Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
Scand J Pain ; 24(1)2024 Jan 01.
Article in English | MEDLINE | ID: mdl-38447036

ABSTRACT

OBJECTIVES: Low back pain is a common musculoskeletal complaint and while prognosis is usually favorable, some patients experience persistent pain despite conservative treatment and invasive treatment to target the root cause of the pain may be necessary. The aim of this study is to evaluate patient outcomes after treatment of lumbar radiculopathy (LR) with quantum molecular resonance radiofrequency coblation disc decompression and percutaneous microdiscectomy with grasper forceps (QMRG). METHODS: This prospective cohort study was carried out in two Spanish hospitals on 58 patients with LR secondary to a contained hydrated lumbar disc hernia or lumbar disc protrusion of more than 6 months of evolution, which persisted despite conservative treatment with analgesia, rehabilitation, and physiotherapy, and/or epidural block, in the previous 2 years. Patients were treated with QMRG and the outcomes were measured mainly using the Douleur Neuropathique en 4 Questions, Numeric Rating Scale, Oswestry Disability Index, SF12: Short Form 12 Health Survey, Patient Global Impression of Improvement, Clinical Global Impression of Improvement, and Medical Outcomes Study Sleep Scale. RESULTS: Patients who received QMRG showed significant improvement in their baseline scores at 6 months post-treatment. The minimal clinically important difference (MCID) threshold was met by 26-98% of patients, depending on the outcome measure, for non-sleep-related outcomes, and between 17 and 62% for sleep-related outcome measures. Of the 14 outcome measures studied, at least 50% of the patients met the MCID threshold in 8 of them. CONCLUSION: Treatment of LR with QMRG appears to be effective at 6 months post-intervention.


Subject(s)
Low Back Pain , Radiculopathy , Humans , Prospective Studies , Radiculopathy/surgery , Follow-Up Studies , Pain Management , Low Back Pain/surgery
2.
Pain Manag ; 12(8): 917-930, 2022 Nov.
Article in English | MEDLINE | ID: mdl-36196857

ABSTRACT

Aims: The aim of this study was to determine whether there exists a difference in efficacy in the treatment of lumbar radiculopathy with quantum molecular resonance coablative radiofrequency and quantum molecular resonance coablative radiofrequency and percutaneous microdiscectomy with grasper forceps (QMRG). Patients & methods: A total of 28 patients from La Fe University and Polytechnic Hospital in Valencia were enrolled in a retrospective cohort. Results: Treatment with QMRG significantly improved non-sleep-related and sleep-related outcome measures. At 6 months post-intervention, treatment with QMRG resulted in significantly better scores in numeric rating scale, Oswestry Disability Index, Short Form 12 Health Survey Physical and Total, Patient Global Impression of Improvement, sleep disturbance and the two sleep problems indexes. Conclusion: Treatment of lumbar radiculopathy with QMRG appears to be more effective at 6 months post-intervention.


Subject(s)
Intervertebral Disc Displacement , Radiculopathy , Humans , Radiculopathy/surgery , Retrospective Studies , Lumbar Vertebrae/surgery , Diskectomy/methods , Cohort Studies , Intervertebral Disc Displacement/complications , Intervertebral Disc Displacement/surgery , Treatment Outcome
3.
Neuromodulation ; 24(3): 448-458, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33462918

ABSTRACT

OBJECTIVE: The objective of this prospective randomized study of cases and controls was to evaluate the efficacy of treatment with low-frequency spinal cord stimulation (LF-SCS) and 10 kHz spinal cord stimulation (10-kHz SCS) in patients diagnosed with complex regional pain syndrome type I (CRPS) with upper limb involvement. MATERIALS AND METHODS: Fifty patients were randomized to receive conventional treatment or SCS with a commercially available low-frequency or 10-kHz system. Patients were assessed at 1, 3, 6, and 12 months. The primary endpoint was at 12-months post permanent implantation of the SCS devices. Outcome measures assessed included: Numerical Rating Scale (NRS), 12-Item Short-Format Health Survey (SF-12), Oswestry Disability Index (ODI), Study Sleep Scale medical outcomes (MOS-SS), Douleur Neuropathique 4 questions pain questionnaire (DN4), Patient Global Impression Scale on the impact of treatment improvement (PGI-I), Clinician Global Impression Scale on the impact of improving the patient (CGI-I). RESULTS: Forty-one patients were finally included in the analysis, 19 patients in the conventional treatment group, 12 in the LF-SCS group, and 10 in the 10-kHz SCS group. At the primary endpoint, patients treated with LF-SCS presented improvements in the NRS and DN4 outcomes around 2.4 and 1.5 times above the minimal clinically important difference (MCID) thresholds. At the primary endpoint, patients treated with 10-kHz SCS presented improvements in the NRS and DN4 outcomes around 2 and 1.4 times above the MCID thresholds. CONCLUSIONS: Patients experienced considerable improvement after SCS. The results show that LF-SCS has very good results when compared with conventional treatment. The results obtained with 10-kHz SCS are encouraging, with the advantages of the absence of paresthesia making it an alternative in the treatment of CRPS.


Subject(s)
Chronic Pain , Complex Regional Pain Syndromes , Spinal Cord Stimulation , Complex Regional Pain Syndromes/therapy , Humans , Pain Measurement , Prospective Studies , Spinal Cord , Treatment Outcome , Upper Extremity
4.
J Cardiothorac Vasc Anesth ; 34(1): 87-96, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31515188

ABSTRACT

OBJECTIVE: To quantify the acute effects of dobutamine in postoperative low cardiac output syndrome (LCOS) using transthoracic echocardiographic, hemodynamic, and blood biomarker monitoring and to assess its association with clinical outcomes. DESIGN: Observational prospective study. SETTING: Single university hospital. PARTICIPANTS: Patients undergoing elective cardiac surgery. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Echocardiographic parameters, hemodynamic data, and plasma biomarkers were obtained before and early after inotrope initiation. The diagnostic value of transthoracic echocardiographic parameters and their association with clinical outcome were evaluated. Thirty-eight LCOS patients and 12 control patients were included. The left ventricular outflow tract velocity time integral was significantly lower in LCOS patients (11.75 v 19.08 cm; p < 0.001) and showed a marked improvement after dobutamine administration (∼37% increase). Dobutamine improved left and right ventricular function, increased mean arterial pressure and urine output, and lowered lactate levels. The duration of dobutamine support, but not in-hospital mortality, was associated with echocardiographic estimates of cardiac performance early after dobutamine initiation. CONCLUSIONS: Early transthoracic echocardiographic assessment and the acute response to inotropic therapy may provide rapid and highly valuable information in the diagnostic workup and risk evaluation of patients with suspected LCOS after cardiac surgery.


Subject(s)
Cardiac Surgical Procedures , Dobutamine , Cardiac Output , Cardiac Output, Low/diagnostic imaging , Cardiac Output, Low/etiology , Cardiac Surgical Procedures/adverse effects , Echocardiography , Humans , Prospective Studies
6.
Paediatr Anaesth ; 26(11): 1097-1105, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27565740

ABSTRACT

BACKGROUND: Pressure recording analytical method (PRAM) is a novel, arterial pulse contour method for measuring cardiac output (CO). Validation studies of PRAM in children are few, and have shown contradictory results. The aim of the study was to compare the MostCare® -PRAM vs the Fick method of cardiac output estimation (reference method). METHODS: This is a single-center, prospective observational study in 52 pediatric patients who underwent diagnostic right and left heart catheterization. Cardiac index (CI) measurements with the MostCare® -PRAM vs the Fick method were obtained under hemodynamically stable conditions. RESULTS: Forty CI measurements were performed. The data showed good agreement between CIFick and CIPRAM : r2 = 0.90 (P < 0.001), mean bias -0.075, limits of agreement from -0.56 to 0.41. The percentage error was 17%. Comparable results were obtained for patients <20 kg (r2 = 0.87, P < 0.001), mean bias -0.135, limits of agreement from -0.35 to 0.62, percentage of error 17%. CONCLUSIONS: In pediatric patients undergoing diagnostic right and left heart catheterization, the MostCare® -PRAM was shown to estimate CI with a good level of agreement with the Fick method measurements.


Subject(s)
Cardiac Catheterization , Monitoring, Physiologic/instrumentation , Monitoring, Physiologic/methods , Adolescent , Cardiac Output , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Reproducibility of Results
SELECTION OF CITATIONS
SEARCH DETAIL
...