Effect on the Duration of Mechanical Ventilation of Identifying Patients Capable of Breathing Spontaneously
E. Wesley Ely, M.D., M.P.H., Albert M. Baker, M.D., Donnie P. Dunagan, M.D., Henry L. Burke, M.D., Allen C. Smith, M.D., Patrick T. Kelly, M.D., Margaret M. Johnson, M.D., Rick W. Browder, M.D., David L. Bowton, M.D., and Edward F. Haponik, M.D.
Background Prompt recognition of the reversal of respiratoryfailure may permit earlier discontinuation of mechanical ventilation,without harm to the patient.
Methods We conducted a randomized, controlled trial in 300 adultpatients receiving mechanical ventilation in medical and coronaryintensive care units. In the intervention group, patients underwentdaily screening of respiratory function by physicians, respiratorytherapists, and nurses to identify those possibly capable ofbreathing spontaneously; successful tests were followed by two-hourtrials of spontaneous breathing in those who met the criteria.Physicians were notified when their patients successfully completedthe trials of spontaneous breathing. The control subjects haddaily screening but no other interventions. In both groups,all clinical decisions, including the decision to discontinuemechanical ventilation, were made by the attending physicians.
Results Although the 149 patients randomly assigned to the interventiongroup had more severe disease, they received mechanical ventilationfor a median of 4.5 days, as compared with 6 days in the 151patients in the control group (P = 0.003). The median intervalbetween the time a patient met the screening criteria and thediscontinuation of mechanical ventilation was one day in theintervention group and three days in the control group (P<0.001).Complications removal of the breathing tube by the patient,reintubation, tracheostomy, and mechanical ventilation for morethan 21 days occurred in 20 percent of the interventiongroup and 41 percent of the control group (P = 0.001). The numberof days of intensive care and hospital care was similar in thetwo groups. Total costs for the intensive care unit were lowerin the intervention group (median, $15,740, vs. $20,890 in thecontrols; P = 0.03); hospital costs were lower, though not significantlyso (median, $26,229 and $29,048, respectively; P = 0.3).
Conclusions Daily screening of the respiratory function of adultsreceiving mechanical ventilation, followed by trials of spontaneousbreathing in appropriate patients and notification of theirphysicians when the trials were successful, can reduce the durationof mechanical ventilation and the cost of intensive care andis associated with fewer complications than usual care.
Source Information
From the Department of Internal Medicine, Section on Pulmonary and Critical Care Medicine, the Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, N.C. (E.W.E., D.P.D., H.L.B., A.C.S., P.T.K., R.W.B., D.L.B., E.F.H.); Lynchburg Pulmonary Associates, Lynchburg, Va. (A.M.B.); and the Mayo Clinic, Jacksonville, Fla. (M.M.J.).
Address reprint requests to Dr. Ely at the Section on Pulmonary and Critical Care, Department of Medicine, Bowman Gray School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157.
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