Infection Sources and Klebsiella pneumoniae Antibiotic Susceptibilities in Endogenous Klebsiella Endophthalmitis
by
, , , , , , and
Kuan-Jen Chen
1,2,*,†
,
Yen-Po Chen
1,2,3,†,
Yi-Hsing Chen
1,2
,
Laura Liu
1,2,
Nan-Kai Wang
4,
An-Ning Chao
1,2,
Wei-Chi Wu
1,2,
Yih-Shiou Hwang
1,2,
Hung-Da Chou
1,2,
Eugene Yu-Chuan Kang
1,2
,
Yen-Ting Chen
1,
Ming-Hui Sun
1,2 and
Chi-Chun Lai
1,2,5 1
Department of Ophthalmology, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan
2
College of Medicine, Chang Gung University, Taoyuan 333, Taiwan
3
Department of Ophthalmology, Tucheng Municipal Hospital, Tucheng, New Taipei 236, Taiwan
4
Department of Ophthalmology, Edward S. Harkness Eye Institute, Columbia University, New York, NY 10032, USA
5
Department of Ophthalmology, Chang Gung Memorial Hospital, Keelung 204, Taiwan
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Antibiotics 2022, 11(7), 866; https://doi.org/10.3390/antibiotics11070866
Submission received: 21 May 2022
/
Revised: 19 June 2022
/
Accepted: 25 June 2022
/
Published: 27 June 2022
Abstract
:Endogenous endophthalmitis is an uncommon intraocular infection with potentially devastating consequences on vision. Klebsiella pneumoniae is highly prevalent in East Asian countries, with an increasing incidence recently worldwide. This retrospective study investigates infection sources and antibiotic susceptibilities of K. pneumoniae in patients with endogenous K. pneumoniae endophthalmitis (EKE) in Northern Taiwan. One hundred and fifty-seven patients with EKE were reviewed between January 1996 and April 2019. Pyogenic liver abscess (120/157, 76.4%) was the most common infection source, followed by pneumonia (13, 8.3%), urinary tract infection (7, 4.5%), and intravenous drug use (4, 2.5%). Bilateral involvement was identified in 12.1% (19/157) of patients, especially in patients with pyogenic liver abscess (16/120, 13.3%), pneumonia (2/13, 15.4%), and urinary tract infection (1/7, 14.3%). The antibiotic susceptibility rates were 98.1%, 92.5%, 97.5%, 96.8%, 100%, 99.3%, and 100% for amikacin, cefuroxime, ceftazidime, ceftriaxone, carbapenems, ciprofloxacin, and levofloxacin, respectively. Four extended-spectrum β-lactamase-producing multidrug-resistant (MDR) K. pneumoniae isolates were identified. In conclusion, pyogenic liver abscess was the major infection source in EKE. In addition, K. pneumoniae was still highly susceptible to ceftazidime and amikacin, and the MDR K. pneumoniae isolates were not common in EKE.
1. Introduction
Endogenous endophthalmitis is an uncommon intraocular infection with potentially devastating consequences on vision. Klebsiella pneumoniae is highly prevalent in East Asian countries [1,2,3,4], with an increasing incidence recently worldwide [5,6,7,8,9,10]. Diabetic patients with K. pneumoniae hepatobiliary infections have a higher risk of developing endogenous K. pneumoniae endophthalmitis (EKE) [1,2,3,4,5,6,7]. EKE has been found in patients with other infections, such as pneumonia and renal abscess [8,9,10,11]. K. pneumoniae isolates are typically susceptible to ceftazidime and amikacin, which are currently used empirically to treat endophthalmitis. Ceftriaxone is also the mainstay treatment for systemic K. pneumoniae infection, including liver abscess [12,13]. In the past, most studies demonstrated the antibiotic susceptibility testing results from patients admitted to the department of internal medicine. However, the details of antibiotic susceptibility testing results are lacking in patients with EKE. Amidst growing concern over the emergence of multidrug-resistant (MDR) bacteria, selecting appropriate antibiotics for infection treatment has become a critical issue [14,15]. Common variants of MDR K. pneumoniae include extended-spectrum β-lactamase (ESBL)-producing and carbapenemase-producing K. pneumoniae [14,15,16]. Although most isolates causing ocular infections are not caused by MDR bacteria, antibiotic susceptibility testing may reveal antibiotic susceptibility and resistance trends.
This retrospective study investigates the infection sources and antibiotic susceptibilities of K. pneumoniae in patients with EKE at a tertiary referral center in Northern Taiwan.
2. Methods and Materials
This study was a retrospective, consecutive case series of patients diagnosed with EKE at any time from January 1996 to April 2019 at a tertiary referral center in Northern Taiwan. The institutional review board of Chang Gung Memorial Hospital in Taoyuan, Taiwan, approved this retrospective study protocol (201900614B0C601, 10 August 2019) and waived the need for written informed consent by these patients. All clinical procedures were conducted according to the principles of the Declaration of Helsinki. The availability of medical records used either manual (1996–2000) or electronic (2001–2019) systems, and the data were collected by K.-J.C. and Y.-P.C. EKE diagnosis was confirmed if patients had signs of posterior ocular inflammation (including vitritis and chorioretinitis with or without choroidal or subretinal abscess as examined using indirect ophthalmoscopy or ultrasonography) and positive K. pneumoniae culture results from the blood, eye (vitreous or aqueous humor), or other extraocular sites, such as aspirated pus from an abscess, sputum, urine, or a wound. Either the primary extraocular source of infection was identified, or the presence of bacteremia was documented without a specific infection focus
All microbiological investigations were performed at the Microbiology Department of Chang Gung Memorial Hospital, Taoyuan, Taiwan. Bacterial culture isolates were identified using conventional microbiological methods between January 1996 and December 2013 and matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS) between January 2014 and April 2019. Conventional microbiological methods included Gram staining and biochemical tests. In MALDI-TOF-MS, automated measurement of the spectrum and comparative analysis against reference bacteria spectra were performed using an Ultraflextreme mass spectrometer and in MALDI Biotyper 3.0 software (Bruker Daltonics, Karlsruhe, Germany). The reliability of identification in the MALDI Biotyper system was expressed in terms of points. A log(score) of ≥2.0 indicated identification to the species level. The antibiotic susceptibility testing results were based on the choice of antibiotics tested in our hospital during the study period. The isolates were tested for susceptibility to various antibiotics using the Kirby–Bauer disc diffusion method on Mueller Hinton blood agar. Clinical and Laboratory Standards Institute (Wayne, PA, USA) standards were used for interpretation and quality control for each corresponding year [13]. Because we reported the visual outcomes in our previous study [2,3], data on visual outcomes were not part of this study. All statistical analyses were performed using SPSS version 23.0 (SPSS IBM Corp., New York, NY, USA).
3. Results
A total of 157 patients were diagnosed with EKE during the study period. The mean age of patients was 51.8 ± 13.6 years (range: 1 month to 87 years). The predominant sex was male (108/157, 68.8%). Immunocompromised status included diabetes mellitus in 105 patients (66.9%), liver cirrhosis in 10 patients (6.4%), alcoholism in 8 patients (5.1%), malignancy with immunosuppressant therapy in 8 patients (5.1%), and end-stage renal failure in 2 patients (1.3%).
3.1. Infectious Source
Table 1 lists the infection sources of EKE. Pyogenic liver abscess was the most common infection source, followed by pneumonia and urinary tract infection. Pyogenic liver abscess progressed with meningitis and endophthalmitis in five patients. Four users of intravenous drugs were identified with EKE. Bilateral involvement was noted in 12.1% (19/157) of patients, especially in those with pyogenic liver abscess (16/120, 13.3%), pneumonia (2/13, 15.4%), and urinary tract infection (1/7, 14.3%). However, there was no significant difference in the rate of bilateral involvement among these three groups. Table 2 shows the distribution of K. pneumoniae as isolated from different samples. The most common positive K. pneumoniae isolates were cultured from blood samples, followed by vitreous samples and aspirated fluid from abscesses.
3.2. Antibiotic Susceptibility Testing
Table 3 presents the antibiotic susceptibility of K. pneumoniae isolates; 98% of K. pneumoniae isolates were susceptible to ceftazidime and amikacin, which are currently used empirically to treat endophthalmitis. The tested antibiotics included penicillins, cephalosporins, aztreonam, fluoroquinolones, aminoglycosides, carbapenems, and sulfamethoxazole-trimethoprim.
Among penicillins, K. pneumoniae tended to be resistant to ampicillin, but more than 90% of K. pneumoniae isolates were susceptible to ampicillin-sulbactam, amoxicillin-clavulanate, and piperacillin-tazobactam. The susceptibility rates to aminoglycosides and sulfamethoxazole-trimethoprim were similar and more than 95%. All K. pneumoniae isolates had a 90–100% susceptibility rate to cephalosporins. All K. pneumoniae isolates were susceptible to carbapenems and levofloxacin.
3.3. Multidrug-Resistant Isolates
Four MDR K. pneumoniae isolates were identified. Table 4 shows the antibiotic susceptibility testing results for multidrug resistance. ESBL production was detected in the four K. pneumoniae isolates, of which only one was susceptible to amikacin. All four isolates were susceptible to carbapenems (imipenem, meropenem, or ertapenem). The four K. pneumoniae isolates were obtained in one user of intravenous drugs and three hospitalized patients, including one patient with splenic abscess and two with pneumonia.
4. Discussion
To the best of our knowledge, this is the largest case series of patients with EKE in a systemic review of the PubMed literature. In the present study, pyogenic liver abscess was the major infection source in cases of EKE, followed by pneumonia, urinary tract infection, and intravenous drug users. K. pneumoniae isolates were highly susceptible to ceftazidime and amikacin. In addition, the MDR K. pneumoniae isolates were uncommon in EKE. Most K. pneumoniae isolates were susceptible to third-generation cephalosporins, carbapenems, and fluoroquinolones. In immunocompromised status, diabetes mellitus was the most important risk factor, followed by liver cirrhosis, alcoholism, malignancy with immunosuppressant therapy, and end-stage renal failure.
Because of the small number of other infection source cases, bilateral eye involvement (13% to 15%) of EKE was only identified in patients with pyogenic liver abscess, pneumonia, or urinary tract infection. There was no significant difference in bilateral eye involvement among these three groups. Six (3.8%) of the patients died during their hospital stay. The causes of death of the six patients were related to pyogenic liver abscess in four patients, pneumonia in one, and peritonitis in one. All six patients died from sepsis and multiorgan failure. The most common positive K. pneumoniae isolates were cultured from blood samples (79%), followed by vitreous samples (41%) and aspirated fluid from abscesses (37%). The lower positive rate of vitreous samples could result from patients treated with systemic antibiotics before EKE was diagnosed.
The increasing incidence of EKE has recently been reported worldwide, and pyogenic liver abscess is the leading cause of EKE. Pyogenic liver abscess accounted for 76.4% of the cases in our study; however, pneumonia, urinary tract infection, and intravenous drug use (IVDU) explained other, less common infection sources. IVDU-related endogenous endophthalmitis is typically caused by Staphylococcus aureus and Candida albicans [17,18,19]. There were some case reports with IVDU-related EKE [20,21]. Our findings suggest that K. pneumoniae should be considered a pathogen for IVDU-related endogenous endophthalmitis. Among four MDR K. pneumoniae strains, three isolates were hospital-acquired infections, including two patients with pneumonia and one with splenic abscess. However, the cause of one MDR K. pneumoniae isolate cultured from IVDU-related endophthalmitis was unknown.
Because the number of ESBL producers and AmpC β-lactamase producers has been increasing, previous studies observed a significant decrease in susceptibilities to third-generation cephalosporins and ciprofloxacin over the two decades of our study period [22]. Additionally, carbapenem-resistant K. pneumoniae, a new major concern emerging during the last decade because of a significantly compromised efficacy of carbapenem agents, has become a focal point of infection control [23,24]. In a case report of carbapenemase-producing K. pneumoniae endophthalmitis by Zhou et al. [25], the K. pneumoniae isolate was resistant to amikacin, ceftazidime, and carbapenems, but susceptible to polymyxin E and tigecycline. The trends of antibiotic susceptibility of K. pneumoniae isolates exhibited no observable change across the decades of our study period. Some sporadic ESBL-producing K. pneumoniae isolates were identified in one patient using intravenous drugs and three hospitalized patients, including one with splenic abscess and two with pneumonia. Moreover, no carbapenem-resistant K. pneumoniae isolate was identified, and four MDR ESBL-producing K. pneumoniae isolates were susceptible to carbapenems (imipenem, meropenem, or ertapenem) in our study.
However, the study has some limitations. First, this was a single-center retrospective case series. Second, K. pneumoniae isolates were not routinely tested at our hospital for susceptibility to the same antibiotics because the review was completed over the course of more than 23 years. Third, we did not retrieve accurate, detailed information on various types of endophthalmitis and visual outcomes, which may interest the readers. Finally, we did not further analyze the MDR bacteria for specific resistance genes. Nevertheless, our findings contribute to the literature in providing a thorough analysis of the antimicrobial susceptibility of K. pneumoniae from all patients diagnosed with EKE over 23 years at a tertiary medical center.
In conclusion, the most common infection source of detected EKE was pyogenic liver abscess. MDR bacterial endophthalmitis was not common. Amikacin and ceftazidime were observed to provide approximately equal gram-negative coverage. In MDR K. pneumoniae isolates, carbapenems and fluoroquinolones may serve as alternative treatments for EKE. The efficacy of multiple antibiotics against ESBL-producing or carbapenemase-producing K. pneumoniae will be tested in experimental and clinical endogenous K. pneumoniae endophthalmitis in future studies.
Author Contributions
Conceptualization, K.-J.C. and Y.-P.C.; Data curation, K.-J.C., M.-H.S., Y.-P.C., H.-D.C., E.Y.-C.K. and Y.-T.C.; Formal analysis, K.-J.C. and Y.-P.C.; Funding acquisition, K.-J.C.; Investigation, K.-J.C.; Methodology, K.-J.C.; Project administration, M.-H.S. and C.-C.L.; Resources, K.-J.C., Y.-P.C., Y.-H.C., N.-K.W., L.L., A.-N.C., W.-C.W., Y.-S.H. and C.-C.L.; Software, K.-J.C.; Writing—original draft, K.-J.C. and Y.-P.C.; Writing—review and editing, K.-J.C., Y.-P.C., Y.-H.C., N.-K.W., L.L., A.-N.C. and W.-C.W. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by a grant from the Taiwan Ministry of Science and Technology MOST 106-2314-B-182A-041, and Chang Gung Memorial Hospital CMRPG3 K1681.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of Chang Gung Memorial Hospital (201900614B0C601, 10 August 2019) in Taoyuan, Taiwan.
Informed Consent Statement
Patient consent was waived by the Institutional Review Board of Chang Gung Memorial Hospital due to a retrospective study.
Data Availability Statement
Not applicable.
Acknowledgments
The authors thank Mao-Cheng Ge for assistance in microbiology.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Yang, C.S.; Tsai, H.Y.; Sung, C.S.; Lin, K.H.; Lee, F.L.; Hsu, W.M. Endogenous Klebsiella endophthalmitis associated with pyogenic liver abscess. Ophthalmology 2007, 114, 876–880. [Google Scholar] [CrossRef]
- Li, Y.H.; Chen, Y.H.; Chen, K.J.; Wang, N.K.; Sun, M.H.; Chao, A.N.; Liu, L.; Lin, Y.J.; Wu, W.C.; Hwang, Y.S.; et al. Infectious Sources, Prognostic Factors, and Visual Outcomes of Endogenous Klebsiella pneumoniae Endophthalmitis. Ophthalmol. Retin. 2018, 2, 771–778. [Google Scholar] [CrossRef]
- Chen, Y.H.; Li, Y.H.; Lin, Y.J.; Chen, Y.P.; Wang, N.K.; Chao, A.N.; Liu, L.; Wu, W.C.; Lai, C.C.; Chen, T.L.; et al. Prognostic Factors and Visual Outcomes of Pyogenic Liver Abscess-Related Endogenous Klebsiella pneumoniae Endophthalmitis: A 20-year retrospective review. Sci. Rep. 2019, 9, 1071. [Google Scholar] [CrossRef]
- Sheu, S.J.; Kung, Y.H.; Wu, T.T.; Chang, F.P.; Horng, Y.H. Risk factors for endogenous endophthalmitis secondary to Klebsiella pneumoniae liver abscess: 20-year experience in Southern Taiwan. Retina 2011, 31, 2026–2031. [Google Scholar] [CrossRef]
- Chen, Y.J.; Kuo, H.K.; Wu, P.C.; Kuo, M.L.; Tsai, H.H.; Liu, C.C.; Chen, C.H. A 10-year comparison of endogenous endophthalmitis outcomes: An east Asian experience with Klebsiella pneumoniae infection. Retina 2004, 24, 383–390. [Google Scholar] [CrossRef]
- Martellosio, J.P.; Gastli, N.; Farhat, R.; Tazi, A.; Duraffour, P.; Rossi, B.; Canouï, E.; Morbieu, C.; Billoët, A.; Mouthon, L.; et al. Hypervirulent Klebsiella pneumoniae, an Emerging Cause of Endogenous Endophthalmitis in A French Center: A Comparative Cohort Study. Ocul. Immunol. Inflamm. 2022, 1–9. [Google Scholar] [CrossRef]
- Serban, D.; Popa Cherecheanu, A.; Dascalu, A.M.; Socea, B.; Vancea, G.; Stana, D.; Smarandache, G.C.; Sabau, A.D.; Costea, D.O. Hypervirulent Klebsiella pneumoniae Endogenous Endophthalmitis-A Global Emerging Disease. Life 2021, 11, 676. [Google Scholar] [CrossRef]
- Chen, K.J.; Hwang, Y.S.; Chen, Y.P.; Lai, C.C.; Chen, T.L.; Wang, N.K. Endogenous Klebsiella endophthalmitis associated with Klebsiella pneumoniae pneumonia. Ocul. Immunol. Inflamm. 2009, 17, 153–159. [Google Scholar] [CrossRef]
- Chen, K.J.; Hwang, Y.S.; Wang, N.K.; Chao, A.N. Endogenous Klebsiella pneumoniae endophthalmitis with renal abscess: Report of two cases. Int. J. Infect. Dis. 2010, 14, e429–e432. [Google Scholar] [CrossRef] [Green Version]
- Wang, F.; Tao, Y.; Sun, B.; Tong, Z.H. Endogenous Klebsiella pneumoniae endophthalmitis associated with Klebsiella pneumoniae pneumonia: 3 cases report and literature review. Zhonghua Jie He He Hu Xi Za Zhi 2019, 42, 438–443. [Google Scholar] [CrossRef]
- Hassanin, F.; Khawjah, D.; Elkhamary, S.; Al Hussain, H. Renal abscesses and endogenous endophthalmitis due to hypermucoviscous hypervirulent Klebsiella pneumoniae (HVKP). IDCases 2021, 24, e01130. [Google Scholar] [CrossRef]
- Seetoh, T.; Lye, D.; Archuleta, S.; Fisher, D. Klebsiella pneumoniae liver abscesses. Lancet Infect. Dis. 2013, 13, 391–392. [Google Scholar] [CrossRef]
- Cheng, H.P.; Siu, L.K.; Chang, F.Y. Extended-spectrum cephalosporin compared to cefazolin for treatment of Klebsiella pneumoniae-caused liver abscess. Antimicrob. Agents Chemother. 2003, 47, 2088–2092. [Google Scholar] [CrossRef] [Green Version]
- Altayb, H.N.; Elbadawi, H.S.; Baothman, O.; Kazmi, I.; Alzahrani, F.A.; Nadeem, M.S.; Hosawi, S.; Chaieb, K. Genomic Analysis of Multidrug-Resistant Hypervirulent (Hypermucoviscous) Klebsiella pneumoniae Strain Lacking the Hypermucoviscous Regulators (rmpA/rmpA2). Antibiotics 2022, 11, 596. [Google Scholar] [CrossRef]
- Lin, Y.T.; Cheng, Y.H.; Chuang, C.; Chou, S.H.; Liu, W.H.; Huang, C.H.; Yang, T.C.; Kreiswirth, B.N.; Chen, L. Molecular and Clinical Characterization of Multidrug-Resistant and Hypervirulent Klebsiella pneumoniae Strains from Liver Abscess in Taiwan. Antimicrob. Agents Chemother. 2020, 64, e00174-20. [Google Scholar] [CrossRef]
- Chiu, S.K.; Wu, T.L.; Chuang, Y.C.; Lin, J.C.; Fung, C.P.; Lu, P.L.; Wang, J.T.; Wang, L.S.; Siu, L.K.; Yeh, K.M. National surveillance study on carbapenem non-susceptible Klebsiella pneumoniae in Taiwan: The emergence and rapid dissemination of KPC-2 carbapenemase. PLoS ONE 2013, 8, e69428. [Google Scholar] [CrossRef]
- Modjtahedi, B.S.; Finn, A.P.; Papakostas, T.D.; Durand, M.; Husain, D.; Eliott, D. Intravenous Drug Use-Associated Endophthalmitis. Ophthalmol. Retina 2017, 1, 192–199. [Google Scholar] [CrossRef]
- Tirpack, A.R.; Duker, J.S.; Baumal, C.R. An Outbreak of Endogenous Fungal Endophthalmitis Among Intravenous Drug Abusers in New England. JAMA Ophthalmol. 2017, 135, 534–540. [Google Scholar] [CrossRef] [Green Version]
- Chen, K.J.; Sun, M.H.; Chen, Y.P.; Wang, N.K.; Wu, W.C.; Lai, C.C. Endogenous Endophthalmitis Caused by Infective Endocarditis in East Asia. Ophthalmol. Retina 2019, 3, 382–384. [Google Scholar] [CrossRef]
- Chen, K.J.; Wu, W.C.; Chen, Y.P.; Liu, L. Intravenous drug use-related endophthalmitis. Clin. Exp. Ophthalmol. 2022. [Google Scholar] [CrossRef]
- Kong, Y.; Tang, X.; Han, Q.; Jiang, H. Endogenous Klebsiella pneumoniae endophthalmitis associated with intravenous drug abuse. Chin. Med. J. 2014, 127, 1594–1595. [Google Scholar]
- Lin, W.P.; Wang, J.T.; Chang, S.C.; Chang, F.Y.; Fung, C.P.; Chuang, Y.C.; Chen, Y.S.; Shiau, Y.R.; Tan, M.C.; Wang, H.Y.; et al. The Antimicrobial Susceptibility of Klebsiella pneumoniae from Community Settings in Taiwan, a Trend Analysis. Sci. Rep. 2016, 6, 36280. [Google Scholar] [CrossRef] [Green Version]
- Jean, S.S.; Lee, N.Y.; Tang, H.J.; Lu, M.C.; Ko, W.C.; Hsueh, P.R. Carbapenem-Resistant Enterobacteriaceae Infections: Taiwan Aspects. Front Microbiol. 2018, 9, 2888. [Google Scholar] [CrossRef]
- Lai, C.C.; Yu, W.L. Klebsiella pneumoniae Harboring Carbapenemase Genes in Taiwan: Its Evolution over 20 Years, 1998–2019. Int. J. Antimicrob. Agents 2021, 58, 106354. [Google Scholar] [CrossRef]
- Zhou, Y.; Wang, X.; Shen, J.; Lu, Z.; Liu, Y. Endogenous Endophthalmitis Caused by Carbapenem-Resistant Hypervirulent Klebsiella pneumoniae: A Case Report and Literature Review. Ocul. Immunol. Inflamm. 2019, 27, 1099–1104. [Google Scholar] [CrossRef]
Table 1.
Infection sources of endogenous Klebsiella pneumoniae endophthalmitis.
| Infectious Source | No. of Patients | Percent | Bilateral Involvement | Percent |
|---|---|---|---|---|
| Pyogenic liver abscess *† | 120 | 76.4% | 16 | 13.3% |
| Pneumonia ‡ | 13 | 8.3% | 2 | 15.4% |
| Urinary tract infection/renal abscess | 7 | 4.5% | 1 | 14.3% |
| Intravenous drug user | 4 | 2.5% | ||
| Necrotizing fasciitis | 1 | 0.6% | ||
| Cellulitis | 1 | 0.6% | ||
| Brain abscess | 1 | 0.6% | ||
| Neck abscess | 1 | 0.6% | ||
| Spleen abscess | 1 | 0.6% | ||
| Retroperitoneal nonorganic abscess | 1 | 0.6% | ||
| Rectal perforation with sepsis | 1 | 0.6% | ||
| Peritonitis | 1 | 0.6% | ||
| Colon cancer with necrosis | 1 | 0.6% | ||
| Not identified | 4 | 2.5% | ||
| Total | 157 | 100% | 19 | 12.1% |
* Three patients with hepatobiliary tract infection but no obvious liver abscess on abdominal echography or computed tomography. † Five patients with meningitis, 20 patients with pneumonia, and one patient with prostate abscess. ‡ Primary infection with pneumonia was not associated with pyogenic liver abscess.
Table 2.
Distribution of Klebsiella pneumoniae isolated from different samples.
| Sample | No. of Patients | % |
|---|---|---|
| Blood | 124 | 79.0 |
| Eye | 65 | 41.4 |
| Abscesses | 58 | 36.9 |
| Urine | 30 | 19.1 |
| Sputum | 13 | 8.3 |
| Wound swab | 3 | 1.9 |
| Plural effusion | 3 | 1.9 |
| Endotracheal aspirates | 2 | 1.3 |
| Ascites | 1 | 0.6 |
| Total | 157 | 100 |
Table 3.
Antibiotic susceptibility of Klebsiella pneumoniae.
| Antibiotics | Tested | Sensitive | Intermediate | Resistant | |
|---|---|---|---|---|---|
| Interval | No. (%) | No. (%) | No. (%) | Diseases (Number) | |
| Ampicillin | 1996–2006 | 75/75 (100%) | All diseases | ||
| Ampicillin-sulbactam | 2007–2010 | 44/46 (95.7%) | 2/46 (4.3%) | Liver abscess (2) | |
| Amoxicillin-clavulanate | 2010–2019 | 22/22 (100%) | |||
| Ticarcillin | 1996–1997 | 4/4 (100%) | Liver abscess (4) | ||
| Piperacillin | 1996–2010 | 75/93 (81.7%) | 5/93 (5.4%) | 13/93 (14.0%) | Liver abscess (9), pneumonia (4) |
| Piperacillin-tazobactam | 2007–2019 | 64/67 (95.5%) | 2/67 (3.1%) | 1/67 (1.5%) | Liver abscess (1) |
| Gentamicin | 1996–2019 | 153/157 (97.5%) | 4/157 (2.5%) | Pneumonia (2), spleen abscess (1), IVDU (1), | |
| Amikacin | 1996–2019 | 154/157 (98.1%) | 3/157 (1.9%) | Pneumonia (2), spleen abscess (1) | |
| Sulfamethoxazole-trimethoprim | 1996–2010 | 91/96 (95.8%) | 5/96 (4.2%) | Pneumonia (2), liver abscess (2),spleen abscess (1) | |
| Cephalothin | 1996–2000 | 20/20 (100%) | |||
| Cefazolin | 1996–2009 | 82/89 (92.1%) | 7/89 (7.9%) | Liver abscess (3), pneumonia (2), spleen abscess (1), IVDU (1), | |
| Cefuroxime | 1999–2019 | 135/146 (92.5%) | 11/146 (7.5%) | Liver abscess (7), pneumonia (2), spleen abscess (1), IVDU (1) | |
| Ceftriaxone | 1996–2019 | 152/157 (96.8%) | 5/157 (3.2%) | Pneumonia (2), spleen abscess (1), IVDU (1), liver abscess (1) | |
| Ceftazidime | 1996–2019 | 153/157 (97.5%) | 4/157 (2.6%) | Pneumonia (2), spleen abscess (1), IVDU (1), | |
| Flomoxef | 2007–2012 | 18/20 (90%) | 2/20 (10%) | Pneumonia (2) | |
| Cefepime | 2008–2013 | 16/16 (100%) | |||
| Cefoperazone-sulbactam | 2016–2019 | 10/10 (100%) | |||
| Aztreonam | 1999–2009 | 90/95 (94.7%) | 5 (5.3%) | Pneumonia (2), spleen abscess (1), IVDU (1), liver abscess (1) | |
| Imipenem | 1996–2006 | 82/82 (100%) | |||
| Ertapenem | 2007–2019 | 71/71 (100%) | |||
| Meropenem | 2007 | 1/1 (100%) | |||
| Ciprofloxacin | 2000–2009 | 130/131 (99.3%) | 1/131 (0.7%) | Pneumonia (1) | |
| Levofloxacin | 2010–2019 | 65/65 (100%) | |||
IVDU, intravenous drug use.
Table 4.
Antibiotic susceptibility testing in multidrug-resistant Klebsiella pneumoniae.
| Antibiotics | Klebsiella pneumoniae | |||
|---|---|---|---|---|
| No. of Isolates | 1 | 2 | 3 | 4 |
| Infection Source | Pneumonia | Pneumonia | Spleen Abscess | IVDU |
| Ampicillin | R | R | R | |
| Amoxicillin-clavulanic acid | S | |||
| Piperacillin | R | R | S | R |
| Piperacillin-tazobactam | S | S | ||
| Gentamicin | R | R | R | R |
| Amikacin | R | R | R | S |
| Cefazolin | R | R | R | R |
| Cefuroxime | R | R | R | R |
| Ceftriaxone | R | R | R | R |
| Ceftazidime | R | R | R | R |
| Floxomef | R | R | S | S |
| Aztreonam | R | R | R | R |
| Trimethoprim-sulfamethoxazole | R | R | R | |
| Ciprofloxacin | S | R | S | S |
| Imipenem | S | S | ||
| Meropenem | S | |||
| Ertapenem | S | |||
IVDU = intravenous drug use; S = susceptible; R = resistant.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Chen, K.-J.; Chen, Y.-P.; Chen, Y.-H.; Liu, L.; Wang, N.-K.; Chao, A.-N.; Wu, W.-C.; Hwang, Y.-S.; Chou, H.-D.; Kang, E.Y.-C.; et al. Infection Sources and Klebsiella pneumoniae Antibiotic Susceptibilities in Endogenous Klebsiella Endophthalmitis. Antibiotics 2022, 11, 866. https://doi.org/10.3390/antibiotics11070866
AMA Style
Chen K-J, Chen Y-P, Chen Y-H, Liu L, Wang N-K, Chao A-N, Wu W-C, Hwang Y-S, Chou H-D, Kang EY-C, et al. Infection Sources and Klebsiella pneumoniae Antibiotic Susceptibilities in Endogenous Klebsiella Endophthalmitis. Antibiotics. 2022; 11(7):866. https://doi.org/10.3390/antibiotics11070866
Chicago/Turabian StyleChen, Kuan-Jen, Yen-Po Chen, Yi-Hsing Chen, Laura Liu, Nan-Kai Wang, An-Ning Chao, Wei-Chi Wu, Yih-Shiou Hwang, Hung-Da Chou, Eugene Yu-Chuan Kang, and et al. 2022. "Infection Sources and Klebsiella pneumoniae Antibiotic Susceptibilities in Endogenous Klebsiella Endophthalmitis" Antibiotics 11, no. 7: 866. https://doi.org/10.3390/antibiotics11070866
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
