LINC: Mechanical chest compressions equally as effective as manual compressions
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AMSTERDAM — Cardiac arrest patients who received mechanical chest compressions with defibrillation during ongoing compressions had similar outcomes as those who received manual compressions during cardiopulmonary resuscitation, according to data presented at ESC Congress 2013.
For the LINC study, Sten Rubertsson, MD, PhD, and colleagues compared a mechanical compression device (LUCAS, Physio-Control Inc.) with manual compressions to determine survival rates after 4 hours and neurological outcomes among survivors up to 6 months.
The researchers studied 2,589 patients from four sites in Sweden, one in England and one in the Netherlands. In all cases, manual chest compressions were performed as soon as emergency personnel arrived. Then, patients were randomly assigned to continued manual compressions (n=1,289) or switched to the mechanical compression device with defibrillation during ongoing compressions (n=1,300).
Sten Rubertsson
Survival rates after 4 hours were similar: 23.6% for the group that received a mechanical compression device vs. 23.7% for the group that received continued manual compressions, Rubertsson, of Uppsala University in Sweden, said during a press conference.
At 6 months, 8.5% of survivors who were assigned a mechanical compression device had positive neurological outcomes, defined as a Cerebral Performance Category Score of 1 or 2, vs. 7.6% of survivors who were assigned manual compressions, Rubertsson said.
“There was no statistically significant difference here,” he said. “What was encouraging, though, was that we had only one patient … with poor neurological outcome in the mechanical device group and six in the manual group.”
Although the findings did not demonstrate superiority for the mechanical compression device, it creates opportunities for further research to explore “situations where it would be preferable to have mechanical assistance,” Rubertsson said. These situations could include CPR during transportation and CPR for extended time periods, he said. – by Katie Kalvaitis and Erik Swain
For more information:
Rubertsson S. Hot Line II: Late breaking trials on intervention and devices. Presented at: the European Society of Cardiology Congress; Aug. 31-Sept. 4, 2013; Amsterdam.
Disclosure: The study was initiated by Uppsala University and sponsored by Physio-Control/Jolife AB. Rubertsson has received consulting income from Physio-Control/Jolife AB. All of the other researchers’ institutions received compensation from Physio-Control/Jolife AB for their work.