Hemoglobin
Transient Red Cell Aplasia
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Transient Red Cell Aplasia
, Aplastic Crisis in Sickle Cell Anemia
See Also
Sickle Cell Anemia
Acute Chest Syndrome
Acute Vaso-Occlusive Episode in Sickle Cell Anemia
Aplastic Crisis in Sickle Cell Anemia
Cerebrovascular Accident in Sickle Cell Anemia
Dactylitis in Sickle Cell Anemia
(
Hand Foot Syndrome in Sickle Cell Anemia
)
Hematuria in Sickle Cell Anemia
Osteomyelitis in Sickle Cell Anemia
Priapism in Sickle Cell Anemia
Pulmonary Hypertension in Sickle Cell Anemia
Septic Arthritis in Sickle Cell Anemia
Sickle Cell Anemia Related Pulmonary Hypertension
Sickle Cell Anemia with Splenic Sequestration
Pathophysiology
Parvovirus B19
infection interrupts
Red Blood Cell
production by affecting erythroid precursors in marrow
Results in high
Red Blood Cell
turn-over
Differential Diagnosis
Sickle Cell Hemolytic Crisis
Splenic Sequestration
Symptoms
Weakness
Shortness of Breath
Fever
Signs
May be fully compensated with normal
Heart Rate
and
Blood Pressure
Pallor
Tachycardia
Hypotension
Labs
Hemoglobin
decreased from baseline
Reticulocyte Count
decreased (approaches 0)
Secondary to decreased
Red Blood Cell
production despite acute
Anemia
Contrast with Sickle Cell Hemolytic Crisis and
Splenic Sequestration
where the
Reticulocyte Count
is increased
Differential Diagnosis
Septic Shock
Splenic Sequestration
Management
Admit with isolation droplet precautions (due to
Parvovirus B19
)
Avoid exposing pregnant women
Consult hematology
Intravenous Immunoglobulin
(IVIG)
Blood Transfusion
may be needed
Blood should be cross-matched,
Leukocyte
depleted, and irradiated
If stable, avoid
Fluid Overload
by slow infusion over 4 hours
Plan to raise
Hemoglobin
by 1 g/dl
Course
Aplasia typically resolves over 1-2 weeks
After infection resolution,
Immunity
to
Parvovirus B19
reduces risk of recurrent aplastic crisis
References
Glassberg and Weingart in Majoewsky (2012) EM: Rap 12(8): 5-6
Lowe and Wang (2018) Crit Dec Emerg Med 32(11): 17-25
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