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PeriOrbital and orbital Infections

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Presentation on theme: "PeriOrbital and orbital Infections"— Presentation transcript:

1 PeriOrbital and orbital Infections

2 Orbital Anatomy

3 Fibrous Membrane separating the orbital and preseptal compartment
Orbital Septum Fibrous Membrane separating the orbital and preseptal compartment

4 Upper Eyelid Extends from the periosteum of the orbital rim to the levator aponeurosis

5 Lower Eyelid Extends from the periosteum of the orbital rim to the inferior border of the tarsal plate

6 Routes of Infection Extension to lids and orbit
Indirect spread venous drainage system shared by cranial and midface structures multiple anastomoses and valveless System

7 Routes of Infection Extension to lids and orbit
Direct spread Ethmoid sinus through lamina papyracea - contained subpereosteal abscess or progressive orbital involvement frontal and maxillary sinus Orbital floor Odontogenic – maxillary sinus - orbit

8 Preseptal cellulitis An infection or inflammatory process of the eyelids and periorbital structures Occurs anterior to and contained by the orbital septum

9 Orbital cellulitis Occurs posterior to the orbital septum
Involves the soft tissue within the bony orbit

10 Cellulitis - Common Etiologies
Spread from adjacent structures – Skin and Sinuses Direct inoculation following Trauma Bacterial spread Upper Respiratory or Middle Ear

11 Preseptal – Associated factors
Hordeola and Chalazia Impetigo/Erysipelas Blepharitis Conjunctivitis Canaliculitis Dacryocystitis Viral dermatitis – herpes simplex & herpes zoster Eyelid swelling both causes and results from impeded venous flow and lymphatic drainage – leading to self-propagating process These are things that can mimic or lead to preseptal and potentially orbital cellulitis

12 Chalazion Most common inflammatory Lesion of eyelid Blocked meibomian gland Inflammatory nodule/cyst Lipogranulomatous Not infectious Typically not painful Oil-producing sebaceous glands located in the tarsal plates of upper and lower lids – chronic libogranulomatous inflammation

13 Chalazion Managed by warm compresses and massage Excision/ Steroid Injection Oil-producing sebaceous glands located in the tarsal plates of upper and lower lids – chronic libogranulomatous inflammation

14 Chalazion Prevention Routine use of warm compresses
Lid margin Cleansing Low dose oral doxycycline Oil-producing sebaceous glands located in the tarsal plates of upper and lower lids – chronic libogranulomatous inflammation

15 Erysipelas Superficial cellulitis Usually group A Strep Intensely erythematous with sharply demarcated border Oil-producing sebaceous glands located in the tarsal plates of upper and lower lids – chronic libogranulomatous inflammation

16 hordeolum Bacterial Infection
mebomian gland or ciliary glands (zeiss or moll) Internal or external Typically painful May lead to preseptal cellulits Meibomian Glands – within tarsal plate Zeis Glands – associated with lash follicles Glands of Moll – apocrine glands associated with eyelash follicles

17 hordeolum Management Staphylococcal - most common etiology
Systemic Antibiotics Lance/Drain Meibomian Glands – within tarsal plate Zeis Glands – associated with lash follicles Glands of Moll – apocrine glands associated with eyelash follicles

18 dacryocystitis Pain, redness and swelling below the medial Canthal tendon Typically associated with blockage of the nasolacrimal System Tear stasis and retention → secondary bacterial infection

19 dacryocystitis Management Antibiotics – systemic Warm compresses
Drainage

20 dacryocystitis Management Oral antibiotics
Gram Positive bacteria most common Consider Gram neg in diabetics, immunocompromised patients IV antibiotics when severe/associated with orbital cellulitis drainage of abscess

21 Herpes Zoster Dermatoblepharitits
Recurrence or reactivation of Varicella Zoster virus Burning, Stabbing pain of forehead/scalp Vesicular Rash in V1 distribution

22 Herpes Zoster Dermatoblepharitits
treat with antivirals Acyclovir if identified within 72 hours of skin lesion onset treat with antivirals Acyclovir if identified within 72 hours of skin lesion onset

23 Preseptal Cellulitis Other Causes of Eyelid Swelling
contact dermatitis Insect bites Thyroid Eye Disease Dacryoadenitis

24 Preseptal Cellulitis Other Causes of Eyelid Swelling
contact dermatitis Thickened, Erythematous, scaly skin

25 Preseptal Cellulitis Other Causes of Eyelid Swelling Insect bites

26 Preseptal Cellulitis Other Causes of Eyelid Swelling
Thyroid Eye Disease Periorbital edema

27 Preseptal Cellulitis Other Causes of Eyelid Swelling Dacryoadenitis
Inflammation of lacrimal gland Superotmeporal pain, swelling, erythema “S” shaped lid deformity

28 Preseptal management Typically outpatient =oral antibiotics
All children < 1 year old should be hospitalized with IV antibiotics Culture when able – more likely after traumatic insult Most common bacteria involved for adults: Staph aurues and Strep pyogenes Most common for children: h influenza type b and strep pneumonia If abscess develops it should be incised and drained

29 Preseptal Management Teenagers and Adults
Usually arises from superficial source (trauma, chalazion) Treated with oral antibiotics Commonly Penicillinase-resistant penicillin or Bactrim Image if: source of infection not determined not responding quickly to treatment orbital process suspected

30 Preseptal Management Children
The most common cause is underlying sinusitis Work up with CT quickly if no source of direct inoculation easily identified Hospitalize and IV antibiotics

31 Orbital Cellulitis Ophthalmic Signs Proptosis Motility Disturbance
Pronounced edema and erythema Impaired vision with afferent pupil defect Conjunctival chemosis and hyperemia Reduced corneal sensation

32 Orbital cellulitis Sources of infection are similar to preseptal
Extension of sinus disease Penetrating trauma Infected adjacent structures Other uncommon sources Scleral buckles, Aqueous drainage devices, endophthalmitis

33 Orbital Cellulitis Noninfectious causes of orbital inflammatory disease Inflammatory and Autoimmune thyroid ophthalmopathy orbital pseudotumor lymphoma dermatomyositis-polymyositis Wegener granulomatosis Sjogren syndrome

34 Orbital Cellulitis Noninfectious causes of orbital inflammatory disease Vascular orbital venous malformation cavernous sinus thrombosis Arteriovenous fistula superior vena cava syndrome

35 Orbital Cellulitis Noninfectious causes of orbital inflammatory disease Neoplasms of orbit and lacrimal gland pediatric: rhabdomyosarcoma, leukemia, metastatic neuroblastoma, retinoblastoma adult: lymphoma

36 Orbital Cellulitis > 90% of all related to underlying sinus disease
In children usually single organism from sinus (s aureus or strep pneumonia) Adolescents and adults have more complex bacteriology (often 2-5 organisms) trauma – Gram - rods Dental – mixed, aggressive aerobes and anaerobes Immunocompromised/Diabetics - fungi

37 Orbital cellulitis Laboratory studies CBC
Nasal swab if purulent material Blood cultures Lumbar puncture if meningeal signs present

38 Orbital cellulitis Imaging Studies Orbital CT
Thin, axial and coronal, without contrast Include orbits, paranasal sinuses, frontal lobes If neurologic involvement include the head when imaging

39 Orbital Cellulitis Significant morbidity if not appropriately treated
orbital apex syndrome blindness cavernous sinus thrombosis cranial nerve palsies meningitis intracranial abscess

40 Orbital Cellulitis Medical Management
Admit for IV antibiotics cephalosporin – Ampicillin or Pipercillin Vancomycin for MRSA Clindamycin for anaerobic coverage Nasal decongestants Transition to outpatient oral antibiotics treatment for 1-3 weeks

41 Surgical Management Orbital Cellulitis If orbital abscess present
Early drainage of involved sinus if orbital signs progressing

42 Differentiating features of cellulitis
Preseptal Orbital Proptosis Absent Present Motility Normal - pain Decreased + pain and double vision Vision Normal Reduced – check vision and color vision Pupillary Reaction +/- APD – check swinging flashlight test Chemosis Rare Common Corneal Sensation May be reduced Systemic Signs Absent/Mild Commonly severe (Fever/Leukocytosis)

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