Pain is one of the most misunderstood, underdiagnosed, and untreated medical problems, particularly in children. New Joint Commission on Accreditation of Health Care Organization regards pain as fifth vital sign and requires caregivers to regularly assess pain. Inadequate pain relief during childhood may have long-term negative effects including harmful neuroendocrine responses disrupted eating and sleep cycles and increased pain perception during subsequent painful experiences. Also, postoperative pain can result in an uncooperative and restless child. Hence, it is preferable to prevent the onset of pain rather than to relieve its existence. Various multimodal techniques have been designed for pediatric pain relief. These include both systemic and regional analgesia. The most commonly used regional technique is caudal epidural block. Advantages of the caudal block are smoother recovery with less distress behavior, early ambulation, decreased the risk of chest infections, decreased postoperative analgesic requirements, and early discharge. In our culture; considerable number of parents still refuses caudal anesthesia fearing from the rare neurological sequelae may occur. This the motive for searching for parenteral surrogate gives clear headed recovery resembles regional analgesia. Dexmedetomidine is an alpha 2 agonist which has sedative, analgesic, and opioid-sparing effect. It prolongs the duration of analgesia by its local vasoconstrictive effect and by increasing the potassium conductance in A-delta and C-fibers. It also exerts its analgesic action centrally via systemic absorption or by diffusion into the cerebrospinal fluid and reaches alpha 2 receptors in the superficial laminae of the spinal cord and brainstem or indirectly activating spinal cholinergic neurons. The sedative effects of dexmedetomidine are mostly due to stimulation of the alpha 2 adrenoceptor in the locus coeruleus
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
135
1 mcg/kg IV over 10 minutes followed by 0.5 mcg/kg/hr
After negative aspiration of blood or cerebrospinal fluid, 2 mg/ kg of bupivacaine at concentration of 0.5% (volume 0.5ml/kg) was given as per the group assigned, then the site of injection was dressed, and the patient was turned supine.
Ahmed Abdelrahman
Tanta, Egypt
quality of recovery of the studied patients
quality of recovery of the studied patients using modified objective pain score
Time frame: in immediate recovery from aneasthesia at postaneathetic care unit up to 2 hours
quality of recovery of the studied patients
change in quality of recovery of the studied patients using modified objective pain score
Time frame: from discharge from PACU up to 6 hours in the surgical ward
concentration of required postoperative analgesic
concentration of postoperative analgesic
Time frame: in immediate recovery from aneasthesia up to 2 hours at postaneathetic care unit
concentration of required postoperative analgesic
concentration of required postoperative analgesic
Time frame: from discharge from PACU up to 6 hours in the surgical ward
concentration of required postoperative sedation
concentration of required postoperative sedation
Time frame: in immediate recovery from aneasthesia up to 2 hours at postaneathetic care unit
concentration of required postoperative sedation
concentration of required postoperative sedation
Time frame: from discharge from PACU up to 6 hours in the surgical ward
number of patients developed perioperative complications.
number of patients developed perioperative complications
Time frame: in immediate recovery from aneasthesia up to 2 hours at postaneathetic care unit
number of patients developed perioperative complications.
number of patients developed perioperative complications
Time frame: from discharge from PACU up to 6 hours in the surgical ward
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