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Impact of Epidural Anesthesia on Low Back Function

2021년 9월 25일 업데이트: Mohamed Gamal Abouelyazeed Ali, South Valley University

Impact of Obstetric Epidural Anesthesia on Mechanical Function of Low Back

Back pain is a common complication after the use of epidural anesthesia in obstetric and non-obstetric surgeries and occurs in 30-45% of cases (Brown, 2005). Certain psychological problems such as depression or unhappiness due to loss of employment may prolong the episode of low back pain (Miller, 2012). According to Egyptian Institution of Health Metrics and Evaluation (IHME), Low Back Pain is the first cause of disability in Egypt from 2007 to 2017.

So, this study will investigate if midline approach of obstetric epidural anaesthesia will be a relative risk for subacute low back mechanical functions as a new way to examine if this type of anaesthesia is involved in the presence of subacute negative effects on the mechanical function of low back or not (to resolve the controversy).

연구 개요

상태

완전한

상세 설명

The lumbar (or lower back) region is made up of five vertebrae (L1-L5), sometimes including the sacrum. Stability of the spine is provided by the ligaments and muscles of the back and abdomen (Floyd and Thompson, 2008).

The primary biomechanical function of the spine is to provide structural support, to allow the body to move freely, and to protect the spinal cord and nerves. Muscles balance external loads to the spine, which supports the load and allows for the motion through its multilevel joint arrangement (Dreischarf et al., 2016).

Low back pain (LBP) is a common minor yet unpleasant complication after epidural anesthesia. Different mechanisms are suggested such as needle trauma and myotoxicity of local anesthetic (Louizos et al., 2005) and incidence of backache after epidural anaesthesia might be expected to be higher than that after spinal anaesthesia (Brown and Elman, 1961).

In most episodes of low back pain, a specific underlying cause is not identified or even looked for, with the pain believed to be due to mechanical problems such as muscle or joint strain (Casazza, 2012). Most cases are idiopathic but usually attributable to muscle strain or ligament injury; found in 65% to 70% of patients with mechanical chronic back pain (Cohen et al., 2008) while totally mechanical low back pain is reported as the cause in about 80% to 95% of patients with low back pain (Cohen et al., 2008) & (Dixit, 2017).

Caesarean section is when a baby is born through an incision in the mother's abdomen and uterine wall. This requires effective anaesthesia which can be regional (epidural or spinal) or a general anaesthetic. With regional epidural anaesthesia, the anaesthetic is infused into the space around the mother's spinal column, whilst with regional spinal anaesthesia, the drug is injected as a single dose into the mother's spinal column. With the two types of regional anaesthesia, the mother is awake for the birth but numbed from the waist down while with general anaesthesia, the mother is unconscious for the birth with the anaesthetic affecting her whole body (Afolabi and Lesi, 2012).

The epidural needle can be placed using the midline or paramedian approach. In both cases, lidocaine 1% is infiltrated in the epidural needle insertion area.

In the midline approach technique, the needle is placed in the midline between 2 spine processes. In the paramedian approach technique, the needle is inserted 1 cm lateral and 1 cm caudal to the lower border of the upper spinous process.

The epidural needle in the medline approach is advanced through ligaments: supraspinous ligament, interspinous ligament, ligamentum flavum and into the target epidural space. Each ligament has different density and texture, which affects the feel of the needle and the resistance to insertion (Vaughan et al., 2013).

Some explanations for Low Back Dysfunction after Epidural Anaesthesia:

The incidence of back pain after epidural anesthesia is over 20% (Rose, 2012) & (Saghafinia et al., 2009) & (Muslu et al., 2009). It occurs rarely after spinal anesthesia (Schwabe and Hopf, 2001). This indicates that back pain may be associated with local trauma and nerve injury caused by the epidural needle, leading to aseptic periosteitis, tendonitis, ligamentous inflammation and/or osteochondritis, which result in lumbar pain (Kalso, 2013).

  • Excessive elongation of spinal ligaments can cause micro-trauma of the ligament fibers and tears or ruptures occur. Also, the interspinous ligaments are the first structures damaged (excessive stretching) when the spine is hyperflexed (Adams et al., 1998).
  • Degeneration and excessive stress on the thoracolumbar fascia may also cause micro-trauma, and resulting in tears. Thoracolumbar fascia may become damaged by over-stretching or excessive stress, potentially eliciting pain (Bogduk, 1983).
  • Other contributing factors include needle trauma, surgical positioning, injection of saline or local anesthetic into the interspinous ligaments and development of a supraspinous hematoma (Covet et al., 1967), (Crawford, 1972).
  • Excessive stretching of ligaments after relaxation of paraspinal muscles and localized trauma to the intervertebral disc has also been implicated in causing back pain (Agarwal and Kishore, 2009).

Visual analogue scale (VAS):

The visual analogue scale is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain." (Delgado et al., 2018).

Pressure algometry:

Pressure algometry has been described as a semi-objective method, or subjective measure and Pain Pressure Threshold (PPT) is a quantitative sensory test of tissue sensitivity, and it is defined as the minimal amount of pressure that produces pain, measured via a pressure algometer (Ylinen, 2007).

Inclinometers:

An inclinometer or tilt meter is an instrument for measuring angles of slope (or tilt), elevation or depression of an object or body segment with respect to gravity (Nielsen et al., 2011).

Oswestry Disability Index:

The Oswestry Disability Index (ODI) is a valid, reliable, and responsive condition-specific assessment tool that is suited for use in clinical practice. It is easy to administer and score, objectifies clients' complaints, and monitors effects of therapy (Vianin, 2008).

Isokinetic dynamometry:

The isokinetic dynamometer is a gold standard instrument for measuring muscle strength and is safe, valid, and reliable, based on the use of kinetic parameters that also include the angular measurement of a corporeal segment throughout the range of motion (Gonosova et al., 2018) & (Habets et al., 2018) & (Roth et al., 2017) & (Guilhem et al., 2014).

Ultrasound Elastography:

Ultrasound elastography (EUS) is a recently developed ultrasound-based method, which allows the qualitative visual or quantitative measurements of the mechanical properties of tissue (Hall, 2003), (Garra, 2007) & (Garra, 2011).

Myoton Pro Device:

A MyotonPRO (Myoton AS, Estonia) is a portable hand-held myotonometer that can assess muscle tone and soft tissue stiffness. According to prior research, the MyotonPRO is a reliable quantitative measurement for assessing the mechanical properties of muscles (Pruyn et al., 2016).

The MyotonPRO can differentiate the viscoelastic properties of a trigger point from a non-trigger point. Our findings support the reliability of this myotonometer. This affordable and portable tool can be used to objectively measure viscoelastic properties of trigger points (Roch et al., 2020).

연구 유형

관찰

등록 (실제)

38

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Cairo, 이집트, 11672
        • Faculty of Physical Therapy - SVU
      • Cairo, 이집트, 11672
        • Faculty of physical therapy, South Valley University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

여성

샘플링 방법

확률 샘플

연구 인구

45 women were enrolled in this study with a 20% rate loss of follow-up (i.e. we need at least 38 participants to complete the study). They were selected from the SVU Teaching Hospitals.

The Participants were classified into 4 groups: -

Group (A):

This group included 6 women. They gave birth through a cesarean delivery using Midline approach epidural anesthesia,

Group (B):

This group included 13 women. They gave birth through a cesarean delivery using Midline approach spinal anesthesia

Group (C):

This group included 7 women. They gave birth through a cesarean delivery using general anesthesia.

Group (D):

This group included 12 women. who are the control group,

설명

Inclusion Criteria:

  • All women gave birth through a cesarean delivery.
  • Their ages will range from 18 to 35 years.
  • All participants will have body mass index (BMI) not more than 30.
  • All participants will be assessed after 6weeks postnatal.
  • All participants will be able to continue all assessment procedures.

Exclusion Criteria:

  • Women who delivered through vaginal delivery.
  • Women who delivered through cesarean delivery but the used anesthetic technique was the paramedian approach of epidural anesthesia.
  • Women who have any non-myofascial low back dysfunctions.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 관찰 모델: 보병대
  • 시간 관점: 회고전

코호트 및 개입

그룹/코호트
Group A
follow up for 6 women who gave birth through a cesarean delivery with Midline approach epidural anesthesia. They will perform all assessment procedures: Visual analog scale (VAS) and Oswestry Disability Index (ODI).
Group B
follow up for 13 women who gave birth through a cesarean delivery with Midline approach spinal anesthesia. They will perform all assessment procedures: Visual analog scale (VAS) and Oswestry Disability Index (ODI).
Group C
follow up for 7 women who gave birth through a cesarean delivery with general anesthesia. They will perform all assessment procedures: Visual analog scale (VAS) and Oswestry Disability Index (ODI).
Group D
follow up for 12 women who are the control group (who did not experience any pregnancy or anesthesia. They will perform all assessment procedures: Visual analog scale (VAS) and Oswestry Disability Index (ODI).

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Subacute Low Back Pain intensity
기간: assessment will be done at 6 weeks after the use of anaesthesia during Cesarean section
Subacute Low Back Pain intensity is assessed by Visual Analogue scale: Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between 0 "no pain" and 10 "worst pain."
assessment will be done at 6 weeks after the use of anaesthesia during Cesarean section

기타 결과 측정

결과 측정
측정값 설명
기간
Low Back functional ability
기간: assessment will be done at 6 weeks after the use of anaesthesia during Cesarean section

Low Back functional ability will be assessed by Oswestry Disability Index: It is a self-administered questionnaire divided into ten sections designed to assess limitations of various activities of daily living. Each section is scored on a 0-5 scale, 5 representing the greatest disability. where as grading system is : 0 - 4 No disability

5 - 14 Mild disability

15 - 24 Moderate disability

25 - 34 Severe disability

35 - 50 Completely disabled

assessment will be done at 6 weeks after the use of anaesthesia during Cesarean section

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Mohamed GA Ali, Msc, South Valley University

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2021년 5월 1일

기본 완료 (실제)

2021년 8월 30일

연구 완료 (실제)

2021년 9월 26일

연구 등록 날짜

최초 제출

2021년 1월 23일

QC 기준을 충족하는 최초 제출

2021년 2월 14일

처음 게시됨 (실제)

2021년 2월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 10월 1일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 9월 25일

마지막으로 확인됨

2021년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • South Valley University

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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