Cold hemolytic anemia: a rare complication of influenza A

Autoimmune hemolytic anemia (AIHA) is characterized by the temperature at which the auto-antibody has the greatest avidity for the target red cell antigen, either warm or cold forms. It is detected by a positive direct antiglobulin test (DAT) also known as the direct Coombs test. DAT is used to determine if red cells have been coated in vivo with immunoglobulin, complement, or both.¹ Some causes of a positive DAT include hemolytic transfusion reactions, hemolytic disease of the fetus and newborn, AIHA, and drug-induced immune hemolysis.

Case presentation and summary

A 58-year-old woman from Brazil with past medical history only significant for cholecystectomy and cesarean section had been visiting in United States for 2 months when she presented to an outside hospital with fever, shortness of breath, and syncope that had resulted in a foot injury. She reported she had been feeling short of breath and had a nonproductive cough and malaise for about 2 weeks before presentation with sick contacts at home. On admission it was noted that she had a hemoglobin level of 7.7 g/dL (normal, 12.0-15.5 g/dL; MCV, 94 fL), total bilirubin of 2.14 mg/dL (normal, 0.2-1.0 mg/dL), and lactate dehydrogenase of 523 U/L (normal, 81-234 U/L). There were no signs of bleeding on her examination. Her DAT was positive and moderate red blood cell agglutination was reported. During the first admission at the outside hospital she was diagnosed with influenza A and completed a full course of oseltamivir (75 mg po twice daily for 5 days). A chest X-ray was negative for infiltrates and showed that the patient’s lung fields were clear. She was transfused 2 units of packed red blood cells with response in hemoglobin up to 9.8 g/dL. The patient was treated with dexamethasone (4 mg IV Q8) as an inpatient and was discharged on a prednisone taper (40 mg, with taper by 10 mg every 3 days) with hemoglobin of 8.1 g/dL.

The patient continued to have nonproductive cough, dyspnea, fevers, chills, and generalized weakness, when she returned to the same outside hospital’s emergency department 2 days after her discharge. At that time, it was noted that she had leucocytosis (white blood cell count, 34.6 x 10⁹ per L), a hemoglobin level of 6.8 g/dL, and her total bilirubin level was 6.9 mg/dL. Her hemodynamics were unstable and she was admitted to their intensive care unit. The results of a chest X-ray revealed right lung consolidation.

The day after this admission, her hemoglobin level fell to 4.7 g/dL, and she was transfused 2 units of packed red blood cells before being transferred to our hospital. A chest X-ray at our hospital confirmed a right lung infiltrate. Vancomycin (1,250 mg IV Q12), levaquin (750 mg IV Q24), and maxipime (1 g IV Q12) were initiated for pneumonia and the patient was transferred to our hospital’s intensive care unit. She was afebrile at 98.3°F, her pulse rate was 84 beats per minute, she was tachypneic with respiratory rate of 26 breaths per minute, her blood pressure was 98/51 mmHg, and she had an oxygen saturation of 99% on 2L oxygen via nasal cannula.

On physical examination she was noted to have scleral icterus and was in mild respiratory distress. A chest X-ray revealed a patchy opacity in the right mid to lower lung. Her initial complete blood panel revealed anemia, with hemoglobin, 6.3 g/dL; white blood cell count, 27 x 10⁹ per L; and platelets, 533 x 10⁹ per L. The patient was then transfused another 2 units of packed red blood cells. She was given intravenous hydration, acetaminophen, and albuterol nebulizer treatments as supportive care. She was provided with blankets to keep warm. In addition to her antibiotics, she was also given prednisone 70 mg for her respiratory symptoms.

Further tests revealed haptoglobin, <30 mg/dL (normal, 36-195 mg/dL); lactate dehydrogenase, 371 U/L (normal, 98-192 U/L); and complements C3, 90 mg/dL (normal, 79-152 mg/dL) and C4, <8 mg/dL (normal, 18-55 mg/dL). Her DAT was positive, and agglutination was seen on peripheral smear (Figure 1). This was her second positive DAT as she had positive one at the outside hospital initially. Her tests for mycoplasma pneumonia, the PCR and IgM, were negative, as were the Monospot for mononucleosis and the ANA for autoimmune disorders. Her cold agglutinin titer was 1:256 (normal, no agglutination <1:64). The patient’s repeat respiratory viral panel was negative given recent full treatment for her influenza A at the previous hospital. Her blood and urine cultures were negative.

The patient was given antibiotics (vancomycin 1,250 mg IV Q12, cefepime 2 g IV Q8, and azithromycin 500 mg daily) for her pneumonia. Her respiratory status improved, and she was transferred to general medical floors after the first day of her admission. Her total bilirubin trended down to 1.9 mg/dL. She remained on prednisone 70 mg daily.

The patient remained in the hospital for an additional 6 days before being discharged home on prednisone. She wanted to return to her home country of Brazil as soon as she was able to and said she would seek outpatient follow-up there with a hematologist. At the time of her discharge, her hemoglobin was 6.6 g/dL and her reticulocyte count, 6.0%. Figures 2 and 3 illustrate her hemoglobin and reticulocyte trend during her admission at our hospital.