Valley Fever

Overview

Fungal infection caused by Coccidioides immitis or C. posadasii that occurs primarily as a respiratory tract infection, although generalized dissemination may occur

Also known as Valley fever or San Joaquin Valley fever

Pathophysiology

After spores are inhaled, cell activation and cytokine formation stimulate inflammatory cells and facilitate killing of the organism, initially infecting the lungs.

In the lungs, the spores change from barrel-shaped spores to spheres and enlarge, eventually changing into individual endospores that are released into the tissues and initiate an inflammatory response.

Normal immune response helps control the infection, although immunosuppression may delay resolution of the infection.

Infection can extend into the lung parenchyma and then spread via lymphatic system, draining into the bloodstream and to distant sites.

The incubation period is 1 to 4 weeks after exposure, with an average of 10 to 16 days; disseminated illness may take weeks to months to occur.

Causes

Inhalation of spores from cultures of infected persons

Inhaled spores of C. immitis or C. posadasii found in the soil

Risk Factors

People who work in fields, on ranches, or in areas where they are exposed to dust from soil

Incidence

Disseminated illness is more common in dark-skinned males, pregnant females, and immunosuppressed individuals.

Coccidioidomycosis is endemic to the southwestern United States, especially between the San Joaquin Valley in California, Arizona (highest number of cases), and southwestern Texas; it's also found in Mexico, Guatemala, Honduras, Venezuela, Colombia, Argentina, and Paraguay.

This disease primarily affects Filipino Americans, Hispanic Americans, Native Americans, and blacks because of population distribution and an occupational link (common in migrant farm laborers).

The disease affects all age groups.

The incidence is highest during the late summer and early fall when the crops have already been harvested, leaving the soil dry.

Complications

Meningitis

Hydrocephalus

Bronchiectasis

Osteomyelitis

Synovitis

Hepatosplenomegaly

Liver failure

Pulmonary scarring

Arthritis

Septic shock

Assessment

History

Possibly asymptomatic (up to 65% of patients)

Living or traveling to an endemic area

Feverchills

Dry cough

Pleuritic chest pain

Dyspnea

Rash

Sore throat

Chills

Malaise

Fatigue

Headache

Joint pain

Night sweats

Weight loss

Physical Findings

Fever

Itchy maculopapular rash

Hemoptysis

Local swelling and redness in involved sites (with musculoskeletal involvement)

Pleural friction rub

Wheezing

Crackles

Decreased breath sounds; dullness on percussion; increased tactile and vocal fremitus

Hepatomegaly and splenomegaly with disseminated disease

Diagnostic Test Results

Laboratory

Complement fixation detects immunoglobulin G antibodies.

Positive serum precipitins (immunoglobulins) may be seen.

C. immitis spores may be detected through immunodiffusion testing of sputum, pus from lesions, and tissue biopsy.

Presence of antibodies in pleural and joint fluid and a rising serum or body fluid antibody titer (indicate dissemination) may be present.

White blood cell count may be increased.

Eosinophil count may be increased.

Erythrocyte sedimentation rate test may be increased.

Imaging

Chest radiography shows bilateral diffuse infiltrates, nodules, mediastinal or hilar adenopathy, or pleural effusion.

Computed tomography scanning (thorax) reveals abnormalities, such as multiple nodules, interlobar septal thickening, and consolidation.

Other

Biopsy of the affected tissue (lung or skin lesion) reveals evidence of a fungus.

Treatment

General

Symptomatic measures

Humidification of environment

Venous thromboembolism (VTE) prophylaxis if hospitalized

Diet

As tolerated

Activity

Activity as tolerated

Medications

IV fluids

Amphotericin B cholesteryl sulfate complex for severe and rapidly progressive disease

Ketoconazole (oral)fluconazole, or itraconazole for nondisseminated disease

Analgesics, such as nonsteroidal anti-inflammatory drugs (NSAIDs) for pleuritic chest pain

Antitussives for cough

Surgery

Reserved for chronic pulmonary coccidioidal infection with complications

Excision or drainage of lesions

Lobectomy for severe pulmonary lesions

Nursing Considerations

Nursing Interventions

Employ standard precautions.

Encourage rest periods as needed.

Apply antiembolism stockings or sequential compression stockings to prevent VTE.

Cluster activities to minimize energy expenditure and oxygen demand.

Encourage the use of energy-conservation measures.

Administer oxygen as ordered based on oxygen saturation levels via pulse oximetry.

Auscultate lung sounds for changes.

Encourage coughing and diaphragmatic breathing exercises, and incentive spirometry to promote lung expansion.

Elevate the head of the bed or encourage the patient to sit up to allow for maximum chest expansion and to ease the work of breathing.

Encourage respiratory hygiene measures.

Maintain a patent airway.

Provide cool mist humidification and other respiratory care measures to relieve cough.

Administer prescribed medications, such as NSAIDs for pain, antitussives for cough, and antifungal agents.

If ketoconazole is ordered, avoid administration of histamine-2 blockers, which decrease the absorption of ketoconazole.

Encourage adequate fluid intake. Offer frequent sips of fluids. Check skin turgor and inspect mucous membranes for moisture.

Obtain specimens for laboratory testing, such as sputum for cultures and blood for complete blood count.

Reposition at least every two hours, and perform skin assessments. Provide skin care measures as indicated.

Monitoring

Fluid balance status

Intake and output

Vital signs

Pain level and effectiveness of interventions

Sputum color, consistency, and amount

Oxygen saturation level

Cardiopulmonary status

Breath sounds

Level of orientation

Associated Nursing Procedures

Alignment and pressure-reducing device application

Antiembolism stocking application, knee-length

Antiembolism stocking application, thigh-length

Coughing and diaphragmatic breathing exercises

Humidifier therapy, bedside

Incentive spirometry

IV bolus injection

IV catheter insertion

IV catheter removal

IV secondary line drug infusion

Neurologic assessment

Oral drug administration

Oxygen administration

Pain assessment

Pain management

Pressure injury prevention

Pulse oximetry

Respiration assessment

Safe medication administration practices, general

Sequential compression therapy

Sputum collection by expectoration

Weight measurement

Patient Teaching

General

Include the patient's family or caregiver in your teaching, when appropriate. Be sure to cover:

disorder, diagnostic testing, underlying cause, and treatment, including medication therapy

prescribed medications, such as antifungal agents, including drugs, dosages, schedule of administration, expected results, and duration of therapy, possibly ranging from 3 to 6 months

possible adverse reactions associated with medication therapy, and signs and symptoms that need to be reported to a practitioner

that most cases are self-limiting and resolve in a few months but that relapse of extrapulmonary or disseminated disease is possible

proper hand hygiene technique and prevention measures to reduce the risk for exposure, especially for patients involved in working with soil (digging, construction)

appropriate skin care measures

that fatigue and lethargy may continue for weeks or months after other symptoms have resolved

importance of continued follow-up care, initially every 2 to 4 weeks and then every 3 to 6 months for up to 2 years to ensure eradication of the infection.

Discharge Planning

Participate in a multidisciplinary team to coordinate discharge planning efforts. The team may include the bedside nurse, a respiratory therapist, physical therapist, social worker, care manager, infection preventionist, and pulmonologist.

Determine the appropriate post-hospital setting to which the patient should be discharged.

Assess patient and family understanding of the diagnosis, treatment, prognosis, follow-up, and warning signs for which to seek medical attention.

Assess the patient's level of independence prior to admission.

Evaluate how the current illness will impact the patient's independence.

Identify the patient's formal and informal supports.

Identify the patient's and family's goals, preferences, comprehension, and concerns about discharge.

Confirm arrangements for transportation to initial follow-ups.

Assess/confirm the patient's and family's understanding of prescribed medication, including dosage, administration, expected results, duration, and possible adverse effects.

Assess/confirm the patient's ability to obtain medications; identify the party responsible for obtaining medications.

Ensure that the patient and caregivers have been given the proper medical contact information.

Provide information on smoking cessation, if appropriate.

Provide contact information regarding local support groups or services.

Document the discharge planning evaluation in the patient's clinical record, including who was present/involved in discharge planning and teaching.

Document the patient's understanding of the teaching provided and if follow-up teaching is needed.