Dosing of ceftriaxone and outcomes after spontaneous bacterial peritonitis

Spontaneous bacterial peritonitis (SBP) is a common, often fatal Background: affliction for cirrhotic patients. Despite all clinical trials of ceftriaxone for SBP using 2g daily, it is often given at 1g daily. We evaluated outcomes of SBP as a function of ceftriaxone dosage. Aim: A retrospective cohort of all patients who received ceftriaxone for Methods: SBP (greater than 250 neutrophils in the ascites). As opposed to 1 gram, median survival is longer for patients receiving Results: 2 grams (228 days vs. 102 days (p = 0.26) and one year survival is significantly higher (p = 0.0034). After adjusting for baseline Model for End Stage Liver Disease (MELD) score, however, this difference was no longer significant. Similarly, there was a significantly shorter length of intensive care for patients receiving 2 g (0.59 ± 1.78 days vs. 3.26 ± 6.9, p = 0.034), odds ratio 0.11 (95% CI 0.02 0.65). This difference, too, was no longer significant after controlling for the MELD score odds ratio 0.21 (95% CI 0.04 1.07). Additionally, 70% of patients received at least one additional antibiotic; over 25 different medications were used in various combinations. We recommend fastidious antibiotic stewardship for patients Conclusions: with cirrhosis and that efforts should be made to standardize the treatment of SBP. The complexity of antibiotic regimens to which cirrhotic patients are exposed must be studied further and rationalized. Patients receiving 2 g of ceftriaxone may require fewer intensive care days and enjoy an improved 1 year survival compared to those receiving 1 g daily. Elliot B. Tapper ( ) Corresponding author: etapper@bidmc.harvard.edu Mazer L, Tapper EB, Piatkowski G and Lai M. How to cite this article: Dosing of ceftriaxone and outcomes after spontaneous bacterial 2014, :57 (doi: ) peritonitis [version 1; referees: 3 approved with reservations] F1000Research 3 10.12688/f1000research.3-57.v1 © 2014 Mazer L . This is an open access article distributed under the terms of the , which Copyright: et al Creative Commons Attribution Licence permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Data associated with the article are available under the terms of the (CC0 1.0 Public domain dedication). Creative Commons Zero "No rights reserved" data waiver The author(s) declared that no grants were involved in supporting this work. Grant information: Competing interests: No competing interests were disclosed. 14 Feb 2014, :57 (doi: ) First published: 3 10.12688/f1000research.3-57.v1 1 2 2


Introduction
Ascites is the most common hepatic decompensation, occurring in 50% of cirrhotic patients followed for over a decade 1 . The development of ascites heralds a vulnerable time of sharply increased mortality for patients with liver disease -related in large part to spontaneous bacterial peritonitis (SBP) 2,3 . SBP is an infection of the ascitic fluid that occurs in 10-30% of patients with ascites 4 . Fatal in as many as 32.6% of cases, SBP can have a profound effect on the tenuous hemodynamics of patients with cirrhosis 5 . Exacerbating the arterial underfilling that results from the splanchnic vasodilation of cirrhosis, SBP may lead to a decrease in cardiac output such that it can no longer satisfy the needs of a kidney that is already vasoconstricted 6 . The result is the hepatorenal syndrome which is often devastating. SBP with renal injury is fatal in 42% of patients 7 .
SBP is caused by translocation of gastrointestinal organisms into the ascitic fluid, most commonly Escherichia coli, Klebsiella pneumoniae and Streptococcus pneumoniae. As such, third generation cephalosporins are amongst the best studied antibiotics in this setting, with ceftriaxone as the drug of choice where cefotaxime is not available. Studied as a treatment for SBP in clinical trials for 25 years, the doses employed were either 1 g every 12 hours or 2 g every 24 hours given intravenously for 5 to 10 day courses [8][9][10][11][12][13][14] .
At our center, we have found that ceftriaxone is often given at 1 g daily either in reference to online resources from other major teaching institutions or because 1 g is the general preset dose for this antibiotic as generated by the electronic ordering system 15 . (http:// clinicalpharmacy.ucsf.edu/idmp/adult_guide/empiric_guide/in-traabd_hosp_frame.htm, last accessed 1-12-2014). The outcomes of SBP as a function of ceftriaxone dosage -1 g daily versus 2 g daily -have never been evaluated. It is unknown what effect the dosage of ceftriaxone has on the control of SBP or on mortality. Neither the American Association for the Study of Liver Disease (AASLD) nor the European Association for the Study of the Liver (EASL) guidelines on SBP management explicitly comment on the dosing of ceftriaxone for this indication 16,17 .
Herein we present the results of a retrospective review of the outcomes of SBP stratified by dose of ceftriaxone. This study aims to determine the additional benefit of the extra gram of ceftriaxone when treating SBP in the clinically relevant terms of renal injury and mortality. , single center review of prospectively maintained medical records for all consecutive patients treated with  ceftriaxone for SBP at the Beth Israel Deaconess Medical Center,  Boston, USA, between January 2003 and December 2011. We searched our clinical database for all patients that received ceftriaxone within 48 hours of a peritoneal fluid cell count and differential drawn in the emergency department or hospital ward. We then limited the population to those with 250 or more neutrophils in the ascites. Patient charts were then examined to exclude those with a prior liver transplant, evidence of intra-abdominal source of infection [abscess, perforation, recent (within 2 weeks) intra-abdominal surgery], peritoneal dialysis, or documentation of a secondary infection (urinary tract infection, pneumonia, blood stream infection, cellulitis, meningitis) for which ceftriaxone was started prior to the peritoneal fluid collection. We collected data on age, sex, Model for End Stage Liver Disease (MELD) score (bilirubin, creatinine and PT/INR) at diagnosis, peritoneal white blood cell count and differential, blood and peritoneal culture data, dose of ceftriaxone, additional antibiotics, duration of antibiotic therapy, creatinine trends, intensive care utilization, length of hospital stay and mortality.

This is a retrospective
Statistics were performed using SAS 9.2 and included student's t-test, multivariate regression analysis, and log-rank testing/survival analysis where appropriate. P-value of 0.05 was considered significant for all analyses. While no prior studies have examined the effect of ceftriaxone dosing in order to determine study power, prior studies of ceftriaxone for SBP may be instructive. For example, in comparing 2 g ceftriaxone to cefonicid, the in-hospital death rate during therapy was 13% versus 30% which, assuming an alpha of 0.05, a sample size of 91 gives an 80% power 13 . However, when examining the broader literature on ceftriaxone, regimens of variable duration (5 vs. 10 days) with 30% vs. 35% 30 day mortality would imply that studies require more than 1600 patients for adequate power 8-14 .

Results
We found 138 patients with SBP treated with ceftriaxone. Of these, 91 patients met our inclusion criteria: 34 patients received 1 g daily and 57 received 2 g (total) daily. There was no significant difference between the groups with respect to age, gender, MELD score, peritoneal culture positivity or other infectious burden (Table 1). hospitalization (74% of those treated with 1 g, and 61% of those treated with 2 g), this difference was not significant. The total course of antibiotics -ceftriaxone or otherwise -was also similar between groups. The group receiving 2 g ceftriaxone daily did have a trend towards a shorter hospital stay, although this did not meet statistical significance (13.24 days vs. 10.28, p = 0.44). We did see a statistically significant shorter average length of intensive unit (ICU) stay in patients who received 2 g ceftriaxone a day (0.59 ± 1.78 days), compared to those who received 1 g ceftriaxone daily (3.26 ± 6.9 days) (p = 0.034). The odds ratio for ICU utilization was 0.11 (95% CI 0.02-0.65). However, this difference was no longer significant after controlling for MELD score -odds ratio 0.21 (95% CI 0.04-1.07). Finally, we examined one-year survival for patients treated with 1 versus 2 g ceftriaxone, and found a significant improvement in survival associated with the 2 g dose (p 0.0034 log rank test) ( Figure 1). Median overall survival was greater for patients treated with the 2 g dose (228 days vs. 102 days, however it was not significant (p = 0.26).
Given the high prevalence of additional antibiotic treatment, we also examined the pattern of antibiotic use. Overall, 70% of patients were treated with at least one additional antibiotic. The duration of antibiotic use, as well as the number and type of antibiotics prescribed were highly variable (Table 3). While vancomycin was the most common concurrent antibiotic, used in 46% of patients, over 25 different medications were used in a variety of combinations.
To further understand the antibiotic regimens observed, we next examined the available culture data. Of 91 patients diagnosed with SBP on neutrophil criteria, 13 were culture-positive. Of these, one patient had a documented infection resistant to ceftriaxone. This patient was excluded from the analysis. 14 patients had evidence of All patients had received a protocol of albumin infusion on days 1 and 3 after the diagnosis of SBP in accordance with best practice 18 .
We next compared the hospital course for patients that received either dose of ceftriaxone (Table 2). While both groups were likely to be treated with at least one additional antibiotic during their

Conclusion
Our study of ceftriaxone dosage for SBP yielded two core findings. First, a total ceftriaxone dose of 2 g daily over 1 g daily exhibited a non-significant reduction of intensive care utilization by cirrhotic patients with SBP, controlling for MELD score. Similarly, there was a trend towards improved mortality with the 2 g dosage. Prospective studies in a larger cohort are indicated to explore the true significance of these results. While it could explain our results, whether the pharmacodynamics of intravenous ceftriaxone are such that the peritoneal drug concentration following a 1 g infusion menu-selection for SBP, our hospital -or any hospital with similar capabilities -may track the disease indications for each antibiotic allowing for audits and outreach.
Our conclusions are limited in a few ways. First, our study is retrospective and therefore we cannot comment on the impact of other treatment decisions that may or may not be associated with the dose of ceftriaxone chosen. Additionally, we cannot exclude the possibility that our study was underpowered to detect a difference between treatment groups. Second, the microbiology of our patients' SBP is unclear given the low rate of culture positivity so we cannot comment on the impact of antimicrobial resistance. Third, follow-up paracenteses to confirm resolution of the SBP after antibiotic treatment were infrequent and thus we cannot comment on the rate of resolution of neutrophilia as function of ceftriaxone dose.
In order to prevent unwanted practice variation, we recommend standardizing the treatment of SBP by automating the dose of ceftriaxone in the provider order entry system. Further research must be aimed at rationalizing the antibiotic regimens employed in the treatment of cirrhotic patients. Programs to this end include fastidious antibiotic stewardship facilitated by computerized audits of indication-based antibiotic usage and improved microbial culture and detection techniques.
results in slower control of infection is unclear from our study 19 . Second, the number, duration and complexity of antibiotic regimens that cirrhotic patients experience is highly variable. The reasons for this finding are unclear and deserve further study in order to understand both the physician and patient factors that increase antibiotic regimen complexity as well as the effect on outcomes including mortality, morbidity and future infection with resistant organisms.
This study emphasizes the need for antibiotic stewardship and treatment standardization in the care of cirrhotic patients. We feel this can be easily achieved by computer programming. For centers that use electronic provider order entry, a preset dose of 2 g of ceftriaxone when prescribing for a diagnosis of SBP can ensure standardized and appropriate dosing. Our findings are inconclusive but suggestive of a benefit from a higher ceftriaxone dose. As a result, we have programmed a prompt into ceftriaxone orders that asks the physician to specify whether the medication is intended to treat SBP. This selection results in an automatic 2 g daily dose (Figure 2). Cirrhotic patients can be admitted to any service of the hospital, including those staffed by hepatologists, internists, surgeons and intensivists. By standardizing care delivery, the healthcare system can ensure that the medications cirrhotic patients receive are dosed appropriately for their needs. Furthermore, by programming a  1.

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We appreciate Dr. Cardenas' comments. As regards to his major points, the first three were easily addressed. First, the title, abstract and introduction have been changed substantially to clarify the aims with the principle focus being patient outcomes. Second, the title has been changed. Third, we clarified that patients on antibiotic prophylaxis were excluded.
As for his fourth, unfortunately it is extremely difficult to determine causes of death when patients often die at other institutions. We do not feel that this is a major limitation for three main reasons. First, we confirm that the patients are alive or dead using a national database. Second, the available prognostics in liver disease, namely the MELD, are capable of predicting all-cause mortality and we adjust for MELD. Third, the causes of death in decompensated cirrhosis are fairly circumscribed and typically closely related to the patients' antecedent clinical course. SBP can result in mortality via sepsis, and renal failure but also, potentially, variceal bleeding, if say the clinician held beta-blockade to preserve renal function.
No competing interests were disclosed. Competing Interests: 1.

4.
I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above. 1.

4.
I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above. The reviewer's comments are well taken.
The language used in the conclusions has been moderated for less sweeping claims. The use of 1 year mortality after one clinical event is frequently described in the literature on cirrhosis. While SBP and 1 year mortality seem disconnected, SBP is a watershed moment for patients with ascites, the prognostic effects of which are well described.
Endpoints have been clarified. Mortality has been included. Infection cure rate is incompletely captured as very few patients received follow up paracentesis; patients with resistant species (very few) and super-infections were specifically excluded from the study. The ascitic culture method is standard.
We add a specific comment on the causes of mortality. Please see our response to Dr. Cardenas. We regret that we cannot provide actual causes of death. However, as the primary outcome was all-cause mortality and we controlled for factors that are validated to predict all-cause mortality, we feel that this outcome is legitimate. Agreed.
No competing interests were disclosed.

Competing Interests:
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