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Comparison of the effects of albumin and crystalloid on mortality in adult patients with severe sepsis and septic shock: a meta-analysis of randomized clinical trials

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Critical Care201418:702

https://doi.org/10.1186/s13054-014-0702-y

©  Xu et al.; licensee BioMed Central. 2014

  • Received: 7 August 2014
  • Accepted: 28 November 2014
  • Published:

Abstract

Introduction

The aim of this study was to examine whether albumin reduced mortality when employed for the resuscitation of adult patients with severe sepsis and septic shock compared with crystalloid by meta-analysis.

Methods

We searched for and gathered data from MEDLINE, Elsevier, Cochrane Central Register of Controlled Trials and Web of Science databases. Studies were eligible if they compared the effects of albumin versus crystalloid therapy on mortality in adult patients with severe sepsis and septic shock. Two reviewers extracted data independently. Disagreements were resolved by discussion with other two reviewers until a consensus was achieved. Data including mortality, sample size of the patients with severe sepsis, sample size of the patients with septic shock and resuscitation endpoints were extracted. Data were analyzed by the methods recommended by the Cochrane Collaboration Review Manager 4.2 software.

Results

A total of 5,534 records were identified through the initial search. Five studies compared albumin with crystalloid. In total, 3,658 severe sepsis and 2,180 septic shock patients were included in the meta-analysis. The heterogeneity was determined to be non-significant (P = 0.86, I2 = 0%). Compared with crystalloid, a trend toward reduced 90-day mortality was observed in severe sepsis patients resuscitated with albumin (odds ratio (OR) 0.88; 95% CI, 0.76 to 1.01; P = 0.08). However, the use of albumin for resuscitation significantly decreased 90-day mortality in septic shock patients (OR 0.81; 95% CI, 0.67 to 0.97; P = 0.03). Compared with saline, the use of albumin for resuscitation slightly improved outcome in severe sepsis patients (OR 0.81; 95% CI, 0.64 to 1.08; P = 0.09).

Conclusions

In this meta-analysis, a trend toward reduced 90-day mortality was observed in severe sepsis patients resuscitated with albumin compared with crystalloid and saline. Moreover, the 90-day mortality of patients with septic shock decreased significantly.

Keywords

  • Septic Shock
  • Severe Sepsis
  • Septic Shock Patient
  • Crystalloid Solution
  • Severe Sepsis Patient

Introduction

Severe sepsis and septic shock are major causes of death in critically ill patients, and fluid management can resuscitate patients in these conditions. Early adequate volume expansion is emphasized as the key elements to be focused on saving lives [1]-[3]. With the advantage of restoring effective volume and maintaining colloid osmotic pressure, albumin is considered to be administered in addition to crystalloid in the initial fluid management of patients with severe sepsis and septic shock [4].

Whether albumin is associated with reduced mortality in the resuscitation of severe sepsis and septic shock compared with crystalloid is a matter of debate. The predefined subgroup analysis of the Saline versus Albumin Fluid Evaluation (SAFE) study suggested albumin potentially resulted in lower mortality in patients with severe sepsis [5],[6]. However, previous meta-analyses that focused on sepsis patients drew nonequivalent results [7],[8]. The large randomized controlled trial, the Albumin Italian Outcome Sepsis (ALBIOS) study also reported contradictory results that albumin provided no improvement at day 28 in patients with severe sepsis [9], while the post hoc analysis of the septic shock subgroup supported a survival benefit to albumin, given the target patient population in this meta-analysis.

As a result of few investigators emphasizing the use of albumin in patients with severe sepsis, let alone septic shock, a meta-analysis is needed to address the outcome of albumin as fluid therapy. Furthermore, as the most commonly used crystalloid, no study stressed the role of albumin when compared with saline in severe sepsis patients.

Our goal was to examine whether albumin reduced mortality when employed in the resuscitation of adult patients with severe sepsis and septic shock compared with crystalloid solutions and saline.

Material and methods

Search strategy for identification of relevant studies

A search of the following databases was conducted: Medline, Elsevier, Cochrane Central Register of Controlled Trials and Web of Science databases. The following keywords were used as searching terms: ‘albumin’ or ‘serum albumin’ or ‘albumin replacement’ or ‘colloid’ or ‘crystalloid’ or ‘crystalloid solution’ or ‘saline’ or ‘normal saline’ or ‘Ringer's solution’ or ‘bicarbonated Ringer’s solution’ or ‘lactated Ringer’s solution’ or ‘isotonic solution’ or ‘hypertonic saline’ and ‘sepsis’ or ‘severe sepsis’ or ‘septic shock’ or ‘shock’ or ‘critical ill’ or ‘critical illness’ or ‘intensive care units’ or ‘intensive care’ or ‘critical care’ or ‘ICU’. No language restrictions were placed on the search. All databases were searched for articles published from inception until March 31, 2014. Additional files and supplementary appendices of the relevant articles were also reviewed. Detailed search strategies are shown in Additional file 1: Search strategy.

Study selection

One reviewer screened the search results, and the full-text manuscripts of all potentially eligible studies were acquired. Then, all of the articles were reviewed by two reviewers independently in accordance with the inclusion criteria. Disagreements between the two reviewers were resolved by consensus and discussion including a third reviewer. When the ‘same author’ or ‘same data’ issue was confronted with, the latest published study was included.

Inclusion and exclusion criteria

We included trials with the following features:
  1. 1.

    Type of trials: randomized controlled clinical and parallel trials.

     
  2. 2.

    Population: trials including adult population with severe sepsis. Severe sepsis was defined as sepsis plus sepsis-induced organ dysfunction or tissue hypoperfusion [4].

     
  3. 3.

    Intervention: patients submitted to albumin for fluid therapy.

     
  4. 4.

    Comparison: crystalloid for fluid therapy.

     
  5. 5.

    Outcome: the primary outcome was all-cause mortality, including 28-day mortality, 90-day mortality or mortality at other time points.

     
Trials with the following features were excluded:
  1. 1.

    They were not published in English or Chinese.

     
  2. 2.

    They were not published as original articles.

     
  3. 3.

    They did not use adult patients.

     
  4. 4.

    They did not compare albumin with crystalloid.

     
  5. 5.

    They included no data on mortality in patients with severe sepsis.

     
  6. 6.

    Full-text articles were not available.

     

Quality assessment

The quality of each article was assessed by two reviewers independently. Disagreements were resolved by consulting a third reviewer. The five-point Jadad scale was calculated to assess the quality of the trial [10]. This scale includes the method of randomization, blinding, and loss to follow-up. In addition, sequences generation, allocation concealment, incomplete outcome data, selective reporting and other bias were also inspected to assess the risk of bias [11]. The latter was reported as low risk, unclear risk, or high risk for each trial. Low risk was defined as low risk of bias in all domains. Unclear risk was defined as unclear risk of bias in at least one domain with no high risk of bias domains. High risk was defined as high risk of bias in one or more domains. The publication bias was assessed by funnel plot techniques.

Data extraction and management

Using a data extraction table, two reviewers independently extracted data. Disagreements were resolved by discussion with other two reviewers until a consensus was achieved. Then, data were proofread by another reviewer. Mortality data, including 28-day or 90-day mortality, were recorded during the data extraction. When 28-day and 90-day morality values were both published in the article, the longest complete follow-up was preferentially used for evaluation in the meta-analysis. However, when 28-day or 90-day mortality values were not presented, ICU or hospital mortality or mortality at other time points were recorded. Other data including the population of each trial, sample size of the trial and patients with severe sepsis, and resuscitation endpoints were extracted. If there was insufficient information in the publications, the contact to the authors was performed.

For studies including a subgroup of septic shock patients, the sample size of septic shock patients and the number of non-survivals were extracted.

Statistical analysis

Data were analyzed by Review Manager 4.2 (The Nordic Cochrane Center, Rigshospitalet, Copenhagen, Denmark). The pooled odds ratio (OR) for dichotomous data and mean differences for continuous data with 95% confidence intervals (CIs) were calculated. The statistical heterogeneity of the data was explored and quantified using the Mantel-Haenszel chi-square test and the I2 test. Heterogeneity was predefined as P <0.05 with the Mantel-Haenszel chi-square test or an I2 value >50%. The random-effects model was used if heterogeneity was observed; otherwise, the fixed-effects model was used. P <0.05 was considered statistically significant.

Results

Study location and selection

A total of 5,534 records were identified through the initial search, and 2,330 records were removed as duplicates. The remainder of the 3,204 records was screened. After assessment of the titles and abstracts, 2,637 articles were excluded as not relevant, and 519 articles were excluded for including pediatric patients. In total, 48 potentially eligible studies were identified for inclusion. Six studies [6],[9],[12]-[15] compared albumin with crystalloid solutions. Of the included trials, two trials [12],[13] were performed and published by the same group in adjacent years. The above factors as well as the similar sample size and mortality rates provided reasonable doubt that the enrolled patients might be the same, and the ‘same author’ or ‘same data’ issue was confronted. Therefore, the latest published study was included, and the trial by Haupt et al. [12] was excluded. Finally, 3,658 severe sepsis and 2,180 septic shock patients were included in the meta-analysis.

Detailed excluded articles are shown in Additional file 2: Excluded articles. The flow diagram is presented in Figure 1.
Figure 1
Figure 1

Flow diagram of the search process and study selection.

Study characteristics

The characteristics of the included studies are shown in Table S1 in Additional file 3. In total, 4 or 5% albumin was used for fluid resuscitation in three trials [6],[13],[15], and 20% albumin was employed for volume expansion in one trial [9]. The remaining one [14] included both concentrations. Normal saline was used as crystalloid in two trials [6],[13], and Ringer’s lactate solution was used as crystalloid in one trial [15]. The remaining two trials [9],[14] included a broad variety of crystalloid products. Mortality was explored for more than one time point, including 28-day mortality and 90-day mortality rates, in two articles, the CRISTAL study [14] and the ALBIOS study [9]. Only 28-day mortality values were published in the SAFE study [6]. The hospital mortality was published in the remaining two trials [13],[15]. Quality assessments of the included studies are shown in Table 1.
Table 1

Quality assessment of the included studies

Authors

Sequences generation

Allocation concealment

Blinding of participants and researchers

Blinding of outcome assessment

Incomplete outcome data

Selective reporting

Other bias

Overall risk of bias

Rackow et al. [13]

Unclear

High

High

High

Low

Unclear

Low

High

Metildi et al. [15]

Low

High

High

High

Low

Unclear

Low

High

The SAFE study investigators [6]

Low

Low

Low

Low

Low

Unclear

Low

Unclear

The CRISTAL study investigators [14]

Low

Low

High

Low

Low

Unclear

Low

High

The ALBIOS study investigators [9]

Low

Low

High

High

Low

Low

Low

High

Sequence generation: Rackow et al. [13] used predetermined randomization schedule. Metildi et al. [15] used random numbers. SAFE [6] used a central minimization algorithm. CRISTAL [14] and ALBIOS [9] used computer-generated sequences. Allocation concealment: no detailed allocation concealment was reported by Metildi et al. [15]. Rackow et al. [13] used a predetermined randomization schedule. SAFE [6] used a central minimization algorithm. CRISTAL [14] used sealed envelopes. ALBIOS [9] used a blinded assignment sequence. Blinding: blinding was not reported in Rackow et al. [13], Metildi et al. [15] and the ALBIOS [9] trial. Blinding was performed in the SAFE [6] trial. Data collection members but not researchers were blinded in the CRISTAL [14] trial. Incomplete outcome data: all trials described the follow-up. Selective reporting: the study protocol of ALBIOS [9] was obtained. Other bias: no evidence of other sources of bias.

The impact on mortality in severe sepsis patients

The effects of resuscitation with albumin on 90-day mortality in patients with severe sepsis was estimated from five trials (Figure 2), and the heterogeneity was also determined to be non-significant (P = 0.86, I2 = 0%). The longest complete follow-up mortality rates of all of the trials were evaluated in the meta-analysis. In two articles [9],[14], mortality rates were explored for more than one time point, and 90-day mortality rates were analyzed for these two trials. A trend toward reduced 90-day mortality was observed in severe sepsis patients resuscitated with albumin compared with crystalloid. However, the finding was not statistically significant (OR 0.88; 95% CI, 0.76 to 1.01; P = 0.08).
Figure 2
Figure 2

The effect of albumin on 90-day mortality in patients with severe sepsis.

The 28-day mortality was also evaluated (Figure 3). Compared with crystalloid, albumin displayed no beneficial effect on 28-day mortality in severe sepsis patients (OR 0.93; 95% CI, 0.80 to 1.08; P = 0.32).
Figure 3
Figure 3

The effect of albumin on 28-day and hospital mortality in patients with severe sepsis.

The impact on 90-day mortality in patients with septic shock

The impact of albumin on 90-day mortality in patients with septic shock was estimated from five trials (Figure 4), the heterogeneity was determined to be non-significant (P = 0.74, I2 = 0%). The longest complete follow-up mortality rates of all the trials were evaluated, including the 90-day mortality values from the CRISTAL study [14] and the ALBIOS study [9], 28-day mortality values from the SAFE study [6] and hospital mortality from the Rackow et al. [13] studies. Compared with crystalloid, the use of albumin for resuscitation significantly decreased the 90-day mortality in septic shock patients (OR 0.81; 95% CI, 0.67 to 0.97; P = 0.03). The studies of septic shock patients included in the meta-analysis are shown in Table 2.
Figure 4
Figure 4

The effect of albumin on 90-day mortality in patients with septic shock.

Table 2

Patients with septic shock included in the meta-analysis

Authors

Year

Definition of septic shock

Sample size of septic shock

Non-survival of septic shock

Non-survival of albumin group with septic shock (events/total)

Non-survival of crystalloid group with septic shock (events/total)

Rackow et al. [13]

1983

Patients were considered septic shock if (1) blood cultures were positive and/or an infected focus was identified, (2) systolic intra-arterial pressure of less than 90 mmHg, or a cardiac index less than 2.2 L/min.m2, or a serum arterial lactate greater than 18 mg/dl, and pulmonary artery wedge pressure less than 15 mmHg.

18

11

5/7

3/4

Metildi et al. [15]

1984

N/A

N/A

N/A

N/A

N/A

The SAFE study investigators [6]

2010

Septic shock was defined by the presence of a defined focus of infection and at least two of the four systemic inflammatory response syndrome criteria and infection-related cardiovascular sequential organ failure assessment score of 3 or 4.

438

160

70/209

90/229

The CRISTAL study investigators [14]

2013

Septic shock was defined by sepsis induced acute hypovolemia. Hypovolemia was defined by the combination of (1) hypotension: systolic arterial pressure of less than 90 mm Hg, mean arterial pressure of less than 60 mm Hg, orthostatic hypotension, or a delta pulse pressure of 13% or higher; (2) evidence for low filling pressures and low cardiac index as assessed either invasively or noninvasively; and (3) signs of tissue hypoperfusion or hypoxia, including at least two of the following clinical symptoms: a Glasgow coma scale score of less than 12, mottled skin, urinary output of less than 25 mL/h, or capillary refilling time of 3 seconds or longer; and arterial lactate levels higher than 2 mmol/L, blood urea nitrogen higher than 56 mg/dL, or a fractional excretion of sodium of less than 1%.

1553

441 (28-day) 538 (90-day)

19/59 (28-day) 22/59 (90-day)

157/557 (28-day) 197/557 (90-day)

The ALBIOS study investigators [9]

2014

Septic shock was defined by the presence of a defined focus of infection and at least two of the four systemic inflammatory response syndrome criteria and infection-related cardiovascular sequential organ failure assessment score of 3 or 4.

1121

524 (90-day)

243/558 (90-day)

281/563 (90-day)

N/A, not applicable. No detailed description of hemodynamic instability in Metildi et al. [15] trial.

Albumin versus saline for the outcome in patients with severe sepsis

The impact of albumin on mortality in patients with severe sepsis compared with saline was estimated from two trials [6],[13] (Figure 5), the heterogeneity was determined to be non-significant (P = 0.99, I2 = 0%). Compared with saline, the use of albumin for resuscitation slightly improved the outcome in severe sepsis patients (OR 0.81; 95% CI, 0.64 to 1.03; P = 0.09); however, the results were not statistically significant.
Figure 5
Figure 5

Albumin versus saline in the resuscitation of patients with severe sepsis.

Discussion

Although previous meta-analyses [7],[8],[16]-[19] have explored the impact of albumin in resuscitating critically ill and sepsis patients, few investigators focused on the use of albumin in patients with severe sepsis, especially with septic shock. Our analysis was the only meta-analysis focusing totally on severe sepsis and septic shock, which are the most important and specific subset of sepsis, and for that the analysis separated from previous meta-analyses studies. Furthermore, to our knowledge, no meta-analysis has compared albumin with saline in severe sepsis patients up to now. In this meta-analysis, the effect of albumin as a resuscitation fluid on mortality in severe sepsis and septic shock was investigated. The results suggested a trend toward reduced 90-day mortality in severe sepsis patients resuscitated with albumin compared with crystalloid and saline. Moreover, the use of albumin for resuscitation significantly decreased the 90-day mortality in septic shock patients.

A meta-analysis is imminent for stressing the role of albumin in resuscitating patients with severe sepsis and septic shock. As the major and specific subsets of sepsis, it was reported the mortality of severe sepsis without shock was 14 to 30%, while in septic shock, the mortality rate raised to 22 to 40% [20]. Therefore, multiple randomized controlled trials have attempted to identify effective treatments to improve the survival of patients with severe sepsis and septic shock, rather than sepsis. However, the latest ALBIOS study published a disappointing result. To determine whether severe sepsis and septic shock patient benefit from the use of albumin for resuscitation compared with crystalloid, and to explore a better solution to improve the outcome, we conducted this meta-analysis to observe the effect of albumin on mortality in the resuscitation of severe sepsis and septic shock patients.

Our results were not equivalent with the recent study published by Patel et al. [8], which showed albumin was ineffective at reducing all-cause mortality. The differences come from: the variant target study population, the more comprehensive included studies, the distinct comparison, the dissimilar results and conclusion. As a result, our manuscript might add new evidence to help guide albumin as an optimal resuscitation fluid for septic shock.

Although the study published by Patel et al. did assess the role of albumin in sepsis of any severity, they did not highlight its role in severe sepsis and septic shock. As a result, the study lacked the detailed description of the characteristics of the included studies. Moreover, the data of septic shock from some important studies (for example the SAFE study) were incomplete owing to the unsuccessful data requests.

The comparison was goals-explicit in our study. As the unsolved, fundamental challenge in resuscitating severe sepsis and septic shock, it is recommended that albumin should be added to the initial resuscitation with crystalloid, and the application of hydroxyethyl starches was against given their role in renal injury [21],[22]. However, there is concern about which agent would improve the outcome of the patients with severe sepsis and septic shock, especially the comparison between albumin and crystalloid. As the most commonly used crystalloid, we also compare albumin with saline.

Compared with the review published by Patel et al., our meta-analysis included more comprehensive studies, which might result a more accurate conclusion. There are four studies included in the British Medical Journal review comparing albumin with crystalloid in patients with septic shock, and half of the included studies were confronted with the ‘same author’ or ‘same data’ issue. Moreover, the data of septic shock in the well-powered SAFE study are not included.

Various reasonable explanations are available for the encouraging results using albumin in septic shock patients. Fluid expansion is a life-saving management for resuscitating septic shock patients. The goal of fluid resuscitation is to expand the intravascular space and restore effective volume. However, fluid often moves into the extravascular space and induces tissue edema in septic patients. While exploiting oncotic pressure gradients [23] to counteract the movement [24], albumin provides intravascular volume expansion more effectively and restores the fluid in the intravascular space. All these above factors affect fluid resuscitation in a more timely and efficient manner. In addition, albumin is a key transporter and binder of active molecules [25],[26]. Albumin also acts as a radical-scavenging antioxidant [27], its role on inhibition of platelet aggregation [28] and maintenance of the capillary membrane permeability [29] also takes a great part in being beneficial to outcome.

This meta-analysis has some limitations that should be noted. First, only five trials were included, and two of these trials had small sample sizes. Second, some included trials were subgroups of large randomized controlled studies with variable methodological quality. Thus, the results are potentially overstated [30]. In addition, the endpoint was different in each study. Some of the trials included both 28-day and 90-day mortality values, whereas one trial only reported 28-day mortality. The remaining trials reported hospital mortality. The mortality rates obtained from various time points may influence the overall results. Finally, the concentration of albumin used in each study was different, and contained two colloid families, the hypooncotic and hyperoncotic albumin. The differences in formulation potentially do not influence the results in the same manner.

There are two other highly anticipated ongoing studies of albumin in patients with septic shock. The Five Percent Albumin vs. Normal Saline as Fluid Resuscitation Strategies for the Management of Early Suspected Septic Shock (NCT00819416) study has enrolled 47 patients up to now. The Early Albumin Resuscitation during Septic Shock (NCT00327704) study completed enrollment of 794 patients in January 2011 though it has not been updated for three years. All the results of the studies above will contribute significantly more to further guidance of the optimal resuscitation fluid for septic shock.

Conclusions

In this meta-analysis, the results suggested a trend toward reduced 90-day mortality in severe sepsis patients resuscitated with albumin compared with crystalloid and saline. Moreover, the 90-day mortality of septic shock patients decreased significantly. Further large randomized controlled trials are necessary to determine the potential benefits of albumin in patients with severe sepsis and septic shock.

Key messages

  • Compared with crystalloid, a trend toward reduced 90-day mortality was observed in adults with severe sepsis resuscitated with albumin.

  • Compared with crystalloid, the use of albumin for resuscitation significantly decreased 90-day mortality in adult septic shock patients.

  • Compared with saline, the use of albumin for resuscitation slightly improved the outcome in adult severe sepsis patients.

Additional files

Abbreviations

ALBIOS study: 

the Albumin Italian Outcome Sepsis study

CI: 

confidence interval

OR: 

odds ratio

SAFE study: 

the Saline versus Albumin Fluid Evaluation study

Declarations

Acknowledgements

The authors thank Prof. Simon Finfer for providing data from the SAFE study.

This work is partially supported by grants from the National Natural Science Foundation of China (81070049, 81000828, 81170057).

Authors’ Affiliations

(1)
Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjiaqiao Rd, Nanjing, 210009, P.R. China

References

  1. Rivers E, Nguyen B, Havstad S, Ressler J, Muzzin A, Knoblich B, Peterson E, Tomlanovich M, Early Goal-Directed Therapy Collaborative Group: Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med. 2001, 345: 1368-1377. 10.1056/NEJMoa010307.View ArticleGoogle Scholar
  2. Yealy DM, Kellum JA, Huang DT, Barnato AE, Weissfeld LA, Pike F, Terndrup T, Wang HE, Hou PC, LoVecchio F, Filbin MR, Shapiro NI, Augus DC, ProCESS Investigators: A randomized trial of protocol-based care for early septic shock. N Engl J Med. 2014, 370: 1683-1693. 10.1056/NEJMoa1401602.View ArticleGoogle Scholar
  3. Lilly CM: The ProCESS trial - a new era of sepsis management. N Engl J Med. 2014, 370: 1750-1751. 10.1056/NEJMe1402564.View ArticleGoogle Scholar
  4. Dellinger RP, Levy MM, Rhodes A, Annane D, Gerlach H, Opal SM, Sevransky JE, Sprung CL, Douglas IS, Jaeschke R, Osborn TM, Nunnally ME, Townsend SR, Reinhart K, Kleinpell RM, Angus DC, Deutschman CS, Machado FR, Rubenfeld GD, Webb SA, Beale RJ, Vincent JL, Moreno R, Surviving Sepsis Campaign Guidelines Committee including the Pediatric Subgroup: Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock, 2012. Crit Care Med. 2013, 41: 580-637. 10.1097/CCM.0b013e31827e83af.View ArticleGoogle Scholar
  5. Finfer S, Bellomo R, Boyce N, French J, Myburgh J, Norton R, SAFE Study Investigators: A comparison of albumin and saline for fluid resuscitation in the intensive care unit. N Engl J Med. 2004, 350: 2247-2256. 10.1056/NEJMoa040232.View ArticleGoogle Scholar
  6. Finfer S, McEvoy S, Bellomo R, McArthur C, Myburgh J, Norton R, SAFE Study Investigators: Impact of albumin compared to saline on organ function and mortality of patients with severe sepsis. Intensive Care Med. 2011, 37: 86-96. 10.1007/s00134-010-2081-4.View ArticleGoogle Scholar
  7. Delaney AP, Dan A, McCaffrey J, Finfer S: The role of albumin as a resuscitation fluid for patients with sepsis: a systematic review and meta-analysis. Crit Care Med. 2011, 39: 386-391. 10.1097/CCM.0b013e3181ffe217.View ArticleGoogle Scholar
  8. Patel A, Laffan MA, Waheed U, Brett SJ: Randomised trials of human albumin for adults with sepsis: systematic review and meta-analysis with trial sequential analysis of all-cause mortality. BMJ. 2014, 349: g4561-10.1136/bmj.g4561.View ArticleGoogle Scholar
  9. Caironi P, Tognoni G, Masson S, Fumagalli R, Pesenti A, Romero M, Fanizza C, Caspani L, Faenza S, Grasselli G, Iapichino G, Antonelli M, Parrini V, Fiore G, Latini R, Gattinoni L, ALBIOS Study Investigators: Albumin replacement in patients with severe sepsis or septic shock. N Engl J Med. 2014, 370: 1412-1421. 10.1056/NEJMoa1305727.View ArticleGoogle Scholar
  10. Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJ, Gavaghan DJ, McQuay HJ: Assessing the quality of reports of randomized clinical trials: is blinding necessary. Control Clin Trials. 1996, 17: 1-12. 10.1016/0197-2456(95)00134-4.View ArticleGoogle Scholar
  11. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, Savovic J, Schulz KF, Weeks L, Sterne JA, Cochrane Bias Methods Group, Cochrane Statistical Methods Group: The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011, 343: d5928-10.1136/bmj.d5928.View ArticleGoogle Scholar
  12. Haupt MT, Rackow EC: Colloid osmotic pressure and fluid resuscitation with hetastarch, albumin, and saline solutions. Crit Care Med. 1982, 10: 159-162. 10.1097/00003246-198203000-00004.View ArticleGoogle Scholar
  13. Rackow EC, Falk JL, Fein IA, Siegel JS, Packman MI, Haupt MT, Kaufman BS, Putnam D: Fluid resuscitation in circulatory shock: a comparison of the cardiorespiratory effects of albumin, hetastarch, and saline solutions in patients with hypovolemic and septic shock. Crit Care Med. 1983, 11: 839-850. 10.1097/00003246-198311000-00001.View ArticleGoogle Scholar
  14. Annane D, Siami S, Jaber S, Martin C, Elatrous S, Declere AD, Preiser JC, Outin H, Troche G, Charpentier C, Trouillet JL, Kimmoun A, Forceville X, Darmon M, Lesur O, Reignier J, Abroug F, Berger P, Clech C, Cousson J, Thibault L, Chevret S, CRISTAL Investigators: Effects of fluid resuscitation with colloids vs crystalloids on mortality in critically ill patients presenting with hypovolemic shock: the CRISTAL randomized trial. JAMA. 2013, 310: 1809-1817. 10.1001/jama.2013.280502.View ArticleGoogle Scholar
  15. Metildi LA, Shackford SR, Virgilio RW, Peters RM: Crystalloid versus colloid in fluid resuscitation of patients with severe pulmonary insufficiency. Surg Gynecol Obstet. 1984, 158: 207-212.Google Scholar
  16. Perel P, Roberts I, Ker K: Colloids versus crystalloids for fluid resuscitation in critically ill patients. Cochrane Database Syst Rev. 2013, 2: CD000567-Google Scholar
  17. Vincent JL, Dubois MJ, Navickis RJ, Wilkes MM: Hypoalbuminemia in acute illness: is there a rationale for intervention? A meta-analysis of cohort studies and controlled trials. Ann Surg. 2003, 237: 319-334.Google Scholar
  18. Wilkes MM, Navickis RJ: Patient survival after human albumin administration. A meta-analysis of randomized, controlled trials. Ann Intern Med. 2001, 135: 149-164. 10.7326/0003-4819-135-3-200108070-00007.View ArticleGoogle Scholar
  19. Cochrane Injuries Group Albumin Reviewers: Human albumin administration in critically ill patients: systematic review of randomised controlled trials. BMJ. 1998, 317: 235-240. 10.1136/bmj.317.7153.235.View ArticleGoogle Scholar
  20. Kaukonen KM, Bailey M, Suzuki S, Pilcher D, Bellomo R: Mortality related to severe sepsis and septic shock among critically ill patients in Australia and New Zealand, 2000–2012. JAMA. 2014, 311: 1308-1316. 10.1001/jama.2014.2637.View ArticleGoogle Scholar
  21. Myburgh JA, Finfer S, Bellomo R, Billot L, Cass A, Gattas D, Glass P, Lipman J, Liu B, McArthur C, McGuinness S, Rajbhandari D, Taylor CB, Webb SA, CHEST Investigators, Australian and New Zealand Intensive Care Society Clinical Trials Group: Hydroxyethyl starch or saline for fluid resuscitation in intensive care. N Engl J Med. 2012, 367: 1901-1911. 10.1056/NEJMoa1209759.View ArticleGoogle Scholar
  22. Brunkhorst FM, Engel C, Bloos F, Meier-Hellmann A, Ragaller M, Weiler N, Moerer O, Gruendling M, Oppert M, Grond S, Olthoff D, Jaschinski U, John S, Rossaint R, Welte T, Schaefer M, Kern P, Kuhnt E, Kiehntopf M, Hartog C, Natanson C, Loeffler M, Reinhart K, German Competence Network Sepsis (SepNet): Intensive insulin therapy and pentastarch resuscitation in severe sepsis. N Engl J Med. 2008, 358: 125-139. 10.1056/NEJMoa070716.View ArticleGoogle Scholar
  23. Weil MH, Henning RJ, Puri VK: Colloid oncotic pressure: clinical significance. Crit Care Med. 1979, 7: 113-116. 10.1097/00003246-197903000-00006.View ArticleGoogle Scholar
  24. American Thoracic Society: Evidence-based colloid use in the critically ill: American Thoracic Society Consensus Statement. Am J Respir Crit Care Med. 2004, 170: 1247-1259. 10.1164/rccm.200208-909ST.View ArticleGoogle Scholar
  25. Sudlow G, Birkett DJ, Wade DN: The characterization of two specific drug binding sites on human serum albumin. Mol Pharmacol. 1975, 11: 824-832.Google Scholar
  26. Quinlan GJ, Margarson MP, Mumby S, Evans TW, Gutteridge JM: Administration of albumin to patients with sepsis syndrome: a possible beneficial role in plasma thiol repletion. Clin Sci (Lond). 1998, 95: 459-465. 10.1042/CS19980191.View ArticleGoogle Scholar
  27. King TP: On the sulfhydryl group of human plasma albumin. J Biol Chem. 1961, 236: C5-Google Scholar
  28. Doweiko JP, Bistrian BR: The effect of glycosylated albumin on platelet aggregation. JPEN J Parenter Enteral Nutr. 1994, 18: 516-520. 10.1177/0148607194018006516.View ArticleGoogle Scholar
  29. Verheij J, van Lingen A, Raijmakers PG, Rijnsburger ER, Veerman DP, Wisselink W, Girbes AR, Groeneveld AB: Effect of fluid loading with saline or colloids on pulmonary permeability, oedema and lung injury score after cardiac and major vascular surgery. Br J Anaesth. 2006, 96: 21-30. 10.1093/bja/aei286.View ArticleGoogle Scholar
  30. Wang R, Lagakos SW, Ware JH, Hunter DJ, Drazen JM: Statistics in medicine–reporting of subgroup analyses in clinical trials. N Engl J Med. 2007, 357: 2189-2194. 10.1056/NEJMsr077003.View ArticleGoogle Scholar

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