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Thoracic Spinal Anesthesia in Awake Breast Surgery

Comparison Between Thoracic Para-vertebral Block and Segmental Thoracic Spinal Anesthesia in Breast Cancer Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03319511
Enrollment
70
Registered
2017-10-24
Start date
2014-11-24
Completion date
2016-11-12
Last updated
2017-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

thoracic spinal, awake mastectomy, paravertebral block, analgesia, ultrasound, breast cancer

Brief summary

General anesthesia is the conventional technique used for breast surgery. breast surgery is associated with a high incidence of postoperative pain, it is estimated that over 50 % of women suffer chronic pain following breast cancer surgery. Regional anesthesia is a good alternative to general anesthesia for breast cancer surgery, providing superior analgesia and fewer side effects related to a standard opiate-based analgesia. there is no evident optimal regional techniques for operative procedures on the breast and axilla, like high thoracic epidural, cervical epidural, paravertebral block, intrerpleural block, PECs block, serratus plane block and segmental thoracic spinal anesthesia. Regional anesthesia decreases operative stress, provides beneficial hemodynamic effects especially for critically ill patients and decreases postoperative morbidity and mortality. Also it reduces post-operative nausea and vomiting and provides prolonged post-operative sensory block, minimizing narcotic requirements. Additionally, this application positively affects the early start of feeding and mobilization.

Detailed description

Thoracic paravertebral block (TPVB) is an alternative method to general anesthesia for patients undergoing breast surgery, because it provides a safe anesthesia with balanced hemodynamic response with unilateral somatic and sympathetic blockade, allows postoperative analgesia lowering narcotic usage , minimal nausea and vomiting rate, early discharge and low cost. Segmental thoracic spinal anesthesia have introduced for cardiac surgery in adults and children in the early 1990's. Kowalewski et al., performed over 10000 cases of spinal injections without a single case of spinal/epidural hematoma or any neurological complications, also segmental thoracic spinal anesthesia has been used successfully for laparoscopic cholecystectomy and abdominal surgeries. It has some advantages when compared with general anesthesia and can be a sole anesthetic in breast cancer surgery with axillary lymph node clearance especially in critical cases. Among its advantages are the quality of postoperative analgesia, lower incidence of nausea and vomiting, and shorter recovery time, with the consequent early hospital discharge. The dose of the anesthetic is exceedingly low, compared with lumbar spinal anesthesia, given the highly specific block to only certain nerve functions along a section of the cord, there is no blockade of the lower extremities. This means that a significantly larger portion of the body experiences no venal dilation, and may offer a compensatory buffer to adverse changes in blood pressure intra-operatively. there was no recorded of neurological complications.The incidence of parasthesia in a study with 300 patients subjected to thoracic spinal puncture at T10-11 was 4.67% in the cut needle group and 8.67% in the pencil point needle group, similar to that reported in lumbar spinal anesthesia.The aim of the present study is the comparison between two sole regional anesthetic techniques, thoracic para-vertebral block and segmental thoracic spinal anesthesia in breast cancer surgery especially for critically ill patients.

Interventions

OTHERspinal group

plain bupivacaine 0.5%,1.5 ml plus dexmedetomidine 5 μg. once injection.

plain bupivacaine 0.5%, 0.3 ml (1.5 mg)/kg plus dexmedetomidine 0.5 μg /kg divided between the T2 and T4 levels.

Sponsors

Alaa Mazy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

a dorsal thoracic gauze cover.

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

ASA II, III, IV patients may have: 1. Cardiovascular disease (e.g., rheumatic heart, systemic hypertension, ischemic heart) 2. Lung disease (e.g., bronchial asthma, COPD) 3. Renal disease (e.g., renal failure, polycystic kidney) 4. Liver disease (e.g., cirrhosis, hepatitis) 5. Endocrine disease (e.g., diabetes mellitus)

Exclusion criteria

1. Patient refusal 2. Contraindication to regional anesthesia (coagulopathy, local infection), 3. Spinal deformities. 4. An allergy to α 2 adrenergic agonist local anesthetic drugs.

Design outcomes

Primary

MeasureTime frameDescription
the block success rate.within 30 min of injectionin number, defined as complete sensory block in all dermatomes (T1-T6 ).

Secondary

MeasureTime frameDescription
The spinal onset of sensory block2, 4, 6, 8, 10, 12, 14 minutes after injection.tested for loss of sensation, with a needle along the anterior axillary line from T1-T6 on the blocked side.
The power of hand grip (T1/ C8)5, 10, 15, 20, 52, 30 minutes after injection.four grades (0-3), 0= no motor block, 1= partial, 2= almost complete, 3= complete motor block.
The power of wrist flexion (C8/C7)5, 10, 15, 20, 52, 30 minutes after injection.four grades (0-3), 0= no motor block, 1= partial, 2= almost complete, 3= complete motor block.
The power of elbow flexion (C6/ C5)5, 10, 15, 20, 52, 30 minutes after injection.four grades (0-3), 0= no motor block, 1= partial, 2= almost complete, 3= complete motor block.
The onset time of lower limb motor block (Bromage 3)5, 10, 15, 20, 25, 30 minutes after injection.in minutes, 3= unable to move legs or feet.
The duration of lower limb motor block (Bromage 0)30, 45, 60, 90,120, 150 minutes after injection.minutes, 0= free movement of legs and feet
Ramsey sedation scale0 (basal), then1, 5, 10, 15, 30, 45, 60, 75, 90, 120 minutes from injection time, then 1, 4, 5, 6, 7, 8, 12, 18, 24 hours starting after the end of operation.(1 = awake, conscious, no sedation; 2 = calm and compose; 3 = awake on verbal command; 4 = brisk response to gentle tactile stimulation; 5 = awake on vigorous shaking; 6 = unarousable).
Heart rate0= basal, then 1, 5, 10, 15, 30, 45, 60, 75, 90, 120 minutes from injection time, then 1, 4, 5, 6, 7, 8, 12, 18, 24 hours starting after the end of operation.beat/minute
Systolic blood pressure0= basal, then 1, 5, 10, 15, 30, 45, 60, 75, 90, 120 minutes from injection time, then 1, 4, 5, 6, 7, 8, 12, 18, 24 hours starting after the end of operation.millimeter mercury
Mean blood pressure0= basal, then 1, 5, 10, 15, 30, 45, 60, 75, 90, 120 minutes from injection time, then 1, 4, 5, 6, 7, 8, 12, 18, 24 hours starting after the end of operation.millimeter mercury
Total ephedrine consumptionintraoperativemilligram, Hypotension defined as 20% drop in baseline blood pressure or systolic pressure below 90 mm Hg)
Total atropine consumptionintraoperativemilligram, Bradycardia defined as heart rate below 50 beat/minute
The paravertebral onset of sensory block5, 10, 15, 20, 52, 30 minutes after injection.tested for loss of sensation, with a needle along the anterior axillary line from T1-T6 on the blocked side.
Hypotension episodesIntraoperative and postoperative for 24 hours.in number. Hypotension (20% drop in baseline blood pressure or systolic pressure below 90 mm Hg).
Bradycardia episodesIntraoperative and postoperative for 24 hours.In number. Bradycardia defined as heart rate below 50 beat/minute
Hypoxia episodesIntraoperative and postoperative for 24 hours.In number. Hypoxia is defined as defined as respiratory rate \<10 breath/ minutes or oxygen saturation less than 90%.
incidence of nauseaIntraoperative and postoperative for 24 hours.In number.
incidence of vomitingIntraoperative and postoperative for 24 hours.In number.
the incidence of pneumothorax.intraoperative and postoperative for 6 hours.in numbers. confirmed by plane X-ray
The incidence of post-dural puncture headache.postoperative for 72 hours.in numbers.
The duration of upper limb motor block,15, 30, 45, 60, 90 minutes after injection.minutes. starting from the time of score 3 to score 0 (0= no motor block).
Visual analog scaleat 0, 4, 5, 6, 7, 8, 12, 18, 24 hours postoperative.a 0-10 cm scale, 0 represents no pain and 10 is the worst pain.
The total mepridine consumption.postoperative for 24 hours.milligram
satisfaction of the patientafter 24 hours from the end of operation.scale from 0-10, 10= the highest.
satisfaction of the surgeonwithin 2 hours from the end of operation.scale from 0-10, 10= the highest.
Total Midazolam consumptionintraoperativemilligram,

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026