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Erschienen in: Journal of Ophthalmic Inflammation and Infection 1/2016

Open Access 01.12.2016 | Original research

Comparison of clinico-microbiological profile and treatment outcome of in-house and referred post cataract surgery endophthalmitis in a tertiary care center in South India

verfasst von: Vikas Ambiya, Taraprasad Das, Savitri Sharma, Jay Chhablani, Vivek Dave, Subhadra Jalali, Raja Narayanan, Joveeta Joseph

Erschienen in: Journal of Ophthalmic Inflammation and Infection | Ausgabe 1/2016

Abstract

Background

The purpose of the study is to compare the clinico-microbiological profile and treatment outcome of in-house vs referred cases of post cataract surgery endophthalmitis in a tertiary eye care facility in South India.

Methods

The clinical records of 50 culture-positive cases each of in-house (group A) and referred (group B) post cataract surgery endophthalmitis were analyzed. The management protocol was similar in both groups.

Results

The time to report to the institute was longer in group B (group B 13.63 [±11.67; 95% CI, 9.95–17.31] days; group A 6.83 [±7.61; 95% CI, 4.57–9.09] days; P = 0.002). The average inflammatory scores in presentation were comparable (group A 17.85 ± 5.83; group B 18.18 ± 7.35; P = 0.243). The final visual outcome was clinically superior in group A (≥20/200-group A 60.42% and group B 44%, P = 0.11; ≤20/400-group A 37.5% and group B 52%, P = 0.62), but statistically not significant. There were more gram-positive organisms in group A (62% vs 38%; P = 0.027) and more gram-negative organisms in group B (52% vs 24%; P = 0.007). Gram-positive bacteria were mostly sensitive to vancomycin (95.24% to 96.67%), but gram-negative bacteria were partly sensitive to ceftazidime (58.33% to 64%).

Conclusions

One could suspect gram-negative infection more often in the referred cases of endophthalmitis. While vancomycin could continue to be the antibiotic of choice in gram-positive bacteria, specific antibiotic following due sensitivity for gram-negative bacteria should replace the empiric use of ceftazidime.
Hinweise
Previously presented at: the 22nd ARVO-India Chapter Annual Meeting, Hyderabad, India as poster on 26 July 2015.

Background

Patients with post cataract surgery endophthalmitis treated by us at a tertiary eye care facility in Hyderabad, India, are a pool of “in-house” and “referred” cases for further management. A decade and half ago, we reported the microbiological profile of these pooled patients [1] in which the gram-positive cocci accounted for less than 50% eyes and gram-negative bacilli were detected in more than 25% eyes. This was contrary to the report of the Endophthalmitis Vitrectomy Study (EVS) [2] results published before our report and also is contrary to the European Society of Cataract and Refractive Surgery (ESCRS) [3] study results published after our report. In view of these differences, we reexamined the microbiological profile and antibiotic sensitivity between two distinct groups of patients, in-house and referred, managed at this facility. We hypothesized that the in-house endophthalmitis profile (both clinical and microbiological) and outcome after treatment could be different.

Methods

The clinical records of all culture-positive cases of post cataract surgery endophthalmitis managed at our institute between January 2010 and December 2014 were reviewed. There were 50 cases of in-house (group A) endophthalmitis. These 50 cases were matched with the first 50 consecutive culture-positive referred cases in the same period (group B; beginning December 2014 backwards and ending March 2010). Two cluster endophthalmitis cases, one in-house (reported earlier) [4] and one referred (reported by another treating center) [5] were excluded from both groups. Institutional review board approval (LEC 09-15-110) was obtained for retrospective data collection and analysis.
A detailed ocular history (cataract surgery, event to onset of symptoms, time to presentation, and previous treatment history in referred cases), the demography (age, gender), laterality, systemic factors (diabetes and immune status) were recorded. Management of all these patients was as per the institutional protocol. Briefly, this consisted of a comprehensive clinical examination (uncorrected and best corrected visual acuity, slit lamp biomicroscopy, applanation/digital tonometry, indirect ophthalmoscopy) and ultrasonography. The severity of inflammation in presentation was measured in all cases by our earlier published inflammatory score [6]. Briefly, this consisted of slit lamp and indirect ophthalmoscopic features of the cornea, anterior chamber, iris, and vitreous in a scale of 0 (no involvement) to 4 (gross involvement) and additional allowance given for any opaque ocular tissues not allowing further examination. The treatment consisted of intraocular antibiotics (vancomycin 1 mg in 0.1 ml normal saline; ceftazidime 2.25 mg in 0.1 ml normal saline) with either vitreous biopsy or core vitrectomy. This was followed with topical antibiotics (every 2 h), topical prednisolone acetate 1% (every 4 h) except in the eyes with significant corneal infiltrate and cycloplegic (every 8 h). The use of intravitreal corticosteroid (typically, dexamethasone 0.4 mg in 0.1 ml) and systemic antibiotics (typically, oral ciprofloxacin 1500 mg/day in two divided doses, in adult) were left to the discretion of the treating faculty. The vitreous sample was plated on the same day for culture. Microbiological work-up of undiluted vitreous included microscopy (after vital dye staining), culture (aerobic, anaerobic, and fungus), and antibiotic sensitivity (Kirby-Bauer disc diffusion). Unlike the current institutional standard, the polymerase chain reaction (PCR) was not done routinely in this period. Any further administration of intravitreal antibiotics with or without corticosteroid was guided by the culture report of the vitreous sample and the sensitivity of the cultured microorganism.

Statistical analysis

The ETDRS visual acuity was converted to logMAR equivalent for statistical analysis. In each group, the mean values of best corrected visual acuity (BCVA) at baseline and at the last follow-up were compared by analysis of variance (ANOVA). The mean values detected in the two groups at each time point were compared by t test. The sensitivity profile of the microorganisms cultured in the two groups was analyzed using the Fisher’s exact test. Values of P < 0.05 were considered statistically significant. The two in-house endophthalmitis patients were excluded from the analysis for final visual outcome and inflammatory score because they received Descemet’s stripping automated endothelial keratoplasty along with cataract surgery but were included in the analysis for microbiological profile.

Results

Baseline characteristics

There were 50 cases each in either group. Between the two groups, there was no statistically significant difference in the demographic profile and in the diabetes status. There was a statistically significant difference between the two groups in the time to report to the institute with endophthalmitis (group A 6.83 [±7.61; 95% CI, 4.57–9.09] days; group B 13.63 [±11.67; 95% CI, 9.95–17.31] days; P = 0.002). There was no significant difference in average inflammatory score at presentation (group A 17.85 ± 5.83; group B 18.18 ± 7.35; P = 0.243). These details are shown in Table 1.
Table 1
Baseline characteristics and final visual outcome
 
Group A. In-house (n = 50)
Group B. Referred (n = 50)
P value
Mean age (years) ± SD
58.13 ± 12.81
58.74 ± 13.29
0.41
Mean baseline BCVA logMAR (ETDRS equivalent) ± SD
1.99 (20/1954) ± 0.61
1.96 (20/1824) ± 0.45
0.48
Male: Female
29: 21
26: 24
0.55
Mean event to report time days (± SD, 95% CI)
6.83 (±7.61; 95% CI, 4.57 – 9.09)
13.63 (±11.67; 95% CI, 9.95 – 17.31)
0.002*
Number of diabetics
6
2
0.14
Inflammatory score (Mean ± SD)
17.85 ± 5.83
18.18 ± 7.35
0. 24
Final best corrected visual acuity
  ≥ 20/200
29 of 48 (60.42%; 95% CI, 45.30-73.89)
22 of 50 (44%; 95% CI, 30.27-58.65)
0.11
  ≤ 20/400
18 of 48 (37.5%; 95% CI, 24.32-54.67)
26 of 50 (52%; 95% CI, 37.58-66.12)
0.62
*Statistically significant

Visual outcome at last visit

The patients were followed up for a mean duration of 7.14 (±6.41; range 1.03–44.3) months in group A and 5.69 (± 5.27; range 1.0–28.73) months in group B (P = 0.37). The improvement in visual acuity of 0.719 logMAR in group A (approximately 7 ETDRS lines; 95% CI, 0.41–1.03, P < 0.001) and of 0.528 logMAR in group B (approximately 5 ETDRS lines; 95% CI, 0.32–0.74, P = 0.001) was statistically significant, but not significantly different between the two groups (P = 0.197). In general, the patients in group A (in-house) had better visual recovery than group B (referred) ≥20/200 in 60.42% (95% CI, 45.30–73.89) instances in group A vs 44% (95% CI, 30.27–58.65) instances in group B, and ≤20/400 in 37.5% (95% CI, 24.32-54.67) instances in group A and 52% (95% CI, 37.58–66.12) instances in group B. These were, however, only clinically significant (Table 1).

Microbiological profile

The microbiological profile is shown in Table 2. Group A had more gram-positive bacteria (n = 31/50, 62%; 95% CI, 47.16–75.00 in group A vs n = 19/50, 38%; 95% CI, 25.00–52.84 in group B; P = 0.027) and there were more gram-negative bacteria in group B (n = 12/50, 24%; 95% CI, 13.52–38.49 in group A vs n = 26/50, 52%; 95% CI, 37.58–66.12 in group B; P = 0.007). Statistically, there was no significant difference in the number of fungal infections (n = 4/50, 8%; 95% CI, 2.59–20.11 each, in groups A and B; P = 1) or in the number of mixed infections (n = 3/50, 6%; 95% CI, 1.56–17.54 in group A vs n = 1/50, 2%; 95% CI, 0.1–12.01 in group B; P = 0.617).
Table 2
Microbiological spectrum
Isolate
Number
Group A In-house (N = 50)
Group B Referred (N = 50)
Gram positive (n = 31 in A, n = 19 in B, P = 0.027a)
Staphylococcus
Coagulase negative Staphylococcus
5
9
Staphylococcus epidermidis
7
2
Staphylococcus aureus
5
0
Total
17
11
Streptococcus
Streptococcus pneumoniae
9
2
Streptococcus species
2
1
Total
11
3
Others
Bacillus species
3
1
Corynebacterium species
0
2
Nocardia species
0
2
Total
3
5
Gram negative (n = 12 in A, n = 26 in B, P = 0.007a)
Pseudomonas
Pseudomonas aeruginosa
8
11
Pseudomonas species
0
5
Total
8
16
Others
Enterobacteriaceae
4
4
Other Gram negative bacteria
0
6
Total
4
10
Others
Fungi
Fungi
4
4
Mixed infections
Multiple bacteria
1
1
Bacterium + Fungus
2
0
Total
3
1
aStatistically significant

Antibiotic-sensitivity profile

The sensitivity profile of the bacteria in the two groups is shown in Figs. 1 and 2. More than 95% gram-positive isolates in both groups (96.67% in group A, 95.24% in group B; P = 1) were sensitive to vancomycin and between 85% and 90% (90.32% gram-positive isolates in group A, and in 85.71% in group B) were sensitive to cefazolin. Only 58.33% of gram-negative isolates in group A and 64% gram-negative isolates in group B were sensitive to ceftazidime. The sensitivity of amikacin compared to ceftazidime in both groups (group A: amikacin 80% vs ceftazidime 58.33% sensitive, P = 0.22; group B: amikacin 73.06% vs ceftazidime 64% sensitive, P = 0.56) was not statistically significant.

Ceftazidime resistance

In group A, 41.67% (5/12) gram-negative isolates were resistant to ceftazidime and, of these five resistant cases, only 40% (2/5) were sensitive to amikacin, but all were sensitive to imipenem. The 3 amikacin resistant isolates in group A belonged to Pseudomonas species. In group B, 36% (9/25) gram-negative isolates were resistant to ceftazidime, and of these, 77.78% (7/9) were sensitive to amikacin (Table 3).
Table 3
Antibiotic sensitivity profile of ceftazidime-resistant gram- negative isolates in groups A and B
S No.
Endophthalmitis isolate
Amikacin
Imipenem
Chloramphenicol
Ciprofloxacin
Gatifloxacin
Moxifloxacin
Ofloxacin
Tobramycin
Group A
1
Eschericia coli
I
S
S
R
I
R
R
NT
2
Enterobacter cloacae
S
S
S
I
S
I
S
R
3
Enterobacter cloacae
S
S
R
I
S
I
S
R
4
Pseudomonas aeruginosa
R
S
R
R
R
R
NT
NT
5
Pseudomonas aeruginosa
R
S
R
R
R
R
NT
NT
Group B
1
Achromobacter xylosoxidans
S
NT
S
S
S
S
S
S
2
Eschericia coli
S
NT
S
S
S
S
S
S
3
Klebsiela pneumoniae
S
S
R
R
R
R
R
S
4
Pseudomonas aeruginosa
R
S
R
R
R
R
R
R
5
Pseudomonas species
S
NT
S
S
S
S
S
S
6
Pseudomonas stutzeri
R
NT
S
S
S
R
S
R
7
Pseudomonas stutzeri
S
R
R
R
R
R
R
S
8
Sphingomonas paucimobilis
S
NT
S
R
S
R
S
S
9
Stenotrphomonas maltophilia
S
NT
S
S
S
S
S
S
I intermediate sensitivity, NT not tested, S sensitive, R resistant

Prior therapy

Five patients had received prior therapy before being referred to us (Table 4). This included four adults and one child. All of them had received vitreous biopsy/core vitrectomy and repeated intravitreal antibiotics. The presenting vision was between light perception (n = 3) to ambulatory vision. Three of them grew Pseudomonas aeroginosa. For the following further treatment, none of the eyes infected with P. aeruginosa recovered vision. Two of the five patients, one infected with Rhizobium radiobacter and one infected with Candida pelliculosa recovered to 6/36 and 6/15, respectively.
Table 4
Baseline profile and outcome of patients with intervention prior to referral (group B)
S no.
Age (years)
Prior intervention
Presenting BCVA
Our intervention
Organism
Sensitivity
Final BCVA
1
70
IOAB
LP
PPV + 2x IOAB
P. aeroginosa
Sensitive to amikacin, ceftazidime, gatifloxacin, moxifloxacin, cirprofloxacin, and ofloxacin
Resistant to chloramphenicol
LP
2
10
2x IOAB
LP
PPV + 2x IOAB
Streptococcus pyogenes
Sensitive to vanomycin, gatifloxacin, moxifloxacin, cirprofloxacin, and ofloxacin
Resistant to amikacin
 
3
64
AC wash + IOAB
LP
Vitreous biopsy + 5x IOAB
P. aeruginosa
Sensitive to amikacin, ceftazidime, gatifloxacin, moxifloxacin, cirprofloxacin, and ofloxacin
Resistant to tobramycin
LP
4
62
Vitreous biosy + IOAB
6/36
PPV + 2x IOAB
R. radiobacter
Sensitive to amikacin, ceftazidime, gatifloxacin, moxifloxacin, cirprofloxacin, ofloxacin
Resistant to chloramphenicol
6/36
5
55
2x IOAB
6/36
PPV + IOAB + 2x Intravitreal Amphoterecin B
C. pelliculosa
6/15
IOAB intraocular (antibacterial) antibiotic injection

Discussion

Endophthalmitis, the most dreaded complication following cataract surgery, has an incidence from 0.04% to 0.13% [711]. Gram-positive bacteria were the predominant isolates in the EVS [2] and the ESCRS [3] studies. We and others in India have reported different microbiological profile of infection where the gram-positive cocci infection was relatively less, and gram-negative bacilli infection was relatively more common [1, 12]. These reports included both in-house and referred cases of endophthalmitis. Two Indian reports have published the in-house endophthalmitis data [13, 14]. In our report [14], culture-positive endophthalmitis was 0.07%; in this cohort 64.8% (n = 24/37) grew gram-positive cocci (n = 16/37, 43.2% were Staphylococcus epidermidis) and 24.3% (n = 9/37) grew gram-negative bacilli (n = 5/37, 13.5% were P. aeruginosa). In the other report, [13] clinical endophthalmitis was 0.09%, but the microbial profile was not part of this report.
Our hypothesis that the profiles of the two groups of endophthalmitis, in-house and referred could be different, was only partly true. There were differences in two areas—one, in the reporting time and two, in the microbiological spectrum. The delay in reporting time of the referred patients was likely because it depended on the referring ophthalmologist. The detection of more gram-positive cocci in the in-house cases and more gram-negative bacilli in referred cases was indeed a surprise (Table 2). The microbial spectrum of in-house endophthalmitis was closer to the EVS [2] and ECRS [3] reports. It is possible that only more fulminant cases that did not respond to initial treatment, invariably caused by gram-negative or similar virulent organisms, were referred to our facility.
The antibiotic sensitivity profile was nearly similar to our earlier report. Gram-positive bacilli had good sensitivity to vancomycin in either group, similar to the EVS report [2], and the gram-negative bacilli had poor sensitivity to ceftazidime in either group, similar to our earlier report [1]. All ceftazidime resistant gram-negative bacilli in group A (in-house cases) were sensitive to imipenem. Additionally, 77.78% of resistant isolates from referred cases were sensitive to amikacin. Imipenem appears to be good choice in gram-negative organisms resistant to ceftazidime and amikacin [1517]. Amikacin could still be an alternative choice, though we have already reported emergence of gram-negative bacteria resistant to both ceftazidime and amikacin [18]. Hence it is prudent to always do a culture-sensitivity test for appropriate management.
The limitations of this study included small number of cases (50 in either group), small number of individual isolates tested for sensitivity, and non-inclusion of PCR as routine basis. The strength of the study is the use of uniform management protocol in both groups. The study clearly demonstrates that the post cataract surgery infection pattern in India may not be significantly different from the ones reported by the EVS and ESCRS reports, though one must employ wiser discretion in treating the in-house and referred patients in a referral facility such as ours.

Conclusions

The study confirms that the gram-positive bacteria are the most common in post cataract surgery endophthalmitis in both in house and referred cases, but the gram-negative bacteria are more common in the referred cases in the teaching tertiary eye care facility in India. P. aeruginosa is the common gram-negative bacteria, and increasingly, they are resistant to commonly used antibiotic, ceftazidime. Hence, a microbiology and antibiotic sensitivity is mandatory while the EVS-based empiric treatment of post cataract surgery endophthalmitis treatment could continue for the time being. It is necessary to weigh the clinical response vis-a-vis the culture sensitivity to make a further decision. This implies seeing the patient 3–4 days after the initial treatment.

Acknowledgements

Authors thank the Hyderabad Eye Research Foundation for supporting the study.

Funding

The study was funded by Hyderabad Eye Research Foundation, Hyderabad, India.

Authors’ contributions

TD for the idea and final manuscript; VA and SS for data collection; VA, TD, SS, VD, JC, SJ, RN, and JJ for data analysis; VA, TD, SS, VD, JC, SJ, RN, and JJ for the manuscript preparation; and SS and JJ for microbiology. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.
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Literatur
1.
Zurück zum Zitat Kunimoto DY, Das T, Sharma S, Jalali S, Majji AB, Gopinathan U et al (1999) Microbiologic spectrum and sensitivity of isolates: part I. Postoperative endophthalmitis. Am J Ophthalmol 128:240–242CrossRefPubMed Kunimoto DY, Das T, Sharma S, Jalali S, Majji AB, Gopinathan U et al (1999) Microbiologic spectrum and sensitivity of isolates: part I. Postoperative endophthalmitis. Am J Ophthalmol 128:240–242CrossRefPubMed
2.
Zurück zum Zitat Han DP, Wisniewski SR, Wilson LA, Barza M, Vine AK, Doft BH et al (1996) Spectrum and susceptibilities of microbiologic isolates in the endophthalmitis vitrectomy study. Am J Ophthalmol 122:1–17CrossRefPubMed Han DP, Wisniewski SR, Wilson LA, Barza M, Vine AK, Doft BH et al (1996) Spectrum and susceptibilities of microbiologic isolates in the endophthalmitis vitrectomy study. Am J Ophthalmol 122:1–17CrossRefPubMed
3.
Zurück zum Zitat Barry P, Gardner S, Seal D, Gettinby G, Lees F, Peterson M, Revie C, ESCRS endophthalmitis study group (2009) Clinical observations associated with proven and unproven cases in the ESCRS study of prophylaxis of postoperative endophthalmitis after cataract surgery. J Cataract Refract Surg 35:1523–1531CrossRefPubMed Barry P, Gardner S, Seal D, Gettinby G, Lees F, Peterson M, Revie C, ESCRS endophthalmitis study group (2009) Clinical observations associated with proven and unproven cases in the ESCRS study of prophylaxis of postoperative endophthalmitis after cataract surgery. J Cataract Refract Surg 35:1523–1531CrossRefPubMed
4.
Zurück zum Zitat Ramappa M, Majji AB, Murthy SI, Balne PK, Nalamada S, Garudadri C et al (2012) An outbreak of acute post-cataract surgery Pseudomonas sp. endophthalmitis caused by contaminated hydrophilic intraocular lens solution. Ophthalmology 119:564–570CrossRefPubMed Ramappa M, Majji AB, Murthy SI, Balne PK, Nalamada S, Garudadri C et al (2012) An outbreak of acute post-cataract surgery Pseudomonas sp. endophthalmitis caused by contaminated hydrophilic intraocular lens solution. Ophthalmology 119:564–570CrossRefPubMed
5.
Zurück zum Zitat Lalitha P, Das M, Purva PS, Karpagam R, Geetha M, Lakshmi Priya J et al (2014) Postoperative endophthalmitis due to Burkholderia cepacia complex from contaminated anaesthetic eye drops. Br J Ophthalmol 98:1498–1502CrossRefPubMed Lalitha P, Das M, Purva PS, Karpagam R, Geetha M, Lakshmi Priya J et al (2014) Postoperative endophthalmitis due to Burkholderia cepacia complex from contaminated anaesthetic eye drops. Br J Ophthalmol 98:1498–1502CrossRefPubMed
6.
Zurück zum Zitat Das T, Jalali S, Gothwal VK, Sharma S, Naduvilath T (1999) Intravitreal dexamethasone in exogenous bacterial endophthalmitis: results of a prospective randomized study. Br J Ophthalmol 83:1050–1055CrossRefPubMedPubMedCentral Das T, Jalali S, Gothwal VK, Sharma S, Naduvilath T (1999) Intravitreal dexamethasone in exogenous bacterial endophthalmitis: results of a prospective randomized study. Br J Ophthalmol 83:1050–1055CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Aaberg TM Jr, Flynn HW Jr, Schiffman J, Newton J (1998) Nosocomial acute-onset postoperative endophthalmitis survey. A 10-year review of incidence and outcomes. Ophthalmology 105:1004–1010CrossRefPubMed Aaberg TM Jr, Flynn HW Jr, Schiffman J, Newton J (1998) Nosocomial acute-onset postoperative endophthalmitis survey. A 10-year review of incidence and outcomes. Ophthalmology 105:1004–1010CrossRefPubMed
8.
Zurück zum Zitat Javitt JC, Vitale S, Canner JK, Street DA, Krakauer H, McBean AM et al (1991) National outcomes of cataract extraction. Endophthalmitis following inpatient surgery. Arch Ophthalmol 109:1085–1089CrossRefPubMed Javitt JC, Vitale S, Canner JK, Street DA, Krakauer H, McBean AM et al (1991) National outcomes of cataract extraction. Endophthalmitis following inpatient surgery. Arch Ophthalmol 109:1085–1089CrossRefPubMed
9.
Zurück zum Zitat Lalitha P, Rajagopalan J, Prakash K, Ramasamy K, Prajna NV, Srinivasan M (2005) Post cataract endophthalmitis in South India: incidence and outcome. Ophthalmology 112:1884–1889CrossRefPubMed Lalitha P, Rajagopalan J, Prakash K, Ramasamy K, Prajna NV, Srinivasan M (2005) Post cataract endophthalmitis in South India: incidence and outcome. Ophthalmology 112:1884–1889CrossRefPubMed
10.
Zurück zum Zitat Miller JJ, Scott IU, Flynn HW Jr, Smiddy WE, Newton J, Miller D (2005) Acute-onset endophthalmitis after cataract surgery (2000-2004): incidence, clinical settings, and visual acuity outcomes after treatment. Am J Ophthalmol 139:983–987CrossRefPubMed Miller JJ, Scott IU, Flynn HW Jr, Smiddy WE, Newton J, Miller D (2005) Acute-onset endophthalmitis after cataract surgery (2000-2004): incidence, clinical settings, and visual acuity outcomes after treatment. Am J Ophthalmol 139:983–987CrossRefPubMed
11.
Zurück zum Zitat Taban M, Behrens A, Newcomb RL, Nobe MY, Saedi G, Sweet PM et al (2005) Acute endophthalmitis following cataract surgery: a systematic review of the literature. Arch Ophthalmol 123:613–620CrossRefPubMed Taban M, Behrens A, Newcomb RL, Nobe MY, Saedi G, Sweet PM et al (2005) Acute endophthalmitis following cataract surgery: a systematic review of the literature. Arch Ophthalmol 123:613–620CrossRefPubMed
12.
Zurück zum Zitat Jambulingam M, Parameswaran SK, Lysa S, Selvaraj M, Madhavan HN (2010) A study on the incidence, microbiological analysis and investigations on the source of infection of postoperative infectious endophthalmitis in a tertiary care ophthalmic hospital: an 8-year study. Indian J Ophthalmol 58:297–302CrossRefPubMedPubMedCentral Jambulingam M, Parameswaran SK, Lysa S, Selvaraj M, Madhavan HN (2010) A study on the incidence, microbiological analysis and investigations on the source of infection of postoperative infectious endophthalmitis in a tertiary care ophthalmic hospital: an 8-year study. Indian J Ophthalmol 58:297–302CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat Ravindran RD, Venkatesh R, Chang DF, Sengupta S, Gyatsho J, Talwar B (2009) Incidence of post-cataract endophthalmitis at Aravind Eye Hospital: outcomes of more than 42,000 consecutive cases using standardized sterilization and prophylaxis protocols. J Cataract Refract Surg 35:629–636CrossRefPubMed Ravindran RD, Venkatesh R, Chang DF, Sengupta S, Gyatsho J, Talwar B (2009) Incidence of post-cataract endophthalmitis at Aravind Eye Hospital: outcomes of more than 42,000 consecutive cases using standardized sterilization and prophylaxis protocols. J Cataract Refract Surg 35:629–636CrossRefPubMed
14.
Zurück zum Zitat Das T, Hussain A, Naduvilath T, Sharama S, Jalali S, Majji AB. Case control analyses of acute endophthalmitis after cataract surgery in South India associated with techniques, patient care, and socio economic status. J Ophthalmol 2012; ID 298459; doi: 10.1155/2012/298459 Das T, Hussain A, Naduvilath T, Sharama S, Jalali S, Majji AB. Case control analyses of acute endophthalmitis after cataract surgery in South India associated with techniques, patient care, and socio economic status. J Ophthalmol 2012; ID 298459; doi: 10.​1155/​2012/​298459
15.
Zurück zum Zitat Alfaro DV 3rd, Hudson SJ, Kasowski EJ, Barton CP, Brucker AJ, Lopez JD et al (1997) Experimental pseudomonal posttraumatic endophthalmitis in a swine model: treatment with ceftazidime, amikacin, and imipenem. Retina 17:139–145CrossRefPubMed Alfaro DV 3rd, Hudson SJ, Kasowski EJ, Barton CP, Brucker AJ, Lopez JD et al (1997) Experimental pseudomonal posttraumatic endophthalmitis in a swine model: treatment with ceftazidime, amikacin, and imipenem. Retina 17:139–145CrossRefPubMed
16.
Zurück zum Zitat Alfaro DV 3rd, Hudson SJ, Offele JJ, Bevin AA, Mines M, Laughlin RM et al (1996) Experimental posttraumatic Bacillus cereus endophthalmitis in a swine model. Efficacy of intravitreal ciprofloxacin, vancomycin, and imipenem. Retina 16:317–323CrossRefPubMed Alfaro DV 3rd, Hudson SJ, Offele JJ, Bevin AA, Mines M, Laughlin RM et al (1996) Experimental posttraumatic Bacillus cereus endophthalmitis in a swine model. Efficacy of intravitreal ciprofloxacin, vancomycin, and imipenem. Retina 16:317–323CrossRefPubMed
17.
Zurück zum Zitat Derick RJ, Paylor R, Peyman GA (1987) Toxicity of imipenem in vitreous replacement fluid. Ann Ophthalmol 19:338–339PubMed Derick RJ, Paylor R, Peyman GA (1987) Toxicity of imipenem in vitreous replacement fluid. Ann Ophthalmol 19:338–339PubMed
18.
Zurück zum Zitat Jindal A, Pathengay A, Khera M, Jalali S, Mathai A, Poppuru RR et al (2013) Combined ceftazidime and amikacin resistance among Gram negative isolates in acute postoperative endophthalmitis: prevalence, antimicrobial susceptibility, and visual acuity outcome. J Ophthalmic Inflamm Infect 25(3(1)):62CrossRef Jindal A, Pathengay A, Khera M, Jalali S, Mathai A, Poppuru RR et al (2013) Combined ceftazidime and amikacin resistance among Gram negative isolates in acute postoperative endophthalmitis: prevalence, antimicrobial susceptibility, and visual acuity outcome. J Ophthalmic Inflamm Infect 25(3(1)):62CrossRef
Metadaten
Titel
Comparison of clinico-microbiological profile and treatment outcome of in-house and referred post cataract surgery endophthalmitis in a tertiary care center in South India
verfasst von
Vikas Ambiya
Taraprasad Das
Savitri Sharma
Jay Chhablani
Vivek Dave
Subhadra Jalali
Raja Narayanan
Joveeta Joseph
Publikationsdatum
01.12.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Ophthalmic Inflammation and Infection / Ausgabe 1/2016
Elektronische ISSN: 1869-5760
DOI
https://doi.org/10.1186/s12348-016-0113-0

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