Neonatal Conjunctivitis |
Reviewed by Simon Rowley and Lesley Voss |
| December 2000 |
Maternal history
Bacterial
culture
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| Chlamydia |
|
| HSV |
|
NB:
Transport all specimens ASAP to Microbiology Laboratory, LabPlus.| Non-Infectious |
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| Infectious | Organism | Age of Onset | Clinical Features | Therapy | |
| Staphylococcus aureus |
2-5 days |
Unilateral, crusted purulent discharge | Topical soframycin drops | ||
| Neisseria gonorrhoeae # |
3 days to 3 weeks |
Bilateral, hyperaemic, chemosis, copious thick white discharge | Ceftriaxone 50mg/kg
IV/IM as a single dose (maximum 125mg),
Saline irrigations hourly until exudate resolves. |
||
| Streptococcus pneumoniae, Haemophilus spp, Enterococci |
2 days |
Mild purulent conjunctivitis | Topical soframycin drops | ||
| Pseudomonas aeruginosa + |
5-18 days |
Oedema and erthyema of lid, purulent discharge. |
IV anti-pseudomonal antibiotics. Topical polymyxin. |
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| Chlamydia trachomatis * |
2-20 weeks |
Unilateral or bilateral, mild conjunctivitis, copious purulent discharge. | PO erythromycin 50mg/kg/day x 14d (bid or qid). | ||
| Herpes simplex | Conjunctivitis with vesicles elsewhere |
Acyclovir 30mg/kg/day IV tid x 14-21d. Topical acyclovir. Isolation. |
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# Uncommon, potential for serious consequences - severe keratitis and endophthalmitis. Requires early recognition and treatment. Needs blood and CSF culture. Consider concomitant chlamydial infection if poor response to cephalosporin. Parents require investigation and screening.
+ Risk of rapid progression from purulent discharge to denuding of corneal epithelium, and perforation of cornea. The anterior chamber can fill with fibrinous exudate, iris can adhere to cornea and later blood vessel invasion. The late ophthalmic complications can be followed by bacteraemia and septic foci.
* Most common pathogen, 20-50% of exposed infants will develop chlamydia conjunctivitis, 10-20% will develop pneumonia. If relapse occurs repeat course of erythromycin for further 14 days. Parents require treatment.
NB: Chloramphenicol in topical therapy can obscure results of tests for chlamydia.
| 1 | Tsang B, Infectious conjunctivitis in childhood. New Ethics Nov 1994, 1-8. |
| 2 | Remington and Klein. Infectious diseases of the fetus and newborn. 4th Ed. 1995. |
|
Generic Name |
Trade Name and Preparation |
Usual susceptibility |
Potential Adverse Effects |
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|
Staphylococci |
Steptococci |
Gram negative bacilli |
Pseudomonas |
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| Chloramphenicol |
Chlomin drops, ointment Chloromycetin drops, ointment Chloroptic drops, ointment Chlorsig drops, ointment Minims drops |
+ |
+ |
+ |
- |
May obscure results of tests for Chlamydia; rarely marrow aplasia. |
| Chloramphenicol/ polymyxin B | Chloromyxin drops, ointment |
+ |
+ |
+ |
+ |
May obscure results of tests for Chlamydia; rarely ototoxicity or marrow aplasia. |
| Framycetin | Soframycin drops, ointment |
+ |
- |
+ |
- |
Sensitisation; development of resistant organisms. |
| Fusidic acid | Fucithalmic drops |
+ |
+ |
- |
- |
Rarely transient stinging. |
| Gentamicin |
Genoptic drops Minims drops |
+ |
- |
+ |
+ |
Sensitisation; development of resistant organisms. |
|
Gramicidin/ neomycin polymyxin B |
Neosporin drops |
+ |
+ |
+ |
+ |
Sensitisation; development of resistant organisms; rarely ototoxicity. |
| Sulphacetamide |
Acetopt drops Bleph Liquifilm drops Minims drops |
+ |
+ |
+ |
- |
Inactivated by pus and tissue breakdown products. |
| Tetracycline | Achromycin ointment |
+ |
+ |
+ |
- |
|
| Tobramycin | Tobrex drops, ointment |
+ |
- |
+ |
+ |
Sensitisation; development of resistant organisms. |