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Lumbar Spine Ultrasound of Patients With Previous Accidental Dural Puncture During Labour Epidural
This study has been completed.
Sponsored by: Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Information provided by: Samuel Lunenfeld Research Institute, Mount Sinai Hospital
ClinicalTrials.gov Identifier: NCT00465166
  Purpose

Accidental dural puncture is a potential complication of epidural analgesia for labour and delivery. When it happens, it may cause debilitating headaches and other symptoms that prevent mothers from talking care of their newborns. Accidental dural puncture is related to the operator performance and to individual anatomical variations of the spine. The purpose of this study is to do a lumbar spine ultrasound on the patients who have had accidental dural punctures and analyze if there is any abnormal anatomy seen. Then, we will compare the position of any spinal abnormality to the position of the dural puncture reported in the anaesthesia record.


Condition Intervention
Postdural Puncture Headache
Procedure: Ultrasound

MedlinePlus related topics: Headache Ultrasound
Drug Information available for: S 1 (Combination)
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Retrospective
Official Title: Lumbar Spine Ultrasound of Patients With Previous Accidental Dural Puncture During Labour Epidural

Further study details as provided by Samuel Lunenfeld Research Institute, Mount Sinai Hospital:

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment: 56
Study Start Date: February 2007
Study Completion Date: July 2007
Groups/Cohorts Assigned Interventions
1
Patients who had a documented, accidental dural puncture during placement of their labor epidural.
Procedure: Ultrasound
Lumbar ultrasound from L1-S1, carried out using a portable ultrasound system equipped with a 2-5 MHz curved array probe.

Detailed Description:

Effective epidural analgesia depends on accurate identification of the epidural space for delivery of analgesic mixtures. The technique of loss of resistance to either saline or air is the most commonly used method to locate the epidural space. Although this technique has a high success rate, it is associated with a significant incidence of accidental dural punctures. Accidental dural punctures might be related to the operator performance or to individual anatomical variations.

A normal ligamentum flavum is fundamental in the loss of resistance technique. However, many cadaver dissection and radiological studies in the literature have showed that the ligamentum flavum may in fact not fuse at the midline; thereby leaving a gap between its left and right portions. Ligamentum flavum midline gaps are thought to be a potential cause of failed recognition of loss of resistance during epidural needle placement and consequently accidental dural puncture. Therefore, if it were feasible to avoid inserting the epidural needle at the same level where a ligamentum flavum midline gap exists, then dural punctures may be less likely.

Lumbar spine ultrasound has been very useful in consistently identifying important anatomical landmarks for epidural needle placement including the ligamentum flavum. It is unknown at this time whether ultrasound is a useful modality to detect abnormal anatomy. Our study will evaluate by ultrasound scan the lumbar vertebral column of patients who have had a previously recognized accidental dural puncture. Our objective is to determine whether or not there is a correlation between accidental dural punctures and abnormalities of ligamentum flavum as seen by ultrasound imaging. Our hypothesis is that patients who have had accidental dural punctures have abnormal anatomy of ligamentum flavum that can be detected by lumbar spine ultrasound.

Lumbar ultrasound imaging from L1-S1 will be performed with the patient in the sitting position. The best possible image captured at the transverse approach for each of the interspaces from L5-S1 to L1-L2 will be saved for analysis of both ligamentum flavum (primary outcome) and symmetry (secondary outcome). A normal ligamentum flavum is described as a hyperechoic continuous midline band, which is aligned with the hyperechoic signal of the transverse processes. An abnormal ligamentum flavum will be described as a non-continuous or even absent signal. The presence of symmetric anatomy is defined as an equal distant between the left and right articular processes and the transverse processes to the midline.

Incidence of abnormal ligamentum flavum and asymmetry will be presented in a descriptive way and the level of anatomical abnormality detected by ultrasound will be correlated to the level of dural puncture reported on the anaesthesia record.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Patients who had a documented, accidental dural puncture during placement of their labor epidural.

Criteria

Inclusion Criteria:

  • Previous dural puncture during labour epidural

Exclusion Criteria:

  • none
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00465166

Locations
Canada, Ontario
Mount Sinai Hospital
Toronto, Ontario, Canada, M5G 1X5
Sponsors and Collaborators
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Investigators
Principal Investigator: Jose CA Carvalho, MD PhD MOUNT SINAI HOSPITAL
  More Information

Responsible Party: Mount Sinai Hospital ( Dr. Jose Carvalho )
Study ID Numbers: 07-05, 07-0002-E
Study First Received: April 23, 2007
Last Updated: December 12, 2007
ClinicalTrials.gov Identifier: NCT00465166  
Health Authority: Canada: Ethics Review Committee

Keywords provided by Samuel Lunenfeld Research Institute, Mount Sinai Hospital:
Accidental dural puncture
Labour epidural
Ultrasound
Ligamentum flavum

Study placed in the following topic categories:
Post-Dural Puncture Headache
Headache Disorders, Secondary
Headache
Neoplasm Metastasis
Central Nervous System Diseases
Brain Diseases
Headache Disorders

Additional relevant MeSH terms:
Nervous System Diseases

ClinicalTrials.gov processed this record on January 16, 2009