TY - JOUR
T1 - A period of immobility after remifentanil administration protects from nausea
T2 - An experimental randomized cross-over study
AU - Heuser, Fabian
AU - Schulz, Christian M.
AU - Hapfelmeier, Alexander
AU - Lehnen, Nadine
AU - Kochs, Eberhard F.
AU - Wagner, Klaus J.
N1 - Publisher Copyright:
© 2016 The Author(s).
PY - 2016/10/10
Y1 - 2016/10/10
N2 - Background: The opioid remifentanil induces a decrease of vestibulo-ocular reflex function, which has been associated with nausea and vomiting when the subjects are moved. The study investigates in healthy female volunteers if immobility after remifentanil administration protects from nausea and vomiting. Methods: In volunteers, a standardized movement intervention (a manually applied head-trunk movement forward, backward and sideward) was started 5 min (session A), 35 min (session B) or 60 min (session C) after cessation of a remifentanil infusion (0.15 μg kg-1 min-1). In a cross-over design, 16 participants were randomized to the early (sessions A and B) or the late intervention group (sessions A and C). Nausea was assessed using a 11-point numerical rating scale before and after each movement intervention. Differences within and between groups were assessed with non-parametric tests for paired and unpaired data. Results: Comparing sessions A, B and C, intensity of nausea was time-dependent after cessation of remifentanil administration (p = 0.015). In the early intervention group, nausea decreased from median 5.0 [IQR 1.5;6.0] in session A to 2.0 [1.0;3.0] in session B (p = 0.094); in the late intervention group nausea decreased from 3.5 [2.0;5.0] in session A to 0.5 [0.0;2.0] in session C (p = 0.031). Conclusions: In summary, in young healthy women, immobility after remifentanil administration protects from nausea and vomiting in a time-dependent manner. In analogy to motion sickness, opioid-induced nausea and vomiting in female volunteers can be triggered by movement. Trial registration: German Clinical Trials Register DRKS00010667. The trial was registered retrospectively on June, 20th 2016.
AB - Background: The opioid remifentanil induces a decrease of vestibulo-ocular reflex function, which has been associated with nausea and vomiting when the subjects are moved. The study investigates in healthy female volunteers if immobility after remifentanil administration protects from nausea and vomiting. Methods: In volunteers, a standardized movement intervention (a manually applied head-trunk movement forward, backward and sideward) was started 5 min (session A), 35 min (session B) or 60 min (session C) after cessation of a remifentanil infusion (0.15 μg kg-1 min-1). In a cross-over design, 16 participants were randomized to the early (sessions A and B) or the late intervention group (sessions A and C). Nausea was assessed using a 11-point numerical rating scale before and after each movement intervention. Differences within and between groups were assessed with non-parametric tests for paired and unpaired data. Results: Comparing sessions A, B and C, intensity of nausea was time-dependent after cessation of remifentanil administration (p = 0.015). In the early intervention group, nausea decreased from median 5.0 [IQR 1.5;6.0] in session A to 2.0 [1.0;3.0] in session B (p = 0.094); in the late intervention group nausea decreased from 3.5 [2.0;5.0] in session A to 0.5 [0.0;2.0] in session C (p = 0.031). Conclusions: In summary, in young healthy women, immobility after remifentanil administration protects from nausea and vomiting in a time-dependent manner. In analogy to motion sickness, opioid-induced nausea and vomiting in female volunteers can be triggered by movement. Trial registration: German Clinical Trials Register DRKS00010667. The trial was registered retrospectively on June, 20th 2016.
KW - Motion sickness
KW - Nausea
KW - Opioid
KW - PONV
KW - Remifentanil
KW - Vestibulo-ocular reflex
KW - Vomiting
UR - http://www.scopus.com/inward/record.url?scp=84990847908&partnerID=8YFLogxK
U2 - 10.1186/s12871-016-0263-5
DO - 10.1186/s12871-016-0263-5
M3 - Article
C2 - 27724859
AN - SCOPUS:84990847908
SN - 1471-2253
VL - 16
JO - BMC Anesthesiology
JF - BMC Anesthesiology
IS - 1
M1 - 90
ER -