Isolate and identify potentially pathogenic aerobic organisms. Susceptibility test is performed at additional charge when organisms isolated meet microbiologic criteria for clinical significance.
Only rapid-growing, nonfastidious aerobic organisms can be recovered and identified by routine methods. Only organisms that predominate will be identified. Unless specifically requested by the physician, fastidious organisms may not be isolated. Anaerobic, fungal, and mycobacterial pathogens should be considered, and appropriate cultures requested if clinically indicated. The procedure will not detect Chlamydia, viruses, fungi, or mycobacteria.
Eye: The major modes of transmission of disease to the conjunctiva include the hands, airborne fomites, and spread for adjacent adnexal infections. Eye infections include eyelid infections, blepharitis, dacryocystitis, orbital cellulitis, conjunctivitis, keratitis, endophthalmitis retinitis, and chorioretinitis. Pinkeye is caused by adenovirus. It presents as bilateral conjunctivitis with a sudden onset. Herpes simplex and zoster present as periorbital or corneal infections. Nontuberculous mycobacterial keratitis may occur following trauma or surgery accompanied by the use of local corticosteroids.1
Wound: Susceptibility testing is usually performed. The majority of bacteria infecting surgical wounds are common airborne microörganisms.2 Effective treatment of wound infection usually includes drainage, removal of foreign bodies, infected prosthetic devices, and retained foreign objects such as suture material. Suction irrigation may be helpful in resolving wound infections. Species commonly recovered from wounds include Escherichia coli, Proteus sp, Klebsiella sp, Pseudomonas sp, Enterobacter sp, enterococci, other streptococci, Bacteroides sp, Prevotella sp, Clostridium sp, Staphylococcus aureus, and coagulase-negative Staphylococcus.
1. Bullington RH Jr, Lanier JD, Font RL. Nontuberculous mycobacterial keratitis. Report of two cases and review of the literature. Arch Ophthalmol. 1992 Apr; 110(4):519-524. PubMed 1562261
2. Whyte W, Hambraeus A, Laurell G, Hoborn J. The relative importance of the routes and sources of wound contamination during general surgery. II. Airborne. J Hosp Infect. 1992 Sep; 22(1):41-54. PubMed 1358946
Baker AS. Ocular infections: Clinical and laboratory considerations. Clin Microbiol Newsl. 1989; 11:97-101.
Cheadle WG. Current perspectives on antibiotic use in the treatment of surgical infections. Am J Surg. 1992 Oct; 164(4A Suppl):44S-47S. PubMed 1443360
Goldstein EJ. Management of human and animal bite wounds. J Am Acad Dermatol. 1989 Dec; 21(6):1275-1279. PubMed 2685062
Jones DB, Leisegang TJ, Robinson NM. Cumitech 17. In: Washington JA, ed. Laboratory Diagnosis of Ocular Infections. Washington, DC: ASM Press;1981 (review).
Kligman EW. Treatment of otitis media. Am Fam Physician. 1992 Jan; 45(1):242-250. PubMed 1728094
Macknin ML. Respiratory infections in children. What helps and what doesn't? Postgrad Med. 1992 Jan; 92(2):242-250. PubMed 1495881
Pollack AV, Evans M. Microbiologic prediction of abdominal surgical wound infection. Arch Surg. 1987 Jan; 122(1):33-37. PubMed 3541852
Randall DA, Fornadley JA, Kennedy KS. Management of recurrent otitis media. Am Fam Physician. 1992 May; 45(5):2117-2123. PubMed 1575107