Updated: Nov 11, 2009
Rocky Mountain spotted fever (RMSF), classically characterized by fever, myalgias, headache, and a petechial rash, is the most common fatal tick-borne disease in the United States. As one of the spotted fevers, it belongs to a large group of tick- and mite-borne infections caused by closely related rickettsiae. These organisms are small, gram-negative bacteria that grow strictly in eukaryotic cells. Rickettsia rickettsii is the organism responsible for RMSF.
The tick that functions as the vector and the reservoir in RMSF is usually the American dog tick (Dermacentor variabilis) in the eastern United States or the Rocky Mountain wood tick (Dermacentor andersoni) in the western United States. However, a 2002-2004 outbreak in Arizona was traced to the common brown dog tick (Rhipicephalus sanguineus), a tick common worldwide but not previously recognized as a vector of disease.
The chance for an individual tick to harbor Rickettsia rickettsii is slight. Although an estimated 4% of the American dog ticks are infected with Rickettsia species, the vast majority of these organisms are nonpathogenic Rickettsia. Therefore, prophylactic treatment of a tick bite is not indicated.
Mortality rates as high as 30% were reported for RMSF in the preantibiotic era. The current mortality rate is 1.4%. A significant portion of this persistent mortality likely is due to delay in diagnosis and treatment.
Rickettsia are introduced into humans after an infected tick feeds for more than 6 hours. The tick bite is painless and frequently goes unnoticed. Rickettsia enter the skin and spread via lymphatics to the bloodstream and attach to their target cells, vascular endothelial cells.
Rickettsia replicate intracellularly and after an average of 1 week (range, 3-12 d), the patient develops clinical manifestations of infection. Illness is characterized by increased vascular permeability with a subsequent host mononuclear cell response. Systemic increase in vascular permeability leads to edema, hypovolemia, and hypoalbuminemia.
In skin, vascular injury initially appears as blanchable erythematous macules (1-5 mm in diameter). Eventually, progression to the classic petechial rash of Rocky Mountain spotted fever (RMSF) usually occurs, although from 10-15% of patients will not have any clinically apparent dermatologic involvement (Rocky Mountain spotless fever).
Central nervous system (CNS) manifestations include encephalitis and meningoencephalitis secondary to vascular injury. Seizures, cranial nerve damage, and permanent blindness and deafness have been documented.
Pulmonary involvement may lead to noncardiogenic pulmonary edema, interstitial pneumonia, and adult respiratory distress syndrome (ARDS), contributing significantly to mortality.
Myocarditis may occur secondary to microcirculatory vasculitis.
Renal manifestations include decreased glomerular filtration rates (GFRs) and prerenal azotemia from hypovolemia.
Focal hepatocellular necrosis occurs in 38% of patients, as evidenced by moderately increased serum aminotransferase levels. Autopsies of patients with RMSF have revealed portal triaditis and vasculitis. However, hepatic failure does not typically occur.
Gastrointestinal (GI) endothelial cell injury leads to abdominal pain, nausea, vomiting, and diarrhea. Many patients have guaiac positive stools. Thirty percent of patients are anemic, and death has been reported from massive GI bleeding.
Remember that RMSF is a multisystem disease. In any particular patient, one organ system may be more affected than the others.
In 2004, 1514 cases were reported—more than 4 times the 365 cases reported in 1998. The reasons for this increase are not known, but wide swings in the incidence of Rocky Mountain spotted fever (RMSF) have occurred since 1920.
Seasonal outbreaks of RMSF parallel the activity of the tick; 90% of cases are reported from April 1 to September 30, with peaks in May and June.
Cases are geographically distributed; North Carolina and Oklahoma account for one third of total cases reported. South Carolina, Tennessee, and Georgia accounted for the third, fourth, and fifth highest number of cases. Less than 2% of the total number of cases are found in the Rocky Mountain states.
Asymptomatic infection may be common; in one study, 12% of children living in high-risk zones had positive serology test results, indicating past exposure to RMSF.1
Rocky Mountain spotted fever has been extensively documented in Canada, Mexico, Central America, Colombia, and Brazil. No reports document RMSF infection outside of the Americas. However, a wide range of related spotted fever group (SFG) rickettsioses has been described across Europe, Africa, Asia, and Oceania. The true incidence of spotted fever infections internationally is not known.
The overall case-fatality rate of Rocky Mountain spotted fever (RMSF) has been reported as 1.4%.2 Children younger than 5 years have a reported fatality rate of 5%.2 Adults older than 70 years have a reported case-fatality rate of 9%.3 Death occurs on average 8 days after onset of symptoms.4 Long-term scarring, blindness, and deafness have been documented.5
Whites have twice the incidence of African Americans. However, African Americans have a higher case-fatality rate, likely due to the greater difficulty of appreciating a rash in highly pigmented individuals.
American Indians are at greater risk for RMSF than the general population.6 From 2001-2005, the average annual incidence of RMSF reported among American Indians was 16.8 per 1,000,000 persons compared with 4.2 for whites, 2.6 for blacks, and 0.5 for Asian/Pacific Islanders. The incidence of RMSF in American Indians increased at a disproportionate rate during this period, though the rate was comparable to those for other races from 1990-2000.7
The male-to-female ratio is 1.7:1.
A high index of suspicion is the most important aspect of diagnosing Rocky Mountain spotted fever (RMSF). Diagnosis is typically delayed. In the case series by Buckingham et al, of 92 patients eventually diagnosed with RMSF, the median delay between first visiting a health care provider and starting antirickettsial therapy was 5 days; only 49% reported a tick bite.8
In other studies, 66% of reported cases had a history of tick attachment 14 days prior to illness. An additional 26% of patients reported being in a tick-infested area.
Children may often present without a known history of tick exposure.
R rickettsii is the organism responsible for Rocky Mountain spotted fever (RMSF).
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Enterovirus infection
Typhoid fever
Bacterial sepsis
Meningococcemia
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Rickettsialpox
Recrudescent typhus
Sylvatic flying squirrel-associated Rickettsia prowazekii infection
Deliver supportive care, including airway support and intravenous fluids, as determined by severity of the patient's condition.
Because the differential diagnosis for Rocky Mountain spotted fever includes many rare diseases, consultations from a dermatologist and/or infectious diseases subspecialists may be needed.
Tetracyclines are the drugs of choice (DOC) for Rocky Mountain spotted fever (RMSF). Despite the risk of teeth staining, tetracycline is now preferred over chloramphenicol for children younger than 9 years. In the review by Holman et al of 6388 cases of RMSF reported between 1981 and 1998, patients treated with chloramphenicol only had an odds ratio for mortality of 5.5, after adjustment for other risk factors.10
Doxycycline therapy11 also treats Lyme disease, ehrlichiosis, and relapsing fever—entities often clinically confused with RMSF.
No human data exist to support use of fluoroquinolones in RMSF. Penicillin, cephalosporins, erythromycin, aminoglycoside, and trimethoprim and sulfamethoxazole are not effective against rickettsia.
Antibiotics usually are administered for 7 days or until the patient is afebrile for 2 days.
Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.
Classically the DOC for adults and children >9 y. Now recommended by the CDC for children <9 y as well, given better efficacy in treating this potentially life-threatening disease. No risk of aplastic anemia exists. Because it binds less strongly to calcium than does tetracycline, it is considered less likely to stain teeth.
200 mg PO/IV divided bid
<100 lb: 2 mg/lb PO/IV divided bid
>100 lb: 200 mg PO/IV divided bid
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
Documented hypersensitivity; severe hepatic dysfunction
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
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
Recommended by the CDC as an alternate drug for the treatment of pregnant women to avoid the risks of tooth and bone malformations. No longer routinely recommended for children because of reduced effectiveness and deleterious side effects.
If administered on an outpatient basis, 30% of patients subsequently will require hospitalization, compared to 11% of patients treated with tetracyclines.
500 mg IV divided qid for 7 d
Not recommended
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
Documented hypersensitivity
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
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)
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Rocky Mountain spotted fever, Rocky Mountain spotted fever symptoms, Rocky Mountain spotted fever treatment, rickettsial infection, tick bite, RMSF, , American dog tick, Dermacentor variabilis, , Rocky Mountain wood tick, , spotted fevers, Rocky Mountain spotless fever
Allon Amitai, MD, International Emergency Medicine Fellow, Rhode Island Hospital; Consulting Staff, Memorial Hospital of Rhode Island; Doctoring Preceptor, Brown University Medical School
Allon Amitai, MD is a member of the following medical societies: American College of Emergency Physicians
Disclosure: Nothing to disclose.
Richard H Sinert, DO, Associate Professor of Emergency Medicine, Clinical Assistant Professor of Medicine, Research Director, State University of New York College of Medicine; Consulting Staff, Department of Emergency Medicine, Kings County Hospital Center
Richard H Sinert, DO is a member of the following medical societies: American College of Physicians and Society for Academic Emergency Medicine
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Peter MC DeBlieux, MD, Professor of Clinical Medicine and Pediatrics, Section of Pulmonary and Critical Care Medicine, Program Director, Department of Emergency Medicine, Louisiana State University Health Sciences Center
Peter MC DeBlieux, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, Radiological Society of North America, and Society of Critical Care Medicine
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John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
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Rick Kulkarni, MD, Assistant Professor of Surgery, Section of Emergency Medicine, Yale-New Haven Hospital
Rick Kulkarni, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
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The authors and editors of eMedicine gratefully acknowledge the contributions of previous editor, Charles V Pollack Jr, MD, and previous author, Richard Medlin Jr, MD, to the development and writing of this article.
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