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Analgesic Efficacy of Intravenous Ibuprofen in the Treatment of Postoperative Acute Pain: A Phase III Multicenter Randomized Placebo-ControlledDouble-Blind Clinical Trial. 静脉注射布洛芬治疗术后急性疼痛的镇痛效果:一项多中心随机安慰剂-对照双盲临床试验。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-01-01 DOI: 10.1155/2023/7768704
Hong-Su Zhou, Ting-Ting Li, Yu Pi, Ting-Hua Wang, Fei Liu, Liu-Lin Xiong

Objective: To evaluate the analgesic efficacy and safety of different does of intravenous ibuprofen (IVIB) in the treatment of postoperative acute pain.

Methods: Patients with an intravenous (IV) patient-controlled analgesia device after abdominal or orthopedic surgery were randomly divided into placebo, IVIB 400 mg, and IVIB 800 mg groups. The first dosage of study medicines was given intravenously 30 minutes (min) before surgery ended, followed by six hours (h) intervals for a total of eight doses following surgery. The demographic characteristics and procedure data, cumulative morphine consumption, the visual analog scale (VAS), the area under the curve (AUC) of VAS, patient satisfaction score (PSS), the rates of treatment failure (RTF), and adverse events (AEs) and serious adverse event (SAEs) were recorded during the period of trial.

Result: A total of 345 patients were enrolled in the full analysis set (FAS), and of 326 participants were valid data set (VDS). Demographic characteristics, disease features, and medical history of patients were not significantly different between groups. Total morphine consumption of the IVIB 400 mg group (11.14 ± 7.14 mg; P = 0.0011) and the IVIB 800 mg group (11.29 ± 6.45 mg; P = 0.0014) was significantly reduced compared with the placebo group (14.51 ± 9.19 mg) for 24 h postoperatively, there was no significant difference between the IVIB 400 mg and IVIB 800 mg groups (P = 0.9997). The placebo group had significantly higher VAS and the AUCs of VAS than those in the IVIB 400 mg and the IVIB 800 mg groups at rest and movement for 24 h postoperatively (P< 0.05), and there was no significant difference between the IVIB 400 mg and IVIB 800 mg groups (P > 0.05). RTF was slightly higher in the placebo group than IVIB 400 mg group and 800 mg group, and no statistical significance (P < 0.690). PSS in the IVIB 400 mg (P = 0.0092) and the IVIB 800 mg groups (P = 0.0011) was higher than the placebo group for pain management, there was also no significant difference between the IVIB 400 mg and IVIB 800 mg groups (P = 0.456). The incidence of RTF (P = 0.690) and AEs (P > 0.05) were not different among the three groups.

Conclusion: Intermittent IV administration of ibuprofen 400 mg or 800 mg within 24 h after surgery in patients undergoing abdominal and orthopedic surgery significantly decreased morphine consumption and relieved pain, without increasing the incidence of AEs.

目的:评价不同剂量静脉注射布洛芬(IVIB)治疗术后急性疼痛的疗效和安全性。方法:将腹部或骨科手术后使用静脉(IV)自控镇痛装置的患者随机分为安慰剂组、IVIB 400 mg组和IVIB 800 mg组。第一剂量研究药物在手术结束前30分钟(min)静脉给予,手术后每隔6小时(h)给药,共给药8次。记录两组患者在试验期间的人口学特征和手术数据、吗啡累积用量、视觉模拟量表(VAS)、VAS曲线下面积(AUC)、患者满意度评分(PSS)、治疗失败率(RTF)、不良事件(ae)和严重不良事件(sae)。结果:全分析集(FAS)纳入345例,有效数据集(VDS)纳入326例。患者的人口学特征、疾病特征和病史在组间无显著差异。IVIB 400 mg组吗啡总用量(11.14±7.14 mg;P = 0.0011), IVIB 800 mg组(11.29±6.45 mg;P = 0.0014)明显低于安慰剂组(14.51±9.19 mg), IVIB 400 mg组与IVIB 800 mg组间差异无统计学意义(P = 0.9997)。术后24 h静息运动时,安慰剂组VAS及auc均高于IVIB 400 mg和IVIB 800 mg组(P < 0.05), IVIB 400 mg和IVIB 800 mg组间差异无统计学意义(P > 0.05)。安慰剂组的RTF略高于IVIB 400 mg组和800 mg组,且无统计学意义(P = 0.0092), IVIB 800 mg组的疼痛管理RTF高于安慰剂组(P = 0.0011), IVIB 400 mg组和IVIB 800 mg组之间也无统计学差异(P = 0.456)。三组RTF发生率(P = 0.690)和ae发生率(P > 0.05)无显著差异。结论:术后24 h内间歇性静脉给予布洛芬400 mg或800 mg可显著减少吗啡消耗,减轻疼痛,且未增加不良反应发生率。
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引用次数: 1
The Effect of Spinal Muscle Fatigue and Psychosocial Factors on Pressure-Pain Threshold in Healthy Adults. 脊髓肌疲劳和心理社会因素对健康成人压痛阈值的影响。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7336477
Susan Mais, Jo Armour Smith

Objective: Pain sensitivity decreases following isometric exercise. It is not clear whether this exercise-induced hypoalgesia (EIH) occurs to the same extent in men and women. It is also unclear if the effect is systemic or local to the exercised musculature. The aim of our study was to investigate whether fatiguing isometric exercise of the spinal and hip extensors would result in increased pressure pain threshold (PPT) at sites local to and remote from the exercised muscles in healthy men and women and whether there is a relationship between central sensitization, psychosocial factors, and PPT.

Subjects: 35 healthy adults (age 27.1 ± 4.5 years, 22 women).

Methods: This was a within-subjects cohort study. Participants completed questionnaires quantifying central sensitization, pain catastrophizing, sleepiness/insomnia, anxiety, and depression. PPT was assessed at the lumbar and thoracic paraspinals, hamstrings, gastrocnemius, wrist, and third digit before and immediately after participants performed the Biering-Sorensen test to failure.

Results: PPT increased postexercise in the thoracic paraspinals, hamstrings, and gastrocnemius in men and women and in the lumbar paraspinals in men only but did not change at the wrist and digit sites. A lower average PPT at baseline was associated with a higher central sensitization scores. A greater increase in average PPT postfatigue was significantly associated with higher average PPT at baseline.

Conclusions: Exercise-induced hypoalgesia occurs at sites overlying the muscles involved in fatiguing exercise, but not at remote sites, and is more evident in males than females. The magnitude of EIH depends upon baseline PPT. Even in healthy individuals, greater central sensitization is associated with lower baseline PPT.

目的:静力运动后疼痛敏感性降低。目前尚不清楚这种运动引起的痛觉减退(EIH)在男性和女性中发生的程度是否相同。目前还不清楚这种影响是全身的还是局部的。本研究的目的是调查在健康男性和女性中,脊柱和髋关节伸肌的疲劳等距运动是否会导致运动肌肉附近和远处部位的压力痛阈值(PPT)增加,以及中枢敏化、社会心理因素和PPT之间是否存在关系。受试者:健康成人35例(年龄27.1±4.5岁,女性22例)。方法:本研究为受试者内队列研究。参与者完成了量化中枢敏化、疼痛灾难化、嗜睡/失眠、焦虑和抑郁的问卷调查。在参与者进行Biering-Sorensen测试之前和之后立即评估腰椎和胸椎旁肌、腘绳肌、腓肠肌、手腕和第三指的PPT。结果:运动后PPT增加了男性和女性的胸椎旁肌、腘绳肌和腓肠肌,男性仅增加了腰椎旁肌,但手腕和手指部位没有改变。基线时较低的平均PPT与较高的中枢致敏评分相关。疲劳后平均PPT的增加与基线时较高的平均PPT显著相关。结论:运动引起的痛觉减退发生在疲劳运动所涉及肌肉的上部部位,而不是远处部位,并且在男性中比女性更明显。EIH的大小取决于基线PPT。即使在健康个体中,较高的中枢致敏与较低的基线PPT相关。
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引用次数: 0
Association of COMT Val158Met Polymorphism with Fibromyalgia in Khartoum State, Sudan. COMT Val158Met多态性与苏丹喀土穆州纤维肌痛的关系
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7313578
Safaa Mamoun Abdelmageid, Faisal Mousa Alamir, Hassan Yousif Abdelrahman, Hind Mohamed Abushama

Fibromyalgia (FM) is a disorder characterized by chronic musculoskeletal pain, fatigue, and cognitive problems. Neurotransmitters, mainly catecholamines, appear to be involved in regulating the etiology of FM. Catechol-O-methyltransferase (COMT) is involved in catabolizing catecholamines such as norepinephrine. The most common variant studied in the COMT gene is the valine (Val) to methionine (Met) substitution at codon 158. This is the first study in Sudan addressing FM cases and genetic susceptibility to the disease. We aimed in this study to investigate the frequency of COMT Val 158 Met polymorphism among patients with FM, rheumatoid arthritis, and in healthy individuals. Genomic DNA from forty female volunteers was analyzed: twenty were from primary and secondary FM patients, ten were from rheumatoid arthritis patients, and ten were from healthy control. FM patients' age was ranging from 25 years to 55 with a mean of 41.14 ± 8.90. The mean age of the rheumatoid arthritis patients and healthy individuals was 31.3 ± 7.5 and 38.6 ± 11.2, respectively. Samples were genotyped for COMT single nucleotide polymorphism rs4680 (Val158Met), using the amplification-refractory mutation system (ARMS-PCR). Genotyping data have been analyzed using the Chi-square and Fisher exact test. The most common genotype among the study participants was the heterozygous Val/Met found in all participants. It was the only genotype found in the healthy participants. The genotype Met/Met was found only in FM patients. The genotype Val/Val was found only in rheumatoid patients. Analyses have shown no association between the Met/Met genotype and FM, and this could be due to a small sample size. In a larger sample size, a significant association could be found as this genotype was shown only by FM patients. Moreover, the Val/Val genotype, which is shown only among rheumatoid patients, might protect them from developing FM symptoms.

纤维肌痛(FM)是一种以慢性肌肉骨骼疼痛、疲劳和认知问题为特征的疾病。神经递质,主要是儿茶酚胺,似乎参与调节FM的病因。儿茶酚o -甲基转移酶(COMT)参与分解代谢儿茶酚胺,如去甲肾上腺素。COMT基因中最常见的变异是密码子158上缬氨酸(Val)与蛋氨酸(Met)的替换。这是苏丹首次针对该病病例和遗传易感性进行的研究。在这项研究中,我们的目的是调查COMT Val 158 Met多态性在FM、类风湿关节炎患者和健康个体中的频率。研究人员分析了40名女性志愿者的基因组DNA: 20名来自原发性和继发性FM患者,10名来自类风湿关节炎患者,10名来自健康对照组。FM患者年龄25 ~ 55岁,平均41.14±8.90岁。类风湿关节炎患者和健康人的平均年龄分别为31.3±7.5岁和38.6±11.2岁。采用扩增-难解突变系统(ARMS-PCR)对样品进行COMT单核苷酸多态性rs4680 (Val158Met)基因分型。使用卡方检验和Fisher精确检验对基因分型数据进行分析。研究参与者中最常见的基因型是在所有参与者中发现的杂合Val/Met。这是在健康参与者中发现的唯一基因型。Met/Met基因型仅在FM患者中发现。Val/Val基因型仅在类风湿患者中发现。分析显示Met/Met基因型与FM之间没有关联,这可能是由于样本量小。在更大的样本量中,可以发现显著的关联,因为该基因型仅在FM患者中显示。此外,Val/Val基因型仅在类风湿患者中显示,可能保护他们免受FM症状的影响。
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引用次数: 0
Transversus Thoracis Muscle Plane Block in Paediatric Patients Who Underwent Minimally Invasive Closure of Transthoracic Ventricular Septal Defect: A Retrospective Study. 经胸室间隔缺损微创闭合术患儿的胸肌平面阻滞:一项回顾性研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/3488552
Qiong Ling, Shuhua Zhao, Yongyong Shi, Xiangyu Li, Ping Li, Gaofeng Zhao, Qianqian Zhu

Objective: Minimally invasive closure of transthoracic ventricular septal defect (VSD) has been widely used in paediatric patients. This retrospective study aimed to explore the use of transversus thoracis muscle plane block (TTMPB) in the minimally invasive closure of transthoracic VSD in paediatric patients.

Methods: From September 28, 2017, to July 25, 2022, a total of 119 paediatric patients scheduled for minimally invasive transthoracic VSD closure were considered for inclusion.

Results: In total, 110 patients were included in the final analysis. Perioperative fentanyl consumption of the TTMPB group was not different from that of the non-TTMPB group (5.90 ± 1.32 μg/kg vs. 6.25 ± 1.74 μg/kg, p = 0.473). Both the time to extubation and postanesthesia care unit (PACU) stay were significantly shorter in the TTMPB group than in the non-TTMPB group (10.94 ± 10.31 min vs. 35.03 ± 23.52 min for extubation, and 42.55 ± 16.83 min vs. 59.98 ± 27.94 min for PACU stay, both p < 0.001). Furthermore, the postoperative paediatric intensive care unit (PICU) stay in the TTMPB group was significantly shorter than in the non-TTMPB group (1.04 ± 0.28 d vs. 1.34 ± 1.05 d, p = 0.005). Multivariate analysis demonstrated that TTMPB was significantly associated with shorter time to extubation (p < 0.001) and PACU stay (p = 0.001) but not postoperative PICU stay (p = 0.094). Discussion. This study showed that TTMPB was a beneficial and safe regional anaesthesia technique for paediatric patients who underwent minimally invasive closure of transthoracic VSD, although prospective randomized controlled trials are needed to confirm the results.

目的:经胸室间隔缺损(VSD)的微创闭合术已广泛应用于儿科患者。本回顾性研究旨在探讨经胸肌平面阻滞(TTMPB)在儿科经胸室间隔缺损微创封闭中的应用。方法:2017年9月28日至2022年7月25日,共纳入119例拟行微创经胸室间隔封堵术的儿科患者。结果:共有110例患者纳入最终分析。TTMPB组围手术期芬太尼用量与非TTMPB组比较差异无统计学意义(5.90±1.32 μg/kg∶6.25±1.74 μg/kg, p = 0.473)。TTMPB组拔管时间和麻醉后护理单位(PACU)停留时间均显著短于非TTMPB组(拔管时间10.94±10.31 min vs. 35.03±23.52 min; PACU停留时间42.55±16.83 min vs. 59.98±27.94 min, p = 0.005)。多因素分析显示,TTMPB与拔管时间缩短(p p = 0.001)显著相关,但与术后PICU停留时间无关(p = 0.094)。讨论。本研究表明,TTMPB是一种有益且安全的区域麻醉技术,适用于经胸室间隔缺损微创闭合术的儿科患者,尽管需要前瞻性随机对照试验来证实结果。
{"title":"Transversus Thoracis Muscle Plane Block in Paediatric Patients Who Underwent Minimally Invasive Closure of Transthoracic Ventricular Septal Defect: A Retrospective Study.","authors":"Qiong Ling,&nbsp;Shuhua Zhao,&nbsp;Yongyong Shi,&nbsp;Xiangyu Li,&nbsp;Ping Li,&nbsp;Gaofeng Zhao,&nbsp;Qianqian Zhu","doi":"10.1155/2023/3488552","DOIUrl":"https://doi.org/10.1155/2023/3488552","url":null,"abstract":"<p><strong>Objective: </strong>Minimally invasive closure of transthoracic ventricular septal defect (VSD) has been widely used in paediatric patients. This retrospective study aimed to explore the use of transversus thoracis muscle plane block (TTMPB) in the minimally invasive closure of transthoracic VSD in paediatric patients.</p><p><strong>Methods: </strong>From September 28, 2017, to July 25, 2022, a total of 119 paediatric patients scheduled for minimally invasive transthoracic VSD closure were considered for inclusion.</p><p><strong>Results: </strong>In total, 110 patients were included in the final analysis. Perioperative fentanyl consumption of the TTMPB group was not different from that of the non-TTMPB group (5.90 ± 1.32 <i>μ</i>g/kg vs. 6.25 ± 1.74 <i>μ</i>g/kg, <i>p</i> = 0.473). Both the time to extubation and postanesthesia care unit (PACU) stay were significantly shorter in the TTMPB group than in the non-TTMPB group (10.94 ± 10.31 min vs. 35.03 ± 23.52 min for extubation, and 42.55 ± 16.83 min vs. 59.98 ± 27.94 min for PACU stay, both <i>p</i> < 0.001). Furthermore, the postoperative paediatric intensive care unit (PICU) stay in the TTMPB group was significantly shorter than in the non-TTMPB group (1.04 ± 0.28 d vs. 1.34 ± 1.05 d, <i>p</i> = 0.005). Multivariate analysis demonstrated that TTMPB was significantly associated with shorter time to extubation (<i>p</i> < 0.001) and PACU stay (<i>p</i> = 0.001) but not postoperative PICU stay (<i>p</i> = 0.094). <i>Discussion</i>. This study showed that TTMPB was a beneficial and safe regional anaesthesia technique for paediatric patients who underwent minimally invasive closure of transthoracic VSD, although prospective randomized controlled trials are needed to confirm the results.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049843/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9698744","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Analgesic Efficacy of Ketoprofen Transdermal Patch versus Ibuprofen Oral Tablet on Postendodontic Pain in Patients with Irreversible Pulpitis: A Randomized Clinical Trial. 酮洛芬透皮贴片与布洛芬口服片对不可逆牙髓炎患者牙髓后疼痛的镇痛效果:一项随机临床试验。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/8549655
Saeede Zadsirjan, Amirhossein Toghrolian, Nazanin Zargar

Materials and methods: In this randomized clinical trial, 64 patients who had mandibular first and second molars with irreversible pulpitis were randomly divided into two groups (n = 32) by stratified permuted block randomization. The experimental group used 60 mg KTP every 6 hours, and the control group received 400 mg ibuprofen tablets every 6 hours for 1 day. The severity of pain experienced by patients was quantified before and at 2, 4, 8, 12, 24, and 48 hours after endodontic treatment, using the numerical rating scale (NRS). Data were analyzed by using the t-test, Mann-Whitney test, and generalized estimating equation (GEE) (alpha = 0.05).

Results: The pain score was not significantly different between the two groups at the baseline or any other postoperative time point (P > 0.05). The reduction in the pain score was significant in both groups from 2 to 10 hours and 10 to 48 hours, postoperatively (P < 0.001). The interaction effect of time and group was not significant on the postoperative pain score in the abovementioned time intervals, and the pattern of pain reduction was the same over time in both groups (P > 0.05).

Conclusion: Both KTP and ibuprofen effectively decreased postendodontic pain. Considering the comparable pattern of pain reduction, KTP can be used as an alternative to ibuprofen tablets for effective pain control after endodontic treatment of mandibular first and second molars with irreversible pulpitis.

材料与方法:采用分层排列块随机法将64例下颌第一磨牙和第二磨牙合并不可逆性牙髓炎患者随机分为两组(n = 32)。实验组每6 h给予KTP 60 mg,对照组每6 h给予布洛芬片400 mg,连用1 d。采用数值评定量表(NRS)对患者在根管治疗前及治疗后2、4、8、12、24、48小时的疼痛程度进行量化。数据分析采用t检验、Mann-Whitney检验和广义估计方程(GEE) (alpha = 0.05)。结果:两组患者在术后基线及其他时间点疼痛评分比较,差异均无统计学意义(P > 0.05)。两组术后2 ~ 10小时和10 ~ 48小时疼痛评分均显著降低(P < 0.001)。在上述时间间隔内,时间和组的交互作用对术后疼痛评分无显著影响,两组疼痛减轻的模式随时间变化相同(P > 0.05)。结论:KTP与布洛芬均能有效减轻牙髓后疼痛。考虑到可比性的疼痛减轻模式,KTP可以作为布洛芬片的替代品,在不可逆牙髓炎的下颌第一和第二磨牙根管治疗后有效地控制疼痛。
{"title":"Analgesic Efficacy of Ketoprofen Transdermal Patch versus Ibuprofen Oral Tablet on Postendodontic Pain in Patients with Irreversible Pulpitis: A Randomized Clinical Trial.","authors":"Saeede Zadsirjan,&nbsp;Amirhossein Toghrolian,&nbsp;Nazanin Zargar","doi":"10.1155/2023/8549655","DOIUrl":"https://doi.org/10.1155/2023/8549655","url":null,"abstract":"<p><strong>Materials and methods: </strong>In this randomized clinical trial, 64 patients who had mandibular first and second molars with irreversible pulpitis were randomly divided into two groups (<i>n</i> = 32) by stratified permuted block randomization. The experimental group used 60 mg KTP every 6 hours, and the control group received 400 mg ibuprofen tablets every 6 hours for 1 day. The severity of pain experienced by patients was quantified before and at 2, 4, 8, 12, 24, and 48 hours after endodontic treatment, using the numerical rating scale (NRS). Data were analyzed by using the <i>t</i>-test, Mann-Whitney test, and generalized estimating equation (GEE) (alpha = 0.05).</p><p><strong>Results: </strong>The pain score was not significantly different between the two groups at the baseline or any other postoperative time point (<i>P</i> > 0.05). The reduction in the pain score was significant in both groups from 2 to 10 hours and 10 to 48 hours, postoperatively (<i>P</i> < 0.001). The interaction effect of time and group was not significant on the postoperative pain score in the abovementioned time intervals, and the pattern of pain reduction was the same over time in both groups (<i>P</i> > 0.05).</p><p><strong>Conclusion: </strong>Both KTP and ibuprofen effectively decreased postendodontic pain. Considering the comparable pattern of pain reduction, KTP can be used as an alternative to ibuprofen tablets for effective pain control after endodontic treatment of mandibular first and second molars with irreversible pulpitis.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266914/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9653946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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: 1
Neuropathic Pain Was Associated with Central Sensitivity Syndrome in Patients with Preoperative Lumbar Spinal Stenosis Using the painDETECT and Central Sensitization Inventory Questionnaires: A Cross-Sectional Study. 通过疼痛检测和中枢致敏性问卷调查发现术前腰椎管狭窄患者神经性疼痛与中枢敏感综合征相关:一项横断面研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9963627
Rintaro Iwasaki, Takahiro Miki, Mizuki Miyazaki, Chifumi Kanetaka, Tetsuryu Mitsuyama, Kaiji Ota

Background: Lumbar spinal stenosis (LSS) patients have been reported to have neuropathic pain and central sensitivity syndrome (CSS). These associations have been reported in other diseases but are unknown in preoperative LSS patients. We aimed to investigate the association between neuropathic pain and CSS in preoperative LSS patients using the painDETECT and the Central Sensitization Inventory (CSI) questionnaires.

Methods: This cross-sectional study was conducted from November 2021 to March 2022. The data were collected regarding demographics and pain, including neuropathic pain, numbness, LSS severity, physical function, quality of life, and CSS. Patients were divided into two groups, patients with acute and chronic pain, and further classified into three categories based on the clinical phenotype of patients in each group. Independent variables included age, gender, type of LSS (bilateral or unilateral symptoms), Numerical Rating Scale of leg pain, CSI, and the Zurich Claudication Questionnaire (ZCQ) for symptom severity and physical function. The dependent variable was painDETECT. Multiple regression analysis using the forced entry method examined the association between painDETECT and CSI.

Results: Of the 119 patients with preoperative LSS, 106 were included. The mean age of the participants was 69.9 years, and 45.3% were female. Neuropathic pain was present in 19.8%, and CSS was present in 10.4%. The CSI (β = 0.468, p < 0.001) and ZCQ for symptom severity (β = 0.304, p < 0.01) were significantly associated with the painDETECT, explaining 47.8% of the variance in the painDETECT score.

Conclusions: There is an association between neuropathic pain and CSS in patients with preoperative LSS using the painDETECT and CSI questionnaires.

背景:腰椎管狭窄症(LSS)患者有神经性疼痛和中枢敏感综合征(CSS)的报道。这些关联在其他疾病中已有报道,但在术前LSS患者中尚不清楚。我们旨在通过painDETECT和中枢致敏量表(CSI)调查LSS患者术前神经性疼痛与CSS之间的关系。方法:本横断面研究于2021年11月至2022年3月进行。收集有关人口统计学和疼痛的数据,包括神经性疼痛、麻木、LSS严重程度、身体功能、生活质量和CSS。将患者分为急性和慢性疼痛患者两组,并根据每组患者的临床表型进一步分为三类。自变量包括年龄、性别、LSS类型(双侧或单侧症状)、腿部疼痛数值评定量表、CSI和苏黎世跛行问卷(ZCQ)的症状严重程度和身体功能。因变量为painDETECT。采用强行进入法进行多元回归分析,检验了painDETECT与CSI之间的关系。结果:119例术前LSS患者中,106例入选。参与者的平均年龄为69.9岁,45.3%为女性。神经性疼痛占19.8%,CSS占10.4%。症状严重程度的CSI (β = 0.468, p < 0.001)和ZCQ (β = 0.304, p < 0.01)与painDETECT得分显著相关,解释了47.8%的painDETECT得分方差。结论:术前LSS患者的神经性疼痛与CSS之间存在关联。
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引用次数: 1
A Novel Scale to Assess Parental Satisfaction of Dental Local Anesthetic Techniques in Children: A Cross-Sectional Study. 一种评估家长对儿童牙科局部麻醉技术满意度的新量表:一项横断面研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9973749
Muaaz Alkhouli, Zuhair Al-Nerabieah, Mayssoon Dashash

Background: Pain control is one of the most important aspects that can affect parental satisfaction of the dental care provided for children. Dental local anesthesia has the highest impact on pain sensation of the children. However, there is no scale in the literature to assess parental satisfaction of dental local anesthetic techniques.

Objectives: This study was aimed to assess the parental satisfaction with dental local anesthetic techniques for their children through designing a scale that reflects satisfaction and to study the validity and reliability of this scale.

Methods: A cross-sectional observational study was conducted on 150 parents (102 mothers and 48 fathers). Two techniques of local anesthesia were used for each child participated in this study (inferior alveolar nerve block and computerized intraosseous anesthesia). The developed scale consisted of 20 items in a 5-point Likert scale. Half of the items were written in a negative format. Internal consistency, validity, and factor analysis were performed in this study. Independent t-test was used to compare between the two techniques of anesthesia, between boys and girls and among fathers and mothers.

Results: Parental satisfaction mean values were higher in the computerized intraosseous anesthesia group in comparison to inferior alveolar nerve block (P value <0.05). The T-test showed that there was no difference between boys and girls regarding parental satisfaction (P value >0.05). Furthermore, fathers show lower satisfaction in the computerized interosseous anesthesia group (P value <0.05). Excellent internal consistency of this scale was resulted as Cronbach's alpha reliability coefficient was 0.985. After factor analysis, seven factor components were retained by using varimax rotation.

Conclusions: Findings of this study reported that the designed parental satisfaction of dental local anesthetic techniques scale (PSLAS) is a valid and reliable scale to be used. Moreover, this study showed that parental satisfaction was higher when computerized intraosseous anesthesia was used in comparison to inferior alveolar nerve block.

背景:疼痛控制是影响父母对儿童牙科护理满意度的最重要方面之一。牙科局部麻醉对儿童疼痛感觉的影响最大。然而,在文献中没有量表来评估父母对牙科局部麻醉技术的满意度。目的:本研究旨在通过设计一份反映儿童牙科局部麻醉技术满意度的量表,来评估家长对儿童牙科局部麻醉技术的满意度,并研究该量表的效度和信度。方法:对150名家长(102名母亲和48名父亲)进行横断面观察研究。本研究对每个患儿采用两种局部麻醉技术(下牙槽神经阻滞和计算机化骨内麻醉)。该量表采用李克特5分制,包括20个项目。一半的题目是用否定的形式写的。本研究进行内部一致性、效度及因子分析。采用独立t检验比较两种麻醉方法之间、男孩和女孩之间以及父亲和母亲之间的差异。结果:计算机化骨内麻醉组家长满意度均值高于下牙槽神经阻滞组(P值t检验显示男女家长满意度无显著差异(P值>0.05)。结论:本研究结果表明,设计的口腔局麻技术家长满意度量表(PSLAS)是一份有效、可靠的可应用的量表。此外,本研究显示,与下牙槽神经阻滞相比,采用计算机化骨内麻醉的家长满意度更高。
{"title":"A Novel Scale to Assess Parental Satisfaction of Dental Local Anesthetic Techniques in Children: A Cross-Sectional Study.","authors":"Muaaz Alkhouli,&nbsp;Zuhair Al-Nerabieah,&nbsp;Mayssoon Dashash","doi":"10.1155/2023/9973749","DOIUrl":"https://doi.org/10.1155/2023/9973749","url":null,"abstract":"<p><strong>Background: </strong>Pain control is one of the most important aspects that can affect parental satisfaction of the dental care provided for children. Dental local anesthesia has the highest impact on pain sensation of the children. However, there is no scale in the literature to assess parental satisfaction of dental local anesthetic techniques.</p><p><strong>Objectives: </strong>This study was aimed to assess the parental satisfaction with dental local anesthetic techniques for their children through designing a scale that reflects satisfaction and to study the validity and reliability of this scale.</p><p><strong>Methods: </strong>A cross-sectional observational study was conducted on 150 parents (102 mothers and 48 fathers). Two techniques of local anesthesia were used for each child participated in this study (inferior alveolar nerve block and computerized intraosseous anesthesia). The developed scale consisted of 20 items in a 5-point Likert scale. Half of the items were written in a negative format. Internal consistency, validity, and factor analysis were performed in this study. Independent <i>t</i>-test was used to compare between the two techniques of anesthesia, between boys and girls and among fathers and mothers.</p><p><strong>Results: </strong>Parental satisfaction mean values were higher in the computerized intraosseous anesthesia group in comparison to inferior alveolar nerve block (<i>P</i> value <0.05). The <i>T</i>-test showed that there was no difference between boys and girls regarding parental satisfaction (<i>P</i> value >0.05). Furthermore, fathers show lower satisfaction in the computerized interosseous anesthesia group (<i>P</i> value <0.05). Excellent internal consistency of this scale was resulted as Cronbach's alpha reliability coefficient was 0.985. After factor analysis, seven factor components were retained by using varimax rotation.</p><p><strong>Conclusions: </strong>Findings of this study reported that the designed parental satisfaction of dental local anesthetic techniques scale (PSLAS) is a valid and reliable scale to be used. Moreover, this study showed that parental satisfaction was higher when computerized intraosseous anesthesia was used in comparison to inferior alveolar nerve block.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219770/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9556195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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: 1
Do Temporomandibular Disorder Patients with Joint Pain Exhibit Forward Head Posture? A Cephalometric Study. 伴有关节疼痛的颞下颌紊乱患者是否表现出前倾的头部姿势?一项头颅测量研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7363412
Chu-Qiao Xiao, Yi-Dan Wan, Ya-Qi Li, Zhe-Bin Yan, Qiao-Yu Cheng, Pei-Di Fan, Yi Huang, Xiao-Yi Wang, Xin Xiong

Purpose: To evaluate head and cervical posture in individuals with or without temporomandibular disorders (TMDs) and to assess the correlations between pain, severity of symptoms, and posture.

Methods: A total of 384 patients (129 males and 255 females) was included. The Fonseca Anamnestic Index (FAI) was used to assess the severity and prevalence of TMD and the presence of temporomandibular joint (TMJ) pain. Patients were divided into three groups: the TMD-free group, TMD without TMJ pain group, and TMD with TMJ pain group. Subsequently, the patients with TMJ pain were further divided into mild TMD and moderate/severe TMD groups. Nine parameters were traced on cephalograms to characterize the head and cervical posture.

Results: TMD patients with TMJ pain showed increased forward head posture (FHP) than patients without TMJ pain and TMD-free subjects. No significant difference was observed between the TMD patients without TMJ pain and TMD-free subjects. In the TMD patients with the TMJ pain group, the moderate/severe TMD patients demonstrated increased FHP compared to mild TMD patients. TMD patients with joint pain had greater CVT/RL (B = 3.099), OPT/RL (B = 2.117), and NSL/C2' (B = 4.646) than the patients without joint pain after adjusting for confounding variables (P < 0.05).

Conclusion: TMD patients with TMJ pain showed increased FHP compared to other groups, and FHP became more significant as TMD severity increased in male patients, indicating the FHP might play an important role in the development of TMJ pain. In the clinical assessment of TMD, the patients' abnormal head and cervical posture might be considered.

目的:评估患有或不患有颞下颌紊乱(TMDs)的个体的头部和颈部姿势,并评估疼痛、症状严重程度和姿势之间的相关性。方法:共纳入384例患者,其中男性129例,女性255例。采用Fonseca记忆指数(FAI)评估TMD的严重程度和患病率以及颞下颌关节(TMJ)疼痛的存在。将患者分为三组:无颞下颌关节疼痛组、无颞下颌关节疼痛组和有颞下颌关节疼痛组。随后将有TMJ疼痛的患者进一步分为轻度TMD组和中/重度TMD组。在脑电图上追踪9个参数,以表征头部和颈部姿势。结果:有TMJ疼痛的TMD患者的前头位(FHP)明显高于无TMJ疼痛和无TMD的患者。无颞下颌关节疼痛的TMD患者与无TMD患者之间无显著差异。在伴有TMJ疼痛的TMD患者中,与轻度TMD患者相比,中度/重度TMD患者表现出更高的FHP。调整混杂变量后,伴有关节疼痛的TMD患者CVT/RL (B = 3.099)、OPT/RL (B = 2.117)、NSL/C2′(B = 4.646)均高于无关节疼痛患者(P < 0.05)。结论:与其他组相比,TMD合并TMJ疼痛患者FHP增高,且男性患者FHP随TMD严重程度的增加而增高,提示FHP可能在TMJ疼痛的发生发展中起重要作用。在临床评价TMD时,可考虑患者的头颈姿势异常。
{"title":"Do Temporomandibular Disorder Patients with Joint Pain Exhibit Forward Head Posture? A Cephalometric Study.","authors":"Chu-Qiao Xiao,&nbsp;Yi-Dan Wan,&nbsp;Ya-Qi Li,&nbsp;Zhe-Bin Yan,&nbsp;Qiao-Yu Cheng,&nbsp;Pei-Di Fan,&nbsp;Yi Huang,&nbsp;Xiao-Yi Wang,&nbsp;Xin Xiong","doi":"10.1155/2023/7363412","DOIUrl":"https://doi.org/10.1155/2023/7363412","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate head and cervical posture in individuals with or without temporomandibular disorders (TMDs) and to assess the correlations between pain, severity of symptoms, and posture.</p><p><strong>Methods: </strong>A total of 384 patients (129 males and 255 females) was included. The Fonseca Anamnestic Index (FAI) was used to assess the severity and prevalence of TMD and the presence of temporomandibular joint (TMJ) pain. Patients were divided into three groups: the TMD-free group, TMD without TMJ pain group, and TMD with TMJ pain group. Subsequently, the patients with TMJ pain were further divided into mild TMD and moderate/severe TMD groups. Nine parameters were traced on cephalograms to characterize the head and cervical posture.</p><p><strong>Results: </strong>TMD patients with TMJ pain showed increased forward head posture (FHP) than patients without TMJ pain and TMD-free subjects. No significant difference was observed between the TMD patients without TMJ pain and TMD-free subjects. In the TMD patients with the TMJ pain group, the moderate/severe TMD patients demonstrated increased FHP compared to mild TMD patients. TMD patients with joint pain had greater CVT/RL (<i>B</i> = 3.099), OPT/RL (<i>B</i> = 2.117), and NSL/C2' (<i>B</i> = 4.646) than the patients without joint pain after adjusting for confounding variables (<i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>TMD patients with TMJ pain showed increased FHP compared to other groups, and FHP became more significant as TMD severity increased in male patients, indicating the FHP might play an important role in the development of TMJ pain. In the clinical assessment of TMD, the patients' abnormal head and cervical posture might be considered.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911253/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10761824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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: 1
Objective Evaluation of Chronic Low-Back Pain Using Serum Lipids: The Role of the Doctor-Patient Relationship. 目的用血脂评价慢性腰痛:医患关系的作用。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9972093
Tomáš Bruthans, Jana Vránová, Anna Yamamotová

Statistical data show that pain intensity in patients with low back pain is associated with a higher BMI, total serum cholesterol, and triacylglycerol levels. The objective of our study was to evaluate how these associations are dependent on the nature of the patient-doctor relationship. Eighty-nine patients hospitalized with chronic low-back pain (50 women, 39 men; average age: 64.5 ± 12.7 years) were assessed over a 3-year period. A serum lipid analysis was conducted (LDL-C, HDL-C, and total cholesterols) at admission in parallel with a subjective evaluation of pain intensity, which was assessed using a numeric rating scale. The participating physician assigned, based on their personal interaction with the patient, an attribute of affinity (positive, neutral, and negative) towards them. Current serum lipid levels and pain intensity were correlated relative to these attributes. Pain intensity did not differ between the groups assigned positive or negative attributes of affinity. In patients belonging to the "positive" group, pain intensity correlated positively with total cholesterol (p=0.01) and LDL cholesterol (p=0.007). No correlations were found in the "negative" group or when the patient-doctor relationship was ignored. We found a significant association between subjectively assessed low back pain intensity and serum levels of total and LDL cholesterol in patients with whom the physician had a positive affinity. A positive affinity with the patients having chronic pain and the patient's trust in their physicians may ultimately mean that the patient's statement about pain is more credible, which may retroactively affect the outcome of therapy.

统计数据显示,腰痛患者的疼痛强度与较高的BMI、血清总胆固醇和三酰甘油水平相关。我们研究的目的是评估这些关联如何依赖于医患关系的性质。89例慢性腰痛住院患者(女性50例,男性39例;平均年龄:64.5±12.7岁,随访3年。入院时进行血脂分析(LDL-C、HDL-C和总胆固醇),同时使用数字评分量表对疼痛强度进行主观评估。参与的医生根据他们与患者的个人互动,对他们分配亲和力属性(积极,中性和消极)。当前的血脂水平和疼痛强度与这些属性相关。疼痛强度在亲和性的正面或负面属性组之间没有差异。在“阳性”组中,疼痛强度与总胆固醇(p=0.01)和低密度脂蛋白胆固醇(p=0.007)呈正相关。在“阴性”组或忽略医患关系时,没有发现相关性。我们发现主观评估的腰痛强度和血清总胆固醇和低密度脂蛋白胆固醇水平之间有显著的关联。与慢性疼痛患者的积极关系和患者对医生的信任可能最终意味着患者关于疼痛的陈述更可信,这可能会追溯影响治疗结果。
{"title":"Objective Evaluation of Chronic Low-Back Pain Using Serum Lipids: The Role of the Doctor-Patient Relationship.","authors":"Tomáš Bruthans,&nbsp;Jana Vránová,&nbsp;Anna Yamamotová","doi":"10.1155/2023/9972093","DOIUrl":"https://doi.org/10.1155/2023/9972093","url":null,"abstract":"<p><p>Statistical data show that pain intensity in patients with low back pain is associated with a higher BMI, total serum cholesterol, and triacylglycerol levels. The objective of our study was to evaluate how these associations are dependent on the nature of the patient-doctor relationship. Eighty-nine patients hospitalized with chronic low-back pain (50 women, 39 men; average age: 64.5 ± 12.7 years) were assessed over a 3-year period. A serum lipid analysis was conducted (LDL-C, HDL-C, and total cholesterols) at admission in parallel with a subjective evaluation of pain intensity, which was assessed using a numeric rating scale. The participating physician assigned, based on their personal interaction with the patient, an attribute of affinity (positive, neutral, and negative) towards them. Current serum lipid levels and pain intensity were correlated relative to these attributes. Pain intensity did not differ between the groups assigned positive or negative attributes of affinity. In patients belonging to the \"positive\" group, pain intensity correlated positively with total cholesterol (<i>p</i>=0.01) and LDL cholesterol (<i>p</i>=0.007). No correlations were found in the \"negative\" group or when the patient-doctor relationship was ignored. We found a significant association between subjectively assessed low back pain intensity and serum levels of total and LDL cholesterol in patients with whom the physician had a positive affinity. A positive affinity with the patients having chronic pain and the patient's trust in their physicians may ultimately mean that the patient's statement about pain is more credible, which may retroactively affect the outcome of therapy.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079384/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9352975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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: 1
Effects of the MR-DTI Characteristics of the Trigeminal Ganglion Target on Radiofrequency Treatment in Patients with Trigeminal Neuralgia: A Retrospective Observational Clinical Study. 三叉神经节靶MR-DTI特征对三叉神经痛射频治疗的影响:回顾性观察性临床研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/1988926
Xu Su, Zhengming Wang, Min Cheng, Yu Tian, Chao Du

Background: In the percutaneous treatment of trigeminal neuralgia (TN), the difficulty in accessing the foramen ovale (FO) has been widely recognized. However, the most efficient percutaneous treatment target is the so-called trigeminal ganglion target (TGT). We propose that the TGT in a puncture can be identified by magnetic resonance diffusion tensor imaging (MR-DTI).

Objectives: To observe the effect of the characteristics of the TGT as detected by MR-DTI on percutaneous stereotactic radiofrequency rhizotomy (PSR) in TN patients.

Methods: In our observational study, we preoperatively performed MR-DTI and/or 3D-CT for 48 TN patients, analyzed the characteristics of the TGT and/or FO, and designed appropriate surgical schemes for producing an accurate PSR trajectory according to these characteristics. The position and size of the TGT aided in adjusting the puncture angle and guiding the approach. Then, we successfully performed a customized PSR guided by the characteristics of the FO or TGT. During the postoperative and follow-up periods, we assessed the effect of treatment with pain scores and MR-DTI findings.

Results: The characteristics of the TGT vary from patient to patient. We performed PSR with a single puncture guided by MR-DTI and 3D-CT in 16 patients, and only one patient required three punctures. All three of these punctures reached the FO target, as confirmed by intraoperative C-arm X-ray. We finally reached the TGT successfully after 2 additional attempts, confirming that the probe reached the TGT that accurately covered the pain territory with an electrophysiology test. The characteristics of the TGT were negatively correlated with the number of PSR punctures. Fewer complications occurred for PSRs guided by the TGT than for PSRs guided by the FO.

Conclusions: The characteristics of the TGT are correlated with the number of punctures in the PSR. The application of MR-DTI for detecting the size of the TGT is an important step in predicting the difficulty of puncture. The PSR approach can be guided by the TGT and FO for TN patients who present with multiple adverse factors and thus may be beneficial in reducing the number of complications.

背景:在经皮治疗三叉神经痛(TN)中,进入卵圆孔(FO)的困难已被广泛认识。然而,最有效的经皮治疗靶点是所谓的三叉神经节靶点(TGT)。我们建议可以通过磁共振扩散张量成像(MR-DTI)来识别穿刺中的TGT。目的:观察MR-DTI检测TGT特征对TN患者经皮立体定向射频根治术(PSR)的影响。方法:在我们的观察性研究中,我们对48例TN患者术前进行MR-DTI和/或3D-CT检查,分析TGT和/或FO的特征,并根据这些特征设计合适的手术方案,以产生准确的PSR轨迹。TGT的位置和大小有助于调整穿刺角度和引导入路。然后,我们成功地根据FO或TGT的特性进行了定制的PSR。在术后和随访期间,我们通过疼痛评分和MR-DTI结果评估治疗效果。结果:TGT的特征因患者而异。我们在MR-DTI和3D-CT引导下对16例患者进行了单次穿刺的PSR,只有1例患者需要三次穿刺。术中c臂x线片证实,所有三次穿刺均达到FO目标。经过两次额外的尝试,我们最终成功到达TGT,通过电生理测试证实探针到达了准确覆盖疼痛区域的TGT。TGT的特征与PSR穿刺次数呈负相关。TGT引导下的psr比FO引导下的psr发生的并发症要少。结论:TGT的特征与PSR穿刺次数有关。应用核磁共振成像技术检测TGT的大小是预测穿刺难度的重要一步。对于存在多种不良因素的TN患者,PSR入路可以在TGT和FO的指导下进行,因此可能有利于减少并发症的数量。
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引用次数: 1
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Pain Research & Management
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