The objective of a study was to compare the
effectiveness and safety of norepinephrine (NE) and phenylephrine (PE)
infusions in preventing post-spinal hypotension during cesarean section (C-section)
under spinal anesthesia (SA).
This was a randomized clinical trial that
enrolled 164 ASA I and II parturients undergoing C-sections under SA. All
participants were prophylactically administered NE (0.05 µg/kg/min) or PE
(0.75µg/kg/min) infusions. The primary outcome was the incidence of post-spinal
hypotension. Secondary outcomes included severe post-spinal hypotension,
reactive hypertension, bradycardia, total vasopressor rescue doses, physician
interventions, nausea and vomiting, and Apgar scores at 1 and 5 minutes.
The results indicated comparable incidences of
post-spinal hypotension and severe post-spinal hypotension between NE and PE
groups. The need for vasopressor rescue doses, incidence of bradycardia, and
reactive hypertension were similar in both groups. Meanwhile, nausea and
vomiting were low and comparable. However, the number of physician
interventions was significantly higher in the PE group (39.02%) compared to the
NE group (28.04%).
The findings showed that the hemodynamics were comparable with NE and PE infusions in preventing hypotension during elective C-section; NE was associated with a lower number of physician interventions compared to PE. The study suggests that NE may be a preferable option for preventing post-spinal hypotension in patients undergoing an elective C-section.
Source: Saharia HK, Barman RK, Mili T, Sarma A, Barman
M, Saikia B, Rajbongshi A. The
New Indian Journal of OBGYN. 2023; 10(1): 46-53.
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