Skip to content
SurgCritCare
Dashboard

Respiratory / Ventilation

Weaning Patients from the Ventilator

Review of ventilator liberation readiness, spontaneous-breathing trials, extubation factors, and evidence-based strategies to reduce duration of mechanical ventilation.

Source
SurgCritCare
Status
review pending
Updated
5/29/2026
On this page
On this page

In the United States, almost 800,000 patients who are hospitalized each year require mechanical ventilation.1 This estimate excludes neonates, and there is little doubt that mechanical ventilation will be increasingly used as the number of patients 65 years of age or older continues to increase.2,3 The majority of patients who receive mechanical ventilation have acute respiratory failure in the postoperative period, pneumonia, congestive heart failure, sepsis, trauma, or the acute respiratory distress syndrome (ARDS).4 Our discussion below assumes that physicians have addressed metabolic, inflammatory, and infectious conditions that may be present and have corrected them to the extent possible. As soon as the condition that caused respiratory failure has started to improve, the transition from full ventilatory support to spontaneous breathing may be initiated. This transition requires sufficient respiratory-muscle strength to sustain breathing and maintain acceptable gas exchange. In most patients, this transition also includes the removal of the endotracheal tube. In patients with prolonged respiratory failure, the term “weaning” may be apropos, since it describes a gradual process of improving the strength-to-load ratio of the respiratory system to enable spontaneous respiration. Unfortunately, although this term is widely used, it is somewhat misleading in the vast majority of patients with acute respiratory failure. “Liberation” from mechanical ventilation is a better description, since it implies rapid removal of a burden that is no longer necessary. Figure 1 shows a typical algorithm used by clinicians to discontinue mechanical ventilation. Patients are assessed daily for their readiness to undergo a trial of spontaneous breathing. In many intensive care units (ICUs), protocol-driven assessments of readiness are carried out by nurses or respiratory therapists. Typical readiness criteria include hemodynamic stability, a ratio of the partial pressure of arterial oxygen (measured in millimeters of mercury) to the fraction of inspired

  • xygen (which is unitless) of more than 200 with the ventilator set to deliver a positive end-expiratory pressure of 5 cm of water or less, and some improvement in the underlying condition that caused the respiratory failure.

Trials of spontaneous breathing assess a patient’s ability to breathe while receiving minimal or no respiratory support. To accomplish this, ventilators are switched from full respiratory support modes such as volume-assist control or pressure control to ventilatory modes such as pressure support, continuous positive airway pressure (CPAP), or ventilation with a T-piece (in which there is no positive endexpiratory pressure). Ideally, a trial of spontaneous breathing is initiated while the patient is awake and not receiving sedative infusions.5 For a spontaneous-breathing trial to be successful, a patient must breathe spontaneously with little or no ventilator support for at least 30 minutes without any of the following: a respiratory rate of more than 35 breaths per minute for more than 5 minutes, an oxygen saturation of less than 90%, a heart rate of more than 140 beats per minute, a sustained change in the heart rate of 20%, systolic blood pressure of more than 180 mm Hg or less than 90 mm Hg, increased anxiety, or diaphoresis. nejm. org Perform daily assessment of patient’s readiness to undergo SBT Not ready Ready SBT for 30 min SBT stopped because of tachypnea, poor gas exchange, or discomfort SBT successful Assess airway, cough, airway secretions, and mentation Factors adequate Extubate Factors inadequate Resume ventilatory support Figure 1. A Common Algorithm for the Transition from Mechanical Ventilation to Spontaneous Breathing. SBT denotes spontaneous-breathing trial. If a trial of spontaneous breathing is successful, several additional factors need to be assessed before removal of the endotracheal tube, including the ability to protect the airway once the tube is removed, the quantity of airway secretions, the strength of cough, and mentation. If these factors are deemed adequate, then the endotracheal tube should be removed. Alternatively, an unsuccessful trial of spontaneous breathing, excessive airway secretions, or inadequate cough and mentation should prompt reinitiation of support with a mechanical ventilator. The mechanism underlying the respiratory failure and the inability

  • f the patient to breathe spontaneously should be determined and addressed daily while the patient continues to receive mechanical ventilation.

Strategies to Reduce the Duration of Mechanical Ventilation

Several studies suggest that the process of discontinuing ventilation after the underlying cause of respiratory failure has been...
Section

Several studies suggest that the process of discontinuing ventilation after the underlying cause of respiratory failure has been addressed accounts for more than half the total duration of mechanical ventilation.6,7 Minimizing the duration of mechanical ventilation is an important consideration for all clinicians who care for critically ill patients. The first textbook on mechanical ventilation, published in 1965, stated, “To know the proper timing and rate of weaning from the respirator requires considerable judgment and experience. As a rule, weaning should start as soon as possible.”8 There is support in the literature for this notion that quick discontinuation of mechanical ventilation is beneficial. In a prospective observational study involving patients with brain injuries, Coplin et al.9 compared discontinuation of mechanical ventilation within 48 hours after readiness criteria had been met with more than a 48-hour delay in discontinuation. There was higher mortality, an increased risk of pneumonia, and a longer hospital stay in the group with delayed discontinuation than in the group in which ventilation was discontinued in a more timely fashion. Thus, clinicians should be motivated to minimize the duration of mechanical ventilation. Table 1 outlines evidence-based treatment strategies to prevent the need for mechanical ventilation as well as interventions to reduce the duration of mechanical ventilation once it has been initiated. Several studies have investigated whether particular methods of ventilatory assistance were associated with earlier discontinuation of mechanical ventilation. Brochard et al.21 and Esteban et al.22 conducted studies that compared a gradual reduction of ventilatory support with spontaneousbreathing trials in patients in medical–surgical ICUs in whom initial spontaneous-breathing trials had been unsuccessful. Although these studies came to different conclusions about which method led to earlier discontinuation of mechanical ventilation, both suggested that subsequent trials of spontaneous breathing were successful in most patients — nearly 76%. These findings provide support for the notion that most patients with acute respiratory failure are quickly able to resume spontaneous respiration if their physicians afford them the opportunity to do so. Efforts to decrease the duration of mechanical ventilation can be divided into two categories: earlier appreciation of readiness for spontaneousbreathing trials and a shorter process of discontinuing mechanical ventilation. Many studies have tried to identify simple measurements that can help clinicians predict which patients are ready for a spontaneous-breathing trial and in which nejm. org Table 1. Strategies to Prevent the Need for Mechanical Ventilation and to Reduce Its Duration. Strategy Source Evidence-based approaches to reduce the need for mechanical ventilation Rivers et al.10 Early goal-directed therapy in the initial treatment of sepsis Use of noninvasive ventilation in selected patients with an acute exacerbation

  • f chronic obstructive pulmonary disease or acute cardiogenic pulmonary edema

Brochard et al.,11 Ram et al.,12 Masip et al.,13 Gray et al.14 Ventilator management and associated care to reduce the duration of mechanical ventilation Use of small tidal volumes (6 ml/kg of ideal body weight) in patients with the acute respiratory distress syndrome The Acute Respiratory Distress Syndrome Network15 Daily interruption of sedative infusion Kress et al.16 Interruption of sedative infusion before spontaneous-breathing trial Girard et al.5 Schweickert et al.17 Early physical and occupational therapy Strøm et al.18 No use of sedatives in patients receiving mechanical ventilation Conservative strategy of fluid management in patients with acute lung injury ARDS Clinical Trials Network19 Strategies to reduce ventilator-associated pneumonia Dezfulian et al.20 patients these trials are most likely to be successful. Yang and Tobin23 found that a ratio of the respiratory rate (expressed in breaths per minute) to tidal volume (expressed in liters) (f: Vt) of 105 breaths per minute per liter or less during a 1-minute trial with the use of a T-piece was quite accurate in identifying patients in whom a subsequent spontaneous-breathing trial would be successful (positive predictive value, 78%; negative predictive value, 95%). However, most experts agree that the best method of determining whether patients are ready to breathe on their own is to perform a trial of spontaneous breathing once they have met readiness criteria.24 Many ICUs use protocols to guide the transition from assisted ventilation to spontaneous breathing and subsequent discontinuation of mechanical ventilation. Most protocols include three components: objective criteria to determine whether a patient is ready to breathe with reduced ventilatory support, structured guidelines for reducing ventilatory support, and a list of criteria to determine whether a patient is ready for extubation. There is also growing consensus that the use of systematic protocols for discontinuation of mechanical ventilation, as compared with usual care, may reduce the duration of mechanical ventilation.25 However, not all studies that use protocols for these strategies have shown improvement

  • ver usual care.26-29 Because there are differences between readiness criteria for spontaneous-breathing trials and algorithms for discontinuation of mechanical ventilation, it is difficult to definitively state which aspect or aspects of these protocols are responsible for a reduction in the duration of mechanical ventilation. Nevertheless, the reproducible benefit shown in studies of various protocols in multiple ICUs suggests that it is the standardized approach to management rather than any specific method of ventilator support, prespecified readiness, or criteria for discontinuation of mechanical ventilation that reduces the duration of mechanical ventilation and improves outcomes. Thus, most guidelines recommend that patients who are receiving mechanical ventilation be assessed daily for their readiness to breathe spontaneously and afforded the opportunity to do so if they meet prespecified criteria.24

Approaches to Spontaneous Breathing Trials

Trials of spontaneous breathing do not succeed for a variety of reasons.
Section

Trials of spontaneous breathing do not succeed for a variety of reasons.

  • (Content truncated — see source.)*