles was used. The primary outcome was assessed using Visual Analogue Scale mean score. Participants were instructed to rate their sensitivity status at follow-ups: 24 hours, one week, and one month. Mann-Whitney U test was employed to compare sensitivity between the two groups.</p><p><strong>Results: </strong>According to results of this trial, a significant difference was observed between two groups after 24 hours (p = 0.004) and one week (p = 0.002). However, no discernible difference was observed after one month (p = 0.643).</p><p><strong>Conclusion: </strong>Post-restorative sensitivity in patients with composite restorations was reduced using titania-reinforced bonding agents as compared to bonding agents without nanoparticles. This shows that inclusion of titania nanoparticles into adhesive dentistry could be beneficial in resolving post-restorative sensitivity occurring with composite restorations.</p>","PeriodicalId":19958,"journal":{"name":"Pakistan Journal of Medical Sciences","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11255811/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141875631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficacy, safety, and quality of life profile of Genotype-3 Chronic Hepatitis-C Pakistani patients receiving ledipasvir plus sofosbuvir treatment. 基因型 3 慢性丙型肝炎巴基斯坦患者接受 ledipasvir 加索非布韦治疗的疗效、安全性和生活质量概况。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.7869
Zahid Yaseen Hashmi, Sandeed Hashmi, Ali Raza

Objective: This study aimed to assess the overall treatment response of Genotype-3 Chronic HCV Pakistani Patients with or without cirrhosis to Ledipasvir plus Sofosbuvir combination.

Method: In this observational study, HCV Genotype-3 patients were enrolled from Liver Center, DHQ Hospital, Faisalabad and divided into two groups, i.e., non-cirrhotic and compensated cirrhotic patients. The study spanned for a period of 24 months (November 2019 - November 2021) from the first enrollment to the last follow up. Non-cirrhotic patients received Ledipasvir/Sofosbuvir (LDV/SOF) 90/400mg for 12 weeks and cirrhotic patients received LDV/SOF with Ribavirin (RBV) for 12 weeks and without RBV for 24 weeks. The treatment efficacy in terms of sustained virological response (SVR12) was monitored 12 weeks post-treatment. The safety profile, and health-related quality of life (HRQoL) were monitored from baseline to follow-up visits.

Results: Two hundred and ninety out of 309 (93.85%) non-cirrhotic and 31 out of 33 (93.94%) compensated cirrhotic patients achieved SVR-12. The safety profile of the non-cirrhotic and compensated cirrhotic patients was comparable throughout the study duration. Fatigue was the most commonly reported adverse event (AE) in non-cirrhotic and compensated cirrhotic patients, followed by headache, nausea, and fever. The HRQoL improved from baseline to follow-up visits among patients of both groups.

Conclusion: It is concluded that LDV and SOF combination regimen is safe and effective for treating Genotype-3 HCV patients without cirrhosis/compensated cirrhosis, and also improves the patient's HRQoL.

研究目的本研究旨在评估有肝硬化或无肝硬化的基因型 3 型慢性 HCV 巴基斯坦患者对莱迪帕韦加索非布韦联合疗法的总体治疗反应:在这项观察性研究中,费萨拉巴德DHQ医院肝脏中心招募了HCV基因型-3患者,并将其分为两组,即非肝硬化患者和代偿期肝硬化患者。研究从首次登记到最后一次随访为期 24 个月(2019 年 11 月至 2021 年 11 月)。非肝硬化患者接受莱迪帕韦/索非布韦(LDV/SOF)90/400mg治疗12周,肝硬化患者接受LDV/SOF联合利巴韦林(RBV)治疗12周和不联合RBV治疗24周。治疗后 12 周监测持续病毒学应答(SVR12)的疗效。从基线到随访,对安全性和健康相关生活质量(HRQoL)进行了监测:309例非肝硬化患者中有290例(93.85%)和33例代偿性肝硬化患者中有31例(93.94%)达到了SVR-12。在整个研究期间,非肝硬化患者和肝硬化代偿期患者的安全性相当。疲劳是非肝硬化患者和肝硬化代偿期患者最常报告的不良事件(AE),其次是头痛、恶心和发热。从基线到随访,两组患者的 HRQoL 均有所改善:结论:LDV和SOF联合疗法对治疗无肝硬化/代偿期肝硬化的基因型3 HCV患者安全有效,并能改善患者的HRQoL。
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引用次数: 0
Comparison of different preoperative fasting times for pediatric elective surgical procedures: A randomized controlled trial. 儿科择期手术不同术前禁食时间的比较:随机对照试验
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.8403
Humna Jasarat, Fatima Naumeri

Objective: To compare the mean residual gastric volume and gastric pH with standard and liberal fasting in children undergoing general anesthesia for elective procedures.

Methods: A randomized controlled trial (NCT05922072) was conducted at Department of Pediatric Surgery, Mayo Hospital Lahore from June 2021 to December 2021 and 120 patients undergoing elective daycare surgical procedures under general anesthesia were enrolled. Patients were divided into Group-A (Standard fasting) and Group-B (Liberal fasting). Group-A with 6-, 4- and 2-hours Nil per oral (NPO) for solids/ formula milk, breast milk and clear fluid, while Group-B with six, four and one hour NPO for solids/ formula milk, breast milk and clear fluid respectively. Residual gastric volume and pH were measured after anesthetizing the patient. Effect modifiers like age, gender, duration of anesthesia and procedure were controlled through stratification. Post-stratification, t-test was applied and p-value less than 0.05 was taken as statistically significant.

Results: In Group-A, mean age was 6.1±4.5 years and 6.4±4.6 years in Group-B. Mean residual gastric volume with standard fasting was 0.67±0.48 ml and liberal fasting 0.80±0.44 ml (p value 0.13). Mean gastric fluid pH with standard fasting was 1.72±0.78 as compared to liberal fasting 1.63±0.70 (p value 0.53).

Conclusion: Free fluid fasting allows for significantly shorter fasting times, though statistically insignificant higher residual gastric volume was recorded in liberal fasting group with a lower pH.

目的比较接受择期手术全身麻醉的儿童在标准禁食和宽松禁食情况下的平均残胃容积和胃pH值:2021 年 6 月至 2021 年 12 月,拉合尔梅奥医院小儿外科开展了一项随机对照试验(NCT05922072),共招募了 120 名在全身麻醉下接受择期日间护理手术的患者。患者被分为 A 组(标准禁食)和 B 组(自由禁食)。A组的固体食物/配方奶、母乳和清流液分别禁食6小时、4小时和2小时,B组的固体食物/配方奶、母乳和清流液分别禁食6小时、4小时和1小时。在对患者进行麻醉后,测量了残胃容积和 pH 值。通过分层控制了年龄、性别、麻醉时间和手术过程等影响因素。分层后采用 t 检验,P 值小于 0.05 为具有统计学意义:结果:A 组平均年龄(6.1±4.5)岁,B 组平均年龄(6.4±4.6)岁。标准空腹时的平均残胃量为 0.67±0.48 ml,自由空腹时的平均残胃量为 0.80±0.44 ml(P 值为 0.13)。标准禁食的平均胃液 pH 值为 1.72±0.78,而自由禁食为 1.63±0.70(P 值为 0.53):结论:自由流体禁食可大大缩短禁食时间,但自由禁食组的残胃量较高且 pH 值较低,这在统计学上并不显著。
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引用次数: 0
Comparison of linear distance of glenoid fossa to frontomaxillary nasal suture in skeletal Class-II and skeletal Class-I malocclusion. 骨骼Ⅱ类和骨骼Ⅰ类错颌畸形患者盂窝至前颌鼻缝线性距离的比较。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.8506
Sadaf Siddiqui, Ambreen Afzal Ehsan, Hasnain Sakrani, Sadia Asif Samdani

Objective: To compare linear distance of glenoid fossa to frontomaxillary nasal suture in skeletal Class-I and II malocclusions.

Methods: This cross-sectional study was conducted at the Department of Orthodontics, Altamash Institute of Dental Medicine, Karachi Pakistan. The duration of study was one year from January, 2019 to January, 2020. After taking informed consent from patient and hospital ethical committee a total of 60 patients were included in the study using WHO sample size calculator. Two groups comprising 30 patients each i.e., Skeletal Class-I malocclusion and Skeletal Class-II malocclusion with mandibular retrusion both having normal vertical relationship were included in the study. The cephalometric measurements SNA, SNB, SNMP, FHMP, GF-FMN, CO-GO, CO GN on lateral cephalograms were measured and compared between the two groups. Independent t test was applied and p value ≤ 0.05 was considered as significant.

Results: In skeletal Class-I malocclusion the mean linear distance of GF-FMN was 70.2 ± 4.02 mm and in skeletal Class-II malocclusion it was 73.4 ± 4.04 mm (p value .004). Glenoid fossa was 3.2 mm distally placed in patients with Class-II malocclusion.

Conclusion: Glenoid fossa position is a diagnostic feature of Class-II malocclusion associated with mandibular retrusion. One of the effective cephalometric measurements to check glenoid fossa position is the distance from the glenoid fossa(GF) to the frontomaxillary nasal suture FMN (GF-FMN).

目的比较Ⅰ类和Ⅱ类骨骼畸形患者盂窝到前颌鼻缝的线性距离:这项横断面研究在巴基斯坦卡拉奇 Altamash 牙科医学院正畸科进行。研究为期一年,从 2019 年 1 月至 2020 年 1 月。在征得患者和医院伦理委员会的知情同意后,使用世界卫生组织样本量计算器将总共 60 名患者纳入研究。研究包括两组患者,每组 30 人,即骨骼 I 类错牙合畸形患者和骨骼 II 类错牙合畸形伴下颌后缩患者,两组患者的垂直关系均正常。研究人员测量了两组患者头颅侧位片上的头形测量值 SNA、SNB、SNMP、FHMP、GF-FMN、CO-GO、CO GN,并进行了比较。采用独立 t 检验,P 值小于 0.05 为差异有显著性:在骨骼Ⅰ类错颌畸形中,GF-FMN的平均直线距离为(70.2 ± 4.02)毫米,在骨骼Ⅱ类错颌畸形中,GF-FMN的平均直线距离为(73.4 ± 4.04)毫米(P值为0.004)。结论:盂窝位置是与下颌后缩相关的II类错颌畸形的诊断特征。检查盂窝位置的有效头形测量方法之一是从盂窝到前颌鼻缝 FMN 的距离(GF-FMN)。
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引用次数: 0
Seizures as the only presentation of Pulmonary Embolism in the absence of Respiratory Symptoms. 在没有呼吸道症状的情况下,癫痫发作是肺栓塞的唯一表现。
IF 1.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-01 DOI: 10.12669/pjms.40.7.9426
Omair Farooq, Amna Maqsood, Muhammad Ahmad, Muhammad Ibrahim Sohail, Maryam Rashid

Pulmonary embolism is a life-threatening emergency. Seizure as the clinical presentation of pulmonary embolism is extremely rare. In this case report a 47-year-old female had an episode of seizure after undergoing total abdominal hysterectomy with bilateral salpingo-oophorectomy due to myometrial uterine fibroids. The patient had no past history of seizure or cardiovascular disease. Based on raised D-Dimers and echocardiography a provisional diagnosis of pulmonary embolism was made, which was confirmed on CT angiogram that showed bilateral saddle pulmonary embolism. Clinicians need to be aware that Pulmonary embolism is a possibility as the differential diagnosis for unexplained, new-onset of seizure activity.

肺栓塞是一种危及生命的急症。以癫痫发作作为肺栓塞的临床表现极为罕见。在本病例报告中,一名 47 岁女性因子宫肌瘤接受了全腹子宫切除术和双侧输卵管切除术,术后癫痫发作。患者既往无癫痫发作史,也无心血管疾病史。根据升高的 D-二聚体和超声心动图,初步诊断为肺栓塞,CT 血管造影证实了这一诊断,并显示双侧鞍状肺栓塞。临床医生需要注意的是,肺栓塞可能是原因不明的新发癫痫活动的鉴别诊断之一。
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引用次数: 0
期刊
Pakistan Journal of Medical Sciences
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