Index
Module 18 • Pulmonology
Pulmonary Disorders I
31%
Data Tables
Pulmonary Disorders I
Grace E. Benanti ~4 min read Module 18 of 20
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Pulmonary Disorders I

d.The 2019 clinical practice guidelines state that ECMO should be considered in patients with severe

ARDS or more specifically with Pao2/Fio2 ratios less than 80 mm Hg and/or in patients with elevated

plateau pressures despite optimizing PEEP, neuromuscular blocking agents (NMBAs), and prone

positioning (BMJ Open Respir Res 2019;6:e000420; Ann Intensive Care 2019;9:69). The 2023

ESICM clinical practice guidelines recommend ECMO use in severe ARDS (as defined in EOLIA

trial eligibility criteria) at an established ECMO center (strong recommendation; moderate level

of evidence in favor) (Intensive Care Med 2023;49:727-59). The 2024 American Thoracic Society

(ATS) guidelines suggest the use of veno-venous ECMO (VV ECMO) in patients early in their

course (less than 7 days) with reversible etiologies of respiratory failure and very severe hypoxemia

(Paco2/Fio2 ratio less than 80 mm Hg) or hypercapnia (pH less than 7.25 with Paco2 60 mm Hg) after

optimizing conventional treatments (Am J Respir Crit Care Med. 2024;209(1):24-36).

Concomitant VV ECMO and prone positioning

A meta-analysis (n=13 studies including only 1 randomized clinical trial) evaluated the clinical

impact of prone positioning and VV ECMO in ARDS compared with VV ECMO alone

(Intensive Care Med 2022;48:270-80).

ii.

Pooled data showed combination VV ECMO and prone positioning 28-day survival was

significantly improved (n=10 studies; RR 1.31; 95% CI, 1.21โ€“1.41). Also, combination therapy

was also associated with significantly improved ICU and in-hospital survival as well as overall

60- and 90-day survival.

iii.

A priori subgroup analyses found improved 28-day survival with concomitant prone positioning

and VV ECMO in both patient cohorts with COVID-19 ARDS patients (n=6 studies; RR 1.32;

95% CI, 1.15โ€“1.50) and ARDS patients without COVID-19 (n=4 studies; RR 1.30; 95% CI,

1.19โ€“1.43).

iv.

Pooled data also showed significant improvements in ventilator-free days at day 28 (n=9 studies;

RR โˆ’1.29; 95% CI, โˆ’2.39 to โˆ’0.19) with prone positioning and VV ECMO over ECMO alone

in ARDS patients

No major complications were reported with either study group.

4

Fluid management

The FACTT trial compared 2 optimal fluid management strategies (conservative (CVP less than

4 mm Hg) and liberal (CVP 10โ€“14 mm Hg) in patients with ARDS and hemodynamic stability

(not requiring vasopressors or MAP greater than 60 mm Hg) (N Engl J Med 2006;354:2564-75).

Diuretics were withheld in patients with shock but were administered according to study protocol

once patients had established hemodynamic stability (discontinuation of vasopressors or MAP

greater than 60 mm Hg). Although 60-day mortality did not differ (p=0.30), the conservative

compared with the liberal strategy was associated with increased ventilator-free days (14.6 ยฑ 0.5 vs.

12.1 ยฑ 0.5, p<0.001) and ICU-free days (28 days) (13.4 ยฑ 0.4 vs. 11.2 ยฑ 0.4, p<0.001).

Fluid strategies were compared (conservative, liberal, and simplified conservative) in a retrospective

comparison among protocols pertaining to ARDS (Crit Care Med 2015;43:288-295). The FACTT

Lite protocol provides fluid management recommendations pertaining to the administration of

furosemide or fluids as well as monitoring without intervention-based CVP, MAP, urinary output,

and pulmonary artery occlusion pressure (optional) (Table 3). No significant differences were found

between the FACTT Lite and the FACTT conservative strategies for ventilator-free days (14.9 vs.

14.6, respectively; p=0.61), ICU-free days (14.4 vs. 13.4, respectively; p=0.054), or death at 60 days

(22% vs. 25%, respectively; p=0.15). Conversely, the FACTT Lite approach had improved outcomes

(ventilator-free, ICU-days, and 60-day mortality) compared with the FACTT liberal approach.

A meta-analysis evaluated the safety and efficacy of conservative versus liberal fluid strategies in

ICU patients with either ARDS or sepsis (Intensive Care Med 2017;43:155-70). No differences in

mortality were found between study groups in the ARDS subgroup (n=5 studies; RR 0.91; 95% CI,

0.77โ€“1.07) or the mixed ARDS and sepsis subgroup (n=2 studies; RR 0.95; 95% CI, 0.80โ€“1.14).

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