Breast Cancer Clinical Trial
Official title:
Evaluation of Post Mastectomy Pain Syndrome After Preoperative Stellate Ganglion Block for Breast Cancer Surgeries, Clinical Randomized Controlled Trial
This study investigate the effect of pre-operative ultrasound guided stellate ganglion block with local anesthetic on the frequency of neuropathic pain syndromes in the first 6-month post cancer breast surgeries with axillary dissection.
In this study Eighty Female patients with a diagnosis of breast cancer, underwent breast
surgery with axillary dissection at National Cancer Institute, Cairo University were included
in this study. Patients will be randomized into two equal comparable groups of patients.
(Group A the study group) was received pre-operative ultrasound guided stellate ganglion
block one hour before surgery and multimodal analgesia and (Group B the control group) was
received multimodal analgesia only.
The present study showed in regards to the acute pain management of the stellate ganglion
block: intraoperative hemodynamics, mean arterial blood pressure and heart rate (MABP, HR)
were statistically significant less in group A (Stellate Group) than group B (Control Group)
and this leads to significant less opioid consumption in Group A (Stellate Group) than Group
B (Control group). In the 1st 24h postoperative opioid consumption measured by number of
rescue dose of morphine 5mg IV were administered when visual analogue score was more than 4
and total requirement per 24 hours was recorded. The results show statistically significant
less opioid consumption in Group A (Stellate Group) with average visual analogue score 3.5 in
1st 24h than Group B (Control group) with average visual analogue score 5.5 in 1st 24h.
The present study showed in regards to the chronic pain management of the stellate ganglion
block that, the 6-month relative frequency of neuropathic pain syndromes, using the grading
system for neuropathic pain (GSNP) shows statistically significance lower frequency of
neuropathic pain syndromes in Group A (Stellate Group) than Group B (Control group).
Assessment of patient daily activity and functional capacity using Eastern cooperative
oncology group (ECOG) scoring showed statistically significance higher performance status
(lower numbers in the score) in Group A (Stellate Group) than Group B (Control group).
Number of patients discharged on tramadol & or Lyrica whom developed Post Mastectomy Pain
syndrome (PMPs) is statically significant lower in Group A (Stellate Group) than Group B
(Control group).
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