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ELECTRONIC ARTICLE |
* Section of Critical Care
Section of Infectious Disease
Section of Cardiology, Department of Pediatrics, West Virginia University, Morgantown, West Virginia
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ABSTRACT |
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 TOP ABSTRACT CASE REPORTSDISCUSSIONCONCLUSIONREFERENCES |
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Key Words: Bordetella pertussis • pulmonary hypertension • hyperleukocytosis • extracorporeal life support • exchange transfusion
Abbreviations: PHT, pulmonary hypertension • ECLS, extracorporeal life support • WBC, white blood cell • FIO2, fraction of inspired oxygen • PaO2, arterial oxygen pressure • NO, nitric oxide
The constellation of bronchopneumonia, extreme leukocytosis, refractory hypoxemia, and pulmonary hypertension (PHT) is well described in severe Bordetella pertussis infection in infants.1,2 The onset of refractory hypoxemia typically is rapid3,4 and responds poorly to advanced ventilation maneuvers, including high-frequency oscillatory ventilation, inhaled nitric oxide, and extracorporeal life support (ECLS).5,6 The mechanism of hypoxemia and pulmonary hypertension in this setting is undetermined; however, several lines of evidence support leukocyte thrombi as the cause. White blood cell (WBC) counts >100 000 in the setting of B pertussis pneumonia are associated with increased mortality.7,8 A leukocyte thrombus in a pulmonary venule has been reported in a fatal case of B pertussis pneumonia.3 Finally, respiratory distress has been described in adults and children with hyperleukocytosis secondary to leukemia.9,10 In the last setting, respiratory distress has resolved after the application of techniques to reduce the leukocyte mass, including leukopheresis and exchange transfusion. We postulated that the application of a similar strategy to reduce leukocyte mass in the setting of B pertussis pneumonia, hypoxemia, and PHT may prevent additional thrombi formation and allow resolution of preexisting thrombi. We report the first use of a double volume exchange transfusion as a therapy for B pertussis pneumonia with PHT and hypoxemia and describe the improvements in oxygenation temporally associated with that therapy.
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CASE REPORTS |
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TOPABSTRACTCASE REPORTSDISCUSSIONCONCLUSIONREFERENCES |
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Her medical history includes preterm birth at 33 weeks via cesarean section as a result of placental abruption. She required mechanical ventilation for 1 week. Her total neonatal intensive care unit stay was 3 weeks. The patient had no surgical history and was not taking any medications. Immunizations given were the first dose of hepatitis B. Family history was significant for multiple family members with cough of 10 to 20 days' duration.
The patient's condition rapidly worsened, necessitating endotracheal intubation. The postintubation arterial blood gas had a pH of 7.18, PCO2 of 95 torr, and PO2 of 85 torr on FIO2 of 1.0.
The patient was referred to our intensive care unit with a presumptive diagnosis of B pertussis pneumonia and respiratory failure. On arrival, she was placed on pressure-control ventilation set at 24 cm of water, end expiratory pressure of 4 cm of water, with a rate of 30 breath/min and FIO2 1.0. Her temperature was 102° F, pulse was 189 beats/min, and blood pressure was 80/50 mm Hg. Lung examination demonstrated diffuse rales and wheezes throughout. Mottling and poor perfusion in her distal extremities responded to a 10-mL/kg bolus of 0.9% saline. Antibiotics were changed to piperacillin/tazobactam and azithromycin. Admission laboratory studies revealed a WBC count of 49 400/mm3 and a venous blood gas of pH 7.25, PCO2 70.3 torr, and PO2 38 torr. The FIO2 was decreased to 0.50 within 4 hours of admission based on pulse oximetry. Initial tracheal aspirate showed very rare WBCs, rare Gram-positive cocci in pairs, and many Gram-negative rods. The tracheal culture grew mixed Gram-negative rods, predominately Pseudomonas aeruginosa, for which gentamicin was added on hospital day 4. Viral cultures of a tracheal aspirate using a shell amplification technique with mink lung mixed cells and human lung carcinoma cells were negative for respiratory syncytial virus; adenovirus; influenza A and B; and parainfluenza 1, 2, and 3. Culture of tracheal secretions on Bordet-Gengou media yielded no growth. Polymerase chain reaction analysis of tracheal secretions demonstrated DNA of B pertussis.
The patient's chest radiograph worsened over the next 3 days, with an increase in the right apical opacity and consolidation in the left apex. The patient had increasing ventilatory requirements necessitating a change to pressure-regulated volume control. Frequent coughing and desaturation episodes were managed with increasing doses of sedatives. Ultimately, she required continuous infusions of fentanyl, midazolam, and vecuronium to maintain adequate oxygenation and ventilation. The patient's FIO2 requirement increased to 0.70 late on hospital day 2 in response to worsening oxygen saturations.
On hospital day 3 the patient's WBC count peaked at 104 000/mm3. An echocardiogram demonstrated dilation of the right ventricle with tricuspid regurgitation, flattened ventricular septum, leftward bowing of the atrial septum, and suprasystemic right ventricular pressure. An arterial catheter was placed. Arterial blood gas analysis demonstrated significantly impaired oxygenation with a arterial oxygen pressure (PaO2)/FIO2 ratio of 120. A repeat arterial blood gas 
3 hours later was essentially unchanged. Faced with the rapid progression of pulmonary dysfunction with severe pulmonary hypertension and the historically poor responses to aggressive support once hypotension and shock have occurred, we proposed a strategy to reduce the leukocyte mass. A double volume exchange transfusion was used, rather than leukopheresis, based on rapid availability within our institution. Parental consent was obtained.
The patient underwent an 800-mL double volume exchange transfusion, in 20-mL aliquots, using cytomegalovirus-negative, leukophor-filtered, irradiated packed red blood cells reconstituted to an estimated hematocrit of 45%. The procedure was performed in 2 hours and was well tolerated. Hypocalcemia was treated with a total of 180 mg/kg calcium chloride during the exchange. The post exchange WBC count fell to 15 200/mm3. The WBC count rose postexchange, peaking on post exchange day 3 at 76 500/mm3; however, the rate of rise was significantly slower than preexchange transfusion (data not shown).
The changes in oxygenation are presented in Fig 1. PaO2/FIO2 ratios during the 3 hours before exchange were stable and consistent with severe respiratory dysfunction (120 and 122). Midway through the exchange, the PaO2/FIO2 ratio had begun to improve (168). With the exception of 1 measurement obtained during a cyanotic spell at 7 hours postexchange, oxygenation continued to improve over the next 31 hours. Mean airway pressure remained 13 to 14 cm water throughout this period. An echocardiogram performed 24 hours after the exchange transfusion demonstrated qualitatively less flattening of the interventricular septum. The estimated right ventricular pressure remained essentially unchanged at 55% of the systemic pressure
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DISCUSSION |
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TOPABSTRACTCASE REPORTSDISCUSSIONCONCLUSIONREFERENCES |
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Once PHT and severe hypoxemia are established, the options for the treatment are limited. The use of nitric oxide (NO) has been described3,5; however, there are no published reports of the hemodynamic or oxygenation response to NO in this setting. Clinical infection with B pertussis is characterized by destruction of ciliated epithelial cells. Heiss et al13 and others have demonstrated that in the presence of tracheal cytotoxin produced by B pertussis, NO synthase is induced and NO is necessary to manifest the ciliated epithelial cell injury seen in the disease. We suggest that NO therefore must be used with caution in this setting. Furthermore, as a vasodilator, NO would be expected to have little effect if the causative basis of the hypoxemia and PHT is leukocyte thrombi in pulmonary capillaries and venules.
The use of ECLS has been described in several series of patients with B pertussis pneumonia, hypoxemia, and PHT. Pooboni et al5 reported a 58% mortality rate in 12 infants who had pertussis and received ECLS in a single British center. Halasa et al6 recently summarized Extracorporeal Life Support Organization's database for patients with a diagnosis of pertussis. Since 1990, 61 children with pertussis have been treated with ECLS, with an overall mortality rate of 70.5%. These reports likely represent the most salvageable cases, with many patients dying before being able to arrive at an ECLS center.
Respiratory distress associated with hyperleukocytosis is well described in the oncology literature. Vernant et al9 described 25 adults with leukemia, respiratory distress, and hyperleukocytosis. He noted that the appearance of respiratory symptoms paralleled the rise in leukocyte count. Thirteen patients died either before receiving therapies to acutely lower the WBC count or before the WBC count decreased. The remaining 12 patients received rapidly acting chemotherapy, and 6 of these patients, those with severe respiratory distress, received leukopheresis. In this series, the resolution of respiratory symptoms paralleled the fall in WBC count, and leukopheresis resulted in "spectacular" improvement in clinical symptoms of respiratory distress and hypoxemia.
Bunin et al10 described a series of children who had leukemia and hyperleukocytosis and were treated with exchange transfusion or leukopheresis. Three of 35 patients presented with respiratory distress, and all experienced improvement in their symptoms after cytoreduction therapy.
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CONCLUSION |
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TOPABSTRACTCASE REPORTSDISCUSSIONCONCLUSIONREFERENCES |
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FOOTNOTES |
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Reprint requests to (M.J.R.) PO Box 9214, Morgantown, WV 26506. E-mail: mromano{at}hsc.wvu.edu
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REFERENCES |
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TOPABSTRACTCASE REPORTSDISCUSSIONCONCLUSIONREFERENCES |
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This article has been cited by other articles:
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  J. Surridge, E. R Segedin, and C. C Grant Pertussis requiring intensive care Arch. Dis. Child., November 1, 2007; 92(11): 970 - 975. [Abstract] [Full Text] [PDF]
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 S. Mattoo and J. D. Cherry Molecular Pathogenesis, Epidemiology, and Clinical Manifestations of Respiratory Infections Due to Bordetella pertussis and Other Bordetella Subspecies Clin. Microbiol. Rev., April 1, 2005; 18(2): 326 - 382. [Abstract] [Full Text] [PDF]
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