EYE

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:

  1. Direct inoculation:
    • Eyelid trauma
    • Infected insect bites
  2. 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
  3. 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)

  1. Preseptal cellulitis
  2. Orbital cellulitis
  3. Subperiosteal abscess
  4. Orbital abscess
  5. 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
FeaturePeriorbital (Preseptal)Orbital (Postseptal)
LocationAnterior to orbital septumPosterior to orbital septum
Systemic featuresMild or absentSystemically unwell, fever common
EyelidUnilateral swellingMore marked swelling, unilateral
ConjunctivaNormalChemosis
Eye movementsNormalPainful, restricted
ProptosisAbsentPresent
DiplopiaAbsentPresent (early sign)
Optic nerve functionNormalMay show ↓ acuity, colour, visual field defects
Common causesTrauma, hordeolum, dacryocystitisSinusitis (esp. ethmoid), trauma, surgery
ComplicationsSpread 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 therapyOral therapyTotal 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 cellulitisNot applicableCefalexin 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

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