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  • 1. Special Articles Surviving Sepsis Campaign guidelines for management of severe sepsis and septic shock R. Phillip Dellinger, MD; Jean M. Carlet, MD; Henry Masur, MD; Herwig Gerlach, MD, PhD; Thierry Calandra, MD; Jonathan Cohen, MD; Juan Gea-Banacloche, MD, PhD; Didier Keh, MD; John C. Marshall, MD; Margaret M. Parker, MD; Graham Ramsay, MD; Janice L. Zimmerman, MD; Jean-Louis Vincent, MD, PhD; Mitchell M. Levy, MD; for the Surviving Sepsis Campaign Management Guidelines Committee Sponsoring Organizations: American Association of Critical-Care Nurses, American College of Chest Physicians, American College of Emergency Physicians, American Thoracic Society, Australian and New Zealand Intensive Care Society, European Society of Clinical Microbiology and Infectious Diseases, European Society of Intensive Care Medicine, European Respiratory Society, International Sepsis Forum, Society of Critical Care Medicine, Surgical Infection Society. Objective: In 2003, critical care and infectious disease experts for death; with resolution of tissue hypoperfusion and in the absence representing 11 international organizations developed management of coronary artery disease or acute hemorrhage, targeting a hemoglobin guidelines for severe sepsis and septic shock that would be of of 7–9 g/dL; appropriate use of fresh frozen plasma and platelets; a low practical use for the bedside clinician, under the auspices of the tidal volume and limitation of inspiratory plateau pressure strategy for Surviving Sepsis Campaign, an international effort to increase aware- acute lung injury and acute respiratory distress syndrome; application of ness and improve outcome in severe sepsis. a minimal amount of positive end-expiratory pressure in acute lung Design: The process included a modified Delphi method, a con- injury/acute respiratory distress syndrome; a semirecumbent bed posi- sensus conference, several subsequent smaller meetings of sub- tion unless contraindicated; protocols for weaning and sedation/analge- groups and key individuals, teleconferences, and electronic-based sia, using either intermittent bolus sedation or continuous infusion se- discussion among subgroups and among the entire committee. dation with daily interruptions/lightening; avoidance of neuromuscular Methods: We used a modified Delphi methodology for grading blockers, if at all possible; maintenance of blood glucose <150 mg/dL recommendations, built on a 2001 publication sponsored by the after initial stabilization; equivalence of continuous veno-veno hemofil- International Sepsis Forum. We undertook a systematic review of the tration and intermittent hemodialysis; lack of utility of bicarbonate use literature graded along five levels to create recommendation grades for pH >7.15; use of deep vein thrombosis/stress ulcer prophylaxis; and from A to E, with A being the highest grade. Pediatric considerations consideration of limitation of support where appropriate. Pediatric con- were provided to contrast adult and pediatric management. siderations included a more likely need for intubation due to low func- Results: Key recommendations, listed by category and not by tional residual capacity; more difficult intravenous access; fluid resus- hierarchy, include early goal-directed resuscitation of the septic citation based on weight with 40 – 60 mL/kg or higher needed; decreased patient during the first 6 hrs after recognition; appropriate diagnostic cardiac output and increased systemic vascular resistance as the most studies to ascertain causative organisms before starting antibiotics; common hemodynamic profile; greater use of physical examination early administration of broad-spectrum antibiotic therapy; reassess- therapeutic end points; unsettled issue of high-dose steroids for therapy ment of antibiotic therapy with microbiology and clinical data to of septic shock; and greater risk of hypoglycemia with aggressive narrow coverage, when appropriate; a usual 7–10 days of antibiotic glucose control. therapy guided by clinical response; source control with attention to Conclusion: Evidence-based recommendations can be made re- the method that balances risks and benefits; equivalence of crystal- garding many aspects of the acute management of sepsis and septic loid and colloid resuscitation; aggressive fluid challenge to restore shock that are hoped to translate into improved outcomes for the mean circulating filling pressure; vasopressor preference for norepi- critically ill patient. The impact of these guidelines will be formally nephrine and dopamine; cautious use of vasopressin pending further tested and guidelines updated annually and even more rapidly as studies; avoiding low-dose dopamine administration for renal protec- some important new knowledge becomes available. (Crit Care Med tion; consideration of dobutamine inotropic therapy in some clinical 2004; 32:858 –873) situations; avoidance of supranormal oxygen delivery as a goal of KEY WORDS: sepsis; severe sepsis; septic shock; sepsis syndrome; therapy; stress-dose steroid therapy for septic shock; use of recom- infection; guidelines; evidence-based medicine; Surviving Sepsis Cam- binant activated protein C in patients with severe sepsis and high risk paign Copyright © 2004 by the Society of Critical Care Medicine DOI: 10.1097/01.CCM.0000117317.18092.E4 858 Crit Care Med 2004 Vol. 32, No. 3
  • 2. T he mortality rate of severe sepsis and septic shock. This process repre- METHODS sepsis (infection-induced or- sented phase II of the Surviving Sepsis The recommendations are graded based on gan dysfunction or hypoper- Campaign, an international effort to in- a modified Delphi methodology with categori- fusion abnormalities) and crease awareness and improve outcome in zation as previously described (Table 1, septic shock (hypotension not reversed severe sepsis. Meeting expenses as well as adapted from Ref. 3). The methods for this with fluid resuscitation and associated staff support for guidelines creation were document build on a 2001 publication spon- with organ dysfunction or hypoperfu- provided by unrestricted industry educa- sored by the International Sepsis Forum and sion abnormalities) in most centers re- tional grants as listed. There were no in- use the same method of grading recommen- mains unacceptably high (1, 2). Similar dustry members of the committee. There dations (4). The supplement submission will to an acute myocardial ischemic attack was no industry input into guidelines de- include background material, questions posed and an acute brain attack, the speed and velopment and no industry presence at any that led to the recommendation, and expanded appropriateness of therapy administered of the meetings. Industry awareness or rationale. This executive summary is targeted in the initial hours after the syndrome de- comment on the recommendations was to be concise and user friendly for the bedside velops likely influence outcome. A group of not allowed. The sponsors of the educa- clinician. The 2001 publication that was used international critical care and infectious tional grants did not see the recommenda- as a starting point for the current process disease experts in the diagnosis and man- tions until the manuscript was peer re- included a MEDLINE search for clinical trials agement of infection and sepsis, represent- viewed and accepted for publication in final in the preceding 10 yrs, supplemented by a ing 11 organizations, came together to de- form. Phase I of the Surviving Sepsis manual search of other relevant journals. Sub- velop guidelines that the bedside clinician topics for each recommendation were cross- Campaign was initiated in October 2002 could use to improve outcome in severe referenced to sepsis, severe sepsis, septic with the Barcelona Declaration to improve shock, sepsis syndrome, and infection. The survival in severe sepsis, and phase III will Surviving Sepsis Campaign guidelines consid- be dedicated to the use of the management ered the evidence in the 2001 publication Surviving Sepsis Campaign Management Guide- lines Committee. Chairs: R. Phillip Dellinger, MD*; guidelines to evaluate the impact on clini- (through 1999) and repeated the process for Henry Masur, MD; Jean M. Carlet, MD; Herwig Gerlach, cal outcome. A comprehensive document 2000 through 2003. The committee process MD, PhD**. Committee Members: Richard J. Beale, created from the deliberations of the com- began in June 2003 with a meeting featuring MD**; Marc Bonten, MD; Christian Brun-Buisson, MD; mittee will be submitted for publication as Thierry Calandra, MD; Joseph A. Carcillo, MD; the first presentations of data and recommen- Jonathan Cohen, MD**; Catherine Cordonnier, MD; E. a supplement. This document represents dations. Recommendations were discussed Patchen Dellinger, MD; Jean-Francois Dhainaut, MD, an executive summary of the consensus and critiqued. Each clinical trial used to sup- PhD; Roger G. Finch, MD; Simon Finfer, MD; Francois process with presentation of key recom- port recommendations was graded based on A. Fourrier, MD; Juan Gea-Banacloche, MD; Maurene mendations. These recommendations are the methodology in Table 1 and included pres- A. Harvey, RN, MPH**; Jan A. Hazelzet, MD; Steven M. ence or absence of important elements such as Hollenberg, MD; James H. Jorgensen, PhD; Didier Keh, intended to provide guidance for the clini- MD; Mitchell M. Levy, MD*; Ronald V. Maier, MD; cian caring for a patient with severe sepsis concealed randomization, blinded outcome Dennis G. Maki, MD; John J. Marini, MD; John C. or septic shock, but they are not applicable adjudication, intention to treat analysis, and Marshall, MD; Steven M. Opal, MD; Tiffany M. Osborn, for all patients. Recommendations from explicit definition of primary outcome. All ar- MD; Margaret M. Parker, MD**; Joseph E. Parrillo, MD; these guidelines cannot replace the clini- ticles were initially reviewed based on sub- Graham Ramsay, MD*; Andrew Rhodes, MD; Jonathan group assignments and typically by two or E. Sevransky, MD; Charles L. Sprung, MD, JD**; Antoni cian’s decision-making capability when he three participants. Survival (28 –30 days) was Torres, MD; Jeffery S. Vender, MD; Jean-Louis Vin- or she is provided with a patient’s unique cent, MD, PhD**; Janice L. Zimmerman, MD. Associate the standard outcome measure used to assess set of clinical variables. Although these rec- outcome benefit, and when an alternative was Members: E. David Bennett, MD; Pierre-Yves Bochud, ommendations are written primarily for used this is stated in the rationale. Where MD; Alain Cariou, MD; Glenn S. Murphy, MD; Martin Nitsun, MD; Joseph W. Szokol, MD; Stephen Trzeciak, the patient in the intensive care unit (ICU) strong trial evidence existed for outcome ben- MD; Christophe Vinsonneau, MD. *Executive Commit- setting, many recommendations are appro- efit in critically ill populations known to con- tee, Surviving Sepsis Campaign. **Steering Commit- priate targets for the pre-ICU setting. It tain a larger number of sepsis patients, these tee, Surviving Sepsis Campaign. The Surviving Sepsis should also be noted that resource limita- Campaign is administered jointly by the European So- trials were considered in determination of rec- ciety of Intensive Care Medicine, International Sepsis tions may prevent physicians from accom- ommendation grading. A strict evidence-based Forum, and the Society of Critical Care Medicine and is plishing a recommendation. methodology with a scoring system was not supported in part by unrestricted educational grants from Baxter Bioscience, Edwards Lifesciences, and Eli Lilly and Company (majority sponsor). Use of trade names or names of commercial Table 1. Grading system sources is for information only and does not imply endorsement by the Society of Critical Care Medicine. Grading of recommendations The authors and the publisher have exercised A. Supported by at least two level I investigations great care to ensure that drug dosages, formulas, and B. Supported by one level I investigation other information presented in this publication are C. Supported by level II investigations only accurate and in accord with the professional standards D. Supported by at least one level III investigation in effect at the time of publication. Readers are, how- E. Supported by level IV or V evidence ever, advised to always check the manufacturer’s Grading of evidence product information sheet that is packaged with the I. Large, randomized trials with clear-cut results; low risk of false-positive (alpha) error of respective products to be fully informed of changes in false-negative (beta) error recommended dosages, contraindications, and the like II. Small, randomized trials with uncertain results; moderate-to-high risk of false-positive before prescribing or administering any drug. (alpha) and/or false-negative (beta) error Also published in Intensive Care Medicine (May). III. Nonrandomized, contemporaneous controls Address requests for reprints to: R. Phillip Del- IV. Nonrandomized, historical controls and expert opinion linger, MD, Cooper Health Systems, One Cooper Plaza, V. Case series, uncontrolled studies, and expert opinion 393 Dorrance, Camden, NJ 08103. Crit Care Med 2004 Vol. 32, No. 3 859
  • 3. used. The goal was total consensus, which was Central venous pressure: 8 –12 mm Hg apy is initiated as the clinical situation reached in all recommendations except two. In Mean arterial pressure 65 mm Hg dictates. those circumstances (recommendations C3 and Urine output 0.5 mL·kg 1·hr 1 H1), the solution was achieved with the inclu- Grade D Central venous (superior vena cava) or mixed sion of subrecommendations that expressed Rationale. Two or more blood cultures are venous oxygen saturation 70% some difference in expert opinion. When there recommended (6). Ideally, at least one blood was difference of opinion about grading of a Grade B culture should be drawn through each lumen clinical trial, an outside epidemiologist was con- of each vascular access device. Obtaining Rationale. Early goal-directed therapy has sulted. This occurred in one circumstance with been shown to improve survival for emergency blood cultures peripherally and through a vas- resolution of differences. Each participant com- department patients presenting with septic cular access device is an important strategy. If pleted a conflict of interest form, and individuals shock in a randomized, controlled, single-- the same organism is recovered from both were not assigned to a subgroup topic if they had center study (5). Resuscitation directed to- cultures, the likelihood that the organism is a potential conflict of interest. A full listing of all ward the previously mentioned goals for the causing the severe sepsis is enhanced. In ad- potential conflicts of interest is included with initial 6-hr period of the resuscitation was able dition, if the culture drawn through the vas- this article. Following that meeting, the process to reduce 28-day mortality rate. The consen- cular access device is positive much earlier continued with further refinement of recom- sus panel judged central venous and mixed than the peripheral blood culture (i.e., 2 hrs mendations through electronic communication venous oxygen saturation to be equivalent. earlier), it may offer support that the vascular among committee members. A second meeting Either intermittent or continuous measure- access device is the source of the infection (7). of core members of the committee occurred in ments of oxygen saturation are judged to be Volume of blood may also be important (8). early October 2003. The document was finalized acceptable. Although lactate measurement 2. Diagnostic studies should be performed and approved by the consensus committee and may be useful, it lacks precision as a measure promptly to determine the source of the by sponsoring organizations in December 2003. of tissue metabolic status. In mechanically infection and the causative organism. Evidence-based approaches are more ventilated patients, a higher target central ve- Imaging studies and sampling of likely readily applied to data from therapeutic trials. nous pressure of 12–15 mm Hg is recom- sources of infection should be per- Evaluation of diagnostic techniques is less mended to account for the increased intratho- formed; however, some patients may be racic pressure. Similar consideration may be well suited to this approach. Readers will note too unstable to warrant certain invasive warranted in circumstances of increased ab- that the majority of the recommendations are procedures or transport outside of the dominal pressure. Although the cause of not supported by high-level evidence. Most are ICU. Bedside studies, such as ultrasound, tachycardia in septic patients may be multi- supported by expert opinion only. In order for may be useful in these circumstances. factorial, a decrease in elevated pulse with a general recommendation to carry a higher fluid resuscitation is often a useful marker of Grade E level of evidence (grades A, B, C, or D), a improving intravascular filling. supporting study or studies must have shown a Rationale. Diagnostic studies may identify a clinical outcome difference. Studies showing 2. During the first 6 hrs of resuscitation of source of infection that must be drained to max- physiologic changes that could be potential sur- severe sepsis or septic shock, if central ve- imize the likelihood of a satisfactory response to rogates of clinical outcome benefit were not nous oxygen saturation or mixed venous therapy. However, even in the most organized used by themselves as pivotal studies but were oxygen saturation of 70% is not achieved and well-staffed healthcare facilities, transport of used to support the validity of studies showing with fluid resuscitation to a central venous patients can be dangerous, as can placing pa- pressure of 8–12 mm Hg, then transfuse tients in outside-unit imaging devices that are an outcome in a clinically important variable packed red blood cells to achieve a hemat- difficult to access and monitor. such as survival or length of ICU stay. A grade of ocrit of 30% and/or administer a dobut- A, B, or C required randomized trials. Recom- amine infusion (up to a maximum of 20 mendations are graded and followed with ratio- g·kg 1·min 1) to achieve this goal. C. Antibiotic Therapy nale. References are provided to support grades A–D. In the committee’s deliberations, the grad- Grade B 1. Intravenous antibiotic therapy should ing of a recommendation did not establish the be started within the first hour of rec- Rationale. The protocol used in the study ognition of severe sepsis, after appropri- level of priority or importance of a specific in- cited previously targeted an increase in mixed tervention, only the degree of literature support. ate cultures have been obtained. venous oxygen saturation to 70%. This was Pediatric considerations are provided at the end achieved by sequential institution of initial fluid Grade E of the document for aspects of management that resuscitation, then packed red blood cells, and differ from adults. Recommendations are then dobutamine. This protocol was associated Rationale. Establishing vascular access and grouped by category and not by hierarchy. with an improvement in survival (5). initiating aggressive fluid resuscitation is the first priority when managing patients with se- vere sepsis or septic shock. However, prompt A. Initial Resuscitation B. Diagnosis infusion of antimicrobial agents is also a logical 1. The resuscitation of a patient in severe 1. Appropriate cultures should always be ob- strategy and may require additional vascular ac- sepsis or sepsis-induced tissue hypoperfu- tained before antimicrobial therapy is ini- cess ports. Establishing a supply of premixed sion (hypotension or lactic acidosis) tiated. To optimize identification of caus- antibiotics in an emergency department or crit- should begin as soon as the syndrome is ative organisms, at least two blood ical care unit for such urgent situations is an recognized and should not be delayed appropriate strategy for enhancing the likeli- cultures should be obtained with at least pending ICU admission. An elevated se- hood that antimicrobial agents will be infused one drawn percutaneously and one drawn rum lactate concentration identifies tis- promptly. Staff should be cognizant that some through each vascular access device, un- sue hypoperfusion in patients at risk who agents require more lengthy infusion time are not hypotensive. During the first 6 hrs less the device was recently ( 48 hrs) whereas others can be rapidly infused or even of resuscitation, the goals of initial resus- inserted. Cultures of other sites such as administered as a bolus. citation of sepsis-induced hypoperfusion urine, cerebrospinal fluid, wounds, respi- should include all of the following as one ratory secretions, or other body fluids 2. Initial empirical anti-infective therapy part of a treatment protocol: should be obtained before antibiotic ther- should include one or more drugs that 860 Crit Care Med 2004 Vol. 32, No. 3
  • 4. have activity against the likely pathogens broad-spectrum therapy usually must be con- Grade E (bacterial or fungal) and that penetrate tinued for the duration of the neutropenia. into the presumed source of sepsis. The 3. When a focus of infection amenable to choice of drugs should be guided by the Grade E source control measures such as an susceptibility patterns of microorganisms intra-abdominal abscess, a gastrointes- Rationale. Use of antimicrobial agents with tinal perforation, cholangitis, or intes- in the community and in the hospital. a more narrow spectrum and reducing the tinal ischemia has been identified as duration of therapy will reduce the likelihood the cause of severe sepsis or septic Grade D that the patient will develop superinfection shock, source control measures should Rationale. The choice of empirical antibi- with pathogenic or resistant organisms such be instituted as soon as possible follow- otics depends on complex issues related to the as Candida species, Clostridium difficile, or ing initial resuscitation. patient’s history (including drug intolerance), vancomycin-resistant Enterococcus faecium. underlying disease, the clinical syndrome, and However, the desire to minimize superinfec- Grade E susceptibility patterns in the patient’s com- tions and other complications should not take Rationale. Case series and expert opinion munity and in the healthcare facility. precedence over the need to give the patient support the principle that rapid correction of a The initial selection of an empirical anti- an adequate course of potent antimicrobials. source of microbial contamination is essential microbial regimen should be broad enough, to maximize survival of the severely septic according to these criteria, covering all likely 4. If the presenting clinical syndrome is determined to be due to a noninfec- patient with acute physiologic deterioration. pathogens since there is little margin for error Intervention should only be undertaken fol- in critically ill patients. There is ample evi- tious cause, antimicrobial therapy should be stopped promptly to mini- lowing adequate resuscitation. Timely and dence that failure to initiate appropriate ther- emergent intervention is particularly impor- apy promptly (i.e., therapy that is active mize the development of resistant pathogens and superinfection with tant for patients with necrotizing soft tissue against the causative pathogen) has adverse infection or intestinal ischemia (19). consequences on outcome (9 –12). other pathogenic organisms. Although restricting the use of antibiotics, Grade E 4. If intravascular access devices are poten- and particularly broad-spectrum antibiotics, is tially the source of severe sepsis or septic important for limiting superinfection and for Rationale. Clinicians should be cognizant shock, they should be promptly removed decreasing the development of antibiotic- that blood cultures will be negative in the after establishing other vascular access. resistant pathogens, patients with severe sep- majority of cases of sepsis or septic shock. sis or septic shock warrant broad-spectrum Thus, the decision to continue, narrow, or Grade E therapy until the causative organism and its stop antimicrobial therapy must be made on antibiotic susceptibilities are defined. At that the basis of clinician judgment and other cul- Rationale. Intravascular access devices are point, restriction of the number of antibiotics ture results. thought to be the source of the majority of and narrowing the spectrum of antimicrobial nosocomial bloodstream infections. When pa- therapy is an important and responsible strat- tients develop sepsis of unknown source, it D. Source Control may be reasonable to leave vascular access egy for minimizing the development of resis- tant pathogens and for containing costs. devices in place until the source of infection 1. Every patient presenting with severe All patients should receive a full loading can be determined. However, when patients sepsis should be evaluated for the pres- dose of each antimicrobial. However, patients ence of a focus on infection amenable to have severe sepsis or septic shock of unknown with sepsis or septic shock often have abnor- source control measures, specifically source, clinicians should consider removal mal renal or hepatic function and may have the drainage of an abscess or local focus and replacement of vascular access devices to abnormal volumes of distribution due to ag- on infection, the debridement of in- be a priority, even if the device is tunneled or gressive fluid resuscitation. The ICU pharma- fected necrotic tissue, the removal of a surgically implanted (20, 21). cist should be consulted to ensure that serum potentially infected device, or the defin- concentrations are attained that maximize ef- itive control of a source of ongoing mi- E. Fluid Therapy ficacy and minimize toxicity, (13–16). crobial contamination (17). (See Appen- dix A for examples of potential sites See initial resuscitation recommendations 3. The antimicrobial regimen should al- needing source control.) (A1–2) for timing of resuscitation. ways be reassessed after 48 –72 hrs on Grade E the basis of microbiological and clinical 1. Fluid resuscitation may consist of natu- data with the aim of using a narrow- Rationale. Healthcare professionals should ral or artificial colloids or crystalloids. spectrum antibiotic to prevent the devel- engage specialists in other disciplines such as There is no evidence-based support for opment of resistance, to reduce toxicity, radiology, surgery, pulmonary medicine, and one type of fluid over another. and to reduce costs. Once a causative gastroenterology to obtain diagnostic samples pathogen is identified, there is no evi- and to drain, debride, or remove the infection Grade C dence that combination therapy is more source as appropriate. effective than monotherapy. The dura- Rationale. Although prospective studies of tion of therapy should typically be 7–10 2. The selection of optimal source control choice of fluid resuscitation in patients with days and guided by clinical response. methods must weigh benefits and risks septic shock only are lacking, meta-analysis of of the specific intervention. Source con- clinical studies comparing crystalloid and col- Grade E trol interventions may cause further loid resuscitation in general and surgical pa- complications such as bleeding, fistulas, tient populations indicate no clinical outcome a. Some experts prefer combination therapy or inadvertent organ injury; in general, difference between colloids and crystalloids for patients with Pseudomonas infections. the intervention that accomplishes the and would appear to be generalizable to sepsis Grade E source control objective with the least populations (22–24). As the volume of distri- physiologic upset should be employed, bution is much larger for crystalloids than for b. Most experts would use combination ther- for example, consideration of percutane- colloids, resuscitation with crystalloids re- apy for neutropenic patients with severe sepsis ous rather than surgical drainage of an quires more fluid to achieve the same end or septic shock. For neutropenic patients, abscess (18). points and results in more edema. Crit Care Med 2004 Vol. 32, No. 3 861
  • 5. 2. Fluid challenge in patients with sus- Grade D 5. Vasopressin use may be considered in pected hypovolemia (suspected inade- patients with refractory shock despite quate arterial circulation) may be given Rationale. Although there is no high- adequate fluid resuscitation and high- at a rate of 500 –1000 mL of crystalloids quality primary evidence to recommend one dose conventional vasopressors. Pending or 300 –500 mL of colloids over 30 mins catecholamine over another, human and an- the outcome of ongoing trials, it is not and repeated based on response (increase imal studies suggest some advantages of recommended as a replacement for nor- in blood pressure and urine output) and norepinephrine and dopamine over epineph- epinephrine or dopamine as a first-line tolerance (evidence of intravascular vol- rine (potential tachycardia, possibly disad- agent. If used in adults, it should be ume overload). vantageous effects on splanchnic circula- administered at infusion rates of 0.01– tion) and phenylephrine (decrease in stroke 0.04 units/min. It may decrease stroke Grade E volume). Phenylephrine is the adrenergic volume. agent least likely to produce tachycardia. Rationale. Fluid challenge must be clearly Dopamine increases mean arterial pressure Grade E separated from an increase in maintenance and cardiac output, primarily due to an in- fluid administration. Fluid challenge is a term crease in stroke volume and heart rate. Nor- Rationale. Low doses of vasopressin may used to describe the initial volume expansion epinephrine increases mean arterial pres- be effective in raising blood pressure in pa- period in which the response of the patient to sure due to its vasoconstrictive effects, with tients refractory to other vasopressors, al- fluid administration is carefully evaluated. little change in heart rate and less increase though no outcome data are available. Un- During this process, large amounts of fluids in stroke volume compared with dopamine. like dopamine and epinephrine, vasopressin may be administered over a short period of Either may be used as a first-line agent to is a direct vasoconstrictor without inotropic time under close monitoring to evaluate the correct hypotension in sepsis. Norepineph- or chronotropic effects and may result in patient’s response and avoid the development rine is more potent than dopamine and may decreased cardiac output and hepato- of pulmonary edema. The degree of intravas- be more effective at reversing hypotension splanchnic flow. Most published reports ex- cular volume deficit in patients with severe in patients with septic shock. Dopamine may clude patients from treatment with vaso- sepsis varies. With venodilation and ongoing be particularly useful in patients with com- pressin if the cardiac index is 2 or 2.5 capillary leak, most patients require continu- promised systolic function but causes more L·min 1·m 2, and it should be used with ing aggressive fluid resuscitation during the tachycardia and may be more arrhythmo- caution in patients with cardiac dysfunction. first 24 hrs of management. Input is typically genic (25, 27–30). Studies show that vasopressin concentra- much greater than output, and input/output tions are elevated in early septic shock, but ratio is of no utility to judge fluid resuscitation 3. Low-dose dopamine should not be used with continued shock, concentrations de- needs during this time period. for renal protection as part of the treat- crease to normal range in the majority of ment of severe sepsis. patients between 24 and 48 hrs (33). This has been called “relative vasopressin defi- F. Vasopressors Grade B ciency” since in the presence of hypoten- sion, vasopressin would be expected to be 1. When an appropriate fluid challenge Rationale. A large randomized trial and a elevated. The significance of this finding is fails to restore adequate blood pres- meta-analysis comparing low-dose dopamine unknown. Doses of vasopressin 0.04 units/ sure and organ perfusion, therapy to placebo in critically ill patients found no min have been associated with myocardial with vasopressor agents should be difference in either primary outcomes (peak ischemia, significant decreases in cardiac started. Vasopressor therapy may also serum creatinine, need for renal replacement be required transiently to sustain life output, and cardiac arrest (34 –36). therapy, urine output, time to recovery of nor- and maintain perfusion in the face of mal renal function) or secondary outcomes life-threatening hypotension, even G. Inotropic Therapy when a fluid challenge is in progress (survival to either ICU or hospital discharge, and hypovolemia has not yet been cor- ICU stay, hospital stay, arrhythmias). Thus, the available data do not support administra- 1. In patients with low cardiac output de- rected. spite adequate fluid resuscitation, dobu- tion of low doses of dopamine to maintain or tamine may be used to increase cardiac Grade E improve renal function (31, 32). output. If used in the presence of low Rationale. Below a certain mean arterial blood pressure, it should be combined 4. All patients requiring vasopressors with vasopressor therapy. pressure, autoregulation in various vascular should have an arterial catheter placed as beds can be lost, and perfusion can become lin- soon as practical if resources are available. Grade E early dependent on pressure. Thus, some pa- tients may require vasopressor therapy to Grade E Rationale. Dobutamine is the first-choice achieve a minimal perfusion pressure and main- inotrope for patients with measured or sus- tain adequate flow. It is important to supple- Rationale. In shock states, measurement pected low cardiac output in the presence of ment goals such as blood pressure with assess- of blood pressure using a cuff is commonly adequate left ventricular filling pressure (or clin- ment of global perfusion such as blood lactate inaccurate, whereas use of an arterial cath- ical assessment of adequate fluid resuscitation) concentrations. Adequate fluid resuscitation is a eter provides a more accurate and reproduc- and adequate mean arterial pressure. In the ab- fundamental aspect of the hemodynamic man- ible measurement of arterial pressure. Mon- sence of measurements of cardiac output, hypo- agement of patients with septic shock and itoring with these catheters also allows beat- tensive patients with severe sepsis may have low, should ideally be achieved before vasopressors to-beat analysis so that decisions regarding normal, or increased cardiac outputs. Therefore, are used, but it is frequently necessary to employ therapy can be based on immediate blood treatment with a combined inotrope/vasopressor vasopressors early as an emergency measure in pressure information (25). Placement of an such as norepinephrine or dopamine is recom- patients with severe shock (25, 26). arterial catheter in the emergency depart- mended. When the capability exists for monitor- ment is typically not possible or practical. It ing cardiac output in addition to blood pressure, 2. Either norepinephrine or dopamine is important to appreciate the complications a vasopressor such as norepinephrine and an (through a central catheter as soon as avail- of arterial catheter placement, which in- inotrope such as dobutamine may be used sep- able) is the first-choice vasopressor agent to clude hemorrhage and damage to arterial arately to target specific levels of mean arterial correct hypotension in septic shock. vessels. pressure and cardiac output. 862 Crit Care Med 2004 Vol. 32, No. 3
  • 6. 2. A strategy of increasing cardiac index to b. Some experts would decrease dosage of syndrome [ARDS]) and with no absolute achieve an arbitrarily predefined elevated steroids after resolution of septic shock. contraindication related to bleeding risk or level is not recommended. relative contraindication that outweighs Grade E the potential benefit of rhAPC (see Appen- Grade A dix B for absolute contraindications and Rationale. There has been no comparative prescription information for warnings). Rationale. Two large prospective clinical study between a fixed duration and clinically trials that included critically ill ICU patients guided regimen. Two RCTs used a fixed dura- Grade B who had severe sepsis failed to demonstrate tion protocol for treatment (39, 41), and inone benefit from increasing oxygen delivery to su- RCT, therapy was decreased after shock reso- Rationale. The inflammatory response in pranormal levels by use of dobutamine (37, lution and discontinued after 6 days (40). severe sepsis is integrally linked to procoagu- 38). The goal of resuscitation should instead lant activity and endothelial activation. The be to achieve adequate levels of oxygen deliv- c. Some experts would consider tapering the inflammatory response in sepsis is procoagu- ery or avoid flow-dependent tissue hypoxia. dose of corticosteroids at the end of therapy. lant in the early stages. rhAPC, an endogenous anticoagulant with anti-inflammatory proper- Grade E ties, has been shown, in a large, multiple- H. Steroids center, randomized, controlled trial (50), to Rationale. One study showed hemody- 1. Intravenous corticosteroids (hydrocortisone namic and immunologic rebound effects after improve survival in patients with sepsis- 200 –300 mg/day, for 7 days in three or abrupt cessation of corticosteroids (46). induced organ dysfunction. four divided doses or by continuous infu- At present, risk assessment is best deter- sion) are recommended in patients with d. Some experts would add fludrocortisone (50 mined by bedside clinical evaluation and judg- septic shock who, despite adequate fluid g orally four times per day) to this regimen. ment. Given the uncertainty of risk assess- replacement, require vasopressor therapy ment and the potential for rapid deterioration Grade E to maintain adequate blood pressure. of patients with severe sepsis and septic shock, Rationale. One study added 50 g of once a patient has been identified as at high Grade C risk of death, treatment should begin as soon fludrocortisone orally (39). Since hydrocorti- Rationale. One multiple-center, random- sone has intrinsic mineralocorticoid activity, as possible. ized, controlled trial (RCT) with patients in se- there is controversy as to whether fludrocor- vere septic shock showed a significant shock tisone should be added. J. Blood Product Administration reversal and reduction of mortality rate in pa- tients with relative adrenal insufficiency (defined 2. Doses of corticosteroids 300 mg hydro- 1. Once tissue hypoperfusion has resolved as post-adrenocorticotropic hormone [ACTH] cortisone daily should not be used in and in the absence of extenuating circum- cortisol increase 9 g/dL) (39). Two additional severe sepsis or septic shock for the pur- stances, such as significant coronary artery smaller RCTs showed significant effects on pose of treating septic shock. disease, acute hemorrhage, or lactic acido- shock reversal (40, 41). In the first study, pa- sis (see recommendations for initial resus- Grade A tients had more severe septic shock (systolic citation), red blood cell transfusion should blood pressure 90 mm Hg despite vasopres- Rationale. Two randomized prospective occur only when hemoglobin decreases to sors) than in the latter two studies (systolic clinical trials and two meta-analyses concluded 7.0 g/dL ( 70 g/L) to target a hemoglo- blood 90 mm Hg with vasopressors). that for therapy of severe sepsis or septic shock, bin of 7.0 –9.0 g/dL. high-dose corticosteroid therapy is ineffective or a. Some experts would use a 250- g ACTH Grade B harmful (47–50). There may be reasons to main- stimulation test to identify responders ( 9 tain higher doses of corticosteroid for medical Rationale. Although the optimum hemo- g/dL increase in cortisol 30 – 60 mins post- conditions other than septic shock. globin for patients with severe sepsis has not ACTH administration) and discontinue been specifically investigated, the Transfusion therapy in these patients. Clinicians should 3. In the absence of shock, corticosteroids Requirements in Critical Care trial suggested not wait for ACTH stimulation results to should not be administered for the treat- that a hemoglobin of 7–9 g/dL (70 –90 g/L) is administer corticosteroids. ment of sepsis. There is, however, no adequate for most critically ill patients. A contraindication to continuing mainte- transfusion threshold of 7.0 g/dL (70 g/L) was Grade E nance steroid therapy or to using stress not associated with increased mortality rate. Rationale. One study demonstrated that an dose steroids if the patient’s history of Red blood cell transfusion in septic patients incremental increase of 9 g/dL after 250- g corticosteroid administration or the pa- increases oxygen delivery but does not usually ACTH stimulation test (responders) identifies tient’s endocrine history warrants. increase oxygen consumption (51–53). This survivors of septic shock (42). A subsequent trial Grade E transfusion threshold contrasts with the tar- demonstrated that stress dose steroids improved get of a hematocrit of 30% in patients with low survival in those patients who failed to produce Rationale. There are no studies document- central venous oxygen saturation during the this increase in cortisol with ACTH (nonre- ing that stress doses of steroids improve the first 6 hrs of resuscitation of septic shock. sponders). Treatment with corticosteroids was outcome of sepsis in the absence of shock ineffective in responders (39). Recommenda- unless the patient requires stress dose replace- 2. Erythropoietin is not recommended as a tions for the identification of relative adrenal ment due to a prior history of steroid therapy specific treatment of anemia associated insufficiency vary based on different cutoff levels or adrenal dysfunction. with severe sepsis but may be used when of random cortisol, peak cortisol after stimula- septic patients have other accepted rea- tion, incremental cortisol increase after stimu- sons for administration of erythropoietin I. Recombinant Human such as renal failure induced compro- lation, and combinations of these criteria (43– Activated Protein C (rhAPC) mise of red blood cell production. 45). In patients with septic shock, clinicians should consider administering a dose of dexa- 1. rhAPC is recommended in patients at high Grade B methasone until such time that an ACTH stim- risk of death (Acute Physiology and Chronic ulation test can be administered because dexa- Health Evaluation II 25, sepsis-induced Rationale. No specific information regard- methasone, unlike hydrocortisone, does not multiple organ failure, septic shock, or ing erythropoietin use in septic patients is avail- interfere with the cortisol assay. sepsis-induced acute respiratory distress able, but clinical trials in critically ill patients Crit Care Med 2004 Vol. 32, No. 3 863
  • 7. show some decrease in red cell transfusion re- with the goal of maintaining end- crease PaO2 when positive end-expiratory pres- quirement with no effect on clinical outcome inspiratory plateau pressures 30 cm sure is applied through either an endotracheal (54, 55). Patients with severe sepsis and septic H2O. (See Appendix C for a formula to tube or a face mask. shock may have coexisting conditions that do calculate predicted body weight.) warrant use of erythropoietin. 4. In facilities with experience, prone posi- Grade B tioning should be considered in ARDS 3. Routine use of fresh frozen plasma to cor- Rationale. Over the past 10 yrs, several patients requiring potentially injurious rect laboratory clotting abnormalities in multiple-center randomized trials have been levels of FIO2 or plateau pressure who are the absence of bleeding or planned invasive performed to evaluate the effects of limiting not at high risk for adverse conse- procedures is not recommended. inspiratory pressure through modulations in quences of positional changes. Grade E tidal volume (60 – 63). These studies showed differing results that may have been caused by Grade E Rationale. Although clinical studies have differences between airway pressures in the not assessed the impact of transfusion of fresh Rationale. Several smaller studies and one treatment and control groups (64, 65). The frozen plasma on outcomes in critically ill larger study have shown that a majority of largest trial of a volume- and pressure-limited patients, professional organizations have rec- patients with ALI/ARDS respond to the prone strategy showed a 9% decrease of all-cause ommended fresh frozen plasma for coagulopa- position with improved oxygenation (72–76). mortality in patients ventilated with tidal vol- thy when there is a documented deficiency of The large multiple-center trial of prone posi- umes of 6 mL/kg of predicted body weight coagulation factors (increased prothrombin tioning for 7 hrs/day did not show improve- (as opposed to 12 mL/kg) while aiming for a time, international normalized ratio, or partial ment in mortality rates in patients with ALI/ plateau pressure 30 cm H2O (66). thromboplastin time) and the presence of ac- ARDS; however, a post hoc analysis suggested tive bleeding or before surgical or invasive improvement in those patients with the most procedures (56 –58). 2. Hypercapnia (allowing PaCO2 to increase severe hypoxemia by PaO2/FIO2 ratio (75). above normal, so-called permissive hy- Prone positioning may be associated with po- 4. Antithrombin administration is not rec- percapnia) can be tolerated in patients tentially life-threatening complications, in- ommended for the treatment of severe with ALI/ARDS if required to minimize cluding accidental dislodgment of the endo- sepsis and septic shock. plateau pressures and tidal volumes. tracheal tube and central venous catheters, Grade B but these complications can usually be Grade C avoided with proper precautions. Rationale. A phase III clinical trial of high- Rationale. An acutely elevated PaCO2 may dose antithrombin did not demonstrate any have physiologic consequences that include 5. Unless contraindicated, mechanically beneficial effect on 28-day all-cause mortality vasodilation as well as an increased heart rate, ventilated patients should be maintained in adults with severe sepsis and septic shock. blood pressure, and cardiac output. Allowing semirecumbent, with the head of the bed High-dose antithrombin was associated with modest hypercapnia in conjunction with lim- raised to 45° to prevent the development an increased risk of bleeding when adminis- iting tidal volume and minute ventilation has of ventilator-associated pneumonia. tered with heparin (59). been demonstrated to be safe in small nonran- 5. In patients with severe sepsis, platelets domized series (67, 68). Patients treated in Grade C should be administered when counts are larger trials that have the goal of limiting tidal volumes and airway pressures have demon- Rationale. The semirecumbent position 5000/mm3 (5 109/L) regardless of has been demonstrated to decrease the inci- apparent bleeding. Platelet transfusion strated improved outcomes, but permissive hypercapnia was not a primary treatment goal dence of ventilator-required pneumonia (77). may be considered when counts are Patients are laid flat for procedures, hemody- 5000 –30,000/mm3 (5–30 109/L) and in these studies (66). The use of hypercarbia is limited in patients with preexisting metabolic namic measurements, and during episodes of there is a significant risk of bleeding. hypotension. Consistent return to semirecum- Higher platelet counts ( 50,000/mm3 acidosis and is contraindicated in patients with increased intracranial pressure. Sodium bent position should be viewed as a quality [50 109/L]) are typically required for indicator in patients receiving mechanical surgery or invasive procedures. bicarbonate infusion may be considered in se- lect patients to facilitate use of permissive ventilation. Grade E hypercarbia. 6. A weaning protocol should be in place Rationale. Guidelines for transfusion of and mechanically ventilated patients 3. A minimum amount of positive end- platelets are derived from consensus opinion should undergo a spontaneous breathing expiratory pressure should be set to pre- and experience in patients undergoing chemo- trial to evaluate the ability to discon- vent lung collapse at end-expiration. Set- therapy. Recommendations take into account tinue mechanical ventilation when they ting positive end-expiratory pressure the etiology of thrombocytopenia, platelet dys- satisfy the following criteria: a) arous- based on severity of oxygenation deficit function, risk of bleeding, and presence of able; b) hemodynamically stable (with- and guided by the FIO2 required to main- concomitant disorders (56, 58). out vasopressor agents); c) no new po- tain adequate oxygenation is one accept- able approach. (See Appendix C.) Some tentially serious conditions; d) low K. Mechanical Ventilation of experts titrate positive end-expiratory ventilatory and end-expiratory pressure Sepsis-Induced Acute Lung pressure according to bedside measure- requirements; and e) requiring levels of ments of thoracopulmonary compliance FIO2 that could be safely delivered with a Injury (ALI)/ARDS face mask or nasal cannula. If the spon- (to obtain the highest compliance, re- 1. High tidal volumes that are coupled with flecting lung recruitment). taneous breathing trial is successful, high plateau pressures should be avoided consideration should be given for extu- in ALI/ARDS. Clinicians should use as a Grade E bation (see Appendix D). Spontaneous starting point a reduction in tidal vol- breathing trial options include a low umes over 1–2 hrs to a “low” tidal vol- Rationale. Raising end-expiratory pressure level of pressure support with continu- ume (6 mL per kilogram of predicted in ALI/ARDS keeps lung units open to partic- ous positive airway pressure 5 cm H2O or body weight) as a goal in conjunction ipate in gas exchange (69 –71). This will in- a T-piece. 864 Crit Care Med 2004 Vol. 32, No. 3
  • 8. Grade A duced if an intermittent assessment of the ier management of fluid balance in depth of neuromuscular blockade is per- hemodynamically unstable septic patients. Rationale. Recent studies demonstrate formed (92, 93). that daily spontaneous breathing trials re- Grade B duce the duration of mechanical ventilation M. Glucose Control Rationale. Studies support the equivalence (78 – 80). Although these studies had limited of continuous and intermittent renal replace- numbers of patients with documented ALI/ 1. Following initial stabilization of patients ment therapies for the treatment of acute re- ARDS, there is no reason to believe that with severe sepsis, maintain blood glu- nal failure in critically ill patients (98, 99).In- ALI/ARDS patients would have different out- cose 150 mg/dL (8.3 mmol/L). Studies termittent hemodialysis may be poorly comes from other critically ill patients. Suc- supporting the role of glycemic control tolerated in hemodynamically unstable pa- cessful completion of spontaneous breath- have used continuous infusion of insulin tients. There is no current evidence to support ing trials leads to a high likelihood of and glucose. With this protocol, glucose the use of continuous venovenous hemofiltra- successful discontinuation of mechanical should be monitored frequently after ini- tion for the treatment of sepsis independent of ventilation. tiation of the protocol (every 30 – 60 renal replacement needs. mins) and on a regular basis (every 4 hrs) L. Sedation, Analgesia, and once the blood glucose concentration has stabilized. O. Bicarbonate Therapy Neuromuscular Blockade in Sepsis Grade D 1. Bicarbonate therapy for the purpose of improving hemodynamics or reducing 1. Protocols should be used when sedation Rationale. A large single-center trial of vasopressor requirements is not recom- of critically ill mechanically ventilated postoperative surgical patients showed signif- mended for treatment of hypoperfusion- patients is required. The protocol should icant improvement in survival when continu- induced lactic acidemia with pH 7.15. include the use of a sedation goal, mea- ous infusion insulin was used to maintain The effect of bicarbonate administration sured by a standardized subjective seda- glucose between 80 and 110 mg/dL (4.4 – 6.1 on hemodynamics and vasopressor re- tion scale. mmol/L) (94). Exogenous glucose was begun quirement at lower pH as well as the simultaneously with insulin with frequent effect on clinical outcome at any pH has Grade B monitoring of glucose (every 1 hr) and inten- not been studied. 2. Either intermittent bolus sedation or sity of monitoring greatest at the time of ini- Grade C continuous infusion sedation to prede- tiation of insulin. Hypoglycemia may occur. There is no reason to think that these data are Rationale. There is no evidence to support termined end points (e.g., sedation not generalizable to all severely septic pa- the use of bicarbonate therapy in the treat- scales) with daily interruption/lighten- ing of continuous infusion sedation with tients. Post hoc data analysis of the trial data ment of hypoperfusion-induced acidemia as- awakening and retitration, if necessary, revealed that although best results were ob- sociated with sepsis. Two studies comparing are recommended methods for sedation tained when glucose was maintained between saline and bicarbonate in patients with pH administration. 80 and 110 mg/dL (4.4 and 6.1 mmol/L), 7.13–7.15 failed to reveal any difference in achieving a goal of 150 mg/dL (8.3 mmol/L) hemodynamic variables or vasopressor re- Grade B also improved outcome when compared with quirements between equimolar concentra- higher concentrations. This goal will likely tions of bicarbonate and normal saline with Rationale (L1 and L2). Mechanically ven- reduce the risk of hypoglycemia. The control either therapy (100, 101). tilated patients receiving continuous sedation may have a significantly longer duration of of the blood glucose concentration appears to mechanical ventilation as well as ICU and hos- be more important than the amount of insulin P. Deep Vein Thrombosis pital length of stay (81). A daily interruption or infused (95, 96). The frequency of blood glu- Prophylaxis lightening of a “continuous” sedative infusion cose determinations may require the use of until the patient is awake may decrease the central or arterial catheters for blood sam- 1. Severe sepsis patients should receive duration of mechanical ventilation and ICU pling. deep vein thrombosis (DVT) prophylaxis stay (82). The use of sedation protocols in with either low-dose unfractionated hep- mechanically ventilated patients has shown a 2. In patients with severe sepsis, a strategy arin or low-molecular weight heparin. of glycemic control should include a nu- For septic patients who have a contrain- reduced duration of mechanical ventilation, trition protocol with the preferential use dication for heparin use (i.e., thrombo- length of stay, and tracheostomy rates (83). of the enteral route. cytopenia, severe coagulopathy, active 3. Neuromuscular blockers should be bleeding, recent intracerebral hemor- avoided if at all possible in the septic Grade E rhage), the use of a mechanical prophy- patient due to the risk of prolonged neu- lactic device (graduated compression Rationale. When a glycemic control strat- stockings or intermittent compression romuscular blockade following discon- egy is initiated, hypoglycemia is minimized by device) is recommended (unless contra- tinuation. If neuromuscular blockers providing a continuous supply of glucose sub- indicated by the presence of peripheral must be used for longer than the first strate. Initially, unless the patient is already vascular disease). In very high-risk pa- hours of mechanical ventilation, either profoundly hyperglycemia, this is accom- tients such as those who have severe intermittent bolus as required or contin- plished with 5% or 10% dextrose infusion and sepsis and history of DVT, a combination uous infusion with monitoring of depth followed by initiation of feeding, preferably by of pharmacologic and mechanical ther- of block with train of four monitoring the enteral route, if tolerated (97). apy is recommended. should be used. Grade A Grade E N. Renal Replacement Rationale. Although no study has been Rationale. Prolonged skeletal muscle 1. In acute renal failure, and in the absence performed specifically in patients with severe weakness has been reported in critically ill of hemodynamic instability, continuous sepsis, large trials confirming the benefit of patients following the use of intermediate- and venovenous hemofiltration and intermit- DVT prophylaxis in general ICU populations long-acting neuromuscular blockers (84 –91). tent hemodialysis are considered equiva- have included significant numbers of septic The risk of prolonged paralysis may be re- lent. Continuous hemofiltration offers eas- patients (102–104). This benefit should be ap- Crit Care Med 2004 Vol. 32, No. 3 865
  • 9. plicable to patients with severe sepsis and sep- ment of intravascular support (110). On the tension of the newborn and sepsis in a tic shock. basis of a number of studies, it is accepted that randomized controlled trial (116). When pedi- aggressive fluid resuscitation with crystalloids atric patients remain in a normotensive low Q. Stress Ulcer Prophylaxis or colloids is of fundamental importance to cardiac output and high vascular resistance survival of septic shock in children (111, 112). state, despite epinephrine and nitrosovasodi- 1. Stress ulcer prophylaxis should be given There is only one randomized, controlled trial lator therapy, then the use of a phosphodies- to all patients with severe sepsis. H2 re- comparing the use of colloid to crystalloid terase inhibitor should be strongly considered ceptor inhibitors are more efficacious resuscitation (dextran, gelatin, lactated Ring- (117–119). Pentoxifylline (not available in the than sucralfate and are the preferred er’s solution, or saline) in children with den- United States) improved outcome in prema- agents. Proton pump inhibitors have not gue shock (111). All these children survived ture neonates with sepsis when given for 6 been assessed in a direct comparison regardless of the fluid used, but the longest hrs/day for 5 days in a randomized, controlled with H2 receptor antagonists and, there- time to recovery from shock occurred in chil- trial (120). fore, their relative efficacy is unknown. dren who received lactated Ringer’s solution. 4. Therapeutic End Points. Therapeutic They do demonstrate equivalency in abil- Among patients with the narrowest pulse pres- end points are capillary refill of 2 secs, nor- ity to increase gastric pH. sure, there was a suggestion that colloids were mal pulses with no differential between pe- Recommendation: Grade A more effective than crystalloids in restoring ripheral and central pulses, warm extremities, normal pulse pressure. Fluid infusion is best urine output 1 mL·kg 1·hr 1, normal men- Rationale. Although no study has been initiated with boluses of 20 mL/kg over 5–10 tal status, decreased lactate and increased base performed specifically in patients with severe mins, titrated to clinical monitors of cardiac deficit, and superior vena cava or mixed ve- sepsis, large trials confirming the benefit of output, including heart rate, urine output, nous oxygen saturation 70%. When employ- stress ulcer prophylaxis in general ICU popu- capillary refill, and level of consciousness. ing measurements to assist in identifying ac- lations have included significant numbers of Children normally have a lower blood pressure ceptable cardiac output in children with septic patients (105–108). This benefit should than adults and can prevent reduction in systemic arterial hypoxemia such as cyanotic be applicable to patients with severe sepsis and blood pressure by vasoconstriction and in- congenital heart disease or severe pulmonary septic shock. In addition, the conditions creasing heart rate. Therefore, blood pressure disease, arterial-venous oxygen content differ- shown to benefit from stress ulcer prophylaxis by itself is not a reliable end point for assess- ence is a better marker than mixed venous (coagulopathy, mechanical ventilation, hypo- ing the adequacy of resuscitation. However, hemoglobin saturation with oxygen. Optimiz- tension) are frequently present in patients once hypotension occurs, cardiovascular col- ing preload optimizes cardiac index. As noted with severe sepsis and septic shock. lapse may soon follow. Hepatomegaly occurs previously, blood pressure by itself is not a in children who are fluid overloaded and can reliable end point for resuscitation. If a pul- R. Consideration for Limitation be a helpful sign of the adequacy of fluid monary artery catheter is used, therapeutic of Support resuscitation. Large fluid deficits typically ex- end points are cardiac index 3.3 and 6.0 ist, and initial volume resuscitation usually L·min 1·m 2 with normal perfusion pressure 1. Advance care planning, including the requires 40 – 60 mL/kg but can be much (mean arterial pressure/central venous pres- communication of likely outcomes and higher (112–114). sure) for age. realistic goals of treatment, should be 3. Vasopressors/Inotropes (Should Only Be 5. Approach to Pediatric Septic Shock. Fig- discussed with patients and families. De- Used After Appropriate Volume Resuscita- ure 1 shows a flow diagram summarizing an cisions for less aggressive support or tion). Children with severe sepsis can present approach to pediatric septic shock (121). withdrawal of support may be in the pa- with low cardiac output and high systemic 6. Steroids. Hydrocortisone therapy should tient’s best interest. vascular resistance, high cardiac output and be reserved for use in children with catechol- low systemic vascular resistance, or low car- amine resistance and suspected or proven ad- Grade E diac output and low systemic vascular resis- renal insufficiency. Patients at risk include Rationale. It is too frequent that inade- tance shock. Depending on which situation children with severe septic shock and purpura quate physician/family communication char- exists, inotropic support should be started in (122, 123), children who have previously re- acterizes end-of-life care in the ICU. The level the case of fluid refractory shock or a combi- ceived steroid therapies for chronic illness, of life support given to ICU patients may not nation of an inotrope together with a vaso- and children with pituitary or adrenal abnor- be consistent with their wishes. Early and fre- pressor or a vasodilator. Dopamine is the first malities. There are no strict definitions, but quent caregiver discussions with patients who choice of support for the pediatric patient with adrenal insufficiency in the case of cate- face death in the ICU and their loved ones may hypotension refractory to fluid resuscitation. cholamine-resistant septic shock is assumed facilitate appropriate application and with- The choice of vasoactive agent is determined at a random total cortisol concentration 18 drawal of life-sustaining therapies. by the clinical examination. Dopamine- g/dL (496 nmol/L). There is no clear consen- refractory shock may reverse with epinephrine sus for the role of steroids or best dose of S. Pediatric Considerations or norepinephrine infusion (114). Pediatric steroids in children with septic shock. A post patients with low cardiac output states may 30- or 60-min ACTH stimulation test increase 1. Mechanical Ventilation. Due to low benefit from use of dobutamine. The use of in cortisol of 9 g/dL (248 nmol/L) also makes functional residual capacity, young infants vasodilators can reverse shock in pediatric pa- that diagnosis. Two randomized controlled trials and neonates with severe sepsis may require tients who remain hemodynamically unstable used “shock dose” hydrocortisone (25 times early intubation (109). The principles of lung- with a high systemic vascular resistance state, higher than the stress dose) in children, both in protective strategies are applied to children as despite fluid resuscitation and implementa- dengue fever. The results were conflicting (124, they are to adults. In premature infants, addi- tion of inotropic support (114, 115). Nitroso- 125). Dose recommendations vary from 1–2 tional attention is paid to avoiding hyperox- vasodilators with a very short half-life (nitro- mg/kg for stress coverage (based on clinical di- emia to prevent retinopathy. prusside or nitroglycerin) are used as first-line agnosis of adrenal insufficiency) to 50 mg/kg for 2. Fluid Resuscitation. Intravenous access therapy for children with epinephrine-resis- empirical therapy of shock followed by the same for fluid resuscitation and inotrope/vasopres- tant low cardiac output and elevated systemic dose as a 24-hr infusion. sor infusion is more difficult to attain in chil- vascular-resistance shock. Inhaled nitric oxide 7. Protein C and Activated Protein C. Pro- dren than in adults. The American Heart As- reduced extracorporeal membrane oxygen- tein C concentrations in children reach adult sociation has developed pediatric advanced life ation (ECMO) use when given to term neo- values at the age of 3 yrs. This might indicate support guidelines for emergency establish- nates with persistent pulmonary artery hyper- that the importance of protein C supplemen- 866 Crit Care Med 2004 Vol. 32, No. 3
  • 10. tation either as protein C concentrate or as rhAPC is even greater in young children than in adults. There has been one dose finding, placebo-controlled study performed using pro- tein C concentrate. This study was not pow- ered to show an effect on mortality rate but did show a positive effect on sepsis-induced coagulation disturbances (126, 127). No ran- domized studies using rhAPC have been per- formed. 8. Granulocyte Macrophage Colony Stim- ulating Factor. Growth factors or white blood cell transfusions are given to patients with neutropenic sepsis secondary to chemother- apy or white blood cell primary immune defi- ciency. A randomized, controlled trial showed improved outcomes in neonates with sepsis and an absolute neutrophil count 1500/ L (1.5 109/L) treated with a 7-day course of granulocyte macrophage colony stimulating factor (128, 129). 9. DVT Prophylaxis. Most DVTs in young children are associated with central venous catheters. Femoral venous catheters are com- monly used in children, and central venous catheter-associated DVT occurs in approximately 25% of children with a femoral central venous catheter. There are no data on use of heparin prophylaxis to prevent DVT in children. 10. Stress Ulcer Prophylaxis. No studies have been performed in children analyzing the effect of stress ulcer prophylaxis. Studies have shown that the rate of clinically important gastrointestinal bleeding in children occurs at rates similar to adults (130, 131). As in adults, coagulopathy and mechanical ventilation are risk factors for clinically important gastroin- testinal bleeding. Stress ulcer prophylaxis strategy is commonly used in mechanically ventilated children, usually with H2 blockers. Its effect is not known. 11. Renal Replacement Therapy. Continu- ous venovenous hemofiltration may be clini- cally useful in children with anuria/severe ol- iguria and fluid overload, but no large RCTs have been performed. 12. Glycemic Control. In general, infants are at risk for developing hypoglycemia Figure 1. Resuscitation of pediatric septic shock. Adapted from Ref. 121. *Normalization of blood when they depend on intravenous fluids. pressure and tissue perfusion; **hypotension, abnormal capillary refill, or extremity coolness. This means that a glucose intake of 4 – 6 mg·kg 1·min 1 or maintenance fluid intake 15. Intravenous Immunoglobulin. Poly- sis on ECMO; eight of the 12 patients survived, with glucose 10% in NaCl 0.45% is advised. clonal intravenous immunoglobulin has with six leading functionally normal lives at a There are no studies in pediatric patients been reported to reduce mortality rate and is median of 1 yr (range, 4 months to 4 yrs) of analyzing the effect of rigid glycemic con- a promising adjuvant in the treatment of follow-up. Children with sepsis on ECMO do trol using insulin. This should only be done sepsis and septic shock. In children, how- not perform worse than children without sep- with frequent glucose monitoring in view of ever, all the trials have been small, and the sis at long-term follow-up (133–135). the risks for hypoglycemia. totality of the evidence is insufficient to 13. Sedation/Analgesia. Appropriate seda- support a robust conclusion of benefit. Ad- tion and analgesia for children who are me- SUMMARY AND FUTURE junctive therapy with monoclonal intrave- chanically ventilated are the standard of care, nous immunoglobulins remains experimen- DIRECTIONS although there are no data supporting any tal (132). particular drugs or drug regimens. Although evidence-based recommenda- 16. ECMO. ECMO has been used in septic 14. Blood Products. In the absence of data, shock in children, but its impact is not clear. tions have been frequently published in the it is reasonable to maintain hemoglobin con- Survival from refractory shock or respiratory medical literature, documentation of im- centration within the normal range for age in failure associated with sepsis is 80% in neo- pact on patient outcome is limited. The children with severe sepsis and septic shock nates and 50% in children. There is one study next phase of the Surviving Sepsis Cam- ( 10 g/dL [100 g/L]). analyzing 12 patients with meningococcal sep- paign is targeted to implement a core set of Crit Care Med 2004 Vol. 32, No. 3 867
  • 11. the previous recommendations in hospital conferences, and website update and amounted Joseph A. Carcillo, MD; Alain Cariou, MD; Jean- environments where change in behavior to approximately $158,758, and were borne by Francois Dhainaut, MD, PhD; Simon Finfer, MD; and clinical impact can be measured. The unrestricted educational grants from Eli Lilly Juan Gea-Banacloche, MD; Herwig Gerlach, MD, first step in this next phase will be a joint (90%) and Edwards (10%). Most of the expense PhD; Maurene A. Harvey, RN, MPH; Steven M. effort with the Institute of Healthcare Im- for this effort has been time by the committee Hollenberg, MD; Ronald V. Maier, MD; John J. provement to deploy a “change bundle” who received no reimbursement. Marini, MD; Martin Nitsun, MD; Graham Ramsay, based on a core set of the previous recom- MD; Jonathan E. Sevransky, MD; Joseph W. Szokol, mendations into the Institute of Healthcare Faculty Disclosures—Potential MD; Christophe Vinsonneau, MD. Improvement collaborative system. Chart Conflicts of Interest review will identify and track change in REFERENCES practice and clinical outcome. Engender- Speakers bureau, consultant fees, or research ing evidence-based change through moti- grants; Richard J. Beale, MD (Eli Lilly, Fresenius 1. Dellinger RP: Cardiovascular management vational strategies while monitoring and Hemocare and Fresenius Kabi); E. David Bennett, of septic shock. Crit Care Med 2003; 31: sharing impact with healthcare practitio- MD (Deltex, Ltd.); Pierre-Yves Bochud, MD 946 –955 ners is the key to improving outcome in (Swiss National Science Foundation); Christian 2. Friedman G, Silva E, Vincent JL: Has the mortality of septic shock changed with severe sepsis. Brun-Buisson, MD (Arrow Int’l, Eli Lilly, Glaxo- time? Crit Care Med 1998; 26:2078 –2086 The reader is reminded that although Smith-Kline, Roche, Wyeth-Lederle); Thierry Ca- 3. Sackett DL: Rules of evidence and clinical this document is static, the optimum landra, MD (Pfizer, Merck, NatImmune); Jean M. recommendations on the use of antithrom- treatment of severe sepsis and septic Carlet, MD (Eli Lilly, Anbics, Novo Nordisk, botic agents. Chest 1989; 95:2S– 4S shock is a dynamic and evolving process. Wyeth Lederle, Fujisawa, Glaxo-Smith-Kline, 4. Sprung CL, Bernard GR, Dellinger RP: In- New interventions will be proven and es- Bayer, Abbott, Intrabiotics); Jonathan Cohen, MD troduction. Intensive Care Med 2001; tablished interventions, as stated in the (Glaxo-Smith-Kline); Catherine Cordonnier, MD 27(Suppl):S1–S2 current recommendations, may need (Gilead Science, Merck, Pfizer, Fujisawa); E. 5. Rivers E, Nguyen B, Havstad S, et al: Early modification. This publication represents Patchen Dellinger, MD (Glaxo-Smith-Kline, goal-directed therapy in the treatment of the start of what will be an ongoing pro- Bayer, Eli Lilly, Merck, Wyeth-Ayerst, Pfizer, Or- severe sepsis and septic shock. N Engl J Med 2001; 345:1368 –1377 cess. The Surviving Sepsis Campaign and tho-McNeil, Chiron, Versicor, InterMune, Penin- 6. Weinstein MP, Reller LP, Murphy JR, et al: the consensus committee members are sula); R. Phillip Dellinger, MD (Aventis, Bayer, The clinical significance of positive blood committed to creating a dynamic, elec- Cubist, Edwards, Eli Lilly, Ortho Biotech, Wyeth- cultures: A comprehensive analysis of 500 tronic, Web-based guideline process. We Ayerst); Roger G. Finch, MD (Cubist, Bayer, episodes of bacteremia and fungemia in foresee that as new evidence becomes Glaxo-Smith-Kline, AstraZeneca, Bristol Myers adults. I. Laboratory and epidemiologic ob- available, revisions will be channeled Squibb, Aventis); Francois A. Fourrier, MD servations. Rev Infect Dis 1983; 5:35–53 through the committee and, following (Laboratoire Francais du fractionnement et des 7. Blot F, Schmidt E, Nitenberg G, et al: Ear- sponsoring organization approval, biotechnologies [LFB]); Jan A. Hazelzet, MD lier positivity of central venous versus pe- changes will be noted on the electronic (Baxter, Eli Lilly); James H. Jorgensen, PhD (bio- ripheral blood cultures is highly predictive guidelines, which are available for post- Merieux Inc., Becton-Dickinson); Didier Keh, MD of catheter-related sepsis. J Clin Microbiol 1998; 36:105–109 ing on all sponsoring organization Web (Deutsche Forschungsgemeinschaft [DFG]); 8. Mermel LA, Maki DG: Detection of bactere- sites. We anticipate a formal updating Mitchell M. Levy, MD (Eli Lilly, Edwards Life- mia in adults: Consequences of culturing an process annually. sciences, OrthoBiotech); Dennis G. Maki, MD (Eli inadequate volume of blood. Ann Intern Lilly, Becton Dickinson, Johnson and Johnson); Med 1993; 119:270 –272 Acknowledgment John C. Marshall, MD (Glaxo-Smith-Kline, Eli 9. McCabe WR, Jackson GG: Gram negative Lilly, Wyeth-Ayerst, Eisai, Centocor, Boehringer- bacteremia. Arch Intern Med 1962; 110: The ESICM, SCCM, and International Sepsis Ingelheim); Henry Masur, MD (Cubist); Glenn S. 92–100 Forum have established the Surviving Sepsis Murphy, MD (Organon, Inc.); Steven M. Opal, MD 10. Kreger BE, Craven DE, McCabe WR: Gram Campaign with the aim of improving the care of (Genetics Institute, Chiron, Eli Lilly); Margaret negative bacteremia. IV. Re-evaluation of septic patients. The first phase of the Campaign M. Parker, MD (Johnson & Johnson [Ortho Bio- clinical features and treatment in 612 pa- tients. Am J Med 1980; 68:344 –355 was built around the Barcelona ESICM meeting tech] – member of Independent Data Monitoring 11. Leibovici L, Shraga I, Drucker M, et al: The in 2002 and included the initial Barcelona Dec- Committee for epo trial); Joseph E. Parrillo, MD benefit of appropriate empirical antibiotic laration, a medical campaign that identified sep- (Eisai American, Inc., Schering-Plough Co., Gl- treatment in patients with bloodstream in- sis as a killer and the need to make progress in axo-Smith-Kline, Medinox, Inc., Chiron Corp., fection. J Intern Med 1998; 244:379 –386 public awareness and to reduce mortality, and Edwards Lifesciences, Ortho Biotech); Andrew 12. Ibrahim EH, Sherman G, Ward S, et al: The two surveys performed among physicians. The Rhodes, MD (Edwards Lifesciences); Charles L. influence of inadequate antimicrobial treat- cost of phase I was approximately $702,598, and Sprung, MD, JD (AstraZeneca, European Com- ment of bloodstream infections on patient was supported by unrestricted educational grants mission, Eli Lilly); Antoni Torres, MD (Aventis, outcomes in the ICU setting. Chest 2000; from Eli Lilly (94%), Edwards (3%), and Baxter Abbott, Bayer); Stephen Trzeciak, MD (Aventis, 118:146 –155 (3%). Producing the present guidelines docu- Eli Lilly, Edwards Lifesciences); Jeffery S. Vender, 13. Hatala R, Dinh T, Cook DJ: Once-daily ami- noglycoside dosing in immunocompetent ment was phase II of the Campaign. For this, the MD (Abbott Pharmaceuticals); Jean-Louis Vin- adults: A meta-analysis. Ann Intern Med sponsor companies have been entirely separated cent, MD, PhD (Baxter, Brahms, BMS, Eli Lilly, 1996; 124:717–725 from the process by which the guidelines were Glaxo-Smith-Kline, Edwards, Pfizer); Janice L. 14. Ali MZ, Goetz MB: A meta-analysis of the developed by the many contributors, whose con- Zimmerman, MD (Glaxo-Smith-Kline, Cubist). relative efficacy and toxicity of single daily flicts of interest have been collected in accor- Direct financial interest – stock ($10,000 or dosing versus multiple daily dosing of ami- dance with SCCM guidance (see below). The costs more) or partial ownership; None. Faculty with noglycosides. Clin Infect Dis 1997; 24: for this phase mainly included the meeting, tele- no relationship to disclose; Marc Bonten, MD; 796 – 809 868 Crit Care Med 2004 Vol. 32, No. 3
  • 12. 15. Amsden GW, Ballow CH, Bertino JS: Phar- randomised trial. Australian and New Zea- sis and septic shock. N Engl J Med 1987; macokinetics and Pharmacodynamcis of land Intensive Care Society (ANZICS) Clin- 317:653– 658 Anti-infective Agents. In: Principles and ical Trials Group. Lancet 2000; 356: 48. Cronin L, Cook DJ, Carlet J, et al: Cortico- Practice of Infectious Diseases. Fifth Edi- 2139 –2143 steroid treatment for sepsis: A critical ap- tion. Mandell GL, Bennett JE, Dolin R 32. Kellum J, Decker J: Use of dopamine in praisal and meta-analysis of the literature. (Eds). Philadelphia, Churchill Livingstone, acute renal failure: A meta-analysis. Crit Crit Care Med 1995; 23:1430 –1439 2000, pp 253–261 Care Med 2001; 29:1526 –1531 49. The Veterans Administration Systemic Sep- 16. Hyatt JM, McKinnon PS, Zimmer GS, et al: 33. Sharshar T, Blanchard A, Paillard M, et al: sis Cooperative Study Group: Effect on The importance of pharmacokinetic/phar- Circulating vasopressin levels in septic high-dose glucocorticoid therapy on mor- macodynamic surrogate markers to out- shock. Crit Care Med 2003; 31:1752–1758 tality in patients with clinical signs of sep- comes. Focus on antibacterial agents. Clin 34. Holmes CL, Patel BM, Russell JA, et al: sis. N Engl J Med 1987; 317:659 – 665 Pharmacokinet 1995; 28:143–160 Physiology of vasopressin relevant to man- 50. Bernard GR, Vincent JL, Laterre PF, et al: 17. Jimenez MF, Marshall JC: Source control in agement of septic shock. Chest 2001; 120: Efficacy and safety of recombinant human the management of sepsis. Intensive Care 989 –1002 activated protein C for severe sepsis. N Engl Med 2001; 27:S49 –S62 35. Malay MB, Ashton RC, Landry DW, et al: J Med 2001; 344:699 –709 18. Bufalari A, Giustozzi G, Moggi L: Postoper- Low-dose vasopressin in the treatment of 51. Hébert PC, Wells G, Blajchman MA, et al: A ative intraabdominal abscesses: Percutane- vasodilatory septic shock. J Trauma 1999; multicenter, randomized, controlled clini- ous versus surgical treatment. Acta Chir 47:699 –705 cal trial of transfusion in critical care. Belg 1996; 96:197–200 36. Holmes CL, Walley KR, Chittock DR, et al: N Engl J Med 1999; 340:409 – 417 19. Moss RL, Musemeche CA, Kosloske AM: Ne- The effects of vasopressin on hemodynam- 52. Marik PE, Sibbald WJ: Effect of stored-blood crotizing fascitis in children: Prompt recog- ics and renal function in severe septic transfusion on oxygen delivery in patients nition and aggressive therapy improve sur- shock: A case series. Intensive Care Med with sepsis. JAMA 1993; 269:3024 –3029 vival. J Pediatr Surg 1996; 31:1142–1146 2001; 27:1416 –1421 53. Lorente JA, Landín L, De Pablo R, et al: 20. Centers for Disease Control and Prevention: 37. Gattinoni L, Brazzi L, Pelosi P, et al: A trial Effects of blood transfusion on oxygen Guidelines for the Prevention of Intravascu- of goal-oriented hemodynamic therapy in transport variables in severe sepsis. Crit lar Catheter-Related Infections. MMWR critically ill patients. N Engl J Med 1995; Care Med 1993; 21:1312–1318 2002; 51:1–29 333:1025–1032 54. Corwin HL, Gettinger A, Rodriguez RM, et 21. O’Grady NP, Alexander M, Dellinger EP, et 38. Hayes MA, Timmins AC, Yau EHS, et al: al: Efficacy of recombinant human erythro- al: Guidelines for the prevention of intra- Elevation of systemic oxygen delivery in the poietin in the critically ill patient: A ran- vascular catheter-related infections. Clin treatment of critically ill patients. N Engl domized double-blind, placebo-controlled Infect Dis 2002; 35:1281–1307 J Med 1994; 330:1717–1722 trial. Crit Care Med 1999; 27:2346 –2350 22. Choi PTL, Yip G, Quinonez LG, et al: Crys- 39. Annane D, Sebille V, Charpentier C, et al: 55. Corwin HL, Gettinger A, Pearl RG, et al: talloids vs. colloids in fluid resuscitation: A Effect of treatment with low doses of hydro- Efficacy of recombinant human erythropoi- systematic review. Crit Care Med 1999; 27: cortisone and fludrocortisone on mortality etin in critically ill patients. JAMA 2002; 200 –210 in patients with septic shock. JAMA 2002; 288:2827–2835 23. Cook D, Guyatt G: Colloid use for fluid 288:862– 871 56. Practice parameter for the use of fresh- resuscitation: Evidence and spin. Ann In- 40. Briegel J, Forst H, Haller M, et al: Stress frozen plasma, cryoprecipitate, and plate- tern Med 2001; 135:205–208 doses of hydrocortisone reverse hyperdy- lets. Fresh-Frozen Plasma, Cryoprecipitate, 24. Schierhout G, Roberts I: Fluid resuscitation namic septic shock: A prospective, random- and Platelets Administration Practice with colloid or crystalloid solutions in crit- ized, double-blind, single-center study. Crit Guidelines Development Task Force of the ically ill patients: A systematic review of Care Med 1999; 27:723–732 College of American Pathologists. JAMA randomized trials. BMJ 1998; 316:961–964 41. Bollaert PE, Charpentier C, Levy B, et al: 1994; 271:777–781 25. Hollenberg SM, Ahrens TS, Astiz ME, et al: Reversal of late septic shock with supra- 57. Guidelines for red blood cell and plasma Practice parameters for hemodynamic sup- physiologic doses of hydrocortisone. Crit transfusion for adults and children. Report port of sepsis in adult patients. Crit Care Care Med 1998; 26:645– 650 of the Working Group. CMAJ 1997; Med 1999; 27:639 – 660 42. Annane D, Sebille V, Troche G, et al: A 156(Suppl):S1–S24 26. LeDoux D, Astiz ME, Carpati CM, et al: 3-level prognostic classification in septic 58. Practice guidelines for blood component Effects of perfusion pressure on tissue per- shock based on cortisol levels and cortisol therapy. A report by the American Society fusion in septic shock. Crit Care Med 2000; response to corticotropin. JAMA 2000; 283: of Anaesthesiologists Task Force on Blood 28:2729 –2732 1038 –1045 Component Therapy. Anesthesiology 1996; 27. Regnier B, Rapin M, Gory G, et al: Haemo- 43. Annane D, Cavaillon JM: Corticosteroids in 84:732–747 dynamic effects of dopamine in septic sepsis: From bench to bedside? Shock 2003; 59. Warren BL, Eid A, Singer P, et al: High-dose shock. Intensive Care Med 1977; 3:47–53 20:197–207 antithrombin III in severe sepsis. A ran- 28. Martin C, Papazian L, Perrin G, et al: Nor- 44. Marik PE, Zaloga GP: Adrenal insufficiency domized controlled trial. JAMA 2001; 286: epinephrine or dopamine for the treatment during septic shock. Crit Care Med 2003; 1869 –1878 of hyperdynamic septic shock? Chest 1993; 31:141–145 60. Amato MB, Barbas CS, Medeiros DM, et al: 103:1826 –1831 45. Cooper MS, Stewart PM: Corticosteroid in- Effect of a protective-ventilation strategy on 29. Martin C, Viviand X, Leone M, et al: Effect of sufficiency in acutely ill patients. N Engl mortality in the acute respiratory distress norepinephrine on the outcome of septic J Med 2003; 348:727–734 syndrome. N Engl J Med 1998; 338:347–354 shock. Crit Care Med 2000; 28:2758 –2765 46. Keh D, Boehnke T, Weber-Carstens S, et al: 61. Stewart TE, Meade MO, Cook DJ, et al: 30. De Backer D, Creteur J, Silva E, et al: Ef- Immunologic and hemodynamic effects of Evaluation of a ventilation strategy to pre- fects of dopamine, norepinephrine, and epi- “low-dose” hydrocortisone in septic shock: vent barotrauma in patients at high risk for nephrine on the splanchnic circulation in A double-blind, randomized, placebo- acute respiratory distress syndrome. Pres- septic shock: Which is best? Crit Care Med controlled, crossover study. Am J Respir sure- and Volume-Limited Ventilation 2003; 31:1659 –1667 Crit Care Med 2003; 167:512–520 Strategy Group. N Engl J Med 1998; 338: 31. Bellomo R, Chapman M, Finfer S, et al: 47. Bone RC, Fisher CJ, Clemmer TP: A con- 355–361 Low-dose dopamine in patients with early trolled clinical trial of high-dose methyl- 62. Brochard L, Roudat-Thoraval F, Roupie E, renal dysfunction: A placebo-controlled prednisolone in the treatment of severe sep- et al: Tidal volume reduction for prevention Crit Care Med 2004 Vol. 32, No. 3 869
  • 13. of ventilator-induced lung injury in acute 76. Chatte G, Sab JM, Dubois JM, et al: Prone and recovery profiles of vecuronium and respiratory distress syndrome. The Multi- position in mechanically ventilated patients cisatracurium 51W89 in intensive care unit center Trial Group on Tidal Volume reduc- with severe acute respiratory failure. Am J patients. Anesth Analg 1995; 81:3–12 tion in ARDS. Am J Respir Crit Care Med Respir Crit Care Med 1997; 155:473– 478 91. Brandom BW, Yellon FF, Lloyd ME, et al: 1998; 158:1831–1838 77. Drakulovic M, Torres A, Bauer T, et al: Su- Recovery from doxacurium infusion admin- 63. Brower RG, Shanholtz CB, Fessler HE, et al: pine body position as a risk factor for nos- istered to produce immobility for more Prospective, randomized, controlled clinical ocomial pneumonia in mechanically venti- than four days in pediatric patients in the trial comparing traditional versus reduced lated patients: A randomised trial. Lancet intensive care unit. Anesth Analg 1997; 84: tidal volume ventilation in acute respiratory 1999; 354:1851–1858 307–314 distress syndrome patients. Crit Care Med 78. Esteban A, Alia I, Tobin MJ, et al: Effect of 92. Rudis MI, Sikora CA, Angus E, et al: A 1999; 27:1492–1498 spontaneous breathing trial duration on prospective, randomized, controlled evalua- 64. Brower RG, Fessler HE: Mechanical venti- outcome of attempts to discontinue me- tion of peripheral nerve stimulation versus lation in acute lung injury and acute respi- chanical ventilation. Spanish Lung Failure standard clinical dosing of neuromuscular ratory distress syndrome. Clin Chest Med Collaborative Group. Am J Respir Crit Care blocking agents in critically ill patients. Crit 2000; 21:491–510 Med 1999; 159:512–518 Care Med 1997; 25:25575–25583 65. Eichacker PQ, Gerstenberger EP, Banks 79. Ely EW, Baker AM, Dunagan DP, et al: Ef- 93. Frankel H, Jeng J, Tilly E, et al: The impact SM, et al: Meta-analysis of acute lung injury fect on the duration of mechanical ventila- of implementation of neuromuscular block- and acute respiratory distress syndrome tri- tion of identifying patients capable of ade monitoring standards in a surgical in- als testing low tidal volumes. Am J Respir breathing spontaneously. N Engl J Med tensive care unit. Am Surg 1996; 62: Crit Care Med 2002; 166:1510 –1514 1996; 335:1864 –1869 503–506 66. Ventilation with lower tidal volumes as 80. Esteban A, Alia I, Gordo F, et al: Extubation 94. van den Berghe G, Wouters P, Weekers F, et compared with traditional tidal volumes for outcome after spontaneous breathing trials al: Intensive insulin therapy in the critically acute lung injury and the acute respiratory with T-tube or pressure support ventilation. ill patients. N Engl J Med 2001; 345: distress syndrome. The Acute Respiratory The Spanish Lung Failure Collaborative 1359 –1367 Distress Syndrome Network. N Engl J Med Group. Am J Respir Crit Care Med 1997; 95. Finney SJ, Zekveld C, Elia A, et al: Glucose 2000; 342:1301–1308 156:459 – 465 control and mortality in critically ill pa- 67. Hickling KG, Walsh J, Henderson S, et al: 81. Kollef MH, Levy NT, Ahrens TS, et al: The tients. JAMA 2003; 2041–2047 Low mortality rate in adult respiratory dis- use of continuous IV sedation is associated 96. Van den Berghe G, Wouters PJ, Bouillon R, tress syndrome using low-volume, pres- with prolongation of mechanical ventila- et al: Outcome benefit of intensive insulin sure-limited ventilation with permissive hy- tion. Chest 1998; 114:541–548 therapy in the critically ill: Insulin dose percapnia: A prospective study. Crit Care 82. Kress JP, Pohlman AS, O’Connor MF, et al: versus glycemic control. Crit Care Med Med 1994; 22:1568 –1578 Daily interruption of sedative infusions in 2003; 31:359 –366 68. Bidani A, Tzouanakis AE, Cardenas VJ, et al: critically ill patients undergoing mechani- 97. Klein S, Kinney J, Jeejeebhoy K, et al: Nu- Permissive hypercapnia in acute respiratory cal ventilation. N Engl J Med 2000; 342: trition support in clinical practice: Review failure. JAMA 272:957–962 1471–1477 of published data and recommendations for 69. Marini JJ, Ravenscraft SA: Mean airway 83. Brook AD, Ahrens TS, Schaiff R, et al: Effect future research directions. A summary of a pressure: Physiologic determinants and of a nursing-implemented sedation protocol conference sponsored by the National Insti- clinical importance—Part I: Physiologic de- on the duration of mechanical ventilation. tutes of Health, American Society for Par- terminants and measurements. Crit Care Crit Care Med 1999; 27:2609 –2615 enteral and Enteral Nutrition, and Ameri- Med 1992; 20:1461–1472 84. Giostra E, Magistris MR, Pizzolato G, et al: can Society for Clinical Nutrition. Am J Clin 70. Gattinoni L, Marcolin R, Caspani ML, et al: Neuromuscular disorder in intensive care Nutr 1997; 66:683–706 Constant mean airway pressure with differ- unit patients treated with pancuronium 98. Mehta RL, McDonald B, Gabbai FB, et al: A ent patterns of positive pressure breathing bromide. Occurrence in a cluster group of randomized clinical trial of continuous ver- during the adult respiratory distress syn- seven patients and two sporadic cases, with sus intermittent dialysis for acute renal fail- drome. Bull Eur Physiopathol Respir 1985; electrophysiologic and histologic examina- ure. Kidney Int 2001; 60:1154 –1163 21:275–279 tion. Chest 1994; 106:210 –220 99. Kellum J, Angus DC, Johnson JP, et al: 71. Pesenti A, Marcolin R, Prato P, et al: Mean 85. Rossiter A, Souney PF, McGowan S, et al: Continuous versus intermittent renal re- airway pressure vs. positive end-expiratory Pancuronium-induced prolonged neuro- placement therapy: A meta-analysis. Inten- pressure during mechanical ventilation. muscular blockade. Crit Care Med 1991; sive Care Med 2002; 28:29 –37 Crit Care Med 1985; 13:34 –37 19:1583–1587 100. Cooper DJ, Walley KR, Wiggs BR, et al: 72. Stocker R, Neff T, Stein S, et al: Prone 86. Partridge BL, Abrams JH, Bazemore C, et al: Bicarbonate does not improve hemody- positioning and low-volume pressure- Prolonged neuromuscular blockade after namics in critically ill patients who have limited ventilation improve survival in pa- long-term infusion of vecuronium bromide lactic acidosis: A prospective, controlled tients with severe ARDS. Chest 1997; 111: in the intensive care unit. Crit Care Med clinical study. Ann Intern Med 1990; 112: 1008 –1017 1990; 18:1177–1179 492– 498 73. Lamm WJ, Graham MM, Albert RK: Mech- 87. Vanderheyden BA, Reynolds HN, Gerold 101. Mathieu D, Neviere R, Billard V, et al: Ef- anism by which prone position improves KB, et al: Prolonged paralysis after long- fects of bicarbonate therapy on hemody- oxygenation in acute lung injury. Am J Re- term vecuronium infusion. Crit Care Med namics and tissue oxygenation in patients spir Crit Care Med 1994; 150:184 –193 1992; 20:304 –307 with lactic acidosis: A prospective, con- 74. Jolliet P, Bulpa P, Chevrolet JC: Effects of 88. Meyer KC, Prielipp RC, Grossman JE, et al: trolled clinical study. Crit Care Med 1991; the prone position on gas exchange and Prolonged weakness after infusion of atra- 19:1352–1356 hemodynamics in severe acute respiratory curium in two intensive care unit patients. 102. Cade JF: High risk of the critically ill for distress syndrome. Crit Care Med 1998; 26: Anesth Analg 1994; 78:772–774 venous thromboembolism. Crit Care Med 1977–1985 89. Manthous CA, Chatila W: Prolonged weak- 1982; 10:448 – 450 75. Gattinoni L, Tognoni G, Pesenti A, et al: ness after withdrawal of atracurium. Am J 103. Belch JJ, Lowe GD, Ward AG, et al: Preven- Effect of prone positioning on the survival Respir Crit Care Med 1994; 150:1441–1443 tion of deep vein thrombosis in medical of patients with acute respiratory failure. 90. Prielipp RC, Coursin DB, Scuderi PE, et al: patients by low-dose heparin. Scott Med J N Engl J Med 2001; 345:568 –573 Comparison of the infusion requirements 1981; 26:115–117 870 Crit Care Med 2004 Vol. 32, No. 3
  • 14. 104. Samama MM, Cohen AT, Darmon JY, et al: and afterload-reducing agents in neonates. gue shock syndrome. Pediatrics 1982; 69: A comparison of enoxaparin with placebo Clin Perinatol 1988; 15:467– 489 45– 49 for the prevention of venous thromboembo- 116. Roberts JD Jr, Fineman JR, Morin FC III, et 126. Hazelzet JA, de Kleijn ED, de Groot R: En- lism in acutely ill medical patients. Prophy- al: Inhaled nitric oxide and persistent pul- dothelial protein C activation in meningo- laxis in Medical Patients with Enoxaparin monary hypertension of the new born. In- coccal sepsis. N Engl J Med 2001; 345: Study Group. N Engl J Med 1999; 341: haled Nitric Oxide Study Group. N Engl 1776 –1777 793– 800 J Med 1997; 336:605– 610 127. de Kleijn ED, de Groot R, Hack CE, et al: 105. Borrero E, Bank S, Margolis I, et al: Com- 117. Barton P, Garcia J, Kouatli A, et al: Hemo- Activation of protein C following infusion of parison of antacid and sucralfate in the pre- dynamic effects of i. v. milrinone lactate in protein C concentrate in children with se- vention of gastrointestinal bleeding in pa- pediatric patients with septic shock. A pro- vere meningococcal sepsis and purpura ful- tients who are critically ill. Am J Med 1985; spective, double-blinded, randomized, pla- minans: A randomized, double-blinded, pla- 79:62– 64 cebo-controlled, interventional study. Chest cebo-controlled, dose-finding study. Crit 106. Bresalier RS, Grendell JH, Cello JP, et al: 1996; 109:1302–1312 Care Med 2003; 31:1839 –1847 Sucralfate versus titrated antacid for the 118. Lindsay CA, Barton P, Lawless S, et al: 128. Bilgin K, Yaramis A, Haspolat K, et al: A prevention of acute stress-related gastroin- Pharmacokinetics and pharmacodynam- randomized trial of granulocyte-macroph- testinal hemorrhage in critically ill pa- ics of milrinone lactate in pediatric pa- age colony-stimulating factor in neonates tients. Am J Med 1987; 83:110 –116 tients with septic shock. J Pediatr 1998; with sepsis and neutropenia. Pediatrics 107. Cook D, Guyatt G, Marshall J, et al: A com- 132:329 –334 2001; 107:36 – 41 parison of sucralfate and ranitidine for the 119. Irazuzta JE, Pretzlaff RK, Rowin ME: Amri- 129. La Gamma EF, De Castro MH: What is prevention of upper gastrointestinal bleed- none in pediatric refractory septic shock: the rationale for the use of granulocyte ing in patients requiring mechanical venti- An open-label pharmacodynamic study. Pe- and granulocyte-macrophage colony- lation. Canadian Critical Care Trials Group. diatr Crit Care Med 2001; 2:24 –28 stimulating factors in the neonatal intensive N Engl J Med 1998; 338:791–797 120. Lauterbach R, Pawlik D, Kowalczyk D, et al: care unit? Acta Paediatr Suppl 2002; 91: 108. Stothert JC, Simonowitz DA, Dellinger EP, Effect of the immunomodulating agent, 109 –116 et al: Randomized prospective evaluation of pentoxifylline, in the treatment of sepsis in 130. Chaïbou M, Tucci M, Dugas MA, et al: Clin- cimetidine and antacid control of gastric pH prematurely delivered infants: A placebo- ically significant upper gastrointestinal in the critically ill. Ann Surg 1980; 192: controlled, double-blind trial. Crit Care bleeding acquired in a pediatric intensive 169 –174 Med 1999; 27:807– 814 care unit: A prospective study. Pediatrics 109. Pollard AJ, Britto J, Nadel S, et al: Emer- 121. Carcillo JA, Fields AI, American College of 1998; 102:933–938 gency management of meningococcal dis- Critical Care Medicine Task Force Commit- 131. Gauvin F, Dugas M, Chaïbou M, et al: The ease. Arch Dis Child 1999; 80:290 –296 tee Members: Clinical practice parameters impact of clinically significant upper gas- 110. Kanter RK, Zimmerman JJ, Strauss RH, et for hemodynamic support of pediatric and trointestinal bleeding in a pediatric inten- al: Pediatric emergency intravenous access. Evaluation of a protocol. Am J Dis Child neonatal patients in septic shock. Crit Care sive care unit. Pediatr Crit Care Med 2001; 1986; 140:132–134 Med 2002; 30:1365–1378 2:294 –298 111. Ngo NT, Cao XT, Kneen R, et al: Acute 122. De Kleijn ED, Joosten KF, Van Rijn B, et al: 132. Alejandria MM, Lansang MA, Dans LF, et al: management of dengue shock syndrome: A Low serum cortisol in combination with Intravenous immunoglobulin for treating randomized double-blind comparison of 4 high adrenocorticotrophic hormone con- sepsis and septic shock. Cochrane Database intravenous fluid regimens in the first centrations are associated with poor out- Syst Rev 2002; (1):CD001090 hour. Clin Infect Dis 2001; 32:204 –213 come in children with severe meningococ- 133. Meyer DM, Jessen ME: Results of extracor- 112. Carcillo JA, Davis AL, Zaritsky A: Role of cal disease. Pediatr Infect Dis J 2002; 21: poreal membrane oxygenation in children early fluid resuscitation in pediatric septic 330 –336 with sepsis. The Extracorporeal LifeSupport shock. JAMA 1991; 266:1242–1245 123. Riordan FA, Thomson AP, Ratcliffe JM, et al: Organization. Ann Thorac Surg 1997; 63: 113. Powell KR, Sugarman LI, Eskenazi AE, et Admission cortisol and adrenocorticotro- 756 –761 al: Normalization of plasma arginine vaso- phic hormone levels in children with me- 134. Goldman AP, Kerr SJ, Butt W, et al: Extra- pressin concentrations when children with ningococcal disease: Evidence of adrenal in- corporeal support for intractable cardiore- meningitis are given maintenance plus re- sufficiency? Crit Care Med 1999; 27: spiratory failure due to meningococcal dis- placement fluid therapy. J Pediatr 1991; 2257–2261 ease. Lancet 1997; 349:466 – 469 117:515–522 124. Min M, U T, Aye M, et al: Hydrocortisone in 135. Brochard L, Rauss A, Benito S, et al: Com- 114. Ceneviva G, Paschall JA, Maffei F, et al: the management of dengue shock syn- parison of three methods of gradual with- Hemodynamic support in fluid-refractory drome. Southeast Asian J Trop Med Public drawal from ventilatory support during pediatric septic shock. Pediatrics 1998; 102: Health 1975; 6:573–579 weaning from mechanical ventilation. e19 125. Sumarmo, Talogo W, Asrin A, et al: Failure Am J Respir Crit Care Med 1994; 150: 115. Keeley SR, Bohn DJ: The use of inotropic of hydrocortisone to affect outcome in den- 896 –903 Crit Care Med 2004 Vol. 32, No. 3 871
  • 15. Appendix A. Source control Source Control Technique Examples Drainage ● Intra-abdominal abscess ● Thoracic empyema ● Septic arthritis ● Pyelonephritis, cholangitis Debridement ● Necrotizing fasciitis ● Infected pancreatic necrosis ● Intestinal infarction ● Mediastinitis Device removal ● Infected vascular catheter ● Urinary catheter ● Colonized endotracheal tube ● Infected intrauterine contraceptive device Definitive control ● Sigmoid resection for diverticulitis ● Cholecystectomy for gangrenous cholecystitis ● Amputation for clostridial myonecrosis Appendix B. Contraindications to use of recombinant human activated protein C (rhAPC)a rhAPC increases the risk of bleeding. rhAPC is contraindicated in patients with the following clinical situations in which bleeding could be associated with a high risk of death or significant morbidity. ● Active internal bleeding ● Recent (within 3 months) hemorrhagic stroke ● Recent (within 2 months) intracranial or intraspinal surgery, or severe head trauma ● Trauma with an increased risk of life-threatening bleeding ● Presence of an epidural catheter ● Intracranial neoplasm or mass lesion or evidence of cerebral herniation See labeling instructions for relative contraindications. a The committee recommends that platelet count be maintained at 30,000 during infusion of rhAPC. Physicians’ Desk Reference. 57th Edition. Montvale, NJ, Thompson PDR, 2003, pp 1875–1876. Appendix C. ARDSNET Ventilator Management (66) ● Assist control mode—volume ventilation ● Reduce tidal volume to 6 mL/kg predicted body weight ● Keep Pplat 30 cm H2O —Reduce Tv as low as 4 mL/kg predicted body weight* to limit Pplat ● Maintain SaO2/SpO2 88–95% ● Anticipated PEEP settings at various FIO2 requirements FIO2 0.3 0.4 0.4 0.5 0.5 0.6 0.7 0.7 0.7 0.8 0.9 0.9 0.9 1.0 PEEP 5 5 8 8 10 10 10 12 14 14 14 16 18 20–24 *Predicted Body Weight Calculation ● Male—50 2.3 [height (inches) 60] or 50 0.91 [height (cm) 152.4] ● Female—45.5 2.3 [height (inches) 60] or 45.5 0.91 [height (cm) 152.4] Tv, tidal volume; SaO2, arterial oxygen saturation; PEEP, positive end-expiratory pressure. 872 Crit Care Med 2004 Vol. 32, No. 3
  • 16. Appendix D. Use of spontaneous breathing trial in weaning ARDS patients Crit Care Med 2004 Vol. 32, No. 3 873