Fulminant bilateral Haemophilus influenzae keratitis in a patient with hypovitaminosis A treated with contaminated autologous serum.

We report on a patient with hypovitaminosis A treated with autologous serum (AS) who had bilateral infectious ulcers positive for Haemophilus influenzae. The patient suffered a perforation of his right eye and total healing of his left eye with a residual leukoma. In cases of severe malnutrition, serum levels of vitamins and bacteriostatic and growth factors are reduced, so AS would not only be ineffective but also increase the risk of secondary corneal infection. The prophylactic use of a topical antibiotic would be useful in treatment with AS, especially in patients who do not use and adequately store the eye drops, as in our patient.

Haemophilus influenzae is an uncommon corneal pathogen that generally affects corneas with risk factors;1 it accounts for <2% of all corneal ulcers2. H. influenzae is a Gram-negative coccobacillus that infects humans. In ophthalmology, H. influenzae has been reported as a cause of endophthalmitis,3 cellulitis, acute bacterial conjunctivitis in children,4 and keratitis and scleritis.5

Autologous serum (AS) has been proven effective and safe in the management of ocular surface disorders6,7 such as Sjögren’s syndrome,8 persistent epithelial defects,9 keratoconjunctivitis sicca, and vitamin A deficiency.10

We report the first bilateral case of corneal ulcers infected by H. influenzae due to the use of contaminated AS in severe hypovitaminosis A.

Hypovitaminosis A must be suspected in cases of severe dry eye in malnourished or alcoholic patients. Although the standard treatment is vitamin supplements, AS has been shown to be beneficial.10

Case report

A 38-year-old man with chronic alcoholism and cachexia presented with long-lasting watering and burning of the eyes. His corrected visual acuity was 20/20 and he exhibited conjunctival keratinization, reduced tear break-up time, moderate superficial keratitis punctata, and Schirmer below 5 mm (Figure 1). Blood levels of vitamin E were reduced (4.3 mg/L), and those of retinol were undetectable.

Figure 1

A) and B) Conjunctival keratinization and moderate superficial keratitis punctata. C) Infectious ulcers with total hipopion. D) Infectious ulcers with 2 mm hypopion. E) Perforation with drainage of purulent content. F) Improvement of infectious keratitis. G) Residual leukoma and disappearance of ocular xerophthalmia. H) Coating with amniotic membrane.

After the poor outcomes obtained using treatment with artificial tears and oral vitamin A (10,000 IU per day), 20% AS 10 times a day was added.

The protocol followed for AS preparation was as follows: 30 mL of the patient’s blood was left to clot at 4°C for 10–12 hours before centrifuging at 4500 rpm for 15 minutes. The serum was separated in a laminar flow cabinet, diluted with sterile saline (0.9%) to a 20% concentration, and aliquoted in 3.0 mL portions clearly labeled with the patient’s details. The vials should have been kept frozen at −20°C and a fresh bottle thawed, stored at 4°C, and used for treatment every week.

After 20 days of treatment, the patient complained of loss of bilateral vision. Bilateral infectious ulcers with total hypopion were seen in the oculus dexter (right eye [OD]) and infectious ulcers with 2 mm hypopyon in the oculus sinister (left eye [OS]) (Figure 1). The patient admitted not storing the eye drops at 4°C.

Treatment with topical 3.5% vancomycin, 5% ceftazidime, and oral linezolid 600 mg every 12 hours was started. Forty-eight hours later, the patient had right perforation with drainage of purulent content and improvement in his OS (Figure 1). The antibiotic schedule was maintained, and urgent coating was performed on the amniotic membrane.

Cultures of corneal scraping and AS were positive for H. influenzae susceptible to ceftazidime and Staphylococcus epidermidis susceptible to vancomycin.

The biochemical analysis of AS resulted in undetectable vitamin E and retinol levels. Immunoglobulin and lysozyme serum levels were also undetectable. AS was discontinued, and oral vitamin supplements were increased (50,000 IU per day).

Three weeks later, vitamin A and E serum levels were restored; the patient had corrected visual acuity of 16/20 in the OS, with residual leukoma not involving the visual axis; disappearance of ocular xerophthalmia; and corrected visual acuity of the OD for light perception, with good coating of the amniotic membrane (Figure 1).

Discussion

AS has been shown to be effective in the management of xerophthalmia10 and other ocular surface disorders.6–9 Its main advantage is the large amount of nutrients, growth factors, and vitamins it contains.7 Its vitamin A levels (46 mg/mL) are higher than the levels of umbilical cord serum (0.23 mg/mL) and natural (0.02 mg/mL) and artificial tears,7 so AS may be useful in vitamin A deficiency.10

However, if serum nutrient levels are low, AS will have the same deficiency; in this case we should evaluate its effectiveness and the need for coadjuvant treatments, or consider the possibility of using blood from a donor.

AS drops have a high protein content, so there is a significant risk of microbial colonization. Nevertheless, toxicity of any added preservatives can negate some of the beneficial effects of AS. AS seems to be a safe treatment; it does not require preservatives, as it contains bacteriostatic factors (immunoglobulins and lysozyme) and has a low risk of contamination, provided that preparation and storage protocols are followed.11

No severe infections secondary to contaminated AS have been reported in previous studies, but indolent infectious keratitis has been described. Tananuvat et al studied 15 eyes treated with AS and described three infectious ulcers: one coagulase-negative Staphylococcus corneal ulcer, one stitch abscess without identified organism, and one Candida infectious crystalline keratopathy, although the persistent epithelial defect had healed.12 Lagnado et al cultured 134 AS samples; 13 samples from six patients were positive for S. epidermidis, Micrococcus, S. viridans, and S. aureus, all of them without clinical repercussion.11

However, in a malnourished subject, serum levels of immunoglobulins will be reduced,13 as in our patient, therefore increasing the probability for secondary corneal infection.

Furthermore, H. influenzae is an opportunistic pathogen with demanding nutritional requirements. It requires factor X and factor V for growth under aerobic conditions.14 Serum has no factor I, V, VIII, or XIII. H. influenzae would not grow in serum for lack of factor V, but should it be colonized by S. epidermidis, as in our case, this would act as a donor of factor V, and H. influenzae would grow.

We do not know whether the contamination was due to the preparation of the AS or due to inadequate storage of the AS by the patient, because the culture was from only one AS bottle, the last of the three obtained in the first and only blood extraction for AS.

In conclusion, the outcome of this patient suggests two major issues. First, if the patient does not adequately use and store eye drops, the risk of infection will increase, with the appearance of severely infectious keratitis. Therefore, the prophylactic use of an antibiotic would be useful. Second, in the case of severe malnutrition, serum levels of vitamins and bacteriostatic and growth factors would be reduced, so AS would not only be ineffective but also increase the risk of secondary corneal infection.