Respiratory syncytial viral infection (RS) is the major cause of lower respiratory tract illness in children  . In infants less than 1 year of age and with lower respiratory infection, up to 80% are due to RS. For most children, an initial RS normally occurred within the first 2 years of life. Clinical manifestations range from mild upper respiratory tract infections to severe lower respiratory tract disorders such as bronchiolitis and/or pneumonia. Well-defined high-risk groups, including infants with prematurity, pre-existing lung disease, congenital heart disease, and immunodeficiencies are more likely to show a prolonged and severe course of RS   . Although some infants need assisted ventilation due to recurrent apnea or respiratory failure, the clinical course of RS is generally good, and some previous studies have shown low mortality rates of 2% - 5%, even for high-risk group patients    .
Acute respiratory distress syndrome (ARDS) secondary to RS has been described in some infants previously   . The disease entity defined as ARDS is an acute and severe parenchymal lung injury characterized by hypoxia, diffuse radiographic infiltrates, decreased pulmonary compliance, and pulmonary edema . The diversity of patients identified as having ARDS makes it difficult for epidemiological and clinical studies to evaluate mortality rates and risk factors, or to measure the benefit of therapeutic interventions including steroid therapy  . In contrast to the overall low mortality rates reported for infants with RS, published data report the mortality rate in pediatric patients with ARDS to be in excess of 24% .
We experienced three infants of RS and developed severe ARDS. Steroid pulse therapy was selected for the treatment of severe ARDS and the clinical course was favorable. The aim of this case report is to show the effectiveness of steroid pulse therapy and the usefulness of plasma surfactant protein D level (SP-D), a serum marker that rapidly and accurately reflects changes in oxygenation in infants with severe ARDS due to RS.
Case 1 was a 1-month-old girl. She had a nasal discharge from 4 days before admission, cough with dyspnea, and poor feeding that worsened days before admission. She was hospitalized with acute bronchopneumonia with hyper-infiltration and restricted regional atelectasis on the lower lobe of the right lung by chest X-ray. She showed retractive breathing, and crackles and wheezing were enhanced in all chest compartments. Vital signs were as follows: body temperature 38.4˚C, respiratory rate 32/min, and SpO2 90% in room air. Laboratory studies demonstrated elevated white blood cells (WBC) 19,100/μL, C-reactive protein (CRP) 4.1 mg/L, and lactose dehydrogenase (LDH) 506 U/L. T/B and NK cell analysis: CD4 37.8%, CD8 31.2%, CD19 15.0%, and CD56 11.2%. IgG/A/M levels were 993, 294, and 219 mg/dL, respectively. Chest computed tomography (CT) showed consolidation with air Broncho gram observed on both dorsal lungs. In addition, granular or patchy shadows were scattered, and thickening of bronchial bundles was recognized as cord-like shadows in the lower lobes of both sides. Invasive mechanical ventilator management was started the day after admission. The partial pressure of arterial oxygen (PaO2)/fraction of inspiratory oxygenation (FiO2) ratio was 142, and KL-6 and SP-D levels were 1304 U/mL and 118 ng/ml, respectively (Table 1). On day 9
Table 1. Changes in KL-6 levels and surfactant protein D levels before and after steroid pulse therapy. KL-6 levels and surfactant protein D levels were associated with the partial pressure of arterial oxygen/fraction of inspiratory oxygenation ratio in all patients before and after steroid pulse therapy. Surfactant protein D levels changed rapidly in parallel with the partial pressure of arterial oxygen/fraction of inspiratory oxygenation ratio; however, KL-6 changes were slightly delayed in all cases. At discharge, surfactant protein D levels in all cases had recovered to normal although KL-6 levels were still high.
*Invasive mechanical ventilation; †Steroid Pulse Therapy; ‡Extubation and non-invasive ventilation; §Discharge; NA: not applicable.
after onset, KL-6 and SP-D levels increased to 1475 U/mL and 177 ng/ml, and the PaO2/FiO2 ratio was reduced to 122. Steroid pulse therapy was started on day 9 after onset.
Case 2 was a 1-year 11-month-old girl with Dandy-Walker syndrome. She was admitted to hospital on day 4 after onset with worsening severe cough, and a loss of appetite for 3 days. Vital signs were as follows: body temperature 37.6˚C, respiratory rate 28/min, and SpO2 89% in room air. Laboratory studies demonstrated elevated WBC of 15,500/μL, CRP 1.5 mg/L, and LDH 310 U/L. Blood tests for immune system components at a previous hospitalization did not show any abnormalities. The amount of IgG was age-appropriate. Because respiratory conditions including retractive breathing gradually worsened, non-invasive ventilator management with a high-flow nasal cannula was started on the day of admission. The day after admission, her respiratory rate was 32/min and there was less wheezing and crackling in the lower chest compared with that at admission. Chest CT showed a large air space along the bottom of the lungs, the mediastinum, and the hilum. An area of increased concentration centered on consolidation with the air Broncho gram spread segmentally into the dorsal part of both lungs. In addition, light ground-glass opacity was diffuse as seen from the hilum (Figure 1). Due to the rapid progressive deterioration of respiratory conditions, invasive mechanical ventilator management was started. Six days after onset, the PaO2/FiO2 ratio rapidly decreased to 112, and KL-6 and SP-D levels were markedly increased at 2003 U/mL and 212 ng/ml, respectively (Table 1). Steroid pulse therapy was started on day 6 after onset.
Case 3 was a 1-year 5-month-old girl with a vertebral defect, anal atresia, cardiac malformations, tracheoesophageal fistula with esophageal atresia, radial dysplasia, renal dysplasia, and limb anomaly (VACTERL association). She had a dry cough for 4 days. Five days after onset, her respiratory condition gradually worsened, and she was hospitalized because of dyspnea. Vital signs were as follows: body temperature 38.1˚C, respiratory rate 32/min, and SpO2 88% in room air. Laboratory studies demonstrated WBC 8900/μL, CRP < 0.1 mg/L, and KL-6 296 U/mL. T/B and NK cell analysis: CD4 35.0%, CD8 22.3%, CD19 15.1%, and CD56 34.0%. IgG/A/M levels were 582, 42, and 97 mg/dL, respectively. Chest CT showed ground-glass shadows or shadows with Broncho gram dominating the dorsal predominance of both lungs. Lung field consolidation indicated strong inflammation (Figure 2). Six days after onset, retractive breathing had worsened, and invasive mechanical ventilation management was started. Seven days after onset, her PaO2/FiO2 ratio had reduced to 156, wheezes were heard in all chest compartments, and KL-6 and SP-D levels were elevated to 2889 U/mL and 451 ng/ml, respectively (Table 1). Steroid pulse therapy started on day 7 after onset.
Figure 1. Case 2, Chest CT image on day 4 after onset. A large air space is observed along the bottom of the lungs, the mediastinum of the mediastinum, and the hilum. An area of increased concentration centered on consolidation with air bronchogram spreads segmentally in the dorsal part of both lungs. In addition, light ground-glass opacity is diffusely seen from the hilum.
Figure 2. Case 3, Chest CT image on day 5 after onset. Ground-glass shadows or even shadows with bronchogram dominate the dorsal predominance of both lungs. Lung field consolidation reflects strong inflammation.
All cases of IgG/A/M levels were age-appropriate and normal ranges of T/B and NK cell subsets were observed. Due to a serious deterioration of respiratory status in all cases, immunodeficiency tests for infection were performed and Pneumocystis jirovecii antigen, HIV Ab/Ag, and β-D-glucan were negative. Antibody measurement with preserved serum demonstrated no co-infection with cytomegalovirus, Legionella, Chlamydia, or Mycoplasma. Echocardiographic findings and blood tests indicated no acute left ventricular cardiac dysfunction or fluid overload upon Pediatrics Intensive Care Unit (PICU) admission. For all cases, viral antigen was detected using a rapid diagnosis kit with a nasal aspiration on the day of admission. In addition, viral gene detection was performed using a one-step RT-PCR standard protocol in Cases 1 and 3. We diagnosed all patients with severe acute respiratory distress syndrome (ARDS) due to RS on the basis of no left heart failure, a PaO2/FiO2 ratio less than 200, and bilateral lung infiltration. Invasive mechanical ventilator management was performed with the aim of improving respiratory support and oxygenation with lung protection after admission. The effectiveness of steroid treatment for ARDS is controversial, depending on when it is started and the amount used. Because of a rapid respiratory deterioration including poor oxygenation, steroid pulse therapy consisting of methylprednisolone 30 mg/kg body weight was continuously administered for 3 days, and then post-treatment with 2 mg/kg was used for 4 days for a total of 7 days as one course. Case 2 post-treatment was extended by one week, and Case 3 was given two courses of steroid therapy. In all cases, steroid pulse therapy was considered to have been highly effective. Clinical symptoms and most laboratory markers improved, even when the clinical course was severe at admission, and returned to normal levels before discharge.
SP-D is mainly synthesized by type II pneumocytes and is an important component of innate pulmonary immunity. Sato et al. reported that adult ARDS patients who died had higher KL-6 levels than survivors . SP-D reflectability of the condition is considered to be generalizable to adults and pediatric ARDS general  - . Changes in SP-D and KL-6 levels before and after steroid treatment were marked, and altered SP-D levels suggested sensitive changes in the interstitial damage of the alveolar epithelial lining, including type II alveolar epithelial cells. This is because changes in SP-D levels paralleled changes in the PaO2/FiO2 ratio without any time lag in all cases. KL-6 levels continued to increase for several days, even after the recovery of oxygenation following steroid treatment. The hypothesis that there is a time lag in serum values between KL-6 and SP-D in infants with ARDS by RS is considered as follows. First, this might be related to differences in the molecular size of SP-D and KL-6. SP-D has a molecular weight of about 500 kDa, whereas KL-6 is much larger, >5000 kDa . SP-D, which has a small molecular size, moves easily from the damaged tissue to the circulating blood, and therefore might better reflect tissue damage without a time lag. Second, the physiological environment for each factor is different. SP-D is a secreted protein and KL-6 is a cell membrane protein . KL-6 can only enter the blood when it is cleaved from the cell membrane via a protease activated by inflammation, suggesting its entry to the blood is slightly delayed. Third, KL-6 and SP-D are produced by type II alveolar epithelial cells; however, KL-6 is also produced by bronchial glands and SP-D is also produced by Clara cells. Differences in KL-6 and SP-D changes may also be related to the number of Clara cells and bronchial glands present. For these reasons, we considered SP-D levels were more sensitive to the pathological conditions than KL-6 levels. SP-D might be a biomarker to evaluate the effect of steroid pulse therapy and associated improvement in oxygenation for ARDS patients due to RS.
Kawasaki et al. reported that at the time of discharge, SP-D levels in infants with acute bronchiolitis due to RS did not recover to normal levels and were similar to those at admission . SP-D levels were maintained until the time of discharge suggesting acute bronchiolitis due to RS continued to promote a partial inflammatory response even during the recovery period. In our cases, SP-D levels decreased to normal after steroid pulse therapy, even in severe ARDS cases, suggesting steroid pulse therapy reduced the inflammation of tissues and cells in which SP-D was present.
No previous reports have evaluated changes in the biomarkers SP-D during the clinical course of infants with ARDS due to RS who were successfully treated with steroid pulse therapy.
Written Informed consent obtained from all patients’ parents.
D. T. contributed to diagnosis management; S. I., T. O., and A. O. also contributed to treatment management; T. Y. provided expert clinical opinion; D. T. wrote the manuscript; S. I., T. O. A. O. and T. Y. clinically reviewed the manuscript and gave technical support. All authors read and approved the final manuscript.
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