01OverviewDefinition, clinical context and the essential points that orientate the chapter.
Endophthalmitis is severe inflammation within the eye, usually caused by infection involving the aqueous and vitreous. Organisms can be introduced during an operation or injection, through a penetrating wound or from an infected cornea. They can also arrive through the circulation from a systemic focus. The resulting inflammatory response can damage delicate retinal tissues quickly. The practical priority is therefore early recognition and delivery of effective treatment inside the eye, not completion of a routine red-eye prescription before seeking help.
Ask about cataract surgery, vitreoretinal surgery, intravitreal injections, glaucoma filtering surgery, trauma and the date symptoms began. Acute postoperative infection often appears during the early days after a procedure, but later infection can occur, including around a filtering bleb or with a slower-growing organism. A patient may initially improve and then deteriorate. Do not use elapsed time alone to exclude infection. A history of immunosuppression, diabetes, systemic illness, vascular access or recent bloodstream infection raises additional questions about an endogenous source.
Clinical findings include reduced acuity, pain, photophobia, conjunctival injection, lid swelling and marked anterior chamber inflammation. A hypopyon is a settled inflammatory cell layer; vitritis may reduce the red reflex and obscure the fundus. Not every patient has dramatic pain or a visible hypopyon, especially in an atypical or endogenous presentation. The specialist examines the anterior and posterior segments and compares the current course with expected postoperative inflammation. Sterile inflammation remains a differential diagnosis, but an uncertain case with significant visual decline must be assessed urgently rather than reassured remotely.
Vitreous sampling allows microscopy, culture and susceptibility testing, with molecular testing where available and appropriate. The laboratory needs prompt notification because the sample is small and handling matters. Aqueous or wound samples may also be selected. Sampling should be followed promptly by empirical intravitreal therapy, without waiting for microbiological confirmation. If the fundus cannot be seen, specialist B-scan ultrasound can assess the posterior segment when globe integrity permits; inability to obtain it immediately should not delay needed treatment.
The cited University Hospitals of North Midlands protocol gives vancomycin 1 mg in 0.1 mL and ceftazidime 2.25 mg in 0.1 mL intravitreally for presumed postoperative bacterial infection. These are a specific NHS protocol's doses rather than a claim that every UK centre uses identical preparations. Ophthalmology and pharmacy must verify the drug, concentration, volume, route and allergy history. Intravitreal administration is off-label, and dilution errors can be sight-threatening. Topical antibiotics alone do not deliver an adequate substitute for this intraocular treatment.
Vitrectomy removes infected and inflammatory vitreous material and can obtain additional specimens. It may be considered early in severe cases, including very poor presenting vision, traumatic or bleb-related infection, or inadequate response. The decision is made by the treating surgeon according to the complete presentation and available view. The cited pathway reviews early response within twenty-four to forty-eight hours and considers surgery if improvement is inadequate. Repeat intravitreal injection is not an automatic timed instruction; selection and timing depend on the specialist protocol, organisms, drug persistence and toxicity risk.
Endogenous infection requires coordinated systemic care. Obtain blood cultures promptly and investigate an appropriate source such as endocarditis, an infected vascular device or another deep focus, guided by symptoms and microbiology. Systemic antibacterial or antifungal treatment is essential to control the source as well as local eye treatment when indicated. Fungal infection changes the intravitreal drug choice and the role of steroids. Corticosteroids, whether topical or systemic, are specialist adjuncts after antimicrobial decisions; an unexamined red eye should not receive an empirical steroid escalation that delays identification of infection.
Key points
- Exogenous infection enters through surgery, injection, injury or an infected ocular surface; endogenous infection reaches the eye through bloodstream spread.
- Reduced vision, pain, redness, lid swelling, hypopyon and vitritis are important findings, but absent pain or absent hypopyon does not exclude infection.
- Diagnosis is initially clinical and treatment must not wait for the result of a vitreous culture.
- The cited NHS postoperative bacterial protocol uses intravitreal vancomycin 1 mg in 0.1 mL plus ceftazidime 2.25 mg in 0.1 mL, administered urgently by ophthalmology.
- Intravitreal preparations and doses are specialist, off-label treatments that differ from ordinary systemic injection doses and cataract prophylaxis.
- Blood cultures and a search for the systemic source are required when endogenous endophthalmitis is suspected, alongside urgent ocular management.
- Daily early reassessment and consideration of vitrectomy depend on presenting vision, infection type and response; a negative culture does not establish that treatment was unnecessary.
02AetiologyUnderlying causes, associations and risk factors, with why each one matters.
Exogenous inoculation
Organisms can enter the eye during surgery or injection, through a penetrating injury, or from contiguous corneal or filtering-bleb infection.
Haematogenous seeding
Bacteria or fungi in the bloodstream can cross into ocular tissues from a distant source, sometimes in association with immunosuppression or vascular devices.
Different pathogen behaviour
Organism virulence and growth rate affect the speed and severity of inflammation, allowing both fulminant acute presentations and more indolent postoperative disease.
03PathophysiologyThe causal sequence from the underlying abnormality to symptoms and harm.
- 1Intraocular microbial proliferation
Microorganisms multiply in normally protected ocular spaces, producing toxins and provoking an inflammatory response within the aqueous and vitreous.
- 2Retinal inflammatory damage
Inflammatory cells and mediators disrupt delicate retinal structures and vascular function, contributing to visual loss beyond the amount of visible anterior inflammation.
- 3Loss of media clarity
Cells, fibrin and vitreous debris scatter light and obscure the fundus, reducing acuity and the ability to inspect posterior tissues directly.
04Clinical features and red flagsSymptoms, examination findings, patterns of presentation and time-critical warnings.
Vision or comfort worsens after an initial recovery from surgery or injection, particularly with increasing inflammation, and requires urgent reassessment.
An anterior chamber cell layer with reduced red reflex or an obscured fundus suggests significant intraocular inflammation rather than simple conjunctivitis.
Absence of severe pain, discharge or a visible hypopyon does not reliably exclude endophthalmitis when vision and intraocular findings are concerning.
Bacteraemia, an infected line, immunosuppression or symptoms of a deep focus can accompany endogenous ocular seeding and need parallel medical assessment.
05InvestigationsWhat to request, why it matters and how to interpret it.
Read from the initial assessment onwards. Tests may run in parallel in urgent care; first-line, preferred, confirmatory, definitive and gold-standard labels appear only when the chapter explicitly states them.
- 01
Urgent acuity and slit-lamp assessmentFirst step - Why
- Establish visual compromise and the extent of intraocular inflammation.
- Interpretation and limitations
- Record acuity, cornea, wound or bleb, anterior chamber and red reflex; diagnosis and the decision to treat are initially clinical.
- 02
Vitreous microbiology with selected additional samples - Why
- Identify the organism and guide targeted antimicrobial treatment.
- Interpretation and limitations
- Obtain samples promptly through ophthalmology and inform microbiology, but do not wait for culture before urgent empirical intravitreal therapy.
- 03
Specialist posterior segment imaging - Why
- Assess vitreous involvement and associated retinal complications when the fundus is obscured.
- Interpretation and limitations
- B-scan can help if globe integrity permits; unavailable immediate imaging should not delay necessary sampling and treatment.
- 04
Blood cultures and systemic source assessment - Why
- Investigate suspected endogenous spread and the underlying infectious focus.
- Interpretation and limitations
- Coordinate cultures and targeted systemic investigations with medical and microbiology teams while arranging eye treatment; a surface swab alone does not investigate bloodstream seeding.
06Differential diagnosisRealistic alternatives and the features that help distinguish them.
Sterile postoperative inflammation
Toxic or immune-mediated inflammation can cause postoperative redness and reduced vision without infection, but the distinction depends on specialist examination and the clinical course.
Severe anterior uveitis
Noninfective inflammation may produce pain, photophobia and a hypopyon while having a different distribution and systemic context from infective vitreous disease.
Microbial keratitis
A primary corneal infiltrate and epithelial defect can cause severe pain and inflammation; advanced infection may extend internally and coexist with endophthalmitis.
07ManagementImmediate care, first-line treatment, alternatives and escalation.
01Emergency referralTreat deterioration after an eye procedure seriouslyFirst stepA patient develops suspicious pain, redness or visual reduction after ocular surgery, injection or penetrating injury.+
- 1Contact emergency ophthalmology immediately, reporting the procedure, timing, acuity change and any systemic illness or immunosuppression.
- 2Arrange prompt examination and specialist sampling and treatment; do not substitute a trial of routine conjunctivitis drops or a delayed postoperative appointment.
- 3Check allergies and relevant medicines and facilitate transfer, ensuring the patient understands the urgency even if pain is modest.
02Ocular infection treatmentSample and deliver intravitreal coverOphthalmic examination supports presumed infective endophthalmitis requiring urgent empirical therapy.+
- 1Take appropriate intraocular specimens and notify the laboratory, then administer protocol-approved intravitreal antimicrobial treatment without waiting for results.
- 2Use specialist-prepared doses and route checks, selecting alternatives with ophthalmology and microbiology where allergy, fungal disease or unusual organisms change the regimen.
- 3EscalationReassess early response and consider vitrectomy or other escalation according to presenting function, source and progression rather than repeating injections automatically.
03Endogenous diseaseManage the eye and systemic source togetherIntraocular infection is suspected in a patient with possible bloodstream spread or a systemic infectious focus.+
- 1Obtain blood cultures and assess for sepsis, an infected device, endocarditis or another plausible source through the appropriate medical team.
- 2Begin source-directed systemic antimicrobial treatment with microbiology advice while ophthalmology determines local intravitreal and surgical requirements.
- 3Review both eyes and ongoing systemic findings, adjusting treatment as cultures, susceptibility and source-control information become available.
Key medicines and prescribing safety2 treatments · regimens, roles and cautions+
Intravitreal vancomycin
The cited NHS postoperative bacterial protocol uses 1 mg in 0.1 mL by intravitreal injection urgently after sampling; further treatment is decided by ophthalmology.This is off-label intravitreal therapy requiring validated preparation and concentration checks; it is not a systemic dose, and repeat injections require assessment of efficacy and retinal toxicity risk.
Intravitreal ceftazidime
In the same NHS protocol, administer 2.25 mg in 0.1 mL intravitreally alongside Gram-positive cover, using specialist preparation and individual review of further doses.Intravitreal use is off-label; verify severe allergy history and the exact preparation with ophthalmology and pharmacy, and select different treatment when fungal or resistant infection is suspected.
08ComplicationsImportant consequences, why they occur and why they matter clinically.
Permanent retinal dysfunction
Infection and inflammation can destroy retinal tissue and leave substantial lasting visual loss despite eradication of the organism.
Structural ocular sequelae
Retinal detachment, cataract, altered pressure or persistent vitreous opacity may complicate recovery and affect the eventual visual result.
Systemic infectious morbidity
In endogenous disease, the same bloodstream source may cause sepsis or other metastatic foci, so the ocular presentation can accompany wider serious illness.
09Monitoring and follow-upTreatment response, safety checks and longer-term review.
- Review the eye at least daily initially under specialist care, recording acuity, inflammation, hypopyon, red reflex and pressure as clinically indicated.
- Assess early improvement within twenty-four to forty-eight hours and escalate persistent or worsening infection rather than waiting for the end of a fixed empirical course.
- Review microbiology actively and communicate unexpected resistance or fungal findings promptly because they can change both drugs and surgical decisions.
- After infection control, assess retinal damage, cataract, pressure and functional vision, supporting adherence, follow-up attendance and rehabilitation where needed.
10Special situationsVariants, exceptions and circumstances that change the usual approach.
Symptoms need not be complete
Waiting for the combination of severe pain and a hypopyon can miss early or atypical infection in an eye with falling vision.
Culture negativity does not exclude infection
Small specimens, prior treatment and organism characteristics can reduce microbiological yield, so results must be interpreted alongside the clinical course.
Treatment routes are different
An intravitreal treatment dose, an intracameral prophylactic dose and an intravenous dose are not interchangeable preparations or prescribing instructions.
The source changes the whole plan
Endogenous infection requires systemic investigation and treatment, while traumatic, bleb-related and fungal presentations may need different ocular interventions from routine postoperative bacterial disease.
11Common pitfallsFrequent interpretation and management errors.
- 01
Prescribing topical antibiotics and delaying referral in a patient with reduced vision after an intraocular procedure.
- 02
Waiting for culture positivity or immediate ultrasound availability before delivering indicated intravitreal treatment.
- 03
Escalating steroid drops for presumed sterile inflammation without assessing a worsening postoperative eye.
- 04
Treating endogenous infection locally while failing to obtain blood cultures or investigate the systemic focus.