Article Figures & Data
Tables
Study type Number of patients Vasopressors Dosea Duration PIVC site Events Retrospective cohort8 202 Norepinephrine (72%), phenylephrine (36%) Median initial to maximum: norepinephrine 0.04–0.13, phenylephrine 25–95 μg/minute Median 11.5 hours, maximum 19 hours Forearm, antecubital fossa, hand 8 events (4%), all local extravasation Randomized controlled trial10 310 (155 early vasopressor, 155 standard treatment) Norepinephrine (67.7%) and epinephrine (17.4%) in early vasopressor group Median (IQR) maximum in early vasopressor group: norepinephrine 0.1 (0.05–0.18), epinephrine 0.41 (0.28–1.2) NR NR 6 events in early vasopressor group (3.8%): 1 skin necrosis, 5 acute limb or intestinal ischemia Unblinded superiority trial11 1,563 (782 restrictive fluid, 781 liberal fluid) NR NR 9.6 hours in restrictive fluid group NR 3 events in PIVC vasopressor group (n = 500), all 3 were site extravasation Prospective cohort13 64 Epinephrine (66%), norepinephrine (41%) Median (IQR): norepinephrine 0.1 (0.01–0.48), epinephrine 0.12 (0.6–0.38) Median (IQR) 19 hours (8.5–37) Antecubital fossa, forearm, hand 2 events (2.9%), extravasation with local tissue swelling Randomized controlled trial14 263 (128 PIVC, 135 CVC) Epinephrine, norepinephrine < 2 mg/hour, if more, crossover to CVC NR NR 133 total events: 56 insertion difficulty, 20 erythema, 19 extravasation, 9 catheter infection Prospective cohort15 635 Norepinephrine Median (IQR) maximum: 10 μg/minute (6–15) Median (IQR) 5.8 hours (2–20) Antecubital fossa 35 extravasationb events (5.5%) Retrospective cohort16 212 patients (39 PIVC, 155 PIVC followed by CVC, 18 CVC only) Phenylephrine (41%), norepinephrine (38%) Median (IQR) maximum in PIVC-only group: phenylephrine 0.17 (0.09–0.27), norepinephrine 0.99 (0.6–1.64) Median (IQR) 10.5 hours (4.7–15.9) in PIVC-only group NR 75 events (35%): 28 leakage, 25 tissued cannula, 19 extravasation, 2 erythema