Periorbital vs Orbital Cellulitis
Preseptal cellulitis is an inflammation of the tissues localized anterior to the orbital septum.
The orbital septum is a fibrous tissue that divides the orbit contents into 2 compartments:
- preseptal (anterior to the septum)
- postseptal (posterior to the septum).
The inflammation that develops posterior to the septum is known as “orbital cellulitis.”
Both entities are caused by an infectious process.
Pathophysiology
Routes of Pathogen Inoculation:
- Direct inoculation:
- Eyelid trauma
- Infected insect bites
- Contiguous spread from adjacent structures:
- Paranasal sinuses (especially ethmoid sinuses via lamina papyracea)
- Chalazion or hordeolum
- Dacryocystitis or dacryoadenitis
- Canaliculitis
- Impetigo, erysipelas
- Herpes simplex/zoster lesions
- Endophthalmitis
- Hematogenous spread:
- From URTI or otitis media via valveless venous systems
Venous Anatomy and Spread:
- Orbit, eyelids, and sinuses drain via superior/inferior orbital veins to the cavernous sinus
- Lack of valves → facilitates bidirectional spread
- Risk of cavernous sinus thrombosis from both preseptal and orbital infections
Classification (Modified Chandler’s Classification)
- Preseptal cellulitis
- Orbital cellulitis
- Subperiosteal abscess
- Orbital abscess
- Cavernous sinus thrombosis
Etiology
Bacterial causes (most common overall):
- Gram-positive cocci:
- Staphylococcus aureus (including trauma-related cases)
- Staphylococcus epidermidis
- Streptococcus pyogenes
- Streptococcus pneumoniae (especially with sinusitis)
- Anaerobes (e.g., Clostridium) → human bite-related cases
- Haemophilus influenzae type b (Hib):
- Historically common in children <5 yrs (now rare with vaccination)
- Still relevant in unvaccinated patients
Viral causes:
- Adenovirus
- Herpes simplex virus (HSV)
- Varicella zoster virus (VZV)
Fungal causes:
- Consider in immunocompromised patients (e.g., mucormycosis)

Diagnosis
General symptoms:
- Eyelid abscess may occur (may need I&D)
- Periorbital vs Orbital Cellulitis
- Eyelid swelling, erythema, warmth
- Low-grade fever, malaise
- Cellulitis may extend to cheek/forehead
Feature | Periorbital (Preseptal) | Orbital (Postseptal) |
---|---|---|
Location | Anterior to orbital septum | Posterior to orbital septum |
Systemic features | Mild or absent | Systemically unwell, fever common |
Eyelid | Unilateral swelling | More marked swelling, unilateral |
Conjunctiva | Normal | Chemosis |
Eye movements | Normal | Painful, restricted |
Proptosis | Absent | Present |
Diplopia | Absent | Present (early sign) |
Optic nerve function | Normal | May show ↓ acuity, colour, visual field defects |
Common causes | Trauma, hordeolum, dacryocystitis | Sinusitis (esp. ethmoid), trauma, surgery |
Complications | Spread to orbit (rare) | Cavernous sinus thrombosis, vision loss, abscess |
Orbital Cellulitis is a Medical Emergency
- Requires urgent imaging (CT orbits/sinuses)
- May lead to intracranial infection, abscess, permanent vision loss
- Admit for IV antibiotics ± surgical drainage
👶 Children <4 years
- Higher risk of orbital cellulitis from posterior spread due to incomplete orbital septum
- Children <3 months: always refer to hospital
Approach to Periorbital Cellulitis
as per eTG
Initial Assessment
- Check for orbital signs: proptosis, ophthalmoplegia, reduced visual acuity
- If unable to examine due to swelling, escalate care
Indications for IV Therapy or Hospital Referral
- Systemically unwell
- Inadequate eye exam (due to swelling or non-cooperation)
- Failure of oral therapy within 48h
- Age <3 months
- High Hib risk (e.g., incomplete vaccination)
Antibiotic Choices for Periorbital Cellulitis
as per eTG 2025
🧑⚕️ Patients without sinusitis/Hib risk:
- Low MRSA risk:
- Dicloxacillin 500 mg PO q6h (child: 12.5 mg/kg up to 500 mg)
- Flucloxacillin 500 mg PO q6h (child: same as above)
- OR Cefalexin 500 mg PO q6h (child: 12.5 mg/kg or 20 mg/kg q8h if poor adherence)
- Penicillin allergy:
- Nonsevere: Cefalexin as above
- Severe: Trimethoprim + Sulfamethoxazole 160+800 mg PO q12h (child: 4+20 mg/kg)
- OR Clindamycin 450 mg PO q8h (child: 10 mg/kg)
- High MRSA risk:
- TMP+SMX or Clindamycin as above
With sinusitis or Hib risk (e.g., <5 yrs not fully vaccinated):
- Low MRSA risk:
- Amoxicillin+clavulanate 875+125 mg PO q12h (child: 22.5+3.2 mg/kg)
- OR Cefuroxime 500 mg PO q12h (child: 15 mg/kg)
- Severe Penicillin allergy:
- TMP+SMX 160+800 mg PO q12h (child: as above)
IV Therapy for Periorbital Cellulitis (when indicated)
- Low MRSA risk:
- Flucloxacillin 2 g IV q6h (child: 50 mg/kg up to 2 g)
- OR Cefazolin 2 g IV q8h (child: 50 mg/kg) if nonsevere penicillin allergy
- Severe allergy:
- Vancomycin IV (dosing per renal function and guidelines)
Duration & Review
- Review within:
- 24 hrs (IV therapy) or 48 hrs (oral therapy)
- Usual duration: 7 days (IV + oral)
- Extend if symptoms persist
Approach to Orbital Cellulitis
Investigations
- Urgent CT orbits + sinuses
- Blood cultures
- 4-hourly visual acuity/pupil checks
Empirical IV Antibiotics
- Standard regimen:
- Ceftriaxone 2 g IV daily + Flucloxacillin 2 g IV q6h
- OR Cefotaxime 2 g IV q8h
- MRSA risk or severe beta-lactam allergy:
- Add or substitute Vancomycin
- If anaerobes suspected: add Metronidazole 500 mg IV q8h
- For severe beta-lactam allergy: Vancomycin + Ciprofloxacin IV
📤 Step Down Oral Therapy (Total 10–14 Days)
- Amoxicillin+clavulanate 875+125 mg PO q12h
- OR Cefuroxime 500 mg PO q12h
- OR TMP+SMX 160+800 mg PO q12h (if MRSA or penicillin allergy)
from RCH
https://www.rch.org.au/clinicalguide/guideline_index/Periorbital_and_orbital_cellulitis
antibiotic treatment
Intravenous therapy | Oral therapy | Total duration | |
Orbital cellulitis | 3rd generation cephalosporin Cefotaxime 50 mg/kg (max 2 g) IV 6 hourly OR Ceftriaxone 100 mg/kg (max 4 g) IV daily If suspected MRSA, add vancomycin (see link for dosing) Duration based on clinical severity and improvement. Usually at least 3-4 days, then switch to oral | Amoxicillin with clavulanic acid (doses based on amoxicillin component) 22.5 mg/kg (max 875 mg) oral bd | 10–14 days |
Severe periorbital cellulitis | |||
Moderate periorbital cellulitis | Cefazolin 50 mg/kg (max 2 g) IV 8 hourly OR Ceftriaxone 50 mg/kg (max 2 g) IV daily (HITH) OR If suspected MRSA, Clindamycin 15 mg/kg (max 600 mg) IV 8 hourly OR oral Duration based on clinical severity and improvement. Usually 1-2 days, then switch to oral | When improving, switch to oral antibiotics as per mild periorbital cellulitis If suspected MRSA:Clindamycin 15 mg/kg (max 600 mg) oral TDS OR Trimethoprim/sulfamethoxazole (8/40 mg/mL) 4/20 mg/kg (max 320/1600 mg) oral BD | 7–10 days |
Mild periorbital cellulitis | Not applicable | Cefalexin 20 mg/kg (max 750 mg) oral TDS OR Cefuroxime 3 months – 2 years: 10 mg/kg (max 125 g), 2 – 12 years: 15 mg/kg (max 250 mg) oral BD | 7-10 days |
Prognosis
- Generally good with prompt diagnosis and treatment.
- Risk of complications remains, even with early and appropriate management.
Complications
1. Orbital Extension
- Orbital cellulitis
- Subperiosteal abscess
- Orbital abscess
- Cavernous sinus thrombosis (via valveless ophthalmic veins)
2. Central Nervous System Involvement
- Occurs secondary to orbital extension
- Meningitis
- Intracranial abscesses: brain, subdural, or extradural
3. Necrotizing Fasciitis
- Rare, but severe
- Typically caused by β-hemolytic Streptococcus
- Clinical features:
- Rapidly spreading cellulitis
- Poorly demarcated margins
- Violaceous skin discoloration
- Risk of necrosis and toxic shock syndrome
- Management:
- Hospital admission
- IV fluid resuscitation
- IV broad-spectrum antibiotics
- Urgent surgical debridement may be required