You are in: eMedicine Specialties > Ophthalmology > INFECTIOUS DISEASE Rocky Mountain Spotted FeverArticle Last Updated: Nov 1, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Byron L Lam, MD, Department of Ophthalmology, Professor, Bascom Palmer Eye Institute, University of Miami School of Medicine Byron L Lam is a member of the following medical societies: Alpha Omega Alpha, American Academy of Ophthalmology, American Medical Association, and Phi Beta Kappa Editors: John D Sheppard, Jr, MD, MMSc, Associate Professor of Ophthalmology, Microbiology and Immunology, Director for Thomas R Lee Center for Ocular Pharmacology, Director, Uveitis Service, Eastern Virginia School of Medicine; Consulting Staff, Virginia Eye Consultants; Simon K Law, MD, PharmD, Assistant Professor of Ophthalmology, Jules Stein Eye Institute; Chief of Section of Ophthalmology Surgical Services, Department of Veterans Affairs Healthcare Center, West Los Angeles; R Christopher Walton, MD, Professor, Director of Uveitis and Ocular Inflammatory Diseases Service, Assistant Department of Ophthalmology, Assistant Dean for Graduate Medical Education and Continuing Education, University of Tennessee College of Medicine; Consulting Staff, Regional Medical Center, Memphis Veterans Affairs Medical Center, St Jude Children's Research Hospital; Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri; Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences Author and Editor Disclosure Synonyms and related keywords: RMSF, rickettsial disease, Rickettsia rickettsii, R rickettsii, Dermacentor andersoni, D andersoni, ticks, wood ticks, dog ticks, Dermacentor variabilis, D variabilis, Amblyomma americanum, A americanum INTRODUCTIONBackgroundRocky Mountain spotted fever (RMSF) is the most common rickettsial disease in the United States; it also occurs throughout the Western hemisphere. RMSF is caused by Rickettsia rickettsii, an obligate intracellular gram-negative coccobacilli that contains both DNA and RNA. Ticks serve as both vectors and reservoirs for RMSF. The organism usually is harbored by the wood tick Dermacentor andersoni in the Rocky Mountain states; the American dog tick Dermacentor variabilis in the eastern, central, southern, and Pacific coastal states; the cayenne tick Amblyomma americanum in Texas and in Central and South America; and the brown dog tick Rhipicephalus sanguineus in Arizona and in Mexico. RMSF is characterized by fever, myalgias, headache, and a petechial rash. Early symptoms are nonspecific. Ocular manifestations include petechial conjunctivitis, anterior uveitis, retinal hemorrhages, cotton-wool spots, retinal vascular engorgement and tortuosity, branch retinal arteriolar occlusion, and optic disc edema. RMSF is a potentially fatal disease with a mortality rate as high as 30% in the preantibiotic era. Early treatment with appropriate antibiotics is the key prognostic factor. Therapy should be instituted as soon as the disease is suspected clinically. Further, RMSF should be considered in family members and contacts who have febrile illness and share environmental exposures with the patient. An ophthalmologist rarely participates in the treatment of patients with RMSF where fulminant systemic symptoms overwhelm mild ocular manifestations. The ocular changes probably are underestimated and underdiagnosed, usually resolving within 3 weeks of systemic antibiotic therapy. PathophysiologyThe disease is transmitted to humans through tick bites, which often occurs unnoticed. The organism invades the endothelial and smooth muscle cells of the blood vessels, producing a systemic vasculitis with increased vascular permeability. Loss of serum proteins, decreased blood volume, and thrombi result in edema, hypovolemia, hypoperfusion, and circulatory failure. Ocular manifestations are due to ischemia and increased vascular permeability. FrequencyUnited StatesAccording to the Centers for Disease Control and Prevention (CDC), approximately 600-800 new cases per year occur, with an annual incidence of 3.8 cases per 1 million persons in 2002. The incidence was lowest among persons younger than 5 years and 10-29 years, and the incidence was highest among adults aged 60-69 years. Seasonal outbreaks parallel tick activity. Most cases occur during the spring and summer with rare sporadic cases throughout the year. Risk factors include exposure to wooded areas and to dogs. Geographic distribution of RMSF shows that more than one half of reported cases are from only 5 states: North Carolina, South Carolina, Tennessee, Oklahoma, and Arkansas. InternationalRMSF is endemic in Central and South America. Mortality/Morbidity
RaceNo racial predilection exists for RMSF. SexThe male-to-female ratio is 1.7:1. AgeIn a survey of children, the findings from immunofluorescence antibody assays suggest infection with R rickettsii or the related spotted fever group rickettsiae may be subclinical and occur more commonly than previously thought. Children have been thought to have a high incidence, perhaps because of a high mortality rate in the young age groups. Data from 1997-2002 from the CDC showed the incidence was lowest among persons younger than 5 years and 10-29 years, and the incidence was highest among adults aged 60-69 years. CLINICALHistoryEarly diagnosis is based on clinical and epidemiologic grounds. The clinician must always have a high index of suspicion, because the early signs and symptoms are nonspecific. A history of tick bite or tick exposure and recent travel to endemic regions are risk factors. The incubation period is 2-14 days following a tick bite.
Physical
CausesR rickettsii causes RMSF. DIFFERENTIALSBranch Retinal Artery Occlusion Branch Retinal Vein Occlusion Central Retinal Artery Occlusion Central Retinal Vein Occlusion Conjunctivitis, Acute Hemorrhagic Conjunctivitis, Viral Eales Disease Headache, Children Neuroretinitis, Diffuse Unilateral Subacute Ocular Ischemic Syndrome Optic Neuritis, Childhood Papilledema Red Eye Evaluation Uveitis, Anterior, Childhood Uveitis, Anterior, Nongranulomatous
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| Drug Name | Doxycycline (Doryx, Bio-Tab, Vibramycin) |
|---|---|
| Description | Inhibits protein synthesis and thus bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. |
| Adult Dose | 200 mg PO/IV divided bid |
| Pediatric Dose | <100 lb: 2 mg/lb divided bid PO/IV >100 lb: 200 mg divided bid PO/IV |
| Contraindications | Documented hypersensitivity; severe hepatic dysfunction |
| Interactions | Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy |
| Pregnancy | D - Unsafe in pregnancy |
| Precautions | Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last one half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines |
| Drug Name | Chloramphenicol (Chloromycetin) |
|---|---|
| Description | Binds to 50 S bacterial-ribosomal subunits and inhibits bacterial growth by inhibiting protein synthesis. Effective against gram-negative and gram-positive bacteria. |
| Adult Dose | Not recommended |
| Pediatric Dose | 50-75 mg/kg PO qid |
| Contraindications | Documented hypersensitivity |
| Interactions | Administered concurrently with barbiturates, chloramphenicol serum levels may decrease while barbiturate levels may increase causing toxicity; manifestations of hypoglycemia may occur with sulfonylureas; rifampin may reduce serum chloramphenicol levels, presumably through hepatic enzyme induction; may increase effects of anticoagulants; may increase serum hydantoin levels, possibly resulting in toxicity; chloramphenicol levels may be increased or decreased |
| Pregnancy | D - Unsafe in pregnancy |
| Precautions | Use only for indicated infections, or as prophylaxis for bacterial infections; serious and fatal blood dyscrasias (aplastic anemia, hypoplastic anemia, thrombocytopenia, granulocytopenia) can occur; evaluate baseline and perform periodic blood studies approximately every 2 d while in therapy; discontinue upon appearance of reticulocytopenia, leukopenia, thrombocytopenia, anemia, or findings attributable to chloramphenicol; adjust dose in liver or kidney dysfunction; caution in pregnancy at term or during labor because of potential toxic effects on fetus (gray syndrome) |
These agents relax any ciliary muscle spasm that can cause a deep aching pain and photophobia. Cycloplegic agents are also mydriatics, and the practitioner should make sure that the patient does not have glaucoma. This medication could provoke an acute angle-closure attack.
| Drug Name | Cyclopentolate 1% (AK-Pentolate, Cyclogyl) |
|---|---|
| Description | DOC in corneal abrasions. Blocks muscle of ciliary body and sphincter muscle of iris from responding to cholinergic stimulation, thus causing mydriasis and cycloplegia. Induces mydriasis in 30-60 min and cycloplegia in 25-75 minutes. These effects last up to 24 hours. |
| Adult Dose | 1 gtt bid/tid in affected eye(s) |
| Pediatric Dose | Administer as in adults; use 0.5% instead of 1% in infants |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma |
| Interactions | Decreases effects of carbachol and cholinesterase inhibitors |
| Pregnancy | A - Safe in pregnancy |
| Precautions | Exercise caution in patients (eg, elderly persons) where increased intraocular pressure may be present; can cause toxic anticholinergic systemic adverse effects (common in children especially infants) but incidence rare when used sparingly; compressing lacrimal sac by digital pressure for 1-3 min, following application, may minimize systemic absorption |
Suppresses active disease, which is assumed to be due to inflammatory mechanisms.
| Drug Name | Prednisolone acetate 1% (AK-Pred, Delta-Cortef, Econopred) |
|---|---|
| Description | Decreases autoimmune reactions, possibly by suppressing key components of immune system. |
| Adult Dose | 1 gtt qd/qid in affected eye(s) |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; viral, fungal, or tubercular infections |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hyperthyroidism, osteoporosis, cirrhosis, nonspecific ulcerative colitis, peptic ulcer, diabetes, and myasthenia gravis |
| Drug Name | Loteprednol etabonate (Lotemax, Alrex) |
|---|---|
| Description | Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability. Topical ester steroid drop with decreased risk of glaucoma. Available in 0.2% and 0.5% drops. |
| Adult Dose | 1 gtt tid up to q1h in both eyes; well shaken to suspend particles |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; viral, fungal, or tubercular infections |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hypertension; known to cause cataract formation with chronic use; fungal invasion should be suspected in any persistent corneal ulceration where a corticosteroid has been used or is in use (fungal cultures should be taken when appropriate) |
Have analgesic and anti-inflammatory activities. Their mechanism of action is not known but may inhibit cyclooxygenase activity and prostaglandin synthesis. Other mechanisms may exist as well, such as inhibition of leukotriene synthesis, lysosomal enzyme release, lipoxygenase activity, neutrophil aggregation, and various cell membrane functions.
| Drug Name | Diclofenac (Voltaren) |
|---|---|
| Description | Inhibits prostaglandin synthesis by decreasing activity of enzyme cyclooxygenase, which in turn decreases formation of prostaglandin precursors. May facilitate outflow of aqueous humor and decreases vascular permeability. |
| Adult Dose | 1 gtt in affected eye(s) qid or prn for pain and photophobia |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; avoid during pregnancy |
| Interactions | Additive effect with systemic NSAIDs may occur |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Corneal thinning may occur (Voltaren from CibaVision, Duluth, GA is not associated with this increased risk) |
| Drug Name | Ketorolac (Acular) |
|---|---|
| Description | Available in preserved bottle as well as PF (preservative free) single dose unit (SDU) containers. |
| Adult Dose | 1 gtt in affected eye(s) qid or prn for pain and photophobia |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Perform ophthalmologic studies in patients who develop eye complaints during therapy; discontinue therapy if changes are noted; changes may include blurred or diminished vision, corneal deposits and retinal disturbances, scotomata, changes in color vision, and macula degeneration |
Rocky Mountain Spotted Fever excerpt
Article Last Updated: Nov 1, 2006