Abstract
Background
The staged laparotomy in the operative management of emergency general surgery (EGS) patients is an extension of trauma surgeons operating on this population. Indications for its application, however, are not well defined, and are currently based on the lethal triad used in physiologically-decompensated trauma patients. This study sought to determine the acute indications for the staged, rapid source control laparotomy (RSCL) in EGS patients.
Methods
All EGS patients undergoing emergent staged RSCL and non-RSCL over 3 years were studied. Demographics, physiologic parameters, perioperative variables, outcomes, and survival were compared. Logistic regression models determined the influence of physiologic parameters on mortality and postoperative complications. EGS-RSCL indications were defined.
Results
215 EGS patients underwent emergent laparotomy; 53 (25 %) were staged RSCL. In the 53 patients who underwent a staged RSCL based on the lethal triad, adjusted multivariable regression analysis shows that when used alone, no component of the lethal triad independently improved survival. Staged RSCL may decrease mortality in patients with preoperative severe sepsis / septic shock, and an elevated lactate (≥3); acidosis (pH ≤ 7.25); elderly (≥70); male gender; and multiple comorbidities (≥3). Of the 162 non-RSCL emergent laparotomies, 27 (17 %) required unplanned re-explorations; of these, 17 (63 %) had sepsis preoperatively and 9 (33 %) died.
Conclusions
The acute physiologic indicators that help guide operative decisions in trauma may not confer a similar survival advantage in EGS. To replace the lethal triad, criteria for application of the staged RSCL in EGS need to be defined. Based on these results, the indications should include severe sepsis / septic shock, lactate, acidosis, gender, age, and pre-existing comorbidities. When correctly applied, the staged RSCL may help to improve survival in decompensated EGS patients.
Keywords: Damage control, Emergency general surgery, EGS, Rapid source control laparotomy, Physiologically decompensated
Background
The staged laparotomy in the operative management of select trauma patients is designed to ensure their immediate survival [1–6]. The damage control (DC) laparotomy is therefore not an operation of last resort; rather, it is a well thought-out stage on a continuum of care which prioritizes the restoration of physiologic normality and homeostasis above definitive organ repair and anatomic reconstruction.
Application of DC principles are based on the clinical recognition of a trauma patient who is physiologically decompensated as defined by the lethal triad seen with hemorrhagic shock: acidosis, coagulopathy, and hypothermia. Decompensated trauma patients must be rescued to avoid progression to irreversible physiologic exhaustion and death; abbreviated operations allow stabilization, correction, and reevaluation of physiologic derangements in an intensive care unit setting [6–13].
Similarly, a select group of emergency general surgery (EGS) patients also present decompensated, near irreversible physiologic exhaustion and death, but for different reasons, often driven by severe sepsis or septic shock [14]. As a natural extension of trauma surgeons operating on the EGS patient-population, DC principles have been widely applied to the operative management of EGS patients.
Indications for DC application in EGS patients, however, are not well defined, and are currently based on the lethal triad used in trauma patients. Because the lethal triad in trauma is founded on patients presenting with hemorrhagic shock – something less commonly seen in EGS patients – its use to guide operative decision making in EGS patients may not be appropriate.
This study sought to determine the acute physiologic indications for the staged, rapid source control laparotomy (RSCL) in EGS patients. Our hypothesis was that application of the lethal triad to EGS patients as criteria for implementation of abbreviated laparotomy would not improve outcomes, and that the definition of a physiologically decompensated EGS patient would be unique from that used in trauma patients.
Methods
This is a retrospective review of consecutive EGS patients undergoing emergent, non-trauma related laparotomies over 3 years, from March 1, 2007 to March 1, 2010, at a tertiary medical center. Emergent operations were defined in accordance with the National Surgical Quality Improvement Program’s (NSQIP) definition of an emergency case: one performed as soon as possible and no later than 12 h after the patient has been admitted to the hospital or after the onset of related preoperative symptomatology [15].
Variables were collected through electronic chart review. Data included demographics, physiologic parameters, perioperative variables, outcomes, and survival. Magnitude of the inflammatory response (four categories: no inflammation, SIRS, sepsis, or severe sepsis/septic shock) was classified based on the NSQIP definition; this definition is in concert with standardized definitions outlined by the American College of Chest Physicians (ACCP), the Society of Critical Care Medicine (SCCM), and the Surgical Infection Society (SIS) [16].
Patients were identified as undergoing a rapid source control laparotomy (RSCL; i.e., damage control laparotomy; planned re-laparotomy) if there was a deliberate, preemptive plan to perform an immediate, limited, staged operation as part of an ongoing continuum of resuscitation. The decision to proceed with staged RSCL was based on the lethal triad used in trauma patients; such RSCL intentions were identified in the operative note, which had to address the planned attempt to reverse the pre-terminal effects of pre-operative physiologic derangements, and/or intra-abdominal hypertension, by means of an abbreviated laparotomy. These patients were left with an open abdomen with a negative pressure dressing at the end of the initial operation, and transferred to the intensive care unit for stabilization. The second operation was then governed by a planned re-laparotomy, once resuscitation and stabilization had been achieved.
Non-RSCL patients were those who underwent non-staged operations, and had their fascia closed at the completion of the initial operation. If these patients subsequently required a re-laparotomy, this would be considered an unplanned re-laparotomy, or an “on-demand re-laparotomy” [17, 18]. For the current analyses, only patients who underwent open operations with colon or small bowel resections were included, based on their high degree of postoperative morbidity and mortality, comparable source for sepsis, and the increased power of the analyses [19–21].
Patient characteristics, physiologic parameters, perioperative variables, outcome metrics, and survival were first compared using univariate techniques. Chi-squared analysis (χ2) or Fisher’s exact test were used to compare differences in proportions of categorical variables; such data were summarized by percentages. Student’s t-tests were used to compare normally distributed continuous variables; such data were summarized by mean values with standard deviations (±SD). Wilcoxon rank sum tests were used to compare non-normally distributed continuous variables; such data were summarized by median values with interquartile ranges.
In hospital mortality was the primary outcome measure. Logistic regression models determined the influence of acute physiologic parameters and other patient characteristics on in-hospital mortality; analyses assessing determinants of postoperative complications were additionally completed. All candidate covariates for multivariable regression were included in a full selection model; variables were not excluded based on their statistical significance. Significance was defined as p-value < 0.05 throughout. EGS-based RSCL indications were defined.
All statistical analyses were conducting using a commercially available statistics software program (SAS 9.2; SAS Institute Inc., Cary, NC). Approval was obtained from the Wake Forest University Baptist Medical Center Institutional Review Board.
Results
215 EGS patients underwent emergent laparotomy during the study period, 162 (75 %) were non-rapid source control laparotomy (non-RSCL) operations and 53 (25 %) were staged rapid source control laparotomy (RSCL; damage control; planned re-laparotomy). Comparing the two operative groups, there were no significant differences in patient characteristics, including gender, race, age, or comorbidities (Table 1).
Table 1.
Patient characteristics and peri-operative physiologic scores & metrics, by operation type
Variablea | non-RSCL (n = 162) | RSCL (n = 53) | p-valueb |
---|---|---|---|
Male gender | 94 (58.0 %) | 29 (54.7 %) | 0.6727 |
Race & Ethnicity: | |||
White | 128 (79.0 %) | 46 (86.8 %) | 0.2107 |
Black | 27 (16.7 %) | 6 (11.2 %) | 0.3486 |
Age, years | 61 (17) | 64 (13) | 0.2336 |
Age (≥70) | 55 (34.0 %) | 19 (35.9 %) | 0.8006 |
Comorbidities: | |||
Number comorbidities, average | 1.9 (2.2) | 2.2 (2.8) | 0.4641 |
No comorbidities | 71 (43.8 %) | 23 (43.4 %) | 0.9562 |
1 comorbidity | 19 (11.7 %) | 2 (3.8 %) | 0.0904 |
2 comorbidities | 14 (8.6 %) | 7 (13.2 %) | 0.3311 |
≥3 comorbidities | 58 (35.8 %) | 21 (39.6 %) | 0.6166 |
Inflammatory status preoperatively: | |||
No inflammation | 75 (46.3 %) | 10 (18.9 %) | 0.0004 |
Sepsis | 59 (36.4 %) | 28 (52.8 %) | 0.0346 |
Severe sepsis/septic shock | 28 (17.3 %) | 15 (28.3 %) | 0.0817 |
Lethal Triad: | |||
Hypothermia (temp ≤ 35C) | 24 (16.8 %) | 7 (14.9 %) | 0.7610 |
Coagulopathy (INR ≥ 1.7) | 13 (11.1 %) | 9 (18.4 %) | 0.2085 |
Acidosis (pH ≤ 7.25) | 24 (22.2 %) | 18 (35.3 %) | 0.0810 |
Patient characteristics: | |||
ASA score, average | 3 (1) | 4 (1) | <0.0001 |
ASA score, 1 or 2 | 23 (14.2 %) | 0 (0.0 %) | 0.0015 |
ASA score, 3 | 65 (40.1 %) | 8 (15.1 %) | 0.0008 |
ASA score, 4 or 5 | 74 (45.7 %) | 45 (84.9 %) | <0.0001 |
Lactate (≥3) | 32 (33.3 %) | 26 (51.0 %) | 0.0372 |
RSCL rapid source control laparotomy, PRBC packed red blood cells, C Celsius, INR international normalized ratio, ASA American Society of Anesthesiologists, L liters
aCategorical variables are presented as number (%); continuous data are presented as mean (± standard deviation); and non-normally distributed continuous variables as median (interquartile range)
b P-values for overall tests of differences between the groups from χ2 or Fisher’s Exact Test for categorical variables and one-way analysis of variance or Kruskal-Wallis test for continuous variables; p-value of <0.05 significant
Peri-operative physiologic scores and metrics, however, did significantly differ (Table 1). Compared with emergent patients in the RSCL cohort, the non-RSCL group was overall healthier, with a significantly higher percentage of patients with no preoperative inflammation and with lower ASA scores (1, 2, or 3). The two groups did not differ significantly with regard to patients with severe sepsis / septic shock, hypothermia, coagulopathy, or acidosis. No patients in either group fit only into the SIRS only classification of preoperative inflammation, indicating that all had a presumed source of infection.
Overall mortality in the RSCL group was significantly higher than in the non-RSCL population (45 % vs 20 %) (Table 2). Specifically, mortality was higher in RSCL compared to non-RSCL patients who were female, white, and without comorbidities. Interestingly, however, mortality between the two operative approaches was no different for patients with sepsis or severe sepsis / septic shock; males; elderly (age ≥70); patients with multiple comorbidities (≥3); patients with hypothermia (temperature ≤35C), coagulopathy (INR ≥1.7), and acidosis (pH ≤ 7.25) (the lethal triad criteria); for all ASA scoring levels; and for elevated lactate levels.
Table 2.
Rates of in-hospital mortality for patient characteristics and peri-operative physiologic metrics, by operation type
Variablea | non-RSCL (n = 162) | RSCL (n = 53) | p-valueb |
---|---|---|---|
All patients: | 33 (20.4 %) | 24 (45.3 %) | 0.0004 |
Inflammatory status preoperatively: | |||
No inflammation | 8 (10.7 %) | 5 (50.0 %) | 0.0012 |
Sepsis | 10 (19.9 %) | 10 (35.7 %) | 0.0520 |
Severe sepsis/septic shock | 15 (53.6 %) | 9 (60.0 %) | 0.6858 |
Patient Characteristics: | |||
Male Gender | 25 (26.6 %) | 13 (44.8 %) | 0.0632 |
Female Gender | 8 (11.7 %) | 11 (45.8 %) | 0.0004 |
Race, White | 27 (21.1 %) | 20 (43.5 %) | 0.0034 |
Age (≥70) | 20 (36.4 %) | 10 (52.6 %) | 0.2131 |
No comorbidities | 17 (23.9 %) | 11 (47.8 %) | 0.0295 |
1 comorbidity | 0 (0.0 %) | 1 (50.0 %) | 0.0016 |
2 comorbidities | 3 (21.4 %) | 3 (42.9 %) | 0.3055 |
≥3 comorbidities | 13 (22.4 %) | 9 (42.9 %) | 0.0733 |
Lethal Triad: | |||
Hypothermia (temp ≤ 35C) | 8 (33.3 %) | 3 (42.9 %) | 0.6431 |
Coagulopathy (INR ≥ 1.7) | 5 (38.5 %) | 5 (55.6 %) | 0.4285 |
Acidosis (pH ≤ 7.25) | 12 (50.0 %) | 10 (55.6 %) | 0.7213 |
Patient characteristics: | |||
ASA score, 1 or 2 | 0 (0.0 %) | 0 (0.0 %) | - |
ASA score, 3 | 5 (7.7 %) | 1 (12.5 %) | 0.6404 |
ASA score, 4 or 5 | 28 (37.8 %) | 23 (51.1 %) | 0.1559 |
Lactate (≥3) | 13 (40.6 %) | 11 (42.3 %) | 0.8970 |
RSCL rapid source control laparotomy, PRBC packed red blood cells, C Celsius, INR international normalized ratio, ASA American Society of Anesthesiologists, L liters
aCategorical variables are presented as number (%); continuous data are presented as mean (± standard deviation); and non-normally distributed continuous variables as median (interquartile range)
b P-values for overall tests of differences between the groups from χ2 or Fisher’s Exact Test for categorical variables and one-way analysis of variance or Kruskal-Wallis test for continuous variables; p-value of <0.05 significant
The application of the lethal triad to guide the use of RSCL did not discriminate between survivors and non-survivors in our multivariable logistic regression models (Table 3). Patients with hypothermia, coagulopathy, and acidosis who underwent damage control procedures had similar rates of mortality compared with the non-RSCL group.
Table 3.
Logistic regression analyses predicting in-hospital mortality for RSCL patients, based only on the lethal triad
Variablea | Unadjusted modela | Adjusted multivariable modelb | ||
---|---|---|---|---|
OR (95 % CI) | p-valuec | OR (95 % CI) | p-valuec | |
Lethal Triad: | ||||
Hypothermia (temp ≤ 35C) | 0.83 (0.16–4.19) | 0.8205 | 0.70 (0.13–3.74) | 0.5330 |
Coagulopathy (INR ≥ 1.7) | 1.53 (0.36–6.55) | 0.5680 | 1.52 (0.34–6.87) | 0.5884 |
Acidosis (pH ≤ 7.25) | 1.92 (0.60–6.15) | 0.2703 | 1.70 (0.47–6.09) | 0.4167 |
RSCL rapid source control laparotomy, C Celsius, INR international normalized ratio
aUnadjusted univariate analyses were used to test an independent variables’s predictive ability on in-hospital mortality
bModel covariates for mortality were chosen by full selection
c P-value of <0.05 significant
In emergent operative patients undergoing non-RSCL (Table 4), multiple variables increased the chances of mortality in the univariate analyses, including severe sepsis/septic shock, male gender, elderly, acidosis, elevated lactate, and ASA score of 4 or 5. Two variables in this group portended an increased likelihood of survival: patients without inflammation and those with an ASA score of 3. The adjusted multivariable logistic regression model confirmed that four variables significantly and independently increased the chances of mortality for non-RSCL operations: patients with severe sepsis / septic shock, male gender, elderly, and acidosis.
Table 4.
Logistic regression analyses predicting in-hospital mortality for non-RSCL patients
Variablea | Unadjusted modela | Adjusted multivariable modelb | ||
---|---|---|---|---|
OR (95 % CI) | p-valuec | OR (95 % CI) | p-valuec | |
Preoperative inflammatory status: | ||||
No inflammation | 0.30 (0.12–0.71) | 0.0060 | 1.00 | - |
Sepsis | 0.71 (0.31–1.62) | 0.4146 | 0.18 (0.02–1.95) | 0.1583 |
Severe sepsis/septic shock | 7.44 (3.04–18.17) | <0.0001 | 12.32 (1.19–127.33) | 0.0350 |
Patient Characteristics: | ||||
Male Gender | 2.72 (1.14–6.47) | 0.0240 | 23.98 (2.00–287.34) | 0.0122 |
Race, White | 1.25 (0.47–3.32) | 0.6579 | 0.25 (0.01–5.64) | 0.3857 |
Age (≥70) | 4.13 (1.86–9.19) | 0.0005 | 13.77 (1.30–145.70) | 0.0293 |
No comorbidities | 1.48 (0.69–3.18) | 0.3201 | 1.00 | - |
1 comorbidity | 0.001 (0.001–999.99) | 0.9546 | 0.001 (0.001–999.99) | 0.9132 |
2 comorbidities | 1.07 (0.284.09) | 0.9181 | 0.04 (0.01–4.13) | 0.1746 |
≥3 comorbidities | 1.21 (0.55–2.66) | 0.6299 | 0.07 (0.01–0.57) | 0.0139 |
Preoperative metrics: | ||||
Acidosis (pH ≤ 7.25) | 3.94 (1.51–10.30) | 0.0052 | 11.08 (1.02–120.64) | 0.0484 |
Lactate (≥3) | 2.68 (1.06–6.82) | 0.0378 | 0.62 (0.08–4.78) | 0.6425 |
Coagulopathy (INR ≥ 1.7) | 2.08 (0.62–6.97) | 0.2333 | 2.11 (0.22–20.43) | 0.5183 |
ASA score, 1 or 2 | 0.001 (0.001–999.99) | 0.9672 | 1.00 | - |
ASA score, 3 | 0.21 (0.08–0.57) | 0.0022 | 999 (0.001–999.99) | 0.9574 |
ASA score, 4 or 5 | 10.10 (3.65–27.95) | <0.0001 | 999 (0.001–999.99) | 0.9416 |
RSCL rapid source control laparotomy, PRBC packed red blood cells, C Celsius, INR international normalized ratio, ASA American Society of Anesthesiologists
aUnadjusted univariate analyses were used to test an independent variables’s predictive ability on in-hospital mortality
bModel covariates for mortality were chosen by full selection
c P-value of <0.05 significant
In contrast to the non-RSCL group, there were no variables in the unadjusted univariate analyses for the RSCL cohort (Table 5) that increased the odds of mortality. In the adjusted multivariable regression, patients had significantly improved chances of survival when undergoing RSCL with two existing factors: elevated preoperative lactate levels or multiple comorbidities. Patients with preoperative acidosis had significant increased risk of death with RSCL, just as in the non-RSCL group.
Table 5.
Logistic regression analyses predicting in-hospital mortality for RSCL patients
Variablea | Unadjusted modela | Adjusted multivariable modelb | ||
---|---|---|---|---|
OR (95 % CI) | p-valuec | OR (95 % CI) | p-valuec | |
Preoperative inflammatory status: | ||||
No inflammation | 1.26 (0.32–5.01) | 0.7397 | 1.00 | - |
Sepsis | 0.44 (0.15–1.32) | 0.1415 | 0.60 (0.07–5.39) | 0.6446 |
Severe sepsis/septic shock | 2.30 (0.68–7.80) | 0.1811 | 3.29 (0.26–41.92) | 0.3596 |
Patient Characteristics: | ||||
Male Gender | 0.96 (0.32–2.85) | 0.9416 | 0.55 (0.07–4.28) | 0.5708 |
Race, White | 0.58 (0.12–2.88) | 0.5022 | 0.26 (0.01–8.47) | 0.4509 |
Age (≥70) | 1.59 (0.51–4.92) | 0.4230 | 5.19 (0.75–35.74) | 0.0942 |
No comorbidities | 1.20 (0.40–3.57) | 0.7448 | 1.00 | - |
1 comorbidity | 1.22 (0.07–20.55) | 0.8915 | 999 (0.001–999.99) | 0.9848 |
2 comorbidities | 0.89 (0.18–4.45) | 0.8900 | 0.58 (0.05–6.08) | 0.6458 |
≥3 comorbidities | 0.85 (0.28–2.58) | 0.7739 | 0.06 (0.01–0.70) | 0.0252 |
Preoperative metrics: | ||||
Acidosis (pH ≤ 7.25) | 1.92 (0.60–6.15) | 0.2703 | 19.42 (1.74–216.65) | 0.0159 |
Lactate (≥3) | 0.79 (0.26–2.40) | 0.6831 | 0.10 (0.01–0.93) | 0.0431 |
Coagulopathy (INR ≥ 1.7) | 1.53 (0.36–6.55) | 0.5680 | 2.14 (0.27–16.83) | 0.4682 |
ASA score, 1 or 2 | - | - | 1.00 | - |
ASA score, 3 | 0.14 (0.02–1.20) | 0.0729 | 1.00 | - |
ASA score, 4 or 5 | 7.32 (0.83–64.43) | 0.0729 | 26.45 (0.82–857.50) | 0.0650 |
RSCL rapid source control laparotomy, PRBC packed red blood cells, C Celsius, INR international normalized ratio, ASA American Society of Anesthesiologists
aUnadjusted univariate analyses were used to test an independent variables’s predictive ability on in-hospital mortality
bModel covariates for mortality were chosen by full selection
c P-value of <0.05 significant
Of the 162 non-RSCL emergent laparotomies, 27 (17 %) required unplanned re-explorations. Mortality in this unplanned take-back group was significantly higher than in the patients who did not require re-exploration (33.3 % vs 17.8 %; p = 0.04). Of the 33 deaths in the non-RSCL cohort, 27.3 % were patients necessitating unplanned re-explorations. Compared to the non-RSCL patients who did not undergo re-exploration, the unplanned take-back group had significantly higher rates of pre-operative severe sepsis / septic shock (44.4 % vs 11.9 %; p < 0.0001). Of all severe sepsis / septic shock patients in the non-RSCL group, 42.9 % (12) required re-exploration (p < 0.0001).
Discussion
The negative downstream consequences of inflammation are well established in acute care surgery. In the trauma patient population, severe physiologic derangements, particularly the lethal triad (hypothermia, acidosis, and coagulopathy), guide management decisions [22]. Research into these postinjury systemic inflammatory states has established the importance, for example, of the damage control (DC) laparotomy for early definitive source control [1–6], and more recently the concept of DC resuscitation [23]. In critically ill patients, the substantial benefits of blunting the proinflammatory immune response has led to such key practices as early goal-directed therapy [24] and standardized treatment protocols for sepsis [25–27].
In EGS patients, upregulation of the systemic inflammatory response leads to a cascade of physiologic insults, and is a prime contributor to death, with mortality rates for severe sepsis / septic shock of over 40 % [14, 19]. However, unlike in trauma and critically ill patients, where physiologic derangements are aggressively acted on with specific corrective interventions, in EGS patients similar preoperative derangements are often recognized but may not be targeted with explicit restorative management techniques [28].
One solution to mitigating the negative downstream effects of physiologic insults seen preoperatively in EGS patients has been the application of DC techniques. Akin to the DC concept in trauma, it has been theorized that EGS patients needing operative intervention may benefit from an abbreviated laparotomy (i.e. rapid source control laparotomy; RSCL) with planned take-back. Such an operation is one of the first stages on a continuum of care that prioritizes the restoration of physiologic normality and homeostasis, and deemphasizes the importance of immediate organ repair and definitive anatomic reconstruction.
To guide the use of the staged RSCL in EGS patients, trauma’s lethal triad has been applied as the standard criteria for operative decision-making. The data to support this, however, is limited [29]. Furthermore, “expert opinion” about the timing of nontraumatic surgical emergencies has been published to guide surgical interventions in EGS patients [30]. To date, no data or empirical evidence has specifically defined a unique set of criteria on which to base the use of RSCL techniques to improve the poor survival rates of physiologically decompensated EGS patients.
Our results represent such data, and suggest that the acute physiologic indicators which help guide operative decisions in trauma patients may not confer a similar survival advantage to decompensated EGS patients undergoing an emergent laparotomy. In the 53 patients who underwent a staged RSCL based on the lethal triad, adjusted multivariable regression analysis shows that when used alone, no component of the lethal triad independently improved survival (Table 3). Therefore, contrary to current practices, application of the lethal triad does not appear to improve survival rates in EGS patients, and may possibly lead to overuse of RSCL with higher mortality rates (Table 2).
These data also illustrate that the indications for performing a staged RSCL in EGS patients should be founded on a set of unique preoperative physiologic parameters, coupled with inherent patient traits, which collectively define an EGS patient as physiologically decompensated (Tables 4 & 5). Our results suggest a profile of a patient who may realize a survival benefit from a RSCL: a patient with preoperative severe sepsis / septic shock, with an elevated lactate (≥3); acidosis (pH ≤ 7.25); elderly (≥70); male gender; and multiple comorbidities (≥3).
Patients with severe sepsis / septic shock had equally high unadjusted mortality rates in both cohorts: 53.6 % in the non-RSCL group and 60.0 % in the RSCL group (Table 2). In the risk-adjusted analyses for the non-RSCL group, presence of severe sepsis / septic shock was independently related to higher mortality rates, with an adjusted odds ratio for death of 12.3 (Table 4). In contrast, in the RSCL group, severe sepsis / septic shock was not independently predictive of increased risk of death (Table 5).
Collectively, our study suggests that emergency operative patients with severe sepsis / septic shock may benefit from a staged, abbreviated laparotomy, and may have an increased risk of death with an unstaged operative approach. Furthermore, in the non-RSCL cohort, 44.4 % of all patients who required unplanned re-explorations had severe sepsis / septic shock preoperatively, compared to only 11.9 % in the patients who were successfully unstaged. These data also document that nearly 50 % of patients with severe sepsis/septic shock undergoing laparotomy with primary fascial closure will require re-exploration (known as an on-demand re-laparotomy).
Similar patterns exist in the data for males and the elderly; these inherent patient traits independently and significantly increased the risk of mortality in emergent non-RSCL, but were not significantly related to mortality in the RSCL cohort (Tables 4 & 5). As such, men and those over the age of 70 may have poorer outcomes when they undergo unstaged, non-RSCL at the time of initial operation. Another inherent patient trait, multiple comorbidities, was independently associated with improved survival for both the non-RSCL and RSCL groups (Tables 4 & 5). Taken together, these data indicated that the elderly (≥70), males, and patients with multiple comorbidities (≥3) may see lower odds of mortality with RSCL emergent operations.
Acidosis (pH ≤ 7.25) and elevations in lactate (≥3) often occur in concert with each other, but presence of one does not necessarily mean presence of the other. We therefore modeled these variables independently from one another, as there was not a significant interaction between these variables in our analyses. In the RSCL group, elevated lactate independently improved chances of survival in patients undergoing abbreviated laparotomies; lactate was not significantly predictive of survival benefit in the non-RSCL cohort. Patients with acidosis (pH ≤ 7.25), on the other hand, have a very poor prognosis across all emergent operations (Table 2). Acidosis was the one variable associated with poor outcomes in both the non-RSCL and RSCL groups (Tables 4 & 5). Because odds of mortality go up significantly and independently with acidosis, and because survival is 50 % in acidotic patients, we have included it as an indication for RSCL.
The data further confirm that certain emergency patients will not benefit from RSCL, and in fact could be harmed by undergoing abbreviated operations. Specifically, patients without physiologic evidence of preoperative inflammation, as defined by the SIRS criteria, should not be considered candidates for RSLC. This cohort can, in most scenarios, safely undergo a non-staged operation; this is akin to the principle of on-demand re-laparotomy [17].
This study has limitations. First, our conclusions are drawn from retrospective data, and are thus constrained by the limitations and biases therein, including selection bias. Second, the definition of an emergency patient is a construct of the study, as well as the individual assessments of the attending surgeon and anesthesiologist. Therefore, generalizing to all emergency surgical patients may not be valid, as definitions of “emergency patient” are not standardized [31]. Thirdly, the data are from one institution, which is a tertiary medical center and large academic hospital; this may not be representative of a national sample from which to make conclusions. Fourth, our conclusions are drawn from a small sample size of 215 patients; we therefore lack the necessary power to show potentially significant differences. And finally, there may be other peri-operative risk factors and physiologic variables not identified here which more accurately predict the need for RSCL in EGS patients.
Conclusions
In conclusion, when correctly applied, the staged RSCL may help to improve survival in decompensated EGS patients. The best candidates for staged RSCL are those patients with severe sepsis / septic shock, who are also male, over age 70 years old, with multiple comorbidities, and have an elevated lactate with acidosis. Use of the staged RSCL can also avoid unplanned re-explorations, which occurred in nearly 50 % patients with severe sepsis / septic shock who underwent primary fascial closure at the initial operation. Patients without evidence of preoperative inflammation may not benefit from staged RSCL. These results further reinforce the concept that EGS patients represent a unique patient-population, and that operative decision-making in these patients should be guided by EGS-specific preoperative and intraoperative physiologic metrics and variables.
Acknowledgements
None.
Abbreviations
- ASA
American Society of Anesthesiologist Score
- DC
Damage control
- EGS
Emergency general surgery
- ICU
Intensive Care Unit
- NSQIP
National surgical quality improvement program
- RSCL
Rapid source control laparotomy
- SIRS
Systemic inflammatory response syndrome
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
Study conception and design: RDB, MCC. Acquisition of data: RDB, JRG, LPN, YS. Analysis and interpretation of data: RDB, ABP, JLS, JRG, LPN, YS, PRM, MCC. Drafting of manuscript: RDB, ABP, JLS, JRG, LPN, YS, PRM, MCC. Critical revision: RDB, ABP, JLS, JRG, LPN, YS, PRM, MCC. All authors read and approved the final manuscript.
Contributor Information
Robert D. Becher, Phone: 203-785-2572, Email: robert.becher@yale.edu
Andrew B. Peitzman, Email: peitzmanab@upmc.edu
Jason L. Sperry, Email: sperryjl@upmc.edu
Jared R. Gallaher, Email: Jared.Gallaher@unchealth.unc.edu
Lucas P. Neff, Email: lucas.neff.2@us.af.mil
Yankai Sun, Email: yankai.sun.7@gmail.com.
Preston R. Miller, Email: pmiller@wakehealth.edu
Michael C. Chang, Email: mchang@wakehealth.edu
References
- 1.Lee JC, Peitzman AB. Damage-control laparotomy. Curr Opin Crit Care. 2006;12:346–350. doi: 10.1097/01.ccx.0000235213.63988.9a. [DOI] [PubMed] [Google Scholar]
- 2.Moore EE, Burch JM, Franciose RJ, Offner PJ, Biffl WL. Staged physiologic restoration and damage control surgery. World J Surg. 1998;22:1184–1190. doi: 10.1007/s002689900542. [DOI] [PubMed] [Google Scholar]
- 3.Asensio JA, McDuffie L, Petrone P, Roldań G, Forno W, Gambaro E, et al. Reliable variables in the exsanguinated patient which indicate damage control and predict outcome. Am J Surg. 2001;182:743–751. doi: 10.1016/S0002-9610(01)00809-1. [DOI] [PubMed] [Google Scholar]
- 4.Rotondo MF, Schwab CW, McGonigal MD, Phillips GR, 3rd, Fruchterman TM, Kauder DR, et al. “Damage control”: an approach for improved survival in exsanguinating penetrating abdominal injury. J Trauma. 1993;35:375–382. doi: 10.1097/00005373-199309000-00008. [DOI] [PubMed] [Google Scholar]
- 5.Johnson JW, Gracias VH, Schwab CW, Reilly PM, Kauder DR, Shapiro MB, et al. Evolution in damage control for exsanguinating penetrating abdominal injury. J Trauma. 2001;51:261–269. doi: 10.1097/00005373-200108000-00007. [DOI] [PubMed] [Google Scholar]
- 6.Burch JM, Ortiz VB, Richardson RJ, Martin RR, Mattox KL, Jordan GL., Jr Abbreviated laparotomy and planned reoperation for critically injured patients. Ann Surg. 1992;215:476–483. doi: 10.1097/00000658-199205000-00010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Rutherford EJ, Morris JA, Jr, Reed GW, Hall KS. Base deficit stratifies mortality and determines therapy. J Trauma. 1992;33:417–423. doi: 10.1097/00005373-199209000-00014. [DOI] [PubMed] [Google Scholar]
- 8.Dunham CM, Siegel JH, Weireter L, Fabian M, Goodarzi S, Guadalupi P, et al. Oxygen debt and metabolic acidemia as quantitative predictors of mortality and the severity of the ischemic insult in hemorrhagic shock. Crit Care Med. 1991;19:231–243. doi: 10.1097/00003246-199102000-00020. [DOI] [PubMed] [Google Scholar]
- 9.Morris JA, Jr, Eddy VA, Blinman TA, Rutherford EJ, Sharp KW. The staged celiotomy for trauma. Issues in unpacking and reconstruction. Ann Surg. 1993;217:576–584. doi: 10.1097/00000658-199305010-00019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Baracco-Gandolfo V, Vidarte O, Baracco-Miller V, del Castillo M. Prolonged closed liver packing in severe hepatic trauma: experience with 36 patients. J Trauma. 1986;26:754–756. doi: 10.1097/00005373-198608000-00012. [DOI] [PubMed] [Google Scholar]
- 11.Bender JS, Bailey CE, Saxe JM, Ledgerwood AM, Lucas CE. The technique of visceral packing: recommended management of difficult fascial closure in trauma patients. J Trauma. 1994;36:182–185. doi: 10.1097/00005373-199402000-00005. [DOI] [PubMed] [Google Scholar]
- 12.Krige JE, Bornman PC, Terblanche J. Therapeutic perihepatic packing in complex liver trauma. Br J Surg. 1992;79:43–46. doi: 10.1002/bjs.1800790114. [DOI] [PubMed] [Google Scholar]
- 13.Sharp KW, Locicero RJ. Abdominal packing for surgically uncontrollable hemorrhage. Ann Surg. 1992;215:467–474. doi: 10.1097/00000658-199205000-00009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Becher RD, Hoth JJ, Miller PR, Meredith JW, Chang MC. Systemic inflammation worsens outcomes in emergency surgical patients. J Trauma Acute Care Surg. 2012;72:1140–1149. doi: 10.1097/TA.0b013e3182516a97. [DOI] [PubMed] [Google Scholar]
- 15.Ameican College of Surgeons (ACS) National Surgical Quality Improvement Program (NSQIP): Data Variables and Definitions from the "User Guide for the 2010 Participant Use Data File," accessed at: https://www.facs.org/~/media/files/quality%20programs/nsqip/ug10.ashx.
- 16.Levy MM, Fink MP, Marshall JC, Abraham E, Angus D, Cook D, et al. SCCM/ESICM/ACCP/ATS/SIS international sepsis definitions conference. Crit Care Med. 2001;2003(31):1250–1256. doi: 10.1097/01.CCM.0000050454.01978.3B. [DOI] [PubMed] [Google Scholar]
- 17.van Ruler O, Mahler CW, Boer KR, Reuland EA, Gooszen HG, Opmeer BC, et al. Comparison of on-demand vs planned relaparotomy strategy in patients with severe peritonitis: a randomized trial. JAMA. 2007;298:865–872. doi: 10.1001/jama.298.8.865. [DOI] [PubMed] [Google Scholar]
- 18.Solomkin JS, Mazuski JE, Bradley JS, Rodvold KA, Goldstein EJC, Baron EJ, et al. Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the Surgical Infection Society and the Infectious Diseases Society of America. Surg Infect (Larchmt) 2010;11:79–109. doi: 10.1089/sur.2009.9930. [DOI] [PubMed] [Google Scholar]
- 19.Becher RD, Hoth JJ, Miller PR, Mowery NT, Chang MC, Meredith JW. A critical assessment of outcomes in emergency versus nonemergency general surgery using the American College of Surgeons National Surgical Quality Improvement Program Database. Am Surg. 2011;77:951–959. [PubMed] [Google Scholar]
- 20.Schilling PL, Dimick JB, Birkmeyer JD. Prioritizing quality improvement in general surgery. J Am Coll Surg. 2008;207:698–704. doi: 10.1016/j.jamcollsurg.2008.06.138. [DOI] [PubMed] [Google Scholar]
- 21.Ingraham AM, Cohen ME, Bilimoria KY, Raval MV, Ko CY, Nathens AB, et al. Comparison of 30-day outcomes after emergency general surgery procedures: potential for targeted improvement. Surgery. 2010;148:217–238. doi: 10.1016/j.surg.2010.05.009. [DOI] [PubMed] [Google Scholar]
- 22.Lenz A, Franklin GA, Cheadle WG. Systemic inflammation after trauma. Injury. 2007;38:1336–1345. doi: 10.1016/j.injury.2007.10.003. [DOI] [PubMed] [Google Scholar]
- 23.Morrison CA, Carrick MM, Norman MA, Scott BG, Welsh FJ, Tsai P, et al. Hypotensive resuscitation strategy reduces transfusion requirements and severe postoperative coagulopathy in trauma patients with hemorrhagic shock: preliminary results of a randomized controlled trial. J Trauma. 2011;70:652–663. doi: 10.1097/TA.0b013e31820e77ea. [DOI] [PubMed] [Google Scholar]
- 24.Rivers E, Nguyen B, Havstad S, Ressler J, Muzzin A, Knoblich B, et al. Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med. 2001;345:1368–1377. doi: 10.1056/NEJMoa010307. [DOI] [PubMed] [Google Scholar]
- 25.Shapiro NI, Howell MD, Talmor D, Lahey D, Ngo L, Buras J, et al. Implementation and outcomes of the Multiple Urgent Sepsis Therapies (MUST) protocol. Crit Care Med. 2006;34:1025–1032. doi: 10.1097/01.CCM.0000206104.18647.A8. [DOI] [PubMed] [Google Scholar]
- 26.Micek ST, Roubinian N, Heuring T, Bode M, Williams J, Harrison C, et al. Before-after study of a standardized hospital order set for the management of septic shock. Crit Care Med. 2006;34:2707–2713. doi: 10.1097/01.CCM.0000241151.25426.D7. [DOI] [PubMed] [Google Scholar]
- 27.ProCESS Investigators. Yealy DM, Kellum JA, Huang DT, Barnato AE, Weissfeld LA, et al. A randomized trial of protocol-based care for early septic shock. N Engl J Med. 2014;370:1683–1693. doi: 10.1056/NEJMoa1401602. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Moore LJ, Moore FA. Early diagnosis and evidence-based care of surgical sepsis. J Intensive Care Med. 2013;28:107–117. doi: 10.1177/0885066611408690. [DOI] [PubMed] [Google Scholar]
- 29.Stawicki SP, Brooks A, Bilski T, Scaff D, Gupta R, Schwab CW, et al. The concept of damage control: extending the paradigm to emergency general surgery. Injury. 2008;39:93–101. doi: 10.1016/j.injury.2007.06.011. [DOI] [PubMed] [Google Scholar]
- 30.Kluger Y, Ben-Ishay O, Sartelli M, Ansaloni L, Abbas AE, Agresta F, et al. World society of emergency surgery study group initiative on Timing of Acute Care Surgery classification (TACS) World J Emerg Surg. 2013;8:17. doi: 10.1186/1749-7922-8-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Becher RD, Meredith JW, Chang MC, Hoth JJ, Beard HR, Miller PR. Creation and implementation of an emergency general surgery registry modeled after the National Trauma Data Bank. J Am Coll Surg. 2012;214:156–163. doi: 10.1016/j.jamcollsurg.2011.11.001. [DOI] [PubMed] [Google Scholar]