Fluid management with a simplified conservative protocol for the acute respiratory distress syndrome*

Colin K Grissom, Eliotte L Hirshberg, Justin B Dickerson, Samuel M Brown, Michael J Lanspa, Kathleen D Liu, David Schoenfeld, Mark Tidswell, R Duncan Hite, Peter Rock, Russell R Miller 3rd, Alan H Morris, National Heart Lung and Blood Institute Acute Respiratory Distress Syndrome Clinical Trials Network, L Hudson, S Gundel, C Hough, M Neff, K Sims, A Ungar, T Watkins, J Steingrub, M Tidswell, E Braden, L DeSouza, J Germain, C Kardos, D Kelley, L Kozikowski, S Ouellette, K Guntupalli, V Bandi, C Pope, C Ross, R Brower, H Fessler, D Hager, P Mendez-Tellez, D Needham, K Oakjones, J Sevransky, A Workneh, C Shanholtz, D Herr, H Howes, G Netzer, P Rock, A Sampaio, J Titus, P Sloane, T Beck, H Highfield, S King, B Lee, N Bolouri, H P Wiedemann, R W Ashton, D A Culver, T Frederick, J A Guzman, J J Komara Jr, A J Reddy, R Hejal, M Andrews, D Haney, A F Connors, S Lasalvia, J D Thornton, E L Warren, M Moss, E L Burnham, L Gray, J Maloney, M Mealer, I Douglas, K Overdier, K Thompson, R Wolken, S Frankel, J McKeehan, M L Warner, T Bost, C Higgins, K Hodgin, N MacIntyre, L Brown, C Cox, M Gentile, J Govert, N Knudsen, S Carson, L Chang, S Choudhury, W Hall, J Lanier, A P Wheeler, G R Bernard, M Hays, S Mogan, T Rice, R D Hite, K Bender, A Harvey, P E Morris, Mary Ragusky, P Wright, S Groce, J McLean, A Overton, J Truwit, K Enfield, M Marshall, A Morris, A Austin, S Barney, S Brown, J Ferguson, H Gallo, T Graydon, C Grissom, E Hirshberg, A Jephson, N Kumar, R Miller, D Murphy, J Orme, A Stowe, L Struck, F Thomas, D Ward, L Weaver, P Bailey, W Beninati, L Bezdijan, T Clemmer, S Rimkus, R Tanaka, C Lawton, D Hanselman, K Sundar, W Alward, C Bishop, D Eckley, T Hill, B Jensen, K Ludwig, D Nielsen, M Pearce, M A Matthay, C Calfee, B Daniel, M Eisner, O Garcia, K Kordesch, K Liu, N Shum, H Zhou, M W Peterson, J Blaauw, K Van Gundy, T Albertson, B Morrissey, E Vlastelin, R Hubmayr, D Brown, M Dubin, E Festic, O Gajic, R Hinds, S Holets, D Kor, A Lee, M Passe, G Simpson, J Wright, B de Boisblanc, A Antoine, D Charbonnet, J Hunt, P Lauto, A Marr, G Meyaski, C Romaine, R Tejedor, S Brierre, J Byrne, T Jagneaux, C LeBlanc, K Moreau, C Thomas, S Jain, D Taylor, L Seoane, C Hebert, J Thompson, F Simeone, J Fearon, D Schoenfeld, M Guha, E Hammond, N Lavery, P Lazar, R Morse, C Oldmixon, N Ringwood, E Smoot, B T Thompson, R Wilson, A Harabin, S Bredow, M Waclawiw, G Weinmann, Colin K Grissom, Eliotte L Hirshberg, Justin B Dickerson, Samuel M Brown, Michael J Lanspa, Kathleen D Liu, David Schoenfeld, Mark Tidswell, R Duncan Hite, Peter Rock, Russell R Miller 3rd, Alan H Morris, National Heart Lung and Blood Institute Acute Respiratory Distress Syndrome Clinical Trials Network, L Hudson, S Gundel, C Hough, M Neff, K Sims, A Ungar, T Watkins, J Steingrub, M Tidswell, E Braden, L DeSouza, J Germain, C Kardos, D Kelley, L Kozikowski, S Ouellette, K Guntupalli, V Bandi, C Pope, C Ross, R Brower, H Fessler, D Hager, P Mendez-Tellez, D Needham, K Oakjones, J Sevransky, A Workneh, C Shanholtz, D Herr, H Howes, G Netzer, P Rock, A Sampaio, J Titus, P Sloane, T Beck, H Highfield, S King, B Lee, N Bolouri, H P Wiedemann, R W Ashton, D A Culver, T Frederick, J A Guzman, J J Komara Jr, A J Reddy, R Hejal, M Andrews, D Haney, A F Connors, S Lasalvia, J D Thornton, E L Warren, M Moss, E L Burnham, L Gray, J Maloney, M Mealer, I Douglas, K Overdier, K Thompson, R Wolken, S Frankel, J McKeehan, M L Warner, T Bost, C Higgins, K Hodgin, N MacIntyre, L Brown, C Cox, M Gentile, J Govert, N Knudsen, S Carson, L Chang, S Choudhury, W Hall, J Lanier, A P Wheeler, G R Bernard, M Hays, S Mogan, T Rice, R D Hite, K Bender, A Harvey, P E Morris, Mary Ragusky, P Wright, S Groce, J McLean, A Overton, J Truwit, K Enfield, M Marshall, A Morris, A Austin, S Barney, S Brown, J Ferguson, H Gallo, T Graydon, C Grissom, E Hirshberg, A Jephson, N Kumar, R Miller, D Murphy, J Orme, A Stowe, L Struck, F Thomas, D Ward, L Weaver, P Bailey, W Beninati, L Bezdijan, T Clemmer, S Rimkus, R Tanaka, C Lawton, D Hanselman, K Sundar, W Alward, C Bishop, D Eckley, T Hill, B Jensen, K Ludwig, D Nielsen, M Pearce, M A Matthay, C Calfee, B Daniel, M Eisner, O Garcia, K Kordesch, K Liu, N Shum, H Zhou, M W Peterson, J Blaauw, K Van Gundy, T Albertson, B Morrissey, E Vlastelin, R Hubmayr, D Brown, M Dubin, E Festic, O Gajic, R Hinds, S Holets, D Kor, A Lee, M Passe, G Simpson, J Wright, B de Boisblanc, A Antoine, D Charbonnet, J Hunt, P Lauto, A Marr, G Meyaski, C Romaine, R Tejedor, S Brierre, J Byrne, T Jagneaux, C LeBlanc, K Moreau, C Thomas, S Jain, D Taylor, L Seoane, C Hebert, J Thompson, F Simeone, J Fearon, D Schoenfeld, M Guha, E Hammond, N Lavery, P Lazar, R Morse, C Oldmixon, N Ringwood, E Smoot, B T Thompson, R Wilson, A Harabin, S Bredow, M Waclawiw, G Weinmann

Abstract

Objectives: In the Fluid and Catheter Treatment Trial (FACTT) of the National Institutes of Health Acute Respiratory Distress Syndrome Network, a conservative fluid protocol (FACTT Conservative) resulted in a lower cumulative fluid balance and better outcomes than a liberal fluid protocol (FACTT Liberal). Subsequent Acute Respiratory Distress Syndrome Network studies used a simplified conservative fluid protocol (FACTT Lite). The objective of this study was to compare the performance of FACTT Lite, FACTT Conservative, and FACTT Liberal protocols.

Design: Retrospective comparison of FACTT Lite, FACTT Conservative, and FACTT Liberal. Primary outcome was cumulative fluid balance over 7 days. Secondary outcomes were 60-day adjusted mortality and ventilator-free days through day 28. Safety outcomes were prevalence of acute kidney injury and new shock.

Setting: ICUs of Acute Respiratory Distress Syndrome Network participating hospitals.

Patients: Five hundred three subjects managed with FACTT Conservative, 497 subjects managed with FACTT Liberal, and 1,124 subjects managed with FACTT Lite.

Interventions: Fluid management by protocol.

Measurements and main results: Cumulative fluid balance was 1,918 ± 323 mL in FACTT Lite, -136 ± 491 mL in FACTT Conservative, and 6,992 ± 502 mL in FACTT Liberal (p < 0.001). Mortality was not different between groups (24% in FACTT Lite, 25% in FACTT Conservative and Liberal, p = 0.84). Ventilator-free days in FACTT Lite (14.9 ± 0.3) were equivalent to FACTT Conservative (14.6 ± 0.5) (p = 0.61) and greater than in FACTT Liberal (12.1 ± 0.5, p < 0.001 vs Lite). Acute kidney injury prevalence was 58% in FACTT Lite and 57% in FACTT Conservative (p = 0.72). Prevalence of new shock in FACTT Lite (9%) was lower than in FACTT Conservative (13%) (p = 0.007 vs Lite) and similar to FACTT Liberal (11%) (p = 0.18 vs Lite).

Conclusions: FACTT Lite had a greater cumulative fluid balance than FACTT Conservative but had equivalent clinical and safety outcomes. FACTT Lite is an alternative to FACTT Conservative for fluid management in Acute Respiratory Distress Syndrome.

Conflict of interest statement

The remaining authors have disclosed that they do not have any potential conflicts of interest.

Figures

Figure 1
Figure 1
A, Cumulative fluid balance for all subjects: Cumulative fluid balance over study days 1 to 7 for the three cohorts. The conservative and liberal fluid protocol groups are from the Fluid and Catheter Treatment Trial (FACTT) of the Acute Respiratory Distress Syndrome (ARDS) Network and are referred to as “FACTT Conservative” and “FACTT Liberal.” The FACTT Lite group is from subsequent ARDS Network studies that used a simplified fluid conservative protocol. Both the FACTT Conservative and FACTT Lite groups had significantly less cumulative fluid balance compared with the FACTT Liberal group (p < 0.001). The FACTT Lite group had significantly greater cumulative fluid balance over 7 days compared with the FACTT Conservative group (p < 0.001). The error bars indicate 95% CIs for cumulative fluid balance on each study day for each group. The number of subjects included in the analysis for each day for the FACTT Conservative and Liberal groups was previously reported (1). The number of subjects included in the analysis for each day for the FACTT Lite group is as follows:n = 1,120 (day 1), n = 1,102 (day 2), n = 1,069 (day 3), n= 1,008 (day 4), n = 921 (day 5),n = 846 (day 6), and n = 773 (day 7). B, Cumulative fluid balance for subjects without baseline shock: Cumulative fluid balance over study days 1 to 7 is shown for subjects without baseline shock in each of the groups. Both the FACTT Conservative and FACTT Lite groups without baseline shock had significantly less cumulative fluid balance compared with the FACTT Liberal group without baseline shock (p < 0.001). The FACTT Lite group had a similar cumulative fluid balance over 7 days compared with the FACTT Conservative group (p = 0.06). The error bars indicate 95% CIs for cumulative fluid balance on each study day for each group.

Source: PubMed

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