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2.
Medicine (Baltimore) ; 103(14): e37659, 2024 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-38579082

RESUMO

Ultrasound-guidance is applied during the administration of Korean medicine (KM) interventions to improve the safety and effectiveness of the interventions. Although many case series and reports on the use of ultrasound-guided KM interventions have been reported, no study has investigated the current use of ultrasound-guidance in clinical practice by doctors of Korean medicine (KMDs). An online survey was conducted with questions examining the status of ultrasound-guidance usage among KMDs practicing in various KM clinical settings. Survey responses from 335 KMDs were collected. Ultrasound started to be widely used in the clinical practice of KM since 2022. The primary objective of using ultrasound-guidance was "To improve the accuracy and efficacy" by 54.6%. Ultrasound-guidance was most frequently applied for shoulder joint diseases, and pharmacopuncture was the most frequently used intervention (76.1% and 90.4%, respectively). The respondents reported that effectiveness could be enhanced the most in nerve entrapment syndromes and especially when used in shoulder joints. Over 90% of KMDs responded that the safety and efficacy of treatment, specialty, and patients' satisfaction were improved after adopting ultrasound-guidance. Moreover, 94.9% of KMDs agreed with the necessity for reimbursement of ultrasound-guidance in KM under national health insurance coverage. Most KMDs responded that they had positive perceptions regarding the clinical use of ultrasound-guidance in KM in terms of treatment effects, safety, and patient satisfaction, and the need for national health insurance coverage of the service. Our findings may provide practice-based evidence for conducting clinical studies.


Assuntos
Hospitais , Padrões de Prática Médica , Humanos , Inquéritos e Questionários , Ultrassonografia de Intervenção/métodos , República da Coreia
3.
Am J Otolaryngol ; 45(1): 104091, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38652678

RESUMO

BACKGROUND: Thyroid nodules are common in the general population. Ultrasonography is the most efficient diagnostic approach to evaluate thyroid nodules. The US FNAC procedure can be performed using either the short axis (perpendicular), or a long axis (parallel) approach to visualize the needle as it is advanced toward the desired nodule. The main aim of this study was to compare the percentage of non-diagnostic results between the long and short axis approach. METHODS: A prospective study that included a randomized controlled trial and was divided into two arms-the short axis and the long axis-was conducted. A total of 245 thyroid nodules were collected through the fine needle aspiration cytology, performed with ultrasound, from march 2021 to march 2022. The patient's demographic information were collected and also nodules characteristics. RESULTS: Of 245 nodules sampled, 122 were sampled with the long axis method, while 123 with the short axis method. There is not significantly less non diagnostic approach with either method compared to the other (11.5 % vs 16.3 % respectively). DISCUSSION: Previous studies came to the conclusion that the long axis method yields fewer non diagnostic samples. This study evaluated the two FNA approaches which were proceeded by the same physician who is expert in both techniques. CONCLUSION: The US FNAC performed in the long axis approach will not produce more conclusive results and less non diagnostic results (Bethesda category 1) than the short axis approach one.


Assuntos
Nódulo da Glândula Tireoide , Humanos , Nódulo da Glândula Tireoide/patologia , Nódulo da Glândula Tireoide/diagnóstico por imagem , Estudos Prospectivos , Feminino , Masculino , Pessoa de Meia-Idade , Biópsia por Agulha Fina/métodos , Adulto , Glândula Tireoide/patologia , Glândula Tireoide/diagnóstico por imagem , Idoso , Biópsia Guiada por Imagem/métodos , Ultrassonografia de Intervenção/métodos , Ultrassonografia/métodos
4.
Curr Opin Anaesthesiol ; 37(3): 259-265, 2024 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-38573182

RESUMO

PURPOSE OF REVIEW: To discuss considerations surrounding the use of point-of-care ultrasound (POCUS) in pediatric anesthesiology. RECENT FINDINGS: POCUS is an indispensable tool in various medical specialties, including pediatric anesthesiology. Credentialing for POCUS should be considered to ensure that practitioners are able to acquire images, interpret them correctly, and use ultrasound to guide procedures safely and effectively. In the absence of formal guidelines for anesthesiology, current practice and oversight varies by institution. In this review, we will explore the significance of POCUS in pediatric anesthesiology, discuss credentialing, and compare the specific requirements and challenges currently associated with using POCUS in pediatric anesthesia. SUMMARY: Point-of-care ultrasound is being utilized by the pediatric anesthesiologist and has the potential to improve patient assessment, procedure guidance, and decision-making. Guidelines increase standardization and quality assurance procedures help maintain high-quality data. Credentialing standards for POCUS in pediatric anesthesiology are essential to ensure that practitioners have the necessary skills and knowledge to use this technology effectively and safely. Currently, there are no national pediatric POCUS guidelines to base credentialing processes on for pediatric anesthesia practices. Further work directed at establishing pediatric-specific curriculum goals and competency standards are needed to train current and future pediatric anesthesia providers and increase overall acceptance of POCUS use.


Assuntos
Anestesiologia , Competência Clínica , Credenciamento , Pediatria , Sistemas Automatizados de Assistência Junto ao Leito , Ultrassonografia , Humanos , Anestesiologia/educação , Anestesiologia/normas , Credenciamento/normas , Sistemas Automatizados de Assistência Junto ao Leito/normas , Criança , Pediatria/educação , Pediatria/normas , Pediatria/métodos , Ultrassonografia/normas , Ultrassonografia/métodos , Competência Clínica/normas , Ultrassonografia de Intervenção/normas , Ultrassonografia de Intervenção/métodos
5.
Rev Assoc Med Bras (1992) ; 70(3): e20230962, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38655995

RESUMO

OBJECTIVE: A new block, namely, modified thoracoabdominal nerves block through perichondrial approach, is administered below the costal cartilage. We sought to compare the analgesic efficacy of the modified thoracoabdominal nerves block through perichondrial approach block with local anesthetic infiltration at the port sites in an adult population who underwent laparoscopic cholecystectomy. METHODS: Patients who will undergo laparoscopic cholecystectomy were randomized to receive bilateral ultrasound-guided modified thoracoabdominal nerves block through perichondrial approach blocks or local anesthetic infiltration at the port insertion sites. The primary outcome was the total amount of tramadol used in the first 12 h postoperatively. The secondary outcomes were total IV tramadol consumption for the first postoperative 24 h and visual analog scale scores. RESULTS: The modified thoracoabdominal nerves block through perichondrial approach group had significantly less tramadol use in the first 12 h postoperatively (p<0.001). The modified thoracoabdominal nerves block through perichondrial approach group's visual analog scale scores at rest (static) and with movement (dynamic) were significantly lower compared with the port infiltration group (p<0.05). CONCLUSION: Patients who received modified thoracoabdominal nerves block through perichondrial approach block had significantly less analgesic consumption and better pain scores than those who received port-site injections after laparoscopic cholecystectomy.


Assuntos
Anestésicos Locais , Colecistectomia Laparoscópica , Bloqueio Nervoso , Medição da Dor , Dor Pós-Operatória , Tramadol , Humanos , Colecistectomia Laparoscópica/métodos , Masculino , Feminino , Bloqueio Nervoso/métodos , Dor Pós-Operatória/prevenção & controle , Adulto , Pessoa de Meia-Idade , Tramadol/administração & dosagem , Tramadol/uso terapêutico , Anestésicos Locais/administração & dosagem , Analgésicos Opioides/administração & dosagem , Analgésicos Opioides/uso terapêutico , Resultado do Tratamento , Ultrassonografia de Intervenção/métodos
6.
Rev Assoc Med Bras (1992) ; 70(3): e20231082, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38656001

RESUMO

OBJECTIVE: Thoracic ultrasonography is widely used in imaging peripheral lesions and invasive interventional procedures. The aim of this study was to assess the diagnostic value of thoracic ultrasonography-guided transthoracic needle aspiration biopsy and the factors affecting the diagnosis of peripheral tumoral lung lesions. METHODS: The lesion size, biopsy needle type, number of blocks, complications, and pathology results were compared in 83 patients between January 2015 and July 2018. The cases with pathological non-diagnosis and definite pathological diagnosis were determined. For the assessment of the factors affecting diagnosis, the size of the lesions and the biopsy needle type were evaluated. Biopsy preparations containing non-diagnostic atypical cells were referred to a cytopathologist. The effect of the cytopathological examination on the diagnosis was also evaluated. RESULTS: Pathological diagnosis was made in 66.3% of the cases; cell type could not be determined in 22.9% of the cases, and they were referred to a cytopathologist. After the cytopathologist's examination, the diagnosis rate increased to 80.7%. Diagnosis rates were higher when using tru-cut than Chiba and higher in cases with tumor size >2 cm than smaller. CONCLUSION: Thoracic ultrasonography-guided transthoracic needle aspiration biopsy is a preferred approach to the diagnosis of peripheral tumoral lung lesions, given its high diagnostic rate, in addition to being cheap, highly suitable for bedside use, and safe, and the lack of radiation exposure.


Assuntos
Biópsia Guiada por Imagem , Neoplasias Pulmonares , Humanos , Neoplasias Pulmonares/patologia , Neoplasias Pulmonares/diagnóstico por imagem , Feminino , Masculino , Pessoa de Meia-Idade , Idoso , Biópsia Guiada por Imagem/métodos , Adulto , Ultrassonografia de Intervenção/métodos , Idoso de 80 Anos ou mais , Estudos Retrospectivos , Biópsia por Agulha Fina/métodos , Reprodutibilidade dos Testes
8.
Artif Cells Nanomed Biotechnol ; 52(1): 218-228, 2024 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-38646876

RESUMO

This study prepared and evaluated polymeric polybutylcyanoacrylate (PBCA) nanoparticles (NPs) that can be used as a new agent for contrast-enhanced intravascular ultrasound (IVUS) imaging with drug delivery capacity. The nanoformulation was successfully developed using suspension polymerisation and characterised in terms of size, size distribution, zeta potential, morphology, stability, toxicity effects, imaging effects and drug release study. The results showed that the nanoparticles were round and hollow, with a particle diameter of 215.8 ± 25.3 nm and a zeta potential of -22.2 ± 4.1 mV. In vitro experiments, the nanoparticles were safe, non-toxic, and stable in nature with the capacity to carry and release drug (ant-miR-126). Moreover, the nanoparticles can match the high-frequency probe of commercially IVUS as a contrast agent to improve the resolution of imaging (the mean echo intensity ratio in the vascular wall increased significantly from 10.89 ± 1.10 at baseline, to 24.51 ± 1.91 during injection and 43.70 ± 0.88 after injection, respectively p < .0001). Overall, a new nano agent with drug-carrying capacity was prepared, which can be used in combination with IVUS for simultaneous diagnosis and targeted therapy of coronary atherosclerosis.


Assuntos
Meios de Contraste , Portadores de Fármacos , Embucrilato , Nanopartículas , Nanopartículas/química , Meios de Contraste/química , Embucrilato/química , Portadores de Fármacos/química , Animais , Ultrassonografia de Intervenção/métodos , Humanos , Liberação Controlada de Fármacos
9.
BMJ Open ; 14(3): e079849, 2024 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-38531566

RESUMO

INTRODUCTION: Ultrasound-guided quadratus lumborum block and erector spinae plane block are widely used for postoperative analgesia in adult patients undergoing abdominal surgeries. This protocol aims to compare the analgesic effects between ultrasound-guided quadratus lumborum block and erector spinae plane block on postoperative pain in abdominal surgeries. METHODS AND ANALYSIS: Four databases, including PubMed, EMBASE, Web of Science and the Cochrane Central Register of Controlled Trials (CENTRAL), will be searched. Randomised controlled trials that compared the analgesic effects between ultrasound-guided quadratus lumborum block and erector spinae plane block on postoperative pain in adult patients will be identified. The primary outcomes are time to the first analgesic request and postoperative analgesic consumption over 24 hours. Secondary outcomes will include postoperative pain scores and the incidence of side effects. RevMan V.5.3 software will be used for data processing and statistical analysis. The Grading of Recommendation, Assessment, Development and Evaluation approach will be used to assess the evidence quality of outcomes. ETHICS AND DISSEMINATION: Ethical approval is not required for this study. Results of this present study will be submitted to a peer-reviewed journal. PROSPERO REGISTRATION NUMBER: CRD42023445802.


Assuntos
Bloqueio Nervoso , Ultrassonografia de Intervenção , Adulto , Humanos , Ultrassonografia de Intervenção/métodos , Revisões Sistemáticas como Assunto , Metanálise como Assunto , Dor Pós-Operatória/tratamento farmacológico , Bloqueio Nervoso/métodos , Analgésicos/uso terapêutico , Analgésicos Opioides/uso terapêutico
10.
Medicine (Baltimore) ; 103(13): e37677, 2024 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-38552057

RESUMO

Simple hepatic cysts (SHC) are generally asymptomatic and incidentally diagnosed using imaging studies. Asymptomatic SHC does not require treatment, but symptomatic SHC warrants treatment using different modalities, including intravenous antibiotic therapy, ultrasound-guided percutaneous catheter drainage (PCD) with sclerotherapy, and surgery. The dissemination of endoscopic ultrasonography (EUS) intervention techniques has enabled the performance of puncture and drainage via the transgastrointestinal route for intra-abdominal abscesses. Despite the development of an EUS-guided drainage method for treating symptomatic SHC, only a few case reports using this method have been reported. This study retrospectively analyzed the safety and feasibility of EUS-guided drainage of symptomatic SHC as well as its clinical outcomes and compared it with combined therapy using PCD and minocycline sclerotherapy. The records of 10 consecutive patients with 11 symptomatic SHCs treated with either EUS-guided drainage or PCD combined with minocycline sclerotherapy at the Musashino Tokushukai Hospital from August 2019 to January 2024 were retrospectively examined. All cases in both groups achieved technical and clinical success, with no reported adverse events. The median reduction rates of the major cyst diameters in the EUS-guided drainage and PCD with sclerotherapy groups were 100% (interquartile range [IQR]: 94%-100%) and 67% (IQR: 48.5%-85%). The length of hospital stay was 7 and 22.5 days in the EUS-guided and PCD with sclerotherapy groups (P = .01). EUS-guided drainage of symptomatic SHC is a safe and effective therapeutic alternative to percutaneous drainage with sclerotherapy and surgery for treating symptomatic SHC.


Assuntos
Cistos , Endossonografia , Hepatopatias , Humanos , Estudos Retrospectivos , Escleroterapia/métodos , Minociclina/uso terapêutico , Drenagem/métodos , Cistos/etiologia , Ultrassonografia de Intervenção/métodos , Resultado do Tratamento
11.
Medicine (Baltimore) ; 103(13): e37597, 2024 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-38552091

RESUMO

Although rectus sheath block (RSB) is routinely used in laparoscopic surgeries to reduce mid-abdominal pain, whether RSB should be performed before or after surgery remains unclear. Herein, the optimal timing for RSB in patients undergoing laparoscopic surgery was investigated. This retrospective cohort study analyzed the data of patients who underwent RSB during laparoscopic procedures at our hospital between January 2013 and December 2018. The primary outcome was the time to rescue analgesia within 24 hours postanesthesia. The patients were divided into preoperative (pre-) and postoperative (post-) RSB groups. A multivariable Cox proportional hazards regression model was used to analyze the time to rescue analgesia in the unmatched and propensity score (PS)-matched patient populations. In total, 609/14,284 patients were included (pre-RSB group, 227 patients; post-RSB group, 382 patients). After PS matching, 97 patients were assigned to both groups. Although the time from extubation to the first analgesic request was not significantly different between the 2 groups (322 vs 294 minutes, P = .57), the patients in the pre-RSB group showed a lower risk of postoperative first analgesic administration after PS matching (adjusted hazard ratio, 0.71; 95% confidence interval, 0.53-0.95; P = .023). Among patients undergoing laparoscopic surgery, those in the pre-RSB group tended to have a longer time to the first analgesic request and had a lower risk of analgesic administration within the first 24 hours than those in the post-RSB group. Thus, performing RSB preoperatively may be preferable.


Assuntos
Laparoscopia , Bloqueio Nervoso , Humanos , Anestésicos Locais , Estudos Retrospectivos , Bloqueio Nervoso/métodos , Reto do Abdome , Ultrassonografia de Intervenção/métodos , Resultado do Tratamento , Dor Pós-Operatória/tratamento farmacológico , Dor Pós-Operatória/etiologia , Dor Pós-Operatória/prevenção & controle , Laparoscopia/efeitos adversos , Analgésicos , Analgésicos Opioides
12.
BMC Med Educ ; 24(1): 351, 2024 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-38553674

RESUMO

BACKGROUND: Simulation-based training is effective for ultrasound (US)-guided procedures. However, commercially developed simulators are costly. This study aims to evaluate the feasibility of a hand-made phantom for US-guided paracentesis. METHODS: We described the recipe to prepare an agar phantom. We collected the US performance data of 50 novices, including 22 postgraduate-year (PGY) residents and 28 undergraduate-year (UGY) students, who used the phantom for training, as well as 12 emergency residents with prior US-guided experience. We obtained the feedback after using the phantom with the Likert 5-point scale. The data were presented with medians and interquartile ranges (IQRs) and analyzed by the Wilcoxon rank sum test. RESULTS: While emergency residents demonstrated superior performance compared to trainees, all trainees exhibited acceptable proficiency (global rating of ≥ 3, 50/50 vs. 12/12, p = 1.000) and comparable needle steadiness [5 (5) vs. 5 (5), p = 0.223]. No significant difference in performance was observed between PGYs [5 (4-5)] and UGYs [5 (4-5), p = 0.825]. No significant differences were observed in terms of image stimulation, puncture texture, needle visualization, drainage simulation, and endurance of the phantom between emergency residents and trainees. However, experienced residents rated puncture texture and draining fluid as "neutral" (3/5 on the Likert scale). The cost of the paracentesis phantom is US$16.00 for at least 30 simulations, reducing it to US$6.00 without a container. CONCLUSIONS: The paracentesis phantom proves to be a practical and cost-effective training tool. It enables novices to acquire paracentesis skills, enhances their US proficiency, and boosts their confidence. Nevertheless, further investigation is needed to assess its long-term impact on clinical performance in real patients. TRIAL REGISTRATION: NCT04792203 at the ClinicalTrials.gov.


Assuntos
Paracentese , Ultrassonografia de Intervenção , Humanos , Paracentese/educação , Estudos de Viabilidade , Ultrassonografia/métodos , Imagens de Fantasmas , Ultrassonografia de Intervenção/métodos , Competência Clínica
13.
Vet J ; 304: 106094, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38452849

RESUMO

This study describes a transversal (TV) ultrasound-guided erector spinae plane (ESP) block technique over the transverse process of T12. And evaluates the distribution of the dye and affected nerves branches compared to a longitudinal (LNG) approach over the transverse process of T12 in canine cadavers. Secondly, it also compares de anatomy and dimensions of the transverse processes of T12 with T9 and T5. For this double-masked, cadaveric experimental study, 12 adult Beagle cadavers were injected with 0.6 mL/kg of dye/contrast. Spread was evaluated by computed tomography (CT) and dissection. Mean bodyweight was 9.76 (±0.59) kg. The TV and LNG approaches stained a median (range) of four (2-6) and three (1-6) medial branches of the dorsal rami of the spinal nerves, three (2-6) and three (2-5) lateral branches, and one (0-3) and one (0-4) ventral branches, respectively. Dye was detected in the epidural space in 55.6% and 66.7% of cases for the TV and LNG approaches, respectively (P=0.63). And in the ventral paravertebral compartment in 22.2% and lymphatics in 88.8% in both approaches. There were no statistical differences for the spread. The dorsolateral edge of the transverse process (TP) was not visible with CT at T12. The mean (±SD) length of the TP was significantly shorter at T12 [3.34 (±0.22)] mm, compared to T9 [6.08 (±0.47)] mm and T5 [5.93 (±0.62)] mm (P <0.001). This study showed similar distribution whether using a TV or LNG approach and differences in the anatomy and length of the T12 TP.


Assuntos
Doenças do Cão , Bloqueio Nervoso , Humanos , Cães , Animais , Bloqueio Nervoso/veterinária , Bloqueio Nervoso/métodos , Vértebras Torácicas , Ultrassonografia/veterinária , Cadáver , Ultrassonografia de Intervenção/veterinária , Ultrassonografia de Intervenção/métodos
15.
Catheter Cardiovasc Interv ; 103(5): 722-730, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38469945

RESUMO

BACKGROUND: The radial first approach in cardiac catheterization is preferred for its benefits in patient comfort and recovery time. Yet, challenges persist due to characteristics like small, deep, calcified, and mobile radial arteries. Utilizing ultrasound before and during procedures can improve success rates. However, the adoption of its use is still limited and subject to debate. AIM: To utilize routine preprocedural ultrasound (US) and compare US guided with palpation guided radial access, focusing on operator efficiency and outcomes. METHODS AND RESULTS: Consenting adult patients undergoing elective radial cardiac catheterization were divided into palpation and US groups. Routine preprocedural assessment of radial artery characteristics was performed using handheld US. Baseline data, US findings, procedural outcomes, and clinical outcomes were compared in 182 participants (91 in each group). US guided radial access had significantly higher first pass success rates (76.92% vs. 49.45%, p 0.0001), fewer number of attempts (1.46 ± 1 vs. 1.99 ± 1.46, p 0.004), and shorter amount of time (93.62 ± 44.04 vs. 120.44 ± 67.1, p 0.002) compared with palpation guidance. The palpation group had significantly higher incidence of spasm (15.38% vs. 3.3%, p 0.0052). Subgroup analysis indicated consistent benefits of US guidance, especially in calcified radial arteries. CONCLUSION: This prospective, nonrandomized, single-center study demonstrated that real-time procedural US improved the operator's time and effort and enhanced patient comfort compared with palpation. US guidance use was particularly favorable in the presence of calcifications observed on baseline preoperative US.


Assuntos
Cateterismo Periférico , Adulto , Humanos , Estudos Prospectivos , Resultado do Tratamento , Cateterismo Periférico/efeitos adversos , Cateterismo Periférico/métodos , Palpação/métodos , Cateterismo Cardíaco/efeitos adversos , Cateterismo Cardíaco/métodos , Artéria Radial/diagnóstico por imagem , Artéria Radial/cirurgia , Ultrassonografia de Intervenção/métodos
16.
World J Surg ; 48(4): 896-902, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38479797

RESUMO

BACKGROUND: Idiopathic granulomatous mastitis (IGM) is a rare inflammatory disease of the breast with clinical features that are often confused with those of breast cancer leading to delayed diagnosis and treatment. This retrospective study aimed to evaluate the therapeutic effectiveness and cosmetic results of drainage surgery using ultrasound-guided vacuum-assisted excision (VAE) for the treatment of IGM at the abscess stage. METHODS: The time of recovery, cases of further surgical intervention, and cosmetic results were retrospectively collected and analyzed from patients who underwent drainage with VAE or conventional drainage between October 2017 and August 2021. RESULTS: A total of 65 patients diagnosed with IGM at the abscess stage who underwent drainage surgery with VAE or conventional drainage surgery were enrolled. Overall, 38 (58.5%) underwent conventional drainage surgery and 27 (41.5%) underwent drainage with VAE. We found that patients who underwent VAE recovered much faster than those who underwent traditional drainage surgery (30.1 vs. 48.0 days). Nine (33.3%) patients in the VAE group required further surgical intervention after drainage, whereas 33 (86.8%) patients in the control group underwent another surgery to resect residual lesions. Additionally, patients in the VAE group were more satisfied with the breast appearance, mainly due to less influence of the scars and better symmetry of their breasts. CONCLUSION: Compared with conventional drainage surgery, drainage surgery using VAE for IGM patients at the abscess stage improved therapeutic and cosmetic outcomes. Furthermore, postoperative management of IGM is crucial.


Assuntos
Neoplasias da Mama , Mastite Granulomatosa , Feminino , Humanos , Estudos Retrospectivos , Mastite Granulomatosa/diagnóstico por imagem , Mastite Granulomatosa/cirurgia , Abscesso/diagnóstico por imagem , Abscesso/cirurgia , Neoplasias da Mama/patologia , Ultrassonografia de Intervenção/métodos , Imunoglobulina M
17.
Comput Methods Programs Biomed ; 247: 108109, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38460346

RESUMO

BACKGROUND AND OBJECTIVE: Automatic needle tip detection is important in real-time ultrasound (US) images that are utilized to guide interventional needle puncture procedures in clinical settings. However, due to the spatial indiscernibility problem caused by the severe background interferences and the tip characteristics of small size, being grayscale and indistinctive appearance patterns, tip detection in US images is challenging. METHODS: To achieve precise tip detection in US images against spatial indiscernibility, a novel multi-keyframe motion-aware framework called TipDet is proposed. It can identify tips based on their short-term spatial-temporal pattern and long-term motion pattern. In TipDet, first, an adaptive keyframe model (AKM) is proposed to decide whether a frame is informative to serve as a keyframe for long-term motion pattern learning. Second, candidate tip detection is conducted using a two-stream backbone (TSB) based on their short-term spatial-temporal pattern. Third, to further identify the true one in the candidate tips, a novel method for learning the long-term motion pattern of the tips is proposed based on the proposed optical-flow-aware multi-head cross-attention (OFA-MHCA). RESULTS: On the clinical human puncture dataset, which includes 4195 B-mode images, the experimental results show that the proposed TipDet can achieve precise tip detection against the spatial indiscernibility problem, achieving 78.7 % AP0.1:0.5 and 8.9 % improvement over the base detector at approximately 20 FPS. Moreover, a tip localization error of 1.3±0.6 % is achieved, exceeding the existing method. CONCLUSIONS: The proposed TipDet can facilitate a wider and easier application of US-guided interventional procedures by providing robust and precise needle tip localization. The codes and data are available at https://github.com/ResonWang/TipDet.


Assuntos
Aprendizagem , Agulhas , Humanos , Ultrassonografia , Movimento (Física) , Ultrassonografia de Intervenção/métodos
18.
Coron Artery Dis ; 35(3): 171-178, 2024 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-38451558

RESUMO

BACKGROUND: In percutaneous coronary intervention (PCI) procedures for patients with unprotected left main coronary artery (ULMCA) lesions, intravascular ultrasonography (IVUS) guidance has shown potential for enhancing clinical outcomes. However, studies confirming its superiority to conventional angiographic-guided PCI remain few. This study aimed to assess if IVUS-guided PCI for patients with unprotected LMCA stenosis improves clinical outcomes compared to angiographic-guided PCI. METHODS: This randomized clinical study enrolled 181 patients with ULMCA lesions scheduled for drug-eluting stent implantation. Patients were split into 90 in the IVUS-guided group and 91 in the conventional group. Procedural characteristics, clinical outcomes, and the incidence of major adverse cardiovascular event (MACE) were evaluated for all patients. The risk reduction associated with IVUS-guided PCI was evaluated using a multivariate Cox regression analysis. RESULTS: Patients who underwent IVUS demonstrated significantly higher pre-dilatation before stenting (88.9% vs. 72.5%, P  = 0.005), post-dilatation balloon diameter (4.46 ±â€…0.48 vs. 4.21 ±â€…0.49, P  < 0.001), stent diameter (3.9 ±â€…0.4 vs. 3.7 ±â€…0.3, P  = 0.002), and pressure for post dilatation (18 ±â€…3 vs. 16 ±â€…2, P  = 0.001). Regarding 12-month outcomes, patients who underwent IVUS demonstrated significantly lower MACE (3.3% vs. 18.7%, P  < 0.001) than those who underwent the conventional method. Multivariate Cox regression analysis revealed that IVUS was related to 84.4% risk reduction of 1-year MACE (HR = 0.156, 95% CI = 0.044-0.556, P  = 0.004). CONCLUSION: Compared to angiographic-guided PCI, IVUS-guided PCI resulted in improved clinical results and a markedly reduced risk of MACE in patients with ULMCA lesions.


Assuntos
Doença da Artéria Coronariana , Stents Farmacológicos , Intervenção Coronária Percutânea , Humanos , Doença da Artéria Coronariana/diagnóstico por imagem , Doença da Artéria Coronariana/terapia , Doença da Artéria Coronariana/etiologia , Intervenção Coronária Percutânea/efeitos adversos , Intervenção Coronária Percutânea/métodos , Angiografia Coronária/métodos , Ultrassonografia de Intervenção/métodos , Resultado do Tratamento
19.
Artigo em Alemão | MEDLINE | ID: mdl-38513640

RESUMO

By implementation of sonography regional anesthesia became more relevant in the daily practice of anesthesia and pain therapy. Due to visualized needle guidance ultrasound supports more safety during needle placement. Thereby new truncal blocks got enabled. Next to the blocking of specific nerve structures, plane blocks got established which can also be described as interfascial compartment blocks. The present review illustrates published and established blocks in daily practice concerning indications and the procedural issues. Moreover, the authors explain potential risks, complications and dosing of local anesthetics.


Assuntos
Anestesia por Condução , Anestesia Local , Humanos , Anestesia por Condução/métodos , Anestésicos Locais , Manejo da Dor/métodos , Abdome/diagnóstico por imagem , Abdome/cirurgia , Ultrassonografia de Intervenção/métodos
20.
Obes Surg ; 34(5): 1505-1512, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38499943

RESUMO

PURPOSE: The external oblique intercostal plane (EOI) block is a novel block technique for anterolateral upper abdominal wall analgesia. The superficial nature of the external oblique intercostal plane allows it to be easily identified even in patients with obesity. The aim of this study was to test the hypothesis that EOI block would reduce IV morphine consumption within 24 h after laparoscopic sleeve gastrectomy. MATERIALS AND METHODS: Patients were randomly assigned to one of two groups: EOI block group and control group. The patients in the EOI block group received ultrasound-guided bilateral EOI block with a total of 40 ml 0.25% bupivacaine after anesthesia induction. The patients in the control group received no intervention. Postoperatively, all the patients were connected to an intravenous patient controlled analgesia (PCA) device containing morphine. The primary outcome of the study was IV morphine consumption in the first postoperative 24 h. RESULTS: The median [interquartile range] morphine consumption at 24 h postoperatively was significantly lower in the EOI block group than in the control group (7.5 [3.5 to 8.5] mg vs 14 [12 to 20] mg, p = 0.0001, respectively). Numerical rating scale (NRS) scores at rest and during movement were lower in the EOI block group than in the control group at 2, 6, and 12 h but were similar at 24 h. No block-related complications were observed in any patients. CONCLUSION: The results of the current study demonstrated that bilateral EOI block reduced postoperative opioid consumption and postoperative pain in patients with obesity undergoing laparoscopic sleeve gastrectomy. TRIAL REGISTRATION: Clinicaltrials.gov identifier: NCT05663658.


Assuntos
Laparoscopia , Bloqueio Nervoso , Obesidade Mórbida , Humanos , Estudos Prospectivos , Bloqueio Nervoso/métodos , Músculos Abdominais , Medição da Dor/efeitos adversos , Obesidade Mórbida/cirurgia , Dor Pós-Operatória/tratamento farmacológico , Dor Pós-Operatória/prevenção & controle , Dor Pós-Operatória/etiologia , Analgésicos Opioides , Morfina , Analgesia Controlada pelo Paciente/efeitos adversos , Analgesia Controlada pelo Paciente/métodos , Laparoscopia/efeitos adversos , Ultrassonografia de Intervenção/métodos , Gastrectomia/métodos
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