Gut and Liver 2020; 14(6): 842-849 https://doi.org/10.5009/gnl19248 Impact of the Sensitivity to Empiric Antibiotics on Clinical Outcomes after Biliary Drainage for Acute Cholangitis
Author Information
Satoshi Kawamura1 , Yuki Karasawa1 , Nobuo Toda1 , Yousuke Nakai2 , Chikako Shibata1 , Ken Kurokawa1 , Junya Arai1 , Kazuyoshi Funato1 , Shigeyuki Kurosaki1 , Shuya Maeshima1 , Mayuko Kondo1 , Kentaro Kojima1 , Takamasa Ohki1 , Michiharu Seki1 , Kazuhiko Koike2 , and Kazumi Tagawa1
1Department of Gastroenterology, Mitsui Memorial Hospital, and 2Department of Gastroenterology, University of Tokyo Hospital, Tokyo, Japan

Nobuo Toda
Department of Gastroenterology, Mitsui Memorial Hospital, Kanda-Izumi-cho 1, Chiyoda-ku, Tokyo 101-8643, Japan
Tel: +81-3-3862-9111, Fax: +81-3-3864-7901, E-mail: ntoda@mitsuihosp.or.jp
© The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. All rights reserved.

Abstract
Background/Aims: Empiric antibiotics are given in combination with biliary drainage for acute cholangitis but sometimes turn out to be insensitive to microorganisms in blood and bile. Clinical outcomes were compared according to sensitivity to microorganisms detected in blood and bile culture to evaluate the impact of sensitivity to empiric antibiotics in cholangitis. Methods: Consecutive patients who underwent biliary drainage for acute cholangitis were retrospectively studied. Clinical outcomes such as 30-day mortality, length of hospital stay and high care unit stay, organ dysfunction and duration of fever were compared in three groups: group A (sensitive to both blood and bile culture), group B (sensitive to blood culture alone) and group C (insensitive to both blood and bile culture). Results: Eighty episodes of cholangitis were classified according to sensitivity results: 42, 32 and six in groups A, B and C. Escherichia coli and Klebsiella were two major pathogens. There were no significant differences in 30-day mortality rate (7%, 0%, and 0%, p=0.244), length of hospital stay (28.5, 21.0, and 20.5 days, p=0.369), organ dysfunction rate (14%, 25%, and 17%, p=0.500), duration of fever (4.3, 3.2, and 3.5 days, p=0.921) and length of high care unit stay (1.4, 1.2, and 1.7 days, p=0.070) in groups A, B and C. Empiric antibiotics were changed in 11 episodes but clinical outcomes appeared to be non-inferior even in 31 episodes of cholangitis who were on inadequate antibiotics throughout the course. Conclusions: Sensitivity of empiric antibiotics was not associated with clinical outcomes in acute cholangitis.
Keywords: Endoscopic retrograde cholangiopancreatography; Cholangitis; Antimicrobial agents
Abstract
Background/Aims: Empiric antibiotics are given in combination with biliary drainage for acute cholangitis but sometimes turn out to be insensitive to microorganisms in blood and bile. Clinical outcomes were compared according to sensitivity to microorganisms detected in blood and bile culture to evaluate the impact of sensitivity to empiric antibiotics in cholangitis. Methods: Consecutive patients who underwent biliary drainage for acute cholangitis were retrospectively studied. Clinical outcomes such as 30-day mortality, length of hospital stay and high care unit stay, organ dysfunction and duration of fever were compared in three groups: group A (sensitive to both blood and bile culture), group B (sensitive to blood culture alone) and group C (insensitive to both blood and bile culture). Results: Eighty episodes of cholangitis were classified according to sensitivity results: 42, 32 and six in groups A, B and C. Escherichia coli and Klebsiella were two major pathogens. There were no significant differences in 30-day mortality rate (7%, 0%, and 0%, p=0.244), length of hospital stay (28.5, 21.0, and 20.5 days, p=0.369), organ dysfunction rate (14%, 25%, and 17%, p=0.500), duration of fever (4.3, 3.2, and 3.5 days, p=0.921) and length of high care unit stay (1.4, 1.2, and 1.7 days, p=0.070) in groups A, B and C. Empiric antibiotics were changed in 11 episodes but clinical outcomes appeared to be non-inferior even in 31 episodes of cholangitis who were on inadequate antibiotics throughout the course. Conclusions: Sensitivity of empiric antibiotics was not associated with clinical outcomes in acute cholangitis.
Keywords: Endoscopic retrograde cholangiopancreatography; Cholangitis; Antimicrobial agents
INTRODUCTION

Acute cholangitis is caused by bacterial infection in the obstructed biliary system due to choledocholithiasis, benign biliary stricture or malignancy and the mortality rate in severe acute cholangitis is reportedly as high as 20%.1 Treatment for acute cholangitis is a combination of biliary drainage and antibiotics2-5 and empiric broad spectrum antibiotics are recommended for cholangitis. However, empiric antibiotics sometimes fail to cover microorganisms subsequently detected in blood or bile culture due to the increase in resistant pathogens in cholangitis.6 While the use of insensitive antimicrobial treatment for bloodstream infections is often related to worse clinical outcomes,7-11 conflicting data are reported about the associations between sensitivity of empiric antibiotics and mortality in cholangitis,6,12,13 depending on the successful biliary drainage.14 Furthermore, microorganisms identified in blood and bile culture sometimes differ in acute cholangitis, though bile culture is more often polymicrobial than blood culture. However, it is still unclear whether sensitivity to microorganisms in blood and/or bile affects clinical outcomes in patients with successful biliary drainage for acute cholangitis.15-17

Therefore, we conducted this retrospective analysis to compare clinical outcomes according to sensitivity to microorganisms detected in blood and bile culture.

MATERIALS AND METHODS

1. Study design and population

This was a single center, retrospective study of patients undergoing biliary drainage for acute cholangitis in a Japanese secondary care hospital. Data on consecutive patients who underwent biliary drainage within 24 hours of the diagnosis of acute cholangitis from January 2010 and December 2015 were extracted from the electrical medical records. Patients with positive blood and/or bile culture were included in our analysis. Patients whose sensitivity analysis of blood and bile culture were not available were excluded from the analysis. Collected data were as follows: age, sex, comorbidity, laboratory data including microorganism evaluation, severity and causes of cholangitis, biliary drainage methods, the timing of cholangitis (nosocomial or not), prior history of biliary drainage, hospitalization (within 30 days) and antibiotics use (within 30 days). This study was approved by the Ethical Committee at Mitsui Memorial Hospital (IRB number: MEC2018-C12).

2. Microbiological assessment and antibiotics use

Bile aspirated during endoscopic retrograde cholangiopancreatography (ERCP) or percutaneous transhepatic biliary drainage was sent for culture. Blood culture was obtained at separate two sites before administration of antibiotics. One set of positive blood culture for skin inhabitants (i.e., Staphylococcus epidermis, Corynebacterium or Bacillus species) was considered contamination.

In general, sulbactam/cefoperazone (SBT/CPZ) was used as the initial empiric antimicrobial therapy to cover gram negative rods and aerobes. Ampicillin was added in patients who were considered as at high risk of Enterococcus spp. infection such as a history of sphincterotomy or an indwelling biliary stent. In cases with a history of ampicillin-resistant Enterococcus spp. infection, vancomycin was added to SBT/CPZ. In cases with a deteriorated general condition, meropenem or doripenem was selected to cover extended-spectrum β-lactamase producing Escherichia coli or Klebsiella spp. Meropenem was also selected in some patients as the initial antibiotics based on the sensitivity analysis of microorganisms detected in the bile aspirate at the previous interventions. Ciprofloxacin or levofloxacin was administrated in patients who were allergic to penicillin or cephalosporin, respectively.

Initial empiric antibiotics were considered as sensitive if they were sensitive to all the microorganisms isolated from blood and/or bile culture. Antibiotics was changed at the discretion of the physicians in cases whose blood or bile culture showed microorganisms insensitive to the empiric antibiotics or in cases without clinical response defined as resolution of fever and jaundice despite successful biliary drainage.

3. Study outcomes

The aim of this study was to evaluate the associations of sensitivity of blood and bile culture with clinical outcomes after successful biliary drainage in patients with acute cholangitis. Patients were categorized into three groups according to sensitivity to the initial empiric antibiotics. The initial empiric antibiotics were sensitive to microorganisms in blood and bile culture (group A), sensitive to microorganisms in blood culture alone (group B) and not sensitive to microorganisms in blood and bile culture (group C). The primary outcome is 30-day mortality and secondary outcomes are the length of hospital stay, the incidence of organ dysfunction, the duration of fever after antibiotics use and the length of high care unit stay.

4. Definitions

The diagnosis and severity assessment of acute cholangitis including organ dysfunction was based on TG13.18 The duration of fever was the period between initiation of antibiotics and the day when a body temperature of <37°C was maintained for 24 hours.19 Nosocomial infection was defined as infection which occurred more than 48 hours after administration or infection which occurred less than 48 hours after admission in patients who had been transferred from another hospital.

5. Statistics

The Mann-Whitney U-test or Student t-test were used for comparison of continuous variables. The chi-square test or Fisher exact test were used for comparison of categorical variables. p-values <0.05 were considered to be statistically significant. JMP version 13 (SAS Institute, Inc, Cary, NC, USA) was used for all statistical analyses.

RESULTS

1. Patients

A total of 263 episodes of acute cholangitis with either positive blood or bile culture were identified during the study period. Among those episodes, biliary drainage was successfully performed within 24 hours in 169 episodes, and either blood or bile culture was positive with sensitivity analysis available in 80 episodes (Fig. 1). Characteristics of these 80 episodes of acute cholangitis are shown in Table 1. The mean age was 74.1 years. Bile duct stones and malignant biliary obstruction were two major causes of cholangitis. Severity of cholangitis was mild in 50%, moderate in 31% and severe in 19%. Biliary drainage was predominantly (84%) performed by ERCP. There were three cases of inappropriate biliary drainage; two endoscopic nasobiliary drainage dislodgement and one uncontrolled cholangitis due to multiple biliary stricture. No antibiotics change was performed in any of three cases.

2. Microbiological evaluation and antibiotics

While the most common isolates in blood culture were E. coli (20%), followed by Klebsiella (15%), the most common isolates in bile culture were Klebsiella (50%) and E. coli (38%) (Table 2). All the isolates in blood culture were identified in the bile as well. Among the microorganisms detected in blood culture, Enterococcus spp. was the most common isolate resistant to the initial empiric antibiotics both in blood (5%) and bile (24%). The second common resistant isolate in bile was Candida spp. (14%).

The empiric antibiotics administered are shown in Table 3. The most common empiric antimicrobial therapy was SBT/CPZ (46%), followed by SBT/CPZ and ampicillin (35%). The empiric antibiotics were sensitive to microorganisms detected in both blood and bile culture in 42 patients (52%, group A), only in blood culture in 32 patients (40%, group B). In six patients, empiric antibiotics were not sensitive to microorganisms detected in blood and bile culture (group C). There were no statistical differences in baseline characteristics among three groups (Table 1). When the sensitivity of microorganisms detected in the groups drained by ERCP and percutaneous transhepatic biliary drainage was compared, there were no significant differences (p=0.725): 52% (35/67) and 54% (7/13) in group A, 39% (26/67) and 46% (6/13) in group B, 9% (6/67) and 0 in group C.

3. Outcomes of cholangitis according to sensitivity to empiric antibiotics

The overall 30-day mortality was 4% in the total cohort (Table 4), which was exclusively observed in group A, but the 30-day mortality did not differ significantly (7%, 0%, and 0% in groups A, B, and C, p=0.244). There were no significant differences in other clinical outcomes, either: the mean length of hospital stay (28.5±3.7, 21.0±4.2, and 20.5±9.8 days in groups A, B and C, p=0.369), the rate of organ dysfunction (14%, 25%, and 17% in groups A, B and C, p=0.500), mean duration of fever (4.3±0.5, 3.2±0.6, and 3.5±1.4 days in groups A, B and C, p=0.921) and mean duration of high care unit stay (1.4±0.4, 1.2±0.5, and 1.7±1.2 days in groups A, B and C, p=0.070).

4. Clinical outcomes by the antibiotics change

During the clinical course of 80 episodes of acute cholangitis, the initial empiric antibiotics were changed in 11 episodes (Fig. 2). Among the remaining 69 episodes of cholangitis without antibiotics change, the initial empiric antibiotics were sensitive in 38 episodes and insensitive in 31 episodes. As shown in Table 5, sensitivity of antibiotics to microorganisms detected in blood or bile culture did not appear to be associated with clinical outcomes, which suggested that sensitivity of empiric antibiotics is not clinically relevant once adequate biliary drainage is achieved for acute cholangitis. Antibiotics given in two mortal cases were sensitive to microorganisms detected in blood and bile culture.

The initial empiric antibiotics were changed in 11 episodes because of the lack of immediate clinical response in seven and despite clinical response in four. Among seven cases without immediate clinical response, antibiotics were changed according to the microorganisms detected in culture only in three cases. In the remaining four cases without clinical response, antibiotics were changed empirically but antibiotics change was eventually unnecessary or inappropriate in terms of sensitivity: Sensitive to sensitive ones in two, sensitive to insensitive ones in one and insensitive to insensitive ones in one. Meanwhile, among four cases with antibiotics change despite clinical response, three cases underwent antibiotics change according to the microbiological analysis, which turned out to be sensitive to sensitive ones. In the remaining one case undergoing antibiotics change for an unknown reason despite clinical response, both the initial and second antibiotics were insensitive to Bacillus and Rhizobium detected in the bile. In summary, antibiotics were changed from sensitive to sensitive ones in three, sensitive to insensitive ones in one and insensitive to sensitive ones in five and insensitive to insensitive ones in two (Fig. 2). In three cases who received insensitive antibiotics even after antibiotics change, the clinical courses of cholangitis were not complicated by the organ function or mortality.

DISCUSSION

While acute cholangitis is managed by a combination of biliary drainage and antibiotics, our retrospective study results suggested that sensitivity of empiric antibiotics to microorganisms detected in blood or bile was not associated with clinical outcomes of acute cholangitis after successful biliary drainage. Empiric antibiotics were only sensitive to blood culture in 40% and not sensitive to bile and blood culture in 8% but there was no significant difference in 30-day mortality in those cases. There were no significant differences in other clinical outcomes such as organ dysfunction and length of hospital stay, either. Although severe acute cholangitis accounted for 19% of our study cohort, the 30-day mortality rate was only 4%, which was exclusively observed in patients who received antibiotics sensitive to microorganisms detected in blood and bile culture.

Among 11 episodes of antibiotics change, antibiotics regimens were changed appropriately (from insensitive to sensitive ones) only in five episodes according to the sensitivity analyses. In the remaining six episodes when antibiotics were not changed based on the sensitivity analyses, antibiotics change was unnecessary or inappropriate (Fig. 2). Therefore, empiric antibiotics should be changed only after antibiotics sensitivity is available. Meanwhile, since sensitivity of empiric antibiotics did not affect clinical outcomes significantly in cases without antibiotics change (Table 5), in cases with clinical response antibiotics change might not be necessary irrespective of sensitivity of the initial antibiotics.

Some studies recommended bile culture should be performed at the time of biliary drainage because bile culture is more polymicrobial than blood culture, based on the assumption that all microorganisms detected in the bile should be covered by antibiotics.15-17 However, clinical outcomes were not discussed in those studies. To the best of our knowledge, this is the first study to compare clinical outcomes according to empiric antibiotics sensitivity to blood and bile culture. Our study suggested that covering all the microorganisms in bile or blood might not be necessarily mandatory in cases with acute cholangitis after successful biliary drainage. However, our study results did not indicate that bile or blood culture is unnecessary in the management of cholangitis. We recommend selecting appropriate antibiotics once susceptibility is available to better manage cholangitis and to avoid further pandemic of resistant bacteria.

In general, insensitive antibiotics for infectious diseases are related to poor clinical outcomes but it depends on primary infection sites.20,21 The mortality rate of biliary tract infection is relatively low probably because of biliary decompression.15 In our study, among 11 cases with antibiotics switch, empiric antibiotics were changed to insensitive ones in three cases but it did not adversely affect clinical outcomes in cholangitis. In line with previous reports, our findings imply that the role of biliary drainage is indispensable in the management of cholangitis.

Several limitations of this study should be acknowledged. First, this is a single center, retrospective study and a large-scale, prospective study is warranted. It should be confirmed whether the use of insensitive antibiotics does not increase rare systemic complications such as infective endocarditis and liver abscess. Of note, in our study cohort, Klebsiella and E. coli are the two major microorganisms and Enterococcus was detected only in 9% of blood culture. In cases with Enterococcal bacteremia, antibiotics should be changed to prevent Enterococcal infective endocarditis according to the recommendations in TG13.22 Although there were no extended-spectrum β-lactamase-producing E. coli and Klebsiella detected in our study cohort, they are increasingly detected in bile culture nowadays. Therefore, large-scale data should be further collected in a multicenter study to evaluate generalizability of our study results. In addition, in some cases with hilar biliary stricture, biliary drainage can be incomplete and antibiotics sensitivity can affect clinical outcomes in those cases. Furthermore, we evaluated the length of hospital stay as one of study endpoints, but some patients had second ERCP for stone extraction in cases with bile duct stones or exchange from endoscopic nasobiliary drainage to stents in case with malignant biliary obstruction. Therefore, the length of hospital stay can be affected not only by clinical response of cholangitis but by the primary causes of cholangitis. Lastly, our study cohort included only those cases who underwent biliary drainage within 24 hours of the onset of cholangitis. However, early biliary drainage is not always available in some centers and elective biliary drainage is performed after the initial empiric antibiotics use. The results of bile culture might be different in those cases undergoing elective biliary drainage compared to our study results.

In conclusion, the sensitivity of empiric antibiotics was not associated with clinical outcomes in patients with acute cholangitis. Our study results suggest that covering all microorganisms detected in blood and bile culture is not always necessary to resolve acute cholangitis once adequate biliary drainage is achieved. However, in cases without clinical response even after biliary drainage, sensitivity of microorganisms detected in bile and blood culture should be evaluated and antibiotics should be changed based on the sensitivity analysis if necessary. Finally, since this is a single center, retrospective study, our study results should be further validated in a large-scale multicenter study.

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

AUTHOR CONTRIBUTIONS

Study concept and design: S.K., N.T. Data acquisition: S.K., Y.K. Data analysis and interpretation: S.K., N.T., Y.N. Drafting of the manuscript: N.T., Y.N. Critical revision of the manuscript for important intellectual content: K. Koike, K.T. Technical and material support: C.S., K. Kurokawa, J.A., K.F., S.K., Y.K., S.M., M.K., K. Kojima, T.O., M.S. All authors contributed to critical revision and approved of the final version.

Figures
Fig. 1. Patient flowchart.
Fig. 2. Change in antibiotics during the clinical course of cholangitis.
Tables

Patient Characteristics

Characteristic Total episodes (n=80) Group A (n=42)* Group B (n=32) Group C (n=6) p-value
Age, yr 74.1±1.3 74.3±1.8 73.2±2.1 78.0±4.8 0.652
Male sex 63 (79) 33 (79) 26 (81) 4 (67) 0.725
Comorbidity
Cerebrovascular disease 19 (24) 9 (21) 9 (28) 1 (17) 0.730
Pulmonary disease 5 (6) 3 (7) 2 (6) 0 0.796
Ischemic heart disease 12 (15) 7 (17) 4 (13) 1 (17) 0.878
Liver disease 6 (8) 5 (12) 1 (3) 0 0.280
Renal disease 3 (4) 1 (2) 2 (6) 0 0.605
Diabetes mellitus 20 (25) 15 (36) 4 (13) 1 (17) 0.066
Hypertension 52 (65) 25 (60) 23 (72) 4 (67) 0.542
Profile
Nosocomial infection 14 (18) 6 (14) 8 (25) 0 0.244
Prior hospitalization 24 (30) 13 (31) 8 (25) 3 (50) 0.462
Prior use of antibiotics 14 (18) 5 (12) 6 (19) 3 (50) 0.069
Prior PTBD or ERCP 39 (49) 19 (45) 15 (47) 5 (83) 0.210
Laboratory data
Total bilirubin, mg/dL 4.38±4.46 4.26±0.68 5.07±0.78 1.58±1.81 0.209
CRP, mg/dL 6.90±6.09 7.81±0.94 6.22±1.07 4.18±2.48 0.286
WBC, ×103/μL 9.55±5.43 10.14±0.84 8.80±0.97 9.38±2.23 0.579
Acute cholangitis severity§ 0.523
Mild 40 (50) 24 (57) 14 (44) 2 (33)
Moderate 25 (31) 12 (29) 10 (31) 3 (50)
Severe 15 (19) 6 (14) 8 (25) 1 (17)
Cause of biliary obstruction 0.676
Stone 40 (50) 24 (57) 14 (44) 2 (33)
Malignancy 38 (48) 17 (40) 17 (53) 4 (67)
Inflammation 2 (2) 1 (3) 1 (3) 0
Biliary drainage method 0.518
ERCP 67 (84) 35 (83) 26 (81) 6 (100)
PTBD 13 (16) 7 (17) 6 (19) 0

Data are presented as mean±SD or number (%).

PTBD, percutaneous transhepatic biliary drainage; ERCP, endoscopic retrograde cholangiopancreatography; CRP, C-reactive protein; WBC, white blood cell.

*Group A, microorganisms in both the blood and bile cultures were sensitive to the antibiotics; Group B, only species in the blood culture were sensitive to the antibiotics; Group C, microorganisms in both the blood and bile cultures were insensitive to the antibiotics; §Severity of acute cholangitis was defined according to the 2013 Tokyo Guidelines.

Microorganisms Detected in Blood and Bile

Microorganism Isolated microorganisms Resistant microorganisms


Blood culture Bile culture Blood culture Bile culture
E. coli 16 (20) 30 (38) 0 0
E. coli ESBL 0 0 0 0
Klebsiella spp. 12 (15) 40 (50) 0 0
Klebsiella ESBL 0 0 0 0
Enterobacter spp. 0 17 (21) 0 1 (1)
Pseudomonas 4 (5) 8 (10) 0 0
Enterococcus spp. 7 (9) 36 (45) 4 (5) 19 (24)
Enterococcus faecium 5 (6) 12 (15) 4 (5) 7 (9)
Enterococcus faecalis 1 (1) 18 (23) 0 7 (9)
Other Enterococcus 2 (2) 9 (11) 0 6 (8)
Citrobacter freundii 0 6 (8) 0 0
Aeromonas hydrophila 1 (1) 8 (10) 1 (1) 9 (11)
Clostridium spp. 1 (1) 8 (10) 0 0
Bacteroides 0 5 (6) 0 2 (3)
Staphylococcus (including MRSA) 1 (1) 6 (8) 0 4 (5)
MRSA 1 (1) 3 (4) 0 2 (2)
Streptococcus 0 8 (10) 0 0
Candida spp. 0 11 (14) 0 11 (14)
Other 1 (1) 17 (21) 1 (1) 6 (8)
Any species 33 (41) 80 (100) 6 (8) 37 (46)

Data are presented as number (%).

E. coli, Escherichia coli; ESBL, extended-spectrum β-lactamase producing species; MRSA, methicillin-resistant Staphylococcus aureus.

Initial Antibiotics Used for Acute Cholangitis

Antibiotics Episode
CMZ 2 (3)
SBT/CPZ 37 (46)
CPFX 1 (1)
MEPM 5 (6)
DRPM 1 (1)
SBT/CPZ+ABPC 28 (35)
SBT/CPZ+VCM 2 (3)
MEPM+ABPC 2 (3)
MEPM+LZD 1 (1)
MEPM+VCM 1 (1)

Data are presented as number (%).

CMZ, cefmetazole; SBT/CPZ, sulbactam/cefoperazone; CPFX, ciprofloxacin; MEPM, meropenem; DRPM, doripenem; ABPC, ampicillin; VCM, vancomycin; LZD, linezolid.

Comparison of Clinical Outcomes among Three Groups According to the Pathogen Sensitivity to the Antibiotics

Clinical outcome Total episode (n=80) Group A (n=42)* Group B (n=32) Group C (n=6) p-value
30-day mortality 3 (4) 3 (7) 0 0 0.244
Length of hospital stay, day 24.9±24 28.5±3.7 21.0±4.2 20.5±9.8 0.369
Organ dysfunction 15 (19) 6 (14) 8 (25) 1 (17) 0.500
Duration of fever, day 3.8±3.5 4.3±0.5 3.2±0.6 3.5±1.4 0.921
Length of HCU stay, day 1.3±2.9 1.4±0.4 1.2±0.5 1.7±1.2 0.070

Data are presented as number (%) or mean±SD.

HCU, high care unit.

*Group A, microorganisms in both the blood and bile cultures were sensitive to the antibiotics; Group B, only species in the blood culture were sensitive to the antibiotics; Group C, microorganisms in both the blood and bile cultures were insensitive to the antibiotics.

Comparison of Clinical Outcomes in Patients without a Change from the Initial Empiric Antibiotics

Clinical outcome The initial antibiotics sensitive to culture (n=38) The initial antibiotics not sensitive to culture (n=31) p-value
30-day mortality 2 (5) 0 0.195
Length of hospital stay, day 28.6±4.0 19.6±4.5 0.136
Organ dysfunction 5 (13) 8 (26) 0.181
Duration of fever, day 3.9±0.5 3.1±0.6 0.363
Length of HCU stay, day 1.3±0.5 1.6±0.5 0.208

Data are presented as number (%) or mean±SD.

HCU, high care unit.

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Tables

Patient Characteristics

Characteristic Total episodes (n=80) Group A (n=42)* Group B (n=32) Group C (n=6) p-value
Age, yr 74.1±1.3 74.3±1.8 73.2±2.1 78.0±4.8 0.652
Male sex 63 (79) 33 (79) 26 (81) 4 (67) 0.725
Comorbidity
Cerebrovascular disease 19 (24) 9 (21) 9 (28) 1 (17) 0.730
Pulmonary disease 5 (6) 3 (7) 2 (6) 0 0.796
Ischemic heart disease 12 (15) 7 (17) 4 (13) 1 (17) 0.878
Liver disease 6 (8) 5 (12) 1 (3) 0 0.280
Renal disease 3 (4) 1 (2) 2 (6) 0 0.605
Diabetes mellitus 20 (25) 15 (36) 4 (13) 1 (17) 0.066
Hypertension 52 (65) 25 (60) 23 (72) 4 (67) 0.542
Profile
Nosocomial infection 14 (18) 6 (14) 8 (25) 0 0.244
Prior hospitalization 24 (30) 13 (31) 8 (25) 3 (50) 0.462
Prior use of antibiotics 14 (18) 5 (12) 6 (19) 3 (50) 0.069
Prior PTBD or ERCP 39 (49) 19 (45) 15 (47) 5 (83) 0.210
Laboratory data
Total bilirubin, mg/dL 4.38±4.46 4.26±0.68 5.07±0.78 1.58±1.81 0.209
CRP, mg/dL 6.90±6.09 7.81±0.94 6.22±1.07 4.18±2.48 0.286
WBC, ×103/μL 9.55±5.43 10.14±0.84 8.80±0.97 9.38±2.23 0.579
Acute cholangitis severity§ 0.523
Mild 40 (50) 24 (57) 14 (44) 2 (33)
Moderate 25 (31) 12 (29) 10 (31) 3 (50)
Severe 15 (19) 6 (14) 8 (25) 1 (17)
Cause of biliary obstruction 0.676
Stone 40 (50) 24 (57) 14 (44) 2 (33)
Malignancy 38 (48) 17 (40) 17 (53) 4 (67)
Inflammation 2 (2) 1 (3) 1 (3) 0
Biliary drainage method 0.518
ERCP 67 (84) 35 (83) 26 (81) 6 (100)
PTBD 13 (16) 7 (17) 6 (19) 0

Data are presented as mean±SD or number (%).

PTBD, percutaneous transhepatic biliary drainage; ERCP, endoscopic retrograde cholangiopancreatography; CRP, C-reactive protein; WBC, white blood cell.

*Group A, microorganisms in both the blood and bile cultures were sensitive to the antibiotics; Group B, only species in the blood culture were sensitive to the antibiotics; Group C, microorganisms in both the blood and bile cultures were insensitive to the antibiotics; §Severity of acute cholangitis was defined according to the 2013 Tokyo Guidelines.

Microorganisms Detected in Blood and Bile

Microorganism Isolated microorganisms Resistant microorganisms


Blood culture Bile culture Blood culture Bile culture
E. coli 16 (20) 30 (38) 0 0
E. coli ESBL 0 0 0 0
Klebsiella spp. 12 (15) 40 (50) 0 0
Klebsiella ESBL 0 0 0 0
Enterobacter spp. 0 17 (21) 0 1 (1)
Pseudomonas 4 (5) 8 (10) 0 0
Enterococcus spp. 7 (9) 36 (45) 4 (5) 19 (24)
Enterococcus faecium 5 (6) 12 (15) 4 (5) 7 (9)
Enterococcus faecalis 1 (1) 18 (23) 0 7 (9)
Other Enterococcus 2 (2) 9 (11) 0 6 (8)
Citrobacter freundii 0 6 (8) 0 0
Aeromonas hydrophila 1 (1) 8 (10) 1 (1) 9 (11)
Clostridium spp. 1 (1) 8 (10) 0 0
Bacteroides 0 5 (6) 0 2 (3)
Staphylococcus (including MRSA) 1 (1) 6 (8) 0 4 (5)
MRSA 1 (1) 3 (4) 0 2 (2)
Streptococcus 0 8 (10) 0 0
Candida spp. 0 11 (14) 0 11 (14)
Other 1 (1) 17 (21) 1 (1) 6 (8)
Any species 33 (41) 80 (100) 6 (8) 37 (46)

Data are presented as number (%).

E. coli, Escherichia coli; ESBL, extended-spectrum β-lactamase producing species; MRSA, methicillin-resistant Staphylococcus aureus.

Initial Antibiotics Used for Acute Cholangitis

Antibiotics Episode
CMZ 2 (3)
SBT/CPZ 37 (46)
CPFX 1 (1)
MEPM 5 (6)
DRPM 1 (1)
SBT/CPZ+ABPC 28 (35)
SBT/CPZ+VCM 2 (3)
MEPM+ABPC 2 (3)
MEPM+LZD 1 (1)
MEPM+VCM 1 (1)

Data are presented as number (%).

CMZ, cefmetazole; SBT/CPZ, sulbactam/cefoperazone; CPFX, ciprofloxacin; MEPM, meropenem; DRPM, doripenem; ABPC, ampicillin; VCM, vancomycin; LZD, linezolid.

Comparison of Clinical Outcomes among Three Groups According to the Pathogen Sensitivity to the Antibiotics

Clinical outcome Total episode (n=80) Group A (n=42)* Group B (n=32) Group C (n=6) p-value
30-day mortality 3 (4) 3 (7) 0 0 0.244
Length of hospital stay, day 24.9±24 28.5±3.7 21.0±4.2 20.5±9.8 0.369
Organ dysfunction 15 (19) 6 (14) 8 (25) 1 (17) 0.500
Duration of fever, day 3.8±3.5 4.3±0.5 3.2±0.6 3.5±1.4 0.921
Length of HCU stay, day 1.3±2.9 1.4±0.4 1.2±0.5 1.7±1.2 0.070

Data are presented as number (%) or mean±SD.

HCU, high care unit.

*Group A, microorganisms in both the blood and bile cultures were sensitive to the antibiotics; Group B, only species in the blood culture were sensitive to the antibiotics; Group C, microorganisms in both the blood and bile cultures were insensitive to the antibiotics.

Comparison of Clinical Outcomes in Patients without a Change from the Initial Empiric Antibiotics

Clinical outcome The initial antibiotics sensitive to culture (n=38) The initial antibiotics not sensitive to culture (n=31) p-value
30-day mortality 2 (5) 0 0.195
Length of hospital stay, day 28.6±4.0 19.6±4.5 0.136
Organ dysfunction 5 (13) 8 (26) 0.181
Duration of fever, day 3.9±0.5 3.1±0.6 0.363
Length of HCU stay, day 1.3±0.5 1.6±0.5 0.208

Data are presented as number (%) or mean±SD.

HCU, high care unit.

Figures
Fig. 1. Patient flowchart.
Fig. 2. Change in antibiotics during the clinical course of cholangitis.
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