None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Elective cardiac surgeries through median sternotomy
Exclusion criteria
Exclusion criteria: 1.history of previous cardiac surgery 2.chronic kidney disease 3.chronic liver disease 4.left ventricular ejection fraction lessthan 35% 5.patients on mechanical ventilator support or inotropes or intra aortic balloon pump preoperatively 6.pregnant and lactating mothers 7,patients who are allergic to study drugs and addicted to narcotis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess and compare the efficacy of preincisional and postincisional parasternal intercostal block on postoperative analgesic requirement in patients undergoing cardiac surgeryTimepoint: 24 hours after shifting to ICU | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To assess and compare intraoperative and postoperative hemodynamic stability after preincisional and postincisional parasternal block 2.To compare duration of postoperative mechanical ventilation after preincisional and postincisional parasternal block 3.To compare postoperative Visual Analogue Scale(VAS) pain scores after preincisional and postincisional parasternal block Timepoint: 1.Heart rate and mean arterial blood pressure will be recorded intraoperatively at baseline, skin incision, sternotomy and sterna retractor placement and post operatively at 0,2,4,6,8,12,24 hours after shifting to ICU 2.Immediately after extubation in ICU 3.VAS score will be noted at the time of first spontaneous eye opening and 12,16,20 and 24 hours after shifting to ICU | — |
Countries
India
Contacts
Jawaharlal Institute of Postgraduate Medical Education and Research