Complications and side effects of cervical and lumbosacral selective nerve root injections

Huston CW, Slipman CW, Garvin C. Complications and side effects of cervical and lumbosacral selective nerve root injections. To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). Prospective, nonrandomized controlled trial o...

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Published inArchives of physical medicine and rehabilitation Vol. 86; no. 2; pp. 277 - 283
Main Authors Huston, Christopher W., Slipman, Curtis W., Garvin, Cyndi
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.02.2005
Elsevier
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Abstract Huston CW, Slipman CW, Garvin C. Complications and side effects of cervical and lumbosacral selective nerve root injections. To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). Prospective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups. Tertiary, academic spine center. Of 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group. Diagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections. Complications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire. There were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P=.001) and lumbar ( P=.005); nonspecific headache, cervical ( P=.019); and nonspinal headache, cervical ( P=.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up. There were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.
AbstractList OBJECTIVE: To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). DESIGN: Prospective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups. SETTING: Tertiary, academic spine center. PARTICIPANTS: Of 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group. INTERVENTIONS: Diagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections. MAIN OUTCOME MEASURES: Complications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire. RESULTS: There were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P =.001) and lumbar ( P =.005); nonspecific headache, cervical ( P =.019); and nonspinal headache, cervical ( P =.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up. CONCLUSIONS: There were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.
Huston CW, Slipman CW, Garvin C. Complications and side effects of cervical and lumbosacral selective nerve root injections. To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). Prospective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups. Tertiary, academic spine center. Of 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group. Diagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections. Complications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire. There were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P=.001) and lumbar ( P=.005); nonspecific headache, cervical ( P=.019); and nonspinal headache, cervical ( P=.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up. There were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.
To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs).OBJECTIVETo determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs).Prospective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups.DESIGNProspective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups.Tertiary, academic spine center.SETTINGTertiary, academic spine center.Of 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group.PARTICIPANTSOf 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group.Diagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections.INTERVENTIONSDiagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections.Complications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire.MAIN OUTCOME MEASURESComplications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire.There were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P =.001) and lumbar ( P =.005); nonspecific headache, cervical ( P =.019); and nonspinal headache, cervical ( P =.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up.RESULTSThere were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P =.001) and lumbar ( P =.005); nonspecific headache, cervical ( P =.019); and nonspinal headache, cervical ( P =.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up.There were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.CONCLUSIONSThere were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.
To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). Prospective, nonrandomized controlled trial of consecutive patients with independent interviews for immediate, 1-week, and 3-month follow-ups. Tertiary, academic spine center. Of 160 patients eligible for SNRI, 151 underwent 306 SNRIs (study group). Sixty patients who had not undergone any intervention served as the control group. Diagnostic and therapeutic fluoroscopically guided cervical and lumbosacral SNRIs. Lidocaine (Xylocaine) was used in the diagnostic injections and a mixture of lidocaine and betamethasone was used in the therapeutic injections. Complications and side effects experienced during the procedure were recorded by the interventionalist. Side effects and complications experienced immediately, 1 week, and 3 months after injection were determined through independent interviews using a questionnaire format. The control group was independently interviewed using the same questionnaire. There were no major complications, such as death, paralysis, spinal nerve injury, infection, or allergic reaction, during the study. Ninety-one percent of subjects had no side effects during the procedure. A positive response on interview was reported by 39.4% of the study subjects immediately after the procedure. Lumbosacral SNRI side effects were as follows: increased pain at the injection site (17.1%); increased radicular pain (8.8%); lightheadedness (6.5%); increased spine pain (5.1%); nausea (3.7%); nonspecific headache (1.4%); and vomiting (0.5%). Immediate side effects from cervical SNRI were as follows: increased pain at injection site (22.7%); increased radicular pain (18.2%); lightheadedness (13.6%); increased spine pain (9.1%); nonspecific headache (4.5%); and nausea (3.4%). At the 1-week interview, comparison of the study and control groups showed statistical significance for the following: pain at injection site, cervical ( P =.001) and lumbar ( P =.005); nonspecific headache, cervical ( P =.019); and nonspinal headache, cervical ( P =.002). At 3 months, 2 subjects complained of increased neck pain and 1 reported heartburn and fluid retention. Two lumbar SNRI subjects were lost to follow-up. There were no major complications with cervical and lumbosacral SNRIs, although various minor side effects occurred.
Author Huston, Christopher W.
Slipman, Curtis W.
Garvin, Cyndi
Author_xml – sequence: 1
  givenname: Christopher W.
  surname: Huston
  fullname: Huston, Christopher W.
  email: cwhuston@cox.net
  organization: Orthopedic Clinic Association, Scottsdale, AZ, USA
– sequence: 2
  givenname: Curtis W.
  surname: Slipman
  fullname: Slipman, Curtis W.
  organization: Penn Spine Center, Department of Rehabilitation Medicine, University of Pennsylvania Medical Center, Philadelphia, PA, USA
– sequence: 3
  givenname: Cyndi
  surname: Garvin
  fullname: Garvin, Cyndi
  organization: College of Medicine, University of Florida, Gainesville, FL, USA
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Issue 2
Keywords Injections
Rehabilitation
Radiculitis
Nerve root disorder
Postoperative complications
Prognosis
Questionnaire
Lumbar spine
Motor system disorder
Toxicity
Diseases of the osteoarticular system
Check
Anticonvulsant
Spine disease
Epidemiology
Interview
Incidence
Prevention
Neck pain
Cervical nerve
Regulation(control)
Vomiting
Secondary effect
Complication
Clinical trial
Diagnosis
Neurological disorder
Human
Corticosteroid
Immunopathology
Nervous system diseases
Mortality
Antiinflammatory agent
Antiarrhythmic agent
Cervical root
Local anesthetic
Treatment
Digestive diseases
Organic amide
Fluorine Organic compounds
Lumbosacral
Betamethasone
Lidocaine
Cervical spine
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
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Snippet Huston CW, Slipman CW, Garvin C. Complications and side effects of cervical and lumbosacral selective nerve root injections. To determine the incidence of...
To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). Prospective, nonrandomized...
To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs).OBJECTIVETo determine the...
OBJECTIVE: To determine the incidence of complications and side effects of cervical and lumbosacral selective nerve root injections (SNRIs). DESIGN:...
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SubjectTerms Adult
Aged
Aged, 80 and over
Anesthetics, Local - administration & dosage
Anti-Inflammatory Agents - administration & dosage
Betamethasone - administration & dosage
Biological and medical sciences
Diseases of the osteoarticular system
Diseases of the spine
Female
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Injections
Injections, Spinal - adverse effects
Lidocaine - administration & dosage
Male
Medical sciences
Middle Aged
Nerve root disorder
Nervous system (semeiology, syndromes)
Nervous system as a whole
Neurology
Postoperative complications
Prospective Studies
Radiculitis
Radiculopathy - drug therapy
Rehabilitation
Spinal Nerve Roots
Title Complications and side effects of cervical and lumbosacral selective nerve root injections
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0003999304003156
https://dx.doi.org/10.1016/j.apmr.2004.02.018
https://www.ncbi.nlm.nih.gov/pubmed/15706554
https://www.proquest.com/docview/67418972
https://www.proquest.com/docview/85318867
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