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Clinical Sciences |

Vitreous and Aqueous Penetration of Orally Administered Gatifloxacin in Humans FREE

Seenu M. Hariprasad, MD; William F. Mieler, MD; Eric R. Holz, MD
[+] Author Affiliations

From the Department of Ophthalmology/Cullen Eye Institute, Baylor College of Medicine, Houston, Tex. The authors have no relevant financial interest in this article.


Arch Ophthalmol. 2003;121(3):345-350. doi:10.1001/archopht.121.3.345.
Text Size: A A A
Published online

Objective  To investigate the penetration of gatifloxacin, a novel extended-spectrum fourth-generation fluoroquinolone antibiotic, into the vitreous and aqueous humor after oral administration.

Methods  A prospective, nonrandomized study of 24 consecutive patients scheduled for pars plana vitrectomy between September 2001 and May 2002 at the Cullen Eye Institute. Aqueous, vitreous, and serum samples were obtained and analyzed from 24 patients after administration of two 400-mg gatifloxacin tablets taken 12 hours apart before the operation. Assays were performed using high-performance liquid chromatography.

Results  Mean ± SD gatifloxacin concentrations in serum (n = 23), vitreous(n = 23), and aqueous (n = 11) were 5.14 ± 1.36 µg/mL, 1.34 ± 0.34 µg/mL, and 1.08 ± 0.54 µg/mL respectively. Mean ± SD sampling times after oral administration of the second gatifloxacin tablet for serum, vitreous, and aqueous were 3.2 ± 1.0 hours, 4.0 ± 1.0 hours, and 3.9 ± 1.1 hours, respectively. The percentages of serum gatifloxacin concentration achieved in the vitreous and aqueous were 26.17% and 21.02%, respectively. Mean inhibitory vitreous and aqueous MIC90 levels were achieved against many pathogens, including Staphylococcus epidermidis, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Propionibacterium acnes, Haemophilus influenzae, Escherichia coli, Bacillus cereus, Proteus mirabilis, and other organisms.

Conclusions  Orally administered gatifloxacin achieves therapeutic levels in the noninflamed human eye, and the activity spectrum appropriately encompass the bacterial species most frequently involved in the various causes of endophthalmitis. Because of its broad-spectrum coverage, low MIC90 levels for the organisms of concern, and good tolerability, gatifloxacin represents a major advance in the prophylaxis or treatment of postoperative, posttraumatic, and bleb-associated bacterial endophthalmitis.

BACTERIAL ENDOPHTHALMITIS is one of the most serious complications of intraocular procedures and open-globe injuries. The microbiological spectrum of infecting organisms in postoperative endophthalmitis was investigated in the Endophthalmitis Vitrectomy Study (EVS). The EVS represents the largest number of postoperative endophthalmitis cases from which bacteriologic data were prospectively obtained. The vast majority of confirmed growth isolates(94.2%) were gram-positive pathogens, most commonly Staphylococcus epidermidis and Staphylococcus aureus. Gram-negative pathogens, the most common being Proteus mirabilis, accounted for only 5.9% of confirmed growth isolates.1 The spectrum of infecting organisms in posttraumatic endophthalmitis differs from that of postoperative endophthalmitis, with Bacillus species playing a more prominent role.2

The EVS investigated the use of intravenous amikacin and ceftazidime in conjunction with intravitreal antibiotic injection for postoperative endophthalmitis and found no improved outcomes with the use of systemic antibiotics.3 Later studies found that amikacin and ceftazidime had very poor intravitreal penetration.4,5 Based on the EVS data, the only conclusion that can be drawn regarding the use of systemic antibiotics is that amikacin and ceftazidime specifically have no role in postoperative endophthalmitis. Since the EVS, there have been major advancements in the development of antibiotics, and the potential uses of these new-generation agents in the treatment of endophthalmitis must be revisited. During the past 10 years, there has been mounting evidence in the literature that agents in the fluoroquinolone class of antibiotics are able to achieve effective concentrations in the vitreous after oral administration.68

Gatifloxacin is a fourth-generation 8-methoxy fluoroquinolone with a spectrum of activity encompassing gram-positive and gram-negative pathogens, including Staphylococcus epidermidis, Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Haemophilus influenzae, Escherichia coli, Bacillus cereus, Neisseria gonorrhoeae, and Proteus mirabilis. Additionally, gatifloxacin has excellent activity against atypical pathogens, such as Mycoplasma, Legionella, and Chlamydia species, as well as the anaerobic organism Propionibacterium acnes.9,10 Gatifloxacin has 96% oral bioavailability, can be administered without regard to food, and reaches peak plasma concentrations 1 to 2 hours after oral dosing. Serum protein binding of gatifloxacin is only 20% and is widely distributed throughout the body into many tissues and fluids. The new fluoroquinolones, such as gatifloxacin, grepafloxacin, moxifloxacin, and trovafloxacin, represent advances in the evolution of this antibiotic class. The more favorable pharmacokinetic properties of the previously mentioned agents are due to alterations of the original fluoroquinolone moiety. For example, gatifloxacin and moxifloxacin possess an 8-methoxy side chain, which may be responsible for their enhanced activity against gram-positive, atypical pathogens and anaerobes while retaining potencies and broad-spectrum coverage against gram-negative organisms comparable to those of older-generation fluoroquinolones.10

We chose to study the intravitreal penetration of orally administered gatifloxacin in humans for 2 reasons. First, older-generation fluoroquinolones, such as ofloxacin, ciprofloxacin, and levofloxacin, have been shown to achieve effective levels in the vitreous after oral administration in the noninflamed eye.68 Second, the mean inhibitory concentrations required to inhibit growth of 90% of bacterial isolates tested (MIC90) for gatifloxacin against the pathogens most commonly responsible for postoperative, posttraumatic, and bleb-associated endophthalmitis were generally lower than those of the other fluoroquinolone antibiotics we surveyed (Table 1).9,10

Table Graphic Jump LocationTable 1. In Vitro Susceptibilities of Gatifloxacin, Levofloxacin, Olfloxacin, and Ciprofloxacin8-10*810,8,7,6,1,2,11,12

The study was conducted with the approval of the Baylor College of Medicine(Houston, Tex) Institutional Review Board. Twenty-four adult patients aged 25 to 82 years (mean ± SD age, 63.7 ± 14.3 years) undergoing elective pars plana vitrectomy between September 2001 and May 2002 at the Cullen Eye Institute, Houston, were included in the study. Exclusion criteria included known sensitivity to fluoroquinolones, renal disease (serum creatinine level greater than 1.8 mg/dL [159.1 µmol/L]), use of any other antibiotics in the preceding 3 weeks, pregnancy or currently breastfeeding, current use of a class IA or III antiarrhythmic agent, fresh vitreous hemorrhage (less than 1 month old) as an indication for vitrectomy, or active endophthalmitis.

After informed consent was obtained, patients were asked to take a total of two 400-mg tablets of gatifloxacin orally, 12 hours apart (loading dosage). Prospectively completed data forms were designed to include medical history, collection times of various samples, and concentrations of gatifloxacin in serum, aqueous, and vitreous. Patients were asked to record on each of the 2 gatifloxacin blister packs the exact time of oral administration. These packs were returned on the day of the operation. Aqueous, vitreous, and serum samples were obtained before infusion of any intravenous or intraocular irrigating solution to obtain pure samples. Approximately 8 to 10 mL of venous blood was collected less than 1 hour before surgery in the preoperative holding area. In the operative suite, approximately 0.1 mL of aqueous fluid was aspirated with a 30-gauge needle attached to a syringe through a paracentesis site in those patients with whom it was felt safe to do so (ie, pseudophakic patients or phakic patients with deep anterior chambers). Within 10 minutes, 0.2 to 0.3 mL of vitreous fluid was obtained by using a vitreous cutting device attached to a syringe via a short length of tubing. Aqueous and vitreous samples were immediately frozen at –20°C. The blood sample was centrifuged, and the serum collected from this was frozen as well. These samples were shipped with dry ice in appropriate packaging material to the Hartford Hospital Laboratory, Hartford, Conn. Gatifloxacin concentrations were determined in each of the samples using a previously described high-performance liquid chromatography technique.13 Serum, aqueous, and vitreous gatifloxacin concentrations were compared with already established in vitro MIC90 data.9,10 A t test was performed to determine if any significant differences existed between various subsets of patients, including diabetic vs nondiabetic patients and phakic status.

Indications for operation in the 24 patients were as follows (Table 2): epiretinal membrane (14 patients), macular hole (5 patients), retinal detachment (3 patients), nonclearing vitreous hemorrhage (1 patient), and tractional retinal detachment secondary to proliferative diabetic retinopathy (1 patient).

Table Graphic Jump LocationTable 2. Patient Characteristics and Gatifloxacin Concentrations After Second Oral Dose

Mean ± SD gatifloxacin concentrations in serum (n = 23), vitreous(n = 23), and aqueous (n = 11) were 5.14 ± 1.36 µg/mL, 1.34 ± 0.34 µg/mL, and 1.08 ± 0.54 µg/mL, respectively. Mean ± SD sampling times after oral administration of the second gatifloxacin tablet for serum, vitreous, and aqueous were 3.2 ± 1.0 hours, 4.0 ± 1.0 hours, and 3.9 ± 1.1 hours, respectively. The percentages of serum gatifloxacin concentration achieved in the vitreous and aqueous were 26.17% and 21.02%, respectively (Table 2).

Patient 16 was removed from the study because no aqueous specimen was collected and there was an insufficient vitreous sample volume to perform high-performance liquid chromatography. Although a serum gatifloxacin concentration was determined for this patient, it was not felt that it added any value to the study, and, therefore, this patient's data were removed from any data analysis (Table 2).

Three of 23 patients were diabetic. The mean ± SD gatifloxacin concentrations in the serum and vitreous for these 3 patients were 6.18 ± 1.10 µg/mL and 1.23 ± 0.13 µg/mL, respectively). These levels were not significantly different from those of the 20 nondiabetic patients whose mean serum and vitreous concentrations were 4.98 ± 1.34 µg/mL and 1.36 ± 0.36 µg/mL, respectively (P =.16 and P = .54, respectively).

Eleven of 23 patients were phakic. The mean ± SD gatifloxacin concentrations in the serum, vitreous, and aqueous for these 11 patients were 5.30 ± 1.44 µg/mL, 1.23 ± 0.28 µg/mL, and 0.62 ± 0.25 µg/mL, respectively. These levels were not significantly different from those of the 1 aphakic and 11 pseudophakic patients whose mean serum, vitreous, and aqueous concentrations were 4.99 ± 1.32 µg/mL, 1.45 ± 0.37 µg/mL, and 1.25 ± 0.52 µg/mL, respectively(P = .59, P = .13, and P = .08, respectively).

No serious adverse reactions were attributed to the antibiotic agent. One patient complained of mild gastrointestinal discomfort, and another patient(patient 7) vomited 30 minutes after taking the second gatifloxacin dose. The concentrations of gatifloxacin in serum and vitreous in this patient were 5.8 µg/mL and 1.4 µg/mL, respectively (Table 2). These values were above the mean of the rest of the group.

Endophthalmitis is one of the most serious complications of intraocular procedures or open-globe trauma. Systemic antibiotics have had an uncertain role in the prophylaxis or treatment of endophthalmitis because the EVS was unable to demonstrate any benefit with the use of intravenous antibiotics in postoperative infection.3 During the past 10 years, the results of several studies have indicated that fluoroquinolone antibiotics achieve significant concentrations in the vitreous after oral administration.68 Unfortunately, many of the older-generation fluoroquinolones achieved intravitreal levels that barely reached the MIC90 against the pathogens most commonly responsible for postoperative, posttraumatic, and bleb-associated endophthalmitis. If one is to consider the use of a systemic antibiotic for the prophylaxis of, or as an adjunct in the treatment of, endophthalmitis, one must find a systemic antibiotic with the highest possible intravitreal penetration, as well as the lowest MIC90 for the organisms of concern. We believe that gatifloxacin may represent a major advance in this regard.

After cataract extraction, bacterial endophthalmitis is most commonly caused by Staphylococcus epidermidis (70% of EVS isolates).1 This typically presents as a moderately severe infection 5 to 7 days postoperatively. Less commonly, 2 other forms of endophthalmitis can develop after cataract extraction. The first is a chronic, indolent endophthalmitis that presents several months postoperatively, usually caused by Propionibacterium acnes.12 A second, less-common form of postoperative endophthalmitis is an early, fulminant type that usually presents 2 to 4 days postoperatively and is caused by Streptococcus or Staphylococcus species as well as gram-negative organisms (most commonly Proteus mirabilis1). In our study, vitreous levels of gatifloxacin were 5.4 times the MIC90 for Staphylococcus epidermidis, 10.3 times the MIC90 for Staphylococcus aureus, 2.7 times the MIC90 for Propionibacterium acnes, 2.7 times the MIC90 for Streptococcus species, and 5.4 times the MIC90 for Proteus mirabilis. Gatifloxacin was unable to achieve intravitreal levels effective against Enterococcus or Pseudomonas species. Fortunately, these 2 organisms are only very rarely encountered in postoperative endophthalmitis.1

The importance of finding a good bacterial endophthalmitis prophylaxis technique for cataract surgery was emphasized in a recent study by Ciulla et al.14 Performing a systematic review of the literature from 1966 to 2000 to assess the bacterial endophthalmitis prophylaxis techniques commonly used in cataract surgery, they found that only preoperative povidone-iodine preparation could receive a moderate clinical recommendation(moderately important to clinical outcome). All other measures received the lowest clinical recommendation (possibly relevant but not definitely related to clinical outcome). Furthermore, the study revealed that no prophylactic technique in the literature could receive the highest of 3 possible clinical recommendations (crucial to clinical outcome).13 Unfortunately, systemic antibacterial agents were not included in this study. Given our findings, one could consider the use of oral gatifloxacin preoperatively and postoperatively as prophylaxis against endophthalmitis. Ciulla et al estimate that there are nearly 2000 cases of endophthalmitis after cataract surgery alone annually in the United States. If all intraocular procedures and cases of open-globe trauma are included, this number is far greater. Therefore, the importance of finding good prophylaxis against postoperative endophthalmitis cannot be underestimated.

Conjunctival filtering bleb-associated endophthalmitis can occur any time after trabeculectomy. Infection of the bleb alone, or "blebitis, " can sometimes be treated with intensive topical or subconjunctival antibiotics. The most common causative organisms in delayed-onset bleb-associated endophthalmitis are Streptococcus and Staphylococcus species.11Haemophilus influenzae is also commonly encountered in this condition. The concentrations of gatifloxacin achieved in the aqueous and vitreous are several-fold higher than the MIC90 for these organisms. Gatifloxacin may prove to be valuable in the treatment of blebitis or as an adjunct in the current treatment of bleb-associated endophthalmitis.

The role of systemic antibiotics in open-globe trauma deserves special attention. Posttraumatic endophthalmitis occurs in 2% to 7% of all open-globe injuries and in 7% to 13% of injuries with retained intraocular foreign bodies.15,16 Injuries that occur in a rural setting result in up to a 30% incidence of endophthalmitis compared with 11% in a nonrural setting.17Staphylococcus, Streptococcus, and Bacillus species are the most commonly encountered organisms in posttraumatic endophthalmitis.18 Although the role and importance of systemic antibiotics in the treatment of infection associated with open-globe trauma remains unresolved, Ariyasu et al19 studied events leading to the development of posttraumatic endophthalmitis by examining the effect of 15 factors on microbial contamination of injured eyes. Only intravenous antibiotic therapy was found to significantly reduce levels of anterior chamber microorganisms at the time of surgical repair, supporting their prophylactic use against the development of posttraumatic endophthalmitis. Based on the findings of Ariyasu et al and the known high incidence of endophthalmitis after open-globe injuries, the prompt and routine use of systemic antibiotics for prophylaxis against infection in the setting of trauma should be further explored. The chosen antibiotic will be one that meets the following criteria: achieves high intravitreal concentrations well above the MIC90 for the specific organisms of concern, is well tolerated, and preferably achieves excellent bioavailability with oral administration. Gatifloxacin fulfills these criteria. The levels achieved in the aqueous and vitreous were several-fold higher than the MIC90 for organisms that are most commonly associated with posttraumatic endophthalmitis (Table 1). In addition, previous studies suggest that intraocular penetration of systemic antibiotics may be higher in an eye that has sustained trauma, is infected, or is inflamed. This may be secondary to disruption of the blood-ocular barrier.20,21

The guidelines set forth by the EVS regarding the treatment of postoperative endophthalmitis should not be translated to posttraumatic endophthalmitis.3 The incidence of endophthalmitis from open-globe trauma is many times greater than after ocular surgical procedures. In addition, as many as 42% of cases from rural areas have more than 1 organism cultured; often, more virulent bacteria are isolated, compared with postoperative endophthalmitis. For example, Bacillus infections are rare in postoperative endophthalmitis but may occur with a frequency of 20% to 46% in posttraumatic cases.17Bacillus species produce severe, rapidly progressive endophthalmitis. Therefore, in the setting of open-globe trauma, rapid administration of an oral antibiotic known to penetrate into the posterior segment may help prevent ocular damage secondary to infection. Based on our data, it appears that oral administration of gatifloxacin may be a promising choice for prophylaxis against endophthalmitis in open-globe injuries before and after surgical intervention.

Two groups have recently studied the fourth-generation fluoroquinolones for possible use in ophthalmology. Mather et al22 have described the fourth-generation fluoroquinolones as "new weapons in the arsenal of ophthalmic antibiotics." They performed an in vitro study determining the differences in susceptibility patterns and potencies of second-, third-, and fourth-generation fluoroquinolones to 93 bacterial endophthalmitis isolates. They demonstrated that coagulase-negative staphylococci that were resistant to second-generation fluoroquinolones (eg, ciprofloxacin and ofloxacin) were statistically most susceptible to fourth-generation fluoroquinolones, specifically gatifloxacin and moxifloxacin. Additionally, Streptococcus viridans and Streptococcus pneumoniae were least susceptible to older-generation fluoroquinolones. Overall, fourth-generation fluoroquinolones retained equivalent potencies to gram-negative bacteria as compared with older-generation fluoroquinolones, such as levofloxacin and ciprofloxacin, while also demonstrating enhanced potencies for gram-positive bacteria.

In another recent study, Garcia-Saenz et al23 investigated the penetration of orally administered moxifloxacin into the human aqueous humor for potential use as a prophylactic agent against bacterial endophthalmitis in cataract surgery. They found that moxifloxacin achieved a mean aqueous concentration of 2.3 ± 0.9 µg/mL; however, their reported MIC90 for Staphylococcus epidermidis was 2.00µg/mL. The concentration achieved is borderline for the most common causative organism in postoperative endophthalmitis. This is not the case with gatifloxacin because intraocular concentrations after oral administration were found to be several times higher than the MIC90 for S epidermidis. Additionally, penetration of moxifloxacin into the vitreous was not investigated; therefore, no conclusions can be made regarding its use in open-globe trauma involving the posterior segment or its use as an adjunctive therapy for endophthalmitis treatment.

Gatifloxacin is very well tolerated, and most adverse reactions are described as mild in nature. The most common adverse reactions include nausea, vaginitis, diarrhea, headache, and dizziness. In our series, one patient complained of mild gastrointestinal discomfort, and another patient vomited 30 minutes after taking the second gatifloxacin dose. The concentrations of gatifloxacin in serum and vitreous in this patient were above the mean level for the rest of the group. The dosage of gatifloxacin recommended by Bristol-Myers Squibb Co (New York, NY) is one 400-mg tablet every 24 hours. In our study design, we chose to use a loading dose of one 400-mg tablet twice a day before sample collection to achieve peak plasma concentrations more rapidly. In the appropriate clinical setting, one may consider using a loading dose of gatifloxacin followed by one 400-mg tablet a day thereafter. Because gatifloxacin is eliminated primarily by renal excretion, a dosage modification is recommended for patients with a creatinine clearance of less than 40 mL/min (<0.07 mL/s). Gatifloxacin should be avoided in patients receiving a class IA (quinidine or procainamide) or class III (amiodarone or sotalol) antiarrhythmic agent because gatifloxacin may have the potential to prolong the QTc interval of the electrocardiogram in some patients.

In summary, orally administered gatifloxacin achieves therapeutic aqueous and vitreous levels in the noninflamed human eye, and the activity spectrum appears to appropriately encompass the bacterial species most often involved in the various causes of endophthalmitis. Because of its broad spectrum of coverage, low MIC90 levels for the organisms of concern, good tolerability, and excellent bioavailability with oral administration, gatifloxacin may represent a major advance in the prophylaxis or treatment of postoperative, posttraumatic, and bleb-associated bacterial endophthalmitis.

Submitted for publication June 11, 2002; final revision received October 24, 2002; accepted November 7, 2002.

This study was supported by a grant from Bristol-Myers Squibb Co and an unrestricted grant from Research to Prevent Blindness, Inc, New York.

This study was presented in part at the 138th Annual Meeting of the American Ophthalmological Society, Sea Island, Ga, May 21, 2002.

Corresponding author and reprints: Eric R. Holz, MD, Department of Ophthalmology/Cullen Eye Institute, Baylor College of Medicine, 6565 Fannin St, NC-205, Houston, TX 77030 (e-mail: seenuh@bcm.tmc.edu).

Han  DPWisniewski  SRWilson  LA  et al.  Spectrum and susceptibilities of microbiologic isolates in the Endophthalmitis Vitrectomy Study. Am J Ophthalmol. 1996;1221- 17
Affeldt  JCFlynn  HW  JrForster  RK  et al.  Microbial endophthalmitis resulting from ocular trauma. Ophthalmology. 1987;94407- 413
Link to Article
Endophthalmitis Vitrectomy Study Group, Results of the Endophthalmitis Vitrectomy Study: a randomized trial of immediate vitrectomy and of intravenous antibiotics for the treatment of postoperative bacterial endophthalmitis. Arch Ophthalmol. 1995;1131479- 1496
Link to Article
el-Massry  AMeredith  TAAguilar  HE  et al.  Aminoglycoside levels in the rabbit vitreous cavity after intravenous administration. Am J Ophthalmol. 1996;122684- 689
Aguilar  HEMeredith  TAShaarawy  A  et al.  Vitreous cavity penetration of ceftazidime after intravenous administration. Retina. 1995;15154- 159
Link to Article
Keren  GAlhalel  ABartov  E  et al.  The intravitreal penetration of orally administered ciprofloxacin in humans. Invest Ophthalmol Vis Sci. 1991;322388- 2392
Fiscella  RGShapiro  MJSolomon  MJ  et al.  Ofloxacin penetration into the eye after intravenous and topical administration. Retina. 1997;17535- 539
Link to Article
Fiscella  RGNguyen  TKCwik  MJ  et al.  Aqueous and vitreous penetration of levofloxacin after oral administration. Ophthalmology. 1999;1062286- 2290
Link to Article
Bauernfeind  A Comparison of the antibacterial activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin, and ciprofloxacin. J Antimicrob Chemother. 1997;40639- 651
Link to Article
Ednie  LMJacobs  MRAppelbaum  PC Activities of gatifloxacin compared to those of 7 other agents against anaerobic organisms. Antimicrob Agents Chemother. 1998;422459- 2462
Song  AScott  IUFlynn  HW  JrBudenz  DL Delayed-onset bleb-associated endophthalmitis: clinical features and visual acuity outcomes. Ophthalmology. 2002;109985- 991
Link to Article
Clark  WLKaiser  PKFlynn  HW  Jr  et al.  Treatment strategies and visual acuity outcomes in chronic postoperative Propionibacterium acnes endophthalmitis. Ophthalmology. 1999;1061665- 1670
Link to Article
Mattoes  HMBanevicius  MLi  D  et al.  Pharmacodynamic assessment of gatifloxacin against Streptococcus pneumoniaeAntimicrob Agents Chemother. 2001;452092- 2097
Link to Article
Ciulla  TAStarr  MBMasket  S Bacterial endophthalmitis prophylaxis for cataract surgery: an evidence-based update. Ophthalmology. 2002;10913- 24
Link to Article
Parrish  CMO'Day  DM Traumatic endophthalmitis. Int Ophthalmol Clin. 1987;27112- 119
Link to Article
Mieler  WFEllis  MKWilliams  DFHan  DP Retained intraocular foreign bodies and endophthalmitis. Ophthalmology. 1990;971532- 1538
Link to Article
Boldt  HCPulido  JSBlodi  CF  et al.  Rural endophthalmitis. Ophthalmology. 1989;961722- 1726
Link to Article
Alfaro  DVRoth  DLiggett  PE Posttraumatic endophthalmitis: causative organisms, treatment, and prevention. Retina. 1994;14206- 211
Link to Article
Ariyasu  RGKumar  SLaBree  LD  et al.  Microorganisms cultured from the anterior chamber of ruptured globes at the time of repair. Am J Ophthalmol. 1995;119181- 188
Martin  DFFicker  LAAguilar  HA  et al.  Vitreous cefazolin levels after intravenous injection: effects of inflammation, repeated antibiotic doses, and surgery. Arch Ophthalmol. 1990;108411- 414
Link to Article
Alfaro  DVHudson  SJRafanan  MM  et al.  The effect of trauma on the ocular penetration of intravenous ciprofloxacin. Am J Ophthalmol. 1996;122678- 683
Mather  RKaranchak  LMRomanowski  EGKowalski  RP Fourth-generation fluoroquinolones: new weapons in the arsenal of ophthalmic antibiotics. Am J Ophthalmol. 2002;133463- 466
Link to Article
Garcia-Saenz  MCArias-Puente  AFresnadillo-Martinez  MJCarrasco-Font  C Human aqueous humor levels of oral ciprofloxacin, levofloxacin, and moxifloxacin. J Cataract Refract Surg. 2001;271969- 1974
Link to Article

Figures

Tables

Table Graphic Jump LocationTable 1. In Vitro Susceptibilities of Gatifloxacin, Levofloxacin, Olfloxacin, and Ciprofloxacin8-10*810,8,7,6,1,2,11,12
Table Graphic Jump LocationTable 2. Patient Characteristics and Gatifloxacin Concentrations After Second Oral Dose

References

Han  DPWisniewski  SRWilson  LA  et al.  Spectrum and susceptibilities of microbiologic isolates in the Endophthalmitis Vitrectomy Study. Am J Ophthalmol. 1996;1221- 17
Affeldt  JCFlynn  HW  JrForster  RK  et al.  Microbial endophthalmitis resulting from ocular trauma. Ophthalmology. 1987;94407- 413
Link to Article
Endophthalmitis Vitrectomy Study Group, Results of the Endophthalmitis Vitrectomy Study: a randomized trial of immediate vitrectomy and of intravenous antibiotics for the treatment of postoperative bacterial endophthalmitis. Arch Ophthalmol. 1995;1131479- 1496
Link to Article
el-Massry  AMeredith  TAAguilar  HE  et al.  Aminoglycoside levels in the rabbit vitreous cavity after intravenous administration. Am J Ophthalmol. 1996;122684- 689
Aguilar  HEMeredith  TAShaarawy  A  et al.  Vitreous cavity penetration of ceftazidime after intravenous administration. Retina. 1995;15154- 159
Link to Article
Keren  GAlhalel  ABartov  E  et al.  The intravitreal penetration of orally administered ciprofloxacin in humans. Invest Ophthalmol Vis Sci. 1991;322388- 2392
Fiscella  RGShapiro  MJSolomon  MJ  et al.  Ofloxacin penetration into the eye after intravenous and topical administration. Retina. 1997;17535- 539
Link to Article
Fiscella  RGNguyen  TKCwik  MJ  et al.  Aqueous and vitreous penetration of levofloxacin after oral administration. Ophthalmology. 1999;1062286- 2290
Link to Article
Bauernfeind  A Comparison of the antibacterial activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin, and ciprofloxacin. J Antimicrob Chemother. 1997;40639- 651
Link to Article
Ednie  LMJacobs  MRAppelbaum  PC Activities of gatifloxacin compared to those of 7 other agents against anaerobic organisms. Antimicrob Agents Chemother. 1998;422459- 2462
Song  AScott  IUFlynn  HW  JrBudenz  DL Delayed-onset bleb-associated endophthalmitis: clinical features and visual acuity outcomes. Ophthalmology. 2002;109985- 991
Link to Article
Clark  WLKaiser  PKFlynn  HW  Jr  et al.  Treatment strategies and visual acuity outcomes in chronic postoperative Propionibacterium acnes endophthalmitis. Ophthalmology. 1999;1061665- 1670
Link to Article
Mattoes  HMBanevicius  MLi  D  et al.  Pharmacodynamic assessment of gatifloxacin against Streptococcus pneumoniaeAntimicrob Agents Chemother. 2001;452092- 2097
Link to Article
Ciulla  TAStarr  MBMasket  S Bacterial endophthalmitis prophylaxis for cataract surgery: an evidence-based update. Ophthalmology. 2002;10913- 24
Link to Article
Parrish  CMO'Day  DM Traumatic endophthalmitis. Int Ophthalmol Clin. 1987;27112- 119
Link to Article
Mieler  WFEllis  MKWilliams  DFHan  DP Retained intraocular foreign bodies and endophthalmitis. Ophthalmology. 1990;971532- 1538
Link to Article
Boldt  HCPulido  JSBlodi  CF  et al.  Rural endophthalmitis. Ophthalmology. 1989;961722- 1726
Link to Article
Alfaro  DVRoth  DLiggett  PE Posttraumatic endophthalmitis: causative organisms, treatment, and prevention. Retina. 1994;14206- 211
Link to Article
Ariyasu  RGKumar  SLaBree  LD  et al.  Microorganisms cultured from the anterior chamber of ruptured globes at the time of repair. Am J Ophthalmol. 1995;119181- 188
Martin  DFFicker  LAAguilar  HA  et al.  Vitreous cefazolin levels after intravenous injection: effects of inflammation, repeated antibiotic doses, and surgery. Arch Ophthalmol. 1990;108411- 414
Link to Article
Alfaro  DVHudson  SJRafanan  MM  et al.  The effect of trauma on the ocular penetration of intravenous ciprofloxacin. Am J Ophthalmol. 1996;122678- 683
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