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  • Research
  • Open Access

Cardiac function during weaning failure: the role of diastolic dysfunction

Contributed equally
Annals of Intensive Care20188:2

  • Received: 27 September 2017
  • Accepted: 26 December 2017
  • Published:



Cardiac dysfunction is a common cause of weaning failure. Weaning shares some similarities with a cardiac stress test and may challenge active phases of the cardiac cycle-like ventricular contractility and relaxation. This study aimed at assessing systolic and diastolic function during the weaning process and scrutinizing their dynamics during weaning trials.


Echocardiography was performed during baseline ventilator settings to assess cardiac function at the initiation of the weaning process and at the start and the end of consecutive weaning trials (performed at day-1, day-2, and before extubation if applicable) to explore the evolution of left ventricle contractility and relaxation in a subset of patients.


Among 67 patients included, weaning was prolonged (≥ 7 days) in 18 (27%) patients and short (< 7 days) in 49 (73%). Prevalence of systolic dysfunction and isolated diastolic dysfunction before the initiation of weaning process were 37 and 17%, respectively. Isolated diastolic dysfunction was more frequent in patients with prolonged weaning as compared to their counterparts. Thirty-one patients were explored by echocardiography during consecutive weaning trials. An increase in filling pressures with an alteration of ventricular relaxation (as assessed by a decrease in tissue Doppler early mitral diastolic wave velocity) was found during failed weaning trials.


Isolated diastolic dysfunction was associated with a prolongation of weaning. Increased filling pressures with left ventricle relaxation impairment may be a key mechanism of weaning trial failure.


  • Weaning
  • Diastolic function
  • Relaxation
  • Diastolic reserve


Weaning from mechanical ventilation is an essential step in the care of critically ill intubated patients, accounting for approximately 40% of the total duration of mechanical ventilation [1]. Given that increased time on mechanical ventilation is associated with higher mortality rates [2], it is crucial to safely wean the patient from the ventilator as soon as possible. Pulmonary edema is one of the main causes of weaning failure [3], and cardiovascular dysfunction during weaning may involve systolic [4] and/or diastolic alterations [5, 6].

In healthy subjects, relaxation enhancement during exercise blunts the increase in venous return to maintain normal filling pressures [7]. However, an impaired relaxation may be unmasked during exercise in patients with mild symptoms of heart failure, irrespective of the presence of diastolic dysfunction at rest [8, 9]. Because weaning shares some similarities with a cardiorespiratory stress test [10, 11], the same pathophysiology is conceivable to explain the increase in filling pressures during weaning failure of cardiac origin. We hypothesized that diastolic dysfunction at baseline or impaired diastolic relaxation during weaning trials may mediate weaning failure.

The present study had two primary aims: first, to assess cardiac function at initiation of the weaning process and evaluate its association with weaning outcomes; second, to assess the dynamics of left ventricle (LV) contractility and relaxation in a subgroup of patients during consecutive weaning trials.


Study population

This ancillary study, planned a priori, was performed in one (Henri Mondor University hospital, Creteil, France) of the nine centers participating in the B-type natriuretic peptide (BNP) for the fluid Management of Weaning (BMW) trial [12]. The BMW study was a randomized, controlled trial comparing a biomarker-guided depletive fluid management strategy to usual care during ventilator weaning. A detailed description of the BMW study design (NCT00473148) has been published previously [12]. Inclusion criteria of the BMW study were those allowing early initiation of ventilator weaning in patients receiving mechanical ventilation for at least 24 h. Permanent non-inclusion criteria were: pregnancy or lactation, age < 18 years, known allergy to furosemide or sulfonamides, tracheostomy at inclusion, hepatic encephalopathy, cerebral edema, acute hydrocephalus, myasthenia gravis, acute idiopathic polyradiculoneuropathy, decision to withdraw life support, and prolonged cardiac arrest with a poor neurological prognosis. The protocol was approved by our institution’s local ethics committee (Comité de Protection des Personnes Ile-de-France IX, approval number 06–035), and informed consent was signed by the patient or a close relative. The main result of the BMW trial was to show that a BNP-driven depletive fluid management strategy decreased the duration of weaning without increasing adverse events [12].

Study protocol

To standardize the weaning process, patients were ventilated using a computer-driven automated weaning system (AWS, Evita Smart Care System, Dräger Medical, Lubeck, Germany), which gradually decreased the pressure support level (while maintaining the patient within a zone of respiratory comfort), as previously described [13]. When the AWS declared the patient ready for separation, extubation was performed as soon as possible (including during the night), provided the patient met the other criteria required for extubation [12].

In a subgroup of 31 patients for whom echocardiography availability allowed consecutive examinations, a daily weaning trial was performed if the patient was still ventilated with the AWS and not ready for separation. The weaning trial lasted one hour and consisted of a low-pressure support trial (10 cm H2O in case of moisture humidifier or 7 cm H2O in case of heated humidifier) with zero-PEEP [11]. Criteria for weaning trial failure were: respiratory rate > 35 breaths/min and/or increased accessory muscle activity, SpO2 < 90%, heart rate > 140 beats/min, systolic blood pressure > 200 or < 80 mmHg, diaphoresis and clinical signs of distress. More information about the study protocol is available in the data supplement (Additional file 1: ESM Study protocol).

Classification of weaning

Successful extubation was defined as patient alive and without reintubation 72 h after extubation. We adapted the WIND study classification of weaning process [2] to the use of the AWS and further summarized this classification into two groups as follows: short weaning (patients successfully extubated within 6 days of AWS) and prolonged weaning (patients still ventilated after 7 days of AWS or more). Patients who died between 1 to 6 days and after 6 days of AWS were classified as short and prolonged weaning, respectively. This dichotomization was driven by the need for parsimony as per the limited sample size, and the fact that prolonged weaning identifies a subgroup of patients at increased risk of mortality, as compared to their counterparts [14].


In all included patients (n = 67), echocardiography was performed to assess cardiac function during baseline ventilator settings (in pressure support ventilation), just before starting the weaning process with the AWS. In addition, we examined in a subset of patients (n = 31) whether weaning trials (low-pressure support with zero-PEEP) could induce an alteration of systolic or diastolic function, independently from their baseline function. In this subgroup, echocardiography was performed at the beginning and end of consecutive weaning trials performed at day-1, day-2, and before extubation. All echocardiographic examinations were performed by a single trained operator (FRC, with competence in advanced critical care echocardiography) not involved in patient care, using a transthoracic ultrasound device (EnVisor, Philips ultrasound, Bothell, WA). Briefly, the following echocardiographic views were examined with the patient in the semi-recumbent position: four-chamber and two-chamber long-axis views to assess left ventricle ejection fraction (LVEF), computed from LV volumes using the bi-plane Simpson method when image quality was suitable, or visually estimated when poor image quality did not allow sufficient identification of the endocardium; tissue Doppler peak systolic (s′) wave at the lateral mitral valve annulus; right ventricle size (a dilated right ventricle was defined by an end-diastolic right ventricle/left ventricle area ratio > 0.6) and function (using the tricuspid annular plane systolic excursion); diastolic function [using pulsed-wave Doppler early (E) and late (A) diastolic wave velocities at the mitral valve, and tissue Doppler early (e′) and late (a′) diastolic wave velocities at the lateral mitral valve annulus]. Systolic dysfunction was defined as LVEF < 50%. Isolated diastolic dysfunction (with preserved LVEF) was defined using the 2016 European Society of Cardiology guidelines (LVEF ≥ 50% with plasma BNP concentration > 35 pg/mL and [E/e′ ratio ≥ 13 or e′ < 9]) [15]. Because there is no single widely accepted definition for diastolic dysfunction, we also assessed, as a sensitivity analysis (available in Additional file 2: Table 1), other definitions proposed by scientific societies and experts, as follows: (1) LVEF ≥ 50% and e′ < 8 cm/s [16]; (2) LVEF ≥ 50% and (E/e′ ratio > 8 or e′/a′ ratio < 1) [17]; or (3) LVEF ≥ 50%, E/e′ ratio > 8 and plasma BNP concentration > 200 pg/mL [18]. Dynamics of LV contractility and relaxation during weaning trials were assessed using the s′ and e′ waves, respectively [1922]. Pulsed-wave Doppler flows were obtained below the aortic valve to assess LV outflow tract for cardiac output computation. Mitral and aortic regurgitation were measured semi-quantitatively using color-flow Doppler and were considered severe at grades III–IV [23]. Echocardiographic images were digitally stored, and a computer-assisted evaluation was performed off-line by two trained operators (EV, AMD). All measures were averaged over a minimum of three cardiac cycles (five to ten in case of non-sinus rhythm).

Statistical analysis

The data were analyzed using SPSS Base 20 (IBM-SPSS Inc, Chicago, IL, USA). Categorical variables were expressed as numbers (percentage) and continuous data as medians (25th–75th percentiles), unless otherwise specified. We used the Chi-squared or Fisher exact test to compare categorical variables between groups and the Student’s T test, Mann–Whitney test or Wilcoxon paired test to compare continuous variables, as appropriate. A p value of < 0.05 was considered statistically significant.


Patient population, cardiac function and weaning outcome

Among the 75 participants enrolled, we have explored cardiac function in 67. Eight patients were excluded because of echocardiography unavailability (Fig. 1). Weaning was prolonged in 18 (27%) patients and short in 49 (73%) patients. All patient characteristics were similar between groups, except for a lower PaO2/FiO2 ratio at inclusion in patients with prolonged weaning as compared to their counterparts (Table 1). Before starting the weaning process, the majority of patients had an impaired cardiac function; overall, the prevalence of systolic dysfunction and isolated diastolic function were 37 and 17%, respectively. Isolated diastolic dysfunction was more frequent in patients with prolonged weaning (≥ 7 days) as compared to their counterparts (Table 1). Tricuspid annular plane systolic excursion was also lower in patients with prolonged weaning as compared to others, while other echocardiographic variables were similar between groups (Table 1). End-diastolic right ventricle/left ventricle area ratio and pulmonary artery systolic pressure were similar in patients with or without isolated diastolic dysfunction: 0.59 [0.58–0.66] versus 0.56 [0.44–0.67], p = 0.46 and 43 [25–61] versus 37 [25–50] mmHg, p = 0.41, respectively. Cardiovascular treatments and weaning outcomes are reported in Table 2. Most patients received diuretics, including all those with prolonged weaning, but the latter group had a more positive fluid balance during weaning as compared to the short weaning group. In comparison with the short weaning group, fewer patients in the prolonged weaning group received vasodilators. Weaning duration, ICU length of stay and mortality were significantly greater in the prolonged weaning group (Table 2).
Fig. 1
Fig. 1

Study flow chart. BMW B-type natriuretic peptide for the fluid management of weaning

Table 1

Patient characteristics and echocardiographic variables just before the weaning process, according to weaning category (n = 67)


All patients

(n = 67)




(n = 49)


(n = 18)

Patient characteristics


Age, year

64 (47–76)

61 (49–75)

69 (44–81)


Male sex

44 (66)

31 (63)

13 (72)


SAPS II at ICU admission

46 (34–53)

44 (34–58)

46 (34–50)





33 (49)

23 (47)

10 (56)



17 (26)

9 (19)

8 (44)


Chronic obstructive pulmonary disease

17 (25)

13 (27)

4 (22)

> 0.99

History of ischemic heart disease

13 (19)

11 (22)

2 (11)


Atrial fibrillation

22 (33)

13 (27)

9 (50)


Reason for intubation




13 (19)

9 (18)

4 (22)


Septic shock

8 (12)

5 (10)

3 (17)


Cardiogenic pulmonary edema

17 (25)

14 (29)

3 (17)



18 (27)

12 (25)

6 (33)


Cardiac arrest

4 (6)

4 (8)

0 (0)



7 (10)

5 (10)

2 (11)


Events between ICU admission and inclusion


Septic shock

33 (49)

25 (51)

8 (44)


Ventilator-associated pneumonia

15 (22)

9 (18)

6 (33)


Acute respiratory distress syndrome

26 (39)

18 (37)

8 (44)


Use of neuromuscular blockers

11 (16)

9 (18)

2 (11)


Cumulative fluid balance before inclusion, mL

4322 (949–7898)

4322 (175–7253)

4228 (1757–17,957)


Duration of invasive MV before inclusion, days

3 (2–6)

3 (2–6)

5 (3–13)


Clinical and biological data at inclusion


SOFA score

4 (3–6)

4 (3–6)

5 (4–6)


Systolic arterial pressure, mmHg

129 (122–144)

132 (113–146)

127 (108–136)


Heart rate, beats/min

93 (82–105)

93 (83–106)

91 (79–104)


Respiratory rate, beats/min

25 (19–30)

23 (18–29)

29 (27–33)


RPP, beats/min·mmHg

12,500 (11,288–15,346)

12,576 (10,744–15,520)

12,423 (12,245–13,035)

> 0.99

Arterial blood gases


 pH, units

7.44 (7.40–7.47)

7.44 (7.40–7.47)

7.44 (7.41–7.47)


 PaO2/FiO2 ratio, mmHg

210 (182–270)

222 (188–277)

186 (153–226)

< 0.01

 PaCO2, mmHg

41 (35–46)

40 (35–46)

42 (37–49)


BNP, pg/ml

331 (114–602)

302 (108–588)

415 (114–842)


Protidemia, g/L

58 (51–66)

58 (54–66)

54 (49–66)


Creatinine, micromol/L

79 (57–101)

81 (59–98)

73 (55–107)


Randomization in the interventional group

34 (51)

25 (51)

9 (50)


Echocardiographic variables


LVEF,  %

55 (40–60)

50 (37–60)

60 (50–62)


Cardiac index, L/min/m2

3.0 (2.2–3.6)

3.1 (2.3–3.6)

2.7 (2.1–3.7)


Systolic dysfunction


LVEF < 50%

25 (37)

21 (43)

4 (22)


Diastolic dysfunction a


LVEF ≥ 50% and BNP > 35 pg/mL and (E/e′ ratio ≥ 13 or e′ < 9)

11 (17)

4 (8)

7 (39)


Heart valve diseaseb

23 (34)

14 (29)

9 (50)


RV/LV area ratio

0.6 (0.5–0.7)

0.6 (0.4–0.7)

0.6 (0.5–0.7)


Tricuspid annular plane systolic excursion, cm

1.9 (1.5–2.6)

2.1 (1.7–2.7)

1.5 (1.3–1.9)


Systolic pulmonary artery pressure, mmHg

38 (25–51)

37 (25–49)

46 (25–66)


SAPS Simplified Acute Physiologic Score, ICU intensive care unit, MV mechanical ventilation, SOFA sequential organ failure assessment, RPP product of heart rate and systolic arterial pressure, FiO 2 fraction of inspired oxygen, BNP B-type natriuretic peptide, LVEF left ventricle ejection fraction, E early diastolic velocity measured using Doppler transmitral flow, A late diastolic velocity measured using Doppler transmitral flow, e′ early peak diastolic velocity of mitral annulus, a′ late peak diastolic velocity of mitral annulus, RV right ventricular end-diastolic area, LV left ventricular end-diastolic area

aDiastolic function could not be assessed in one patient for e′ and in two patients for E/e′ ratio

bHeart valve disease is defined as a severe aortic or mitral regurgitation (grade III/IV). Data are presented as n (%) or median (1st quartile–3rd quartile)

Table 2

Cardiovascular treatments and outcomes according to weaning category (n = 67)


All patients

(n = 67)




(n = 49)


(n = 18)

Cardiovascular treatments during weaning



56 (84)

38 (78)

18 (100)



19 (28)

15 (31)

4 (22)



30 (45)

26 (53)

4 (22)



19 (28)

13 (27)

6 (33)


Any cardiovascular treatment

62 (93)

44 (90)

18 (100)


Average daily furosemide dose during weaning, mg

25 (4–59)

30 (1–59)

22 (6–56)


Average daily fluid balance during weaning, mL

− 757 (− 2016 to − 81)

− 1202 (− 2342 to − 477)

51 (− 638 to 449)

< 0.01

Average daily urine output during weaning, mL

2588 (1971 to 3863)

2950 (2205 to 4167)

1967 (1649 to 2912)




Time to first successful extubation, days

2 (1–6)

1 (1–2)

13 (10–32)

< 0.01

Ventilator free days at day-28, days

24 (18–27)

27 (25–27)

0 (0–16)

< 0.01

Time to discharge from ICU, days

9 (5–18)

7 (4–10)

31 (15–53)

< 0.01

Time to discharge from hospital, days

28 (15–53)

22 (13–32)

39 (22–53)


ICU mortality

9 (13)

2 (4)

7 (39)

< 0.01

Hospital mortality

10 (15)

3 (6)

7 (39)

< 0.01

Data are presented as n (%) or median (1st quartile–3rd quartile). Patient who died before day-28 had 0 ventilator free days

ICU intensive care unit

Dynamics of LV contractility and relaxation during weaning trials

Among the 67 patients included, 31 were explored during consecutive weaning trials (Additional file 2: Table 2). Sixteen of these patients (52%) successfully passed the first weaning trial (day-1), whereas 15 (48%) failed. The evolution of cardiac clinical parameters and echocardiographic parameters during consecutive weaning trials (day-1, day-2, and before extubation) are displayed in Figs. 2 and 3, respectively. Failure of weaning trial was more often associated with an increase in systolic arterial pressure, heart rate and their product (pressure-rate product), as compared with weaning trial successes (Fig. 2). A marked increase in LV filling pressures (as assessed by E/e′ ratio) concomitant with an alteration of diastolic relaxation (as assessed by e′ velocity) were found in failed weaning trials (Fig. 3, Table 3). The e′ velocity increased in fewer (6.7%) and decreased in greater (93.3%) number of patients who failed weaning trials, as compared to successes (p < 0.001).
Fig. 2
Fig. 2

Systolic arterial pressure (a), heart rate (b) and pressure-rate product (c) at the start (white square) and the end (black square) of consecutive weaning trials during the weaning process (n = 31), according to first trial outcome (success or failure). #p value < 0.05 as compared to the start of weaning trial (Wilcoxon test)

Fig. 3
Fig. 3

Tissue Doppler s′ wave (a), e′ wave (b) and E/e′ ratio (c), recorded with echocardiography at the start (white square) and the end (black square) of consecutive weaning trials during the weaning process (n = 31), according to first trial outcome (success or failure). #p value < 0.05 as compared to the start of weaning trial (Wilcoxon test)

Table 3

Percent change in echocardiographic variables between the start and the end of the first weaning trial (n = 31), according to outcome (success or failure)



n = 31


n = 16


n = 15


Delta sa

− 3% (− 12%; 9%)

− 3% (− 7%; 5%)

− 2% (− 15%; 9%)


Delta e

− 3% (− 12%; − 4%)

3% (− 9%; 6%)

− 6% (− 18%; − 3%)


Delta E

13% (8%; 19%)

12% (7%; 16%)

14% (11%; 23%)


Delta E/e

16% (9%; 25%)

10% (4%; 14%)

26% (20%; 28%)

< 0.01

Data are presented as median (1st quartile; 3rd quartile)

s′ peak systolic velocity at the lateral mitral valve annulus, e′ early peak diastolic velocity of mitral annulus, E early diastolic velocity measured using Doppler transmitral flow

as′ could not be assessed in three patients


We herein report a high prevalence of cardiac dysfunction at initiation of weaning. Prolonged weaning was associated with a predominantly isolated diastolic rather than systolic dysfunction in our cohort. Echocardiographic exploration suggested that LV relaxation impairment with increased filling pressures may be a key mechanism of failed weaning trials.

Cardiac dysfunction before the initiation of weaning

Cardiac dysfunction plays a critical role in weaning outcome. In patients with prolonged weaning (≥ 7 days) in our series, systolic and isolated diastolic dysfunction were found in 22 and 39% of patients, respectively. Systolic dysfunction is a known risk factor for extubation failure [4]. However, in patients with preserved LVEF, increase in preload (volume status) and afterload (arterial stiffness) during weaning may also impair LV compliance and provoke pulmonary edema, especially in case of pre-existing diastolic dysfunction [24]. Our results are consistent with some previous reports describing diastolic dysfunction as a risk factor for weaning failure [5, 6, 25]. The heterogeneity of diastolic dysfunction definitions may explain the variability of its incidence and prevalence in critically ill patients [26].

Cardiac dynamics during weaning

During weaning, removal of positive-pressure ventilation increases LV preload and afterload, inducing some physiologic changes similar to those observed during a cardiovascular stress test. Tachycardia and hypertension are two major determinants of diastolic dysfunction. They were more pronounced during weaning failure in our series and have been reported as frequent features of weaning-induced cardiac dysfunction [27]. Pressure-rate product was significantly increased during failed weaning trials, as compared to successes. Tachycardia could participate in the alteration of diastolic function by reducing diastolic filling time and/or decreasing coronary perfusion [28]. In addition, LV diastolic performance has been shown to be strongly influenced by the hypertensive response to exercise. Hypertension is well known to exacerbate heart failure in patients with preserved ejection fraction [29].

The fall in LV pressure during relaxation is a key determinant of diastolic function, and depends on intrinsic (contractility, LV stiffness) and extrinsic (preload, afterload) factors [30, 31]. The E wave velocity of mitral inflow assesses the early diastolic filling of LV, primarily reflecting the driving pressure between the left atrium and the left ventricle, and is therefore affected by preload and relaxation. The e′ velocity, measured with tissue Doppler at the lateral mitral valve annulus, is usually used to correct for the effect of LV relaxation on E wave [21, 22, 32]. Thus, the E/e′ ratio is considered a reliable measure of LV filling pressure, with minimal influence of intrinsic relaxation or age [33]. Although the assessment of diastolic function with these validated Doppler indices is usually highly reproducible [21, 32, 34], the detection of small changes may be challenging for non-experts in routine practice.

We found an increase in E/e′ ratio during weaning trial, which is compatible with an elevation of filling pressures, as previously demonstrated [25, 35]. Several studies have found an independent association between e′ and LV relaxation [22, 33, 36]. As compared to the E wave velocity, preload may have a minimal effect on e′ [21, 22, 37], especially in patients with diastolic dysfunction [38]. Our finding that e′ velocity tends to reduce during failed weaning trials is therefore compatible with an impaired diastolic relaxation in these patients, although a causality cannot be ascertained. This phenomenon is compatible with a lack of diastolic reserve, which may prevent the ability of LV to improve diastolic function and maintain normal filling pressures during stress [3941]. Several studies evaluated the diastolic reserve with echocardiography in patients with heart failure and preserved ejection fraction [8, 9]. A decrease in e′ wave, together with a concomitant increase in E/e′ ratio, was the strongest markers of impaired diastolic reserve in these patients. Similar results were found in our study during failed weaning trials. A dynamic alteration of diastolic function during weaning stress in patients lacking diastolic reserve could be a possible mechanism of weaning failure, independently from the cardiac function at baseline. This hypothesis is in accordance with a previous work by Moschietto et al., who suggested the evolution of the LV relaxation rate during a spontaneous breathing trial (SBT) as the key factor in weaning outcome. However, the decrease in e′ velocity during failed weaning trials is in contrast with this former study which found no significant variation during SBT. This discrepancy may be explained by the timing of the second echocardiography. These authors repeated echocardiographic examination only 10 min after starting the weaning trial, whatever its total duration [25], whereas we rather assessed dynamic changes at the end of the weaning trial. The modality of weaning trial may also play a critical role [11].

Therapeutic implications

The key mechanism of weaning failure did not seem to involve systolic dysfunction in our study, as also suggested by others [5, 25, 35]. Inotropic support could hypothetically exacerbate stress-induced diastolic dysfunction by increasing heart rate and/or myocardial oxygen demand. Dobutamine was even used as a stress test to diagnose heart failure with preserved ejection fraction [42]. Isolated diastolic dysfunction is frequent in ICU patients, especially in the elderly [43], and its diagnosis may deserve a specific therapeutic management in case of complicated weaning. Conservative and depletive fluid management are known to decrease the duration of ventilator support [44] and weaning [12], respectively. In our series, we could not assess the specific role of diuretics on SBT-induced cardiovascular burden because the vast majority of patients in the entire cohort received diuretics. Despite the use of diuretics in all patients with prolonged weaning, the urine output was lower and the fluid balance was higher in this group. The control of volume overload during diastolic heart failure may require higher doses of furosemide and/or the association of thiazide-like diuretics [29]; these strategies should be tested in future trials of fluid management during weaning. Fewer patients with prolonged weaning were treated with vasodilators as compared to those with short weaning. Vasodilators may be used to blunt the hypertensive response to weaning and expedite separation from the ventilator [45]. Future trials are needed to determine the optimal blood pressure target during ventilator weaning. Whether aerobic exercise training in ventilated patients could improve the diastolic reserve [46], ameliorate the tolerance of weaning trials and fasten the weaning process also needs to be explored in future studies.

Strengths and limitations

Strengths of our study include its prospective design and the detailed cardiac assessment using echocardiography. In particular, our study comprehensively assessed diastolic function at weaning start and its dynamics during consecutive weaning trials. Limitations include the monocentric setting and the limited sample size, which precluded any multivariable analysis of factors associated with prolonged weaning. Also, only a minority of patients explored consecutively fulfilled our definition of diastolic dysfunction, preventing any evaluation of the relationship between diastolic dysfunction at baseline and relaxation dynamics during weaning trials. The lack of a single gold standard definition of diastolic dysfunction complicated the analysis of our data, inasmuch as there was some patient heterogeneity concerning the changes in diastolic indices. Last, the characterization of the cardiac origin of weaning failure with tools like the pulmonary artery catheter or cardiac biomarkers would have strengthened our findings.


Isolated diastolic dysfunction is more frequent in patients with prolonged weaning (≥ 7 days), as compared to those with a shorter weaning. In addition, failure of weaning trial seems associated with an elevation of filling pressures mediated by a stress-induced impairment of diastolic relaxation, which is compatible with a lack of diastolic reserve. Documentation of diastolic dysfunction as a cause of weaning failure is critical, as it may require specific management (especially vasodilators to blunt the hypertensive response to the weaning cardiovascular stress).




late diastolic velocity measured using pulsed-wave Doppler transmitral flow


tissue Doppler late diastolic wave velocities at the lateral mitral valve annulus


automated weaning system


B-type natriuretic peptide


early diastolic velocity measured using pulsed-wave Doppler transmitral flow


tissue Doppler early diastolic wave velocities at the lateral mitral valve annulus


intensive care unit


left ventricle


left ventricle ejection fraction


positive end-expiratory pressure


tissue Doppler peak systolic wave velocity at the lateral mitral valve annulus


peripheral oxygen saturation


spontaneous breathing trial


Authors’ contributions

AMD have full access to all data and take responsibility for the integrity of the data and the accuracy of the data analysis. FRC, EV, LB and AMD contributed to initial study design, data analysis and interpretation, drafting of the manuscript, critical revisions for intellectual content, and final approval of the version to be published. AB contributed to data analysis and interpretation, drafting and critical revisions of the manuscript, and final approval of the version to be published. All authors read and approved the final manuscript

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

Clinical datasets are available from the corresponding author on personal demand.

Ethics approval and consent to participate

The protocol was approved by our institution’s local ethics committee (Comité de Protection des Personnes Ile-de-France IX, Approval Number 06-035), and informed consent was signed by the patient or a close relative.

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Authors’ Affiliations

Service de Réanimation Médicale, DHU A-TVB, Hôpitaux Universitaires Henri Mondor, Assistance Publique – Hôpitaux de Paris, 51 Avenue du Maréchal de Lattre de Tassigny, 94010 Créteil Cedex, France
Servei de Medicina Intensiva, Hospital Verge de la Cinta, Tortosa, Tarragona, Spain
Groupe de Recherche Clinique CARMAS, Institut Mondor de Recherche Biomédicale, Faculté de Médecine de Créteil, Université Paris Est Créteil, 94010 Créteil, France
Service de Réanimation Polyvalente, Centre hospitalier Saint-Joseph Saint-Luc, Lyon, France
Keenan Research Centre and Critical Care Department, St Michael’s Hospital, Toronto, Canada
Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Canada


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