ESSENTIAL WORKUP
- Diagnose via:
- Isolation of organism:
- Blood
- CSF for encephalitis
- Bronchoalveolar lavage for pneumonitis
- Amniotic fluid
- Aqueous humor
- Detection of tachyzoites in tissues or body fluids
- Demonstrating characteristic lymph node pathology
- Thorough ocular exam:
- Retinal exam
- Visual acuity
DIAGNOSIS TESTS & NTERPRETATION
Lab
- LDH >600/UL associated with toxoplasmosis
- CBC:
- ABG/pulse oximetry for pulmonary symptoms
- IgG antibodies:
- High number of false-positive and false-negative results
- Common tests:
- Sabin–Feldman dye test
- Indirect fluorescent antibody
- Agglutination
- Enzyme-linked immunosorbent assay test
- Immunoglobulin M (IgM) antibodies:
- Absence excludes diagnosis in immunocompetent host
- Reference labs may be helpful, such as Remington (650-853-4828 Toxoplasma Serology Laboratory) (
www.pamf.org/serology
)
- Diagnoses acute infection
- Appear in 5 days
- Disappear in weeks to months
- Neonatal testing differentiates from maternal infection
Imaging
- Chest radiograph for pulmonary symptoms:
- Pneumonitis associated with reticulonodular pattern
- CT head with contrast:
- Multiple bilateral hypodense ring-enhancing lesions
- MRI brain:
- High signal abnormalities on T2-weighted images
- Serial fetal ultrasonography can be useful in exploring congenital infection of the CNS or other signs.
Diagnostic Procedures/Surgery
Brain biopsy for encephalitis—definitive diagnosis
DIFFERENTIAL DIAGNOSIS
- Cryptococcal meningitis
- CNS lymphoma
- Pneumocystis carinii
pneumonia
- Cytomegalovirus retinitis
- Mycobacterial infection
TREATMENT
INITIAL STABILIZATION/THERAPY
- Treat seizures in standard fashion with diazepam and phenytoin.
- Initiate oxygen if hypoxia due to pneumonitis.
ED TREATMENT/PROCEDURES
Immunocompetent
Toxoplasmic lymphadenitis:
- No antibiotics unless symptoms severe and persistent
- Treat symptomatic patients with pyrimethamine and folinic acid plus sulfadiazine or clindamycin for 3–4 wk
- Clindamycin may be a useful alternative to sulfadiazine because of the side effects of the latter and in those who are hypersensitive to sulfa
- Pyrimethamine and sulfadiazine (Eon Labs 800-526-0225) is available as a combination drug.
- Corticosteroids may be useful for ocular complications and CNS disease.
- Reassess to determine if longer therapy needed.
Immunocompromised
- Confirmed acute infection by serology/symptoms:
- Treat with pyrimethamine and folinic acid + sulfadiazine or clindamycin for 4–6 wk after resolution of symptoms.
- Alternative medications:
- Trimethoprim–sulfamethoxazole
- Pyrimethamine and folinic acid + dapsone
- CNS symptoms + a lesion on CT or MRI:
- Treat empirically with pyrimethamine and folinic acid + sulfadiazine or clindamycin.
- Brain biopsy or CSF to confirm diagnosis
- Administer anticonvulsants only if confirmed prior seizures:
- Poorer outcome for patients on anticonvulsants
- Chronic asymptomatic infection:
- No therapy required
- Prophylaxis options for toxoplasmosis in AIDS and immunosuppressed patients:
- Trimethoprim–sulfamethoxazole; lifelong prophylaxis should be considered in HIV patients after consultation.
- Pyrimethamine (75 mg/wk) and dapsone (200 mg/wk) and leucovorin 10–25 mg with each dose pyrimethamine
Ocular
- Treat with pyrimethamine and sulfadiazine for 1 mo.
- May add clindamycin
- Administer systemic steroids with macular or optic nerve involvement.
Acute Acquired Infection in Pregnancy
- Initially treat with spiramycin pending confirmatory tests and consultation (FDA, Division of Special Pathograns and Transplant Drug Products 301-796-1600 or CDC at 404-718-4745).
- After the infection is documented, initiate treatment after consultation:
- Spiramycin in the 1st 17 wk
- Pyrimethamine and sulfadiazine after 17 wk
- Spiramycin may reduce congenital transmission but does not treat fetus if infection is in placenta; maternal therapy may decrease severity of congenital disease.
- Treat congenital infection with sulfadiazine, pyrimethamine, and folinic acid for 12 mo.
- Prevention of exposure in seronegative pregnant women is important when contacting cats or their excrement.
MEDICATION
- Clindamycin:
- 600 mg (peds: 20–40 mg/kg/24 h) IV q6h
- 300 mg (peds: 8–20 mg/kg/24 h) PO q6h
- Useful if patient hypersensitive to sulfa
- Dapsone: 50 mg PO per day or 200 mg PO per week (child >1 mo: 2 mg/kg PO per day)
- Folinic acid: 5–25 mg PO daily in conjunction with pyrimethamine therapy
- Pyrimethamine: 100 mg BID on 1st day loading dose, then 25–50 mg PO per day
- Spiramycin: FDA authorization required
- Sulfadiazine: 500 mg–2 g (peds: 100–200 mg/kg/24 h div. BID) PO q6h
- Trimethoprim–sulfamethoxazole: 5 mg/kg of trimethoprim component IV or PO q12h
FOLLOW-UP
DISPOSITION
Admission Criteria
- Acute infection with severe systemic symptoms
- Immunocompromised patients with:
- Toxoplasmosis encephalitis
- Pneumonitis
- Sepsis
Discharge Criteria
- Immunocompetent patients with:
- Maternal/congenital infection with mild symptoms
Issues for Referral
Infectious disease consultant
ADDITIONAL READING
- American Academy of Pediatrics.
Red Book 2012 Report of the Committee on Infectious Diseases
. Elk Grove, IL: AAP; 2012.
- Centers for Disease Control and Prevention. Guidelines for prevention and treatment of opportunistic infections in HIV infected adults and adolescents.
MMWR
. 2009;58:1–207.
http://www.cdc.gov/mmwr/pdf/rr/rr58e324.pdf
.
- Jones JL, Dargelas V, Roberts J, et al. Risk factors for
Toxoplasma gondii
infection in the United States.
Clin Infect Dis.
2009;49:878–884.
- Kaplan JE, Benson C, Holmes KK, et al. Guidelines for prevention and treatment of opportunistic infections in HIV-infected adults and adolescents: Recommendations from CDC, the National Institutes of Health, and the HIV Medicine Association of the Infectious Diseases Society of America.
MMWR Recomm Rep.
2009;58:1–207.
- Sciammarella J. Toxoplasmosis. Available at
http://www.emedicine.com/emerg/topic601.htm
. Accessed on July 6, 2002.
CODES
ICD9
- 130.0 Meningoencephalitis due to toxoplasmosis
- 130.4 Pneumonitis due to toxoplasmosis
- 130.9 Toxoplasmosis, unspecified
ICD10
- B58.2 Toxoplasma meningoencephalitis
- B58.3 Pulmonary toxoplasmosis
- B58.9 Toxoplasmosis, unspecified
TRANSFUSION COMPLICATIONS
Philip Shayne
BASICS
EPIDEMIOLOGY
- Of 39 million hospital discharges in US, 5.8% (2.3 million) were associated with blood transfusions (2004).
- In 2011 there were 30 deaths in US fully attributable to transfusion complications.
- Some type of transfusion reaction occurs in 2% of units transfused within 24 hr of use.
- Noninfectious complications:
- Febrile nonhemolytic reaction: RBCs 1 in 500 transfusions, platelets 1 in 900
- Allergic reaction (nonanaphylactic): 1 in 3 to 1 in 300
- Anaphylaxis: 1 in 20,000 to 1 in 50,000
- Acute hemolytic reaction: 1 in 38,000 to 1 in 70,000
- Delayed hemolytic reaction: 1 in 4,000 to 1 in 11,000
- Transfusion-associated circulatory overload (TACO): 1 in 100, but as high as 10% in susceptible populations
- Alloimmunization: 1 in 10 to 1 in 100
- Graft-versus-host disease: 1 in 400,000; rare but has >90% mortality.
- Transfusion-related lung injury (TRALI): 1 in 5,000 to 1 in 190,000; represents 13% of reported transfusion-related deaths
- Iron overload: Unknown incidence, depends on volume of blood, often occurs after >100 RBC units
- Hypocalcemia: Unknown incidence
- Hyperkalemia: Unknown incidence
- Infectious complications:
- Bacterial contamination: RBCs 1 in 65,000 to 1 in 500,000; platelets 1 in 1,000 to 1 in 10,000:
- Most common bacterial agents:
Yersinia enterocolitica
,
Pseudomonas spp
,
Serratia spp
.
- Leading cause of mortality among infectious complications; 17–22% of all cases
- Hepatitis C: 1 in 1.6 million
- Hepatitis B: 1 in 100,000 to 1 in 400,000
- HTLV I and II: 1 in 500,000 to 1 in 3 million
- HIV: 1 in 1.4 million to 1 in 4.7 million
- HAV: 1 in 1,000,000
- B19 parvovirus: 1 in 40,000; post-transfusion anemia rare with scattered case reports
- Parasites:
Babesia
and malaria: <1 in 1 million
- Parasites:
Trypanosoma cruzi
: 1 in 42,000
- Case reports of Epstein–Barr virus, Lyme disease, brucellosis, human herpesvirus, Creutzfeldt–Jakob disease