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Spinal Stenosis

Spinal Stenosis is a medical condition characterized by the narrowing of the spinal canal, often resulting in compression of the spinal cord or nerve roots.
This can lead to pain, numbness, and weakness in the back, legs, and feet.
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Most cited protocols related to «Spinal Stenosis»

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Publication 2014
Back Pain Chronic Pain Diagnosis Dietary Supplements Medical Devices Pain Pharmaceutical Preparations Phenotype Physical Examination Sciatica Spinal Stenosis Vertebral Column

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Publication 2018
Cells Cell Separation Ethics Committees Females Formaldehyde Freezing Homo sapiens Intervertebral Disc Degeneration Intervertebral Disk Displacement Lumbar Region Males Nitrogen Operative Surgical Procedures Paraffin Embedding Patients Proteins Scoliosis Spinal Fusions Spinal Stenosis Stenosis Tail Tissues Western Blot
We previously published the Mind-Body Approaches to Pain (MAP) trial protocol [15 (link)]. The primary source of participants was Group Health (GH), a large integrated healthcare system in Washington State. Letters describing the trial and inviting participation were mailed to GH members who met the electronic medical record (EMR) inclusion/exclusion criteria, and to random samples of residents in communities served by GH. Individuals who responded to the invitations were screened and enrolled by telephone (Figure 1). Potential participants were told that they would be randomized to one of “two different widely-used pain self-management programs that have been found helpful for reducing pain and making it easier to carry out daily activities” or to continued usual care plus $50. Those assigned to MBSR or CBT were not informed of their treatment allocation until they attended the first session. We recruited participants from 6 cities in 10 separate waves.
We recruited individuals 20 to 70 years of age with non-specific low back pain persisting at least 3 months. Persons with back pain associated with a specific diagnosis (e.g., spinal stenosis), with compensation or litigation issues, who would have difficulty participating (e.g., unable to speak English, unable to attend classes at the scheduled time and location), or who rated pain bothersomeness <4 and/or pain interference with activities <3 on 0–10 scales were excluded. Inclusion and exclusion criteria were assessed using EMR data for the previous year (for GH enrollees) and screening interviews. Participants were enrolled between September 2012 and April 2014. Due to slow enrollment, after 99 participants were enrolled, we stopped excluding persons 64–70 years old, GH members without recent visits for back pain, and patients with sciatica. The trial protocol was approved by the GH Human Subjects Review Committee. All participants gave informed consent.
Publication 2016
Back Pain Diagnosis Encounter Groups Healthy Volunteers Human Body Litigation Management, Pain Pain Patients Respiratory Diaphragm Sciatica Self-Management Spinal Stenosis
Sociodemographic characteristics assessed in the home interview included age, sex, race (self-identified), and years of education. Race was included because our prior work found Black race associated with polyarticular pain.22 (link) Cognitive status was assessed using the MMSE, scored 0–30.17 (link) We used the validated Physical Activity Scale for the Elderly (PASE) to measure physical activity in the previous week.28 (link) Participants were asked about doctor-diagnosed major medical conditions. Heart disease included report of heart attack, congestive heart failure, angina, pacemaker or cardiac arrhythmia. Other self-reported diagnoses included stroke, Parkinson’s Disease, rheumatoid arthritis, and spinal stenosis/disc disease. Peripheral neuropathy was assessed using Semmes-Weinstein monofilament testing.29 (link) Peripheral arterial disease was defined using an algorithm, based on an ankle-arm index <0.90 and the Rose Intermittent Claudication questionnaire.23 (link) Diabetes was defined using an algorithm based on self-reported diabetes, use of antidiabetic medications, and laboratory measures from the baseline clinic visit including random glucose (≥200mg/dl) and hemoglobin A1c (>7%). American College of Rheumatology (ACR) clinical criteria for osteoarthritis(OA) of the hand and knee30 (link), 31 (link) were assessed in the clinic examination by experienced nurses trained by the study rheumatologist (R.H.S.). Depression was assessed using Eaton’s method based on a modification of the 20-item Centers for Epidemiologic Studies Depression (CESD) scale.32 , 33 Distant vision was measured at 10-feet using a letter chart, the Good-Lite Chart Model 600A. Body mass index (BMI, height in cm2/weight in kilograms) was calculated from measured height and weight. Standing balance was scored using 4 timed tests (side-by-side, semi-tandem, tandem and one-leg stands).34 (link) For the timed chair stands test, participants were asked to fold their arms across their chest and stand up and down from a chair 5 times as quickly as possible.34 (link) Gait speed was based on the shortest time of 2 trials of a usual-paced 4-meter walk.
Publication 2009
Aged Angina Pectoris Antidiabetics Arm, Upper Cardiac Conduction System Disease Cerebrovascular Accident Chest Clinic Visits Cognition Congestive Heart Failure Diabetes Mellitus Diagnosis Foot Glucose Heart Diseases Hemoglobin A, Glycosylated Index, Body Mass Indices, Ankle-Brachial Intermittent Claudication Mini Mental State Examination Myocardial Infarction Negroes Nurses Pacemaker, Artificial Cardiac Pain Peripheral Nervous System Diseases Peripheral Vascular Diseases Physical Examination Physicians Rheumatoid Arthritis Rheumatologist Spinal Diseases Spinal Stenosis Stenosis Vision
We did the systematic review by following the Cochrane Collaboration guidelines.6 (link)
13 We included only randomised controlled trials published in full text in peer reviewed journals. We included trials published in any language that enrolled adults with chronic low back pain, defined as pain between the 12th rib and buttock crease. Where samples included patients with spinal pain at any level, we included the study if more than 75% of patients had low back pain. We defined chronic low back pain as pain that had persisted for longer than three months. Where the sample also included patients with symptoms of less than three months’ duration, we included the study if more than 75% had chronic low back pain. We excluded trials if they recruited patients with specific low back pain caused by infection, neoplasm, metastasis, rheumatoid arthritis or other inflammatory articular conditions (such as ankylosing spondylitis), spinal stenosis, or fractures. We included trials that reported on patients with diagnoses such as disc degeneration or bulging discs, facet joint dysfunction, or sacroiliac joint pain. The protocol for the original version of this review was published on the Cochrane website in advance of publication of the full review,12 and only minor amendments were made to that protocol before we began this review. These amendments were not published.
We defined multidisciplinary rehabilitation in alignment with the biopsychosocial model. A study was eligible for inclusion if the multidisciplinary rehabilitation intervention involved a physical component and one or both of a psychological component or a social/work targeted component. Furthermore, the different components had to be delivered by clinicians with different professional backgrounds, but no specific professional backgrounds were required. Multidisciplinary rehabilitation interventions could be of any intensity and rehabilitation approach and could be provided in inpatient or outpatient settings. Randomised controlled trials that tested multidisciplinary rehabilitation programmes versus any other treatment were eligible for inclusion. We categorised control interventions as usual care, physical treatment, surgery, and waiting list.
The primary outcomes were pain, disability, and work absenteeism. Secondary outcomes were psychological functioning, quality of life, adverse events, and health service utilisation. We split outcomes into short term (three months’ follow-up or less), medium (three to less than 12 months), and long term (12 months or more). We considered long term outcomes to be primary.
Publication 2015
Adult Ankylosing Spondylitis Arthralgia Arthropathy Buttocks Diagnosis Disabled Persons Facet Joint Fracture, Bone Infection Inflammation Inpatient Intervertebral Disc Degeneration Low Back Pain Neoplasms Operative Surgical Procedures Outpatients Pain Patients Physical Examination Rehabilitation Rheumatoid Arthritis Sacroiliac Joint Spinal Stenosis

Most recents protocols related to «Spinal Stenosis»

Following the institutional review board approval for the study (number: 119/2019; Muğla Sıtkı Koçman University Ethical Committee), a retrospective cohort analysis was performed using the medical records of patients. For the current study, patient consent is not required. All procedures executed involving human participants were in accordance with the ethical standards of the institutional ethical committee and with the 1964 Helsinki declaration.
A total of 146 patients who applied to the neurosurgery outpatient clinic with a recent abdominal CT (max three months) because of a lower back pain complaint were included in the study. Patients with a previous history of surgery or a vertebral fracture were excluded. After excluded patients, a total of 146 patients were included in the study, of whom 90 were female (61.6%) and 56 were male (38.4%). The mean age of the patients was 51.42±13.91 (20-82) years.
Lumbar vertebra CT scans of all patients were reviewed retrospectively. CT images at the level from L3-L4 intervertebral disc were analyzed for body composition of fat tissue and muscle mass volume through the dedicated CT software (Syngo.via, SOMATOM Definition Flash: Siemens Healthcare, Forchheim, Germany). The L3-L4 level was selected in sagittal reformat CT images with the software (Figure 1).
The density range of -200, -40 HU was selected for the fat density measurement in the cross-section with the "region grooving" application in the angled axial images obtained parallel to the disc plane at this level. First, the fat volume in the whole section was measured (visceral and subcutaneous). Then, only the visceral adipose tissue volume was calculated by drawing borders to exclude subcutaneous adipose tissue (Figure 2). The subcutaneous fat tissue volume was obtained by subtracting the visceral fat tissue volume from the total fat volume (Figure 3).
With the same application, muscle density was selected and paravertebral muscle tissue volume was calculated (bilateral musculus psoas major, musculus quadratus lumborum, musculus iliocostalis, musculus longissimus, musculus multifidus volumes). A Spearman correlation model was used to analyze visceral adiposity, subcutaneous fat, and muscle mass.
In CT images, each intervertebral disc space was evaluated in terms of the presence of osteophytes, loss of disc height, sclerosis in the end plates, and spinal stenosis (spinal canal narrowing under 15 mm AP diameter) to investigate the presence of degeneration. Each level was scored according to the presence of findings, with 1 point for the presence of osteophytes, loss of disc height, sclerosis in the end plates, and spinal stenosis. The total score at all levels (L1-S1) was calculated for each patient.
Statistical analyses were performed using IBM SPSS version 20.0 software (IBM Corp., Armonk, NY). The conformity of the data to normal distribution was assessed using the Shapiro-Wilk test. Normally distributed variables were presented as mean±standard deviation and those not showing normal distribution as median (minimum-maximum) values. Categorical variables were presented as numbers (n) and percentages (%). The Spearman's rank correlation coefficient test was used to determine the correlation between the measured parameters in various vertebral pathologies. Continuous variables were compared using the Mann-Whitney U test. The receiver operating characteristic (ROC) analysis was used to detect the area under the curve (AUC) and define the cutoff values with their sensitivities and specificities of the measurements. An alpha value of p<0.05 was accepted as statistically significant.
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Publication 2023
Abdomen Cone-Beam Computed Tomography Ethics Committees, Research Homo sapiens Intervertebral Disc Low Back Pain Males Multifidus Muscle Tissue Neurosurgical Procedures Obesity, Visceral Operative Surgical Procedures Osteophyte Patients Psoas Muscles Pulp Canals Sclerosis Spinal Fractures Spinal Stenosis Subcutaneous Fat Vertebra Vertebrae, Lumbar Visceral Fat Woman X-Ray Computed Tomography
This study was approved by the Committee of Medical Ethics and the Institutional Review Boards of our hospital (2022, Reviewed, No. 13).We retrospectively reviewed the clinical data of patients who underwent UBE-ULBD and OLD in a single academic institution between February 2019 and July 2021. Written informed consent was waived due to the retrospective nature of the study. Data for OLD were derived from 2019 to 2021, whereas data for UBE-ULBD were from 2020 to 2021 when the UBE-ULBD technique was used for severe DLSS. The inclusion criteria were: (1) aged >18 years; (2) Single level DLSS; (3) minimum of 1 year of follow-up; (4) Schizas Grade C or D (severe central stenosis) on preoperative MRI [Grade A, cerebrospinal fluid (CSF) is clearly visible inside the dural sac; Grade B, rootlets occupy the entire dural sac but can still be individualized; Grade C, rootlets cannot be individualized with posterior epidural fat and invisible CSF; Grade D, rootlets cannot be individualized without posterior epidural fat]; (5) All patients had symptoms associated with lower limb neurological impairment with failure to respond to conservative treatment for at least 3 month. Patients were excluded for the following reasons: (1) Previous history of lumbar surgery; (2) Presence of lumbar spondylolisthesis, lumbar instability, or degenerative deformity with Cobb angle >20°;(3) Spinal stenosis caused by lumbar tumors, tuberculosis or fractures; (4) Severe illness affecting anesthesia or surgery; (5) The follow-up period was shorter than 1 year. Consequently, this study included 51 patients (operated at 51 vertebral levels; UBE-ULBD group) who underwent unilateral biportal endoscopy unilateral laminectomy bilateral decompression (UBE-ULBD) and 59 patients (operated at 59 vertebral levels; OLN group) who underwent conventional open lumbar discectomy (OLD).All surgeries were performed by a single spinal surgeon.
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Publication 2023
Anesthesia Cerebrospinal Fluid Congenital Abnormality Conservative Treatment Decompression Diskectomy Endoscopy, Gastrointestinal Ethics Committees, Research Fracture, Bone Laminectomy Lower Extremity Lumbar Region Neoplasms Operative Surgical Procedures Patients Spinal Stenosis Spondylolisthesis Stenosis Surgeons Tuberculosis Vertebra
This study used a retrospective design and a convenience sampling method. It included patients who underwent standing film and MRI examinations and were diagnosed with DLD at this hospital between 1 January 2015 and 1 June 2016. The Institutional Review Board approved the study (approval number: ID:2014–426), and each patient gave written consent. The inclusion criteria were as follows: (1) patients with lumbar spinal stenosis, lumbar disc hernia or lumbar spondylolisthesis; (2) age ≥ 50 years; (3) no underlying congenital or neurological abnormalities; (4) no leg length discrepancy > 2 cm; (5) Cobb angle < 20°; (6) no more than 1 month between the standing x-ray and MRI. The exclusion criteria were as follows: (1) previous spinal surgery; (2) incomplete clinical and imaging data; (3) nondegenerative spine pathologies; (4) fracture of a vertebra. The standing radiographs were taken with a digital flat panel detector system, and the MRI was obtained with a 1.5 T MRI scanner (Siemens, Germany). All radiographic and MRI images were assessed by means of the picture archiving and communication system (PACS) workstation of our hospital.
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Publication 2023
Ethics Committees, Research Fingers Hernia Lumbar Region Nervous System Abnormality Operative Surgical Procedures Patients Physical Examination Radiography Spinal Fractures Spinal Stenosis Spondylolisthesis Vertebral Column X-Rays, Diagnostic
All procedures and protocols were conducted in accordance with the principles of Helsinki Declaration, written informed consent was obtained from all participants in accordance with standard operative procedures. The study was approved by the Clinical Hospital Center Zemun- Belgrade by the number of approval 8946.
The present study was an observational cohort study of 60 patients who were prospectively recruited and divided into two groups. Patients were hospitalized at the Department of Neurosurgery at Clinical Hospital Center Zemun between 2020 and 2021 and were operated with surgical indications of lumbar disc herniation (LDH) and lumbar spinal stenosis (LSS). All patients fulfilled the following criteria: 1. Age > 18 years, 2. No previous surgery on spine, 3. Diagnosis was verified by magnetic resonance imaging. Patients with history of osteoporosis, immunosuppression, chronic corticosteroid use, intravenous drug use, fever of unknown origin, history of malignancy, unexplained weight loss, or progressive/disabling symptoms were excluded from the study. All patients were operated by one neurosurgeon (V. A.). The LF samples were obtained from the 60 patients randomized in 2 groups. The first group underwent micro-discectomy for LDH and included LF samples from 30 patients (LDH group). The second group underwent decompressive surgery without instrumented fusion for LSS and included LF samples from 30 patients (LSS group). In the patients with multisegmental stenosis, samples were taken from the radiologically determined site of greatest stenosis. While every effort was made to remove the LF en-bloc, in the majority of cases, the LF was removed piecemeal.
Demographic and clinical data were obtained using a pre-prepared questionnaire as well as data from medical history. Morphological/radiological data were obtained by measuring specific parameters on magnetic resonance imaging—T2 sequences, performed by two experienced radiologists, after several repeated measurements. The examined morphological/radiological parameters measured on the sagittal image projection of the lumbosacral spine region were presence of Schmorl's nodes, vertebral body hemangioma, spondylolisthesis, and value of lumbar lordosis angle. Other measurements were performed at the axial image section where the degree of discal herniation or spinal stenosis were most prominent and included: interfacet distance, thickness of LF on both sides, dural laterolateral (LL) diameter and anteroposterior (AP) diameter of dural sac, average facet joint angle, and dural sac surface. The scoliosis angle was also determined using the standard Cobbs method on the coronary sections of spine magnetic resonance imaging of the patients30 (link). Spondylolisthesis was determined as a percentage of vertebral body slippage. Lumbar lordosis angle was also determined using the standard Cobbs method30 (link). The determination of the other mentioned parameters is shown in Fig. 2.

Measurement of (A) ligamentous interfacet distance, (B) anteroposterior diameter of dural sac, (C) laterolateral diameter of dural sac, (D) thickness of LF on both sides, (E) average facet joint angle measured according to formula: (a + b)/2, (F) dural sac surface.

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Publication 2023
Adrenal Cortex Hormones Diagnosis Diskectomy Facet Joint Fever of Unknown Origin Heart Hemangioma Immunosuppression Intervertebral Disk Displacement Laminectomy Ligaments Lordosis Lumbar Region Lumbosacral Region Malignant Neoplasms Neurosurgeon Neurosurgical Procedures Operative Surgical Procedures Osteoporosis Patients Pharmaceutical Preparations Radiologist Scoliosis Spinal Stenosis Spondylolisthesis Stenosis Vertebral Body Vertebral Column X-Rays, Diagnostic
We analyzed prospectively collected NORspine data on patients operated for lumbar spinal stenosis (LSS) at four hospitals between January 1st, 2015 and December 31st, 2016. Patients who consented to participate in NORspine completed questionnaires at baseline. The NORspine registry then mailed similar questionnaires to patients at 12 months postoperatively. Patients responded directly to NORspine without the involvement of the treating center. NORspine routinely sends one postal reminder to those who do not respond before they are considered non-respondents. We engaged the NORspine office to reach out to those who did not respond at 12 months after surgery. The 12 months postoperative questionnaire was sent once again. We also sent one reminder by mail and one by SMS to those who still did not respond. Patients that responded at 12 months postoperatively are termed respondents, while those who did not respond are termed non-respondents. Those who finally responded are termed “responsive non-respondents”, and those who never responded to any contact are termed “resistant non-respondents”.
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Publication 2023
Lumbar Region Operative Surgical Procedures Patients Spinal Stenosis

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More about "Spinal Stenosis"

Spinal stenosis is a medical condition characterized by the narrowing of the spinal canal, often resulting in compression of the spinal cord or nerve roots.
This can lead to a variety of symptoms, including back pain, numbness, weakness, and tingling in the legs and feet.
The condition is sometimes referred to as vertebral canal stenosis or central canal stenosis.
Researchers and clinicians often utilize a range of tools and techniques to diagnose and manage spinal stenosis.
For example, imaging tests such as MRI (e.g., 1.5T MRI scanner) and CT scans can be used to visualize the spinal structures and assess the degree of narrowing.
Laboratory tests, such as those involving the use of INNOTEST or DMEM/F12 cell culture media, may also be employed to gather additional information about the patient's condition.
In terms of treatment, various interventions may be recommended, depending on the severity of the stenosis and the individual's symptoms.
Conservative approaches, such as physical therapy, medications, and the use of devices like the Active style Pro HJA-350IT, may be the first line of treatment.
In more severe cases, surgical options, such as decompression procedures or the use of Collagenase type II or SURGICEL Absorbable Hemostat, may be considered.
To support research and clinical decision-making, tools like SPSS version 18.0 and the Lunar Prodigy bone densitometry system can be valuable.
Additionally, resources like PubCompare.ai's AI-powered platform can help researchers efficiently locate and compare the best protocols and products related to spinal stenosis, enhancing their understanding and facilitating the advancement of treatment options.
By incorporating a range of relevant terms, including synonyms, abbreviations, and subtopics, this content aims to provide a comprehensive and informative overview of spinal stenosis, its diagnosis, and its management, empowering researchers and clinicians in their efforts to improve patient outcomes.