ABSTRACT
Conclusion:
An increase in serum BNP levels may be seen in patients with moderate to severe bronchiolitis without myocardial dysfunction. It was argued that this BNP increase may be related to the degree of deterioration of gas exchange associated with the disease. Plasma BNP level is a potential prognostic factor in moderate to severe bronchiolitis.
Results:
The mean basal plasma BNP level in the patients was significantly higher than in controls (61.75±65 pg/mL vs. 13.99±8.79 pg/mL; p=0.001). There was no significant difference in ejection fraction and fractional shortening values between the patients with normal and high BNP levels and controls (p>0.05). Patients with high BNP levels had higher mean partial carbon dioxide values than patients with normal BNP levels (p=0.037). There was a positive correlation between plasma BNP level and length of hospital stay (r=0.286; p=0.007) and intensive care unit stay (r=0.645; p=0.000).
Methods:
The study was conducted prospectively on 37 patients aged 1-24 months with a modified Wang respiratory score of 6 and above and diagnosed with bronchiolitis. The patients with high (>100 pg/mL, n=6) and normal (≤100 pg/mL, n=31) serum BNP levels were compared in terms of left ventricular systolic functions, and vital, laboratory, and radiological findings. The relationship between serum BNP level and prognosis was evaluated.
Introduction:
We have limited information about the clinical importance of plasma B-type natriuretic peptide (BNP) level and its prognostic value in children with bronchiolitis. In this study, we aimed to determine basal plasma BNP levels and their relationship with left ventricular systolic functions and prognosis in patients hospitalized with moderate to severe bronchiolitis.
Introduction
Acute bronchiolitis is the most common lower respiratory tract disease seen during infancy. It has been reported that although the frequency is not fully known, cardiac involvement may develop at varying degrees during this disease, which is caused by numerous viral agents, mainly respiratory syncytial virus (RSV). It is known that cardiac damage can occur in different degrees of severity, ranging from subclinical electrical and functional myocardial dysfunction to severe conduction disorders and widespread myocardial injury.1-5 Therefore, it is very important that the cardiac involvement which can develop in patients with acute bronchiolitis is not clinically overlooked and that it is detected early.
Symptoms and signs such as tachypnea, tachycardia, loss of appetite and fatigue, which are among the clinical findings of heart failure, can be seen in many patients diagnosed with bronchiolitis. Differential diagnosis of heart failure may become more difficult in patients with accompanied pneumonia who manifest rales in pulmonary auscultation. In recent years, plasma B-type natriuretic peptide (BNP) has been used more widely as a specific biomarker in the diagnosis of acute cardiac diseases and evaluating the prognosis and response to treatment in pediatric patients as well as in adults.6-11 Aside from heart diseases, BNP plasma levels have also been found to be elevated in acute bronchiolitis, which is involved in the differential diagnosis of dyspnea.11,12 However, our knowledge on the relation of BNP with prognosis in patients with isolated acute bronchiolitis is quite limited.
This study was conducted to determine the baseline plasma BNP levels, to assess the relationship between left ventricular systolic functions and plasma BNP levels, and to investigate the prognostic value of plasma BNP level in children aged 1 to 24 months who were diagnosed as having moderate to severe isolated bronchiolitis without additional disease in a pediatric emergency unit of a tertiary care hospital.
Materials and Methods
The present study was conducted prospectively on 37 patients hospitalized due to moderate-severe bronchiolitis during three bronchiolitis seasons between 2014 and 2017. This study was approved by the ethics committee of the hospital (İstanbul Medeniyet University Göztepe Training and Research Hospital, decision number: 2014/0132, date: 26.08.2014). Before enrollment in the study, parents of all patients were informed in detail about the study and their consent was obtained.
The diagnosis of bronchiolitis was made by evaluation of criteria including wheezing, restlessness, feeding difficulties, tachypnea, use of auxiliary respiratory muscles (all starting as prodromal symptoms of upper respiratory tract infection) in infants between 1 and 24 months of age and history of contact with an infected person or staying in day care homes.13 Modified Wang breathing score was used to determine the severity of the bronchiolitis. The respiratory score was evaluated as ≤5 points: mild, 6-10 points: moderate, and 10 points: severe bronchiolitis (see Appendix).14,15 Criteria for inclusion were as follows: patients who were between 1 and 24 months of age, who had bronchiolitis for the first time, and who had a modified Wang respiratory score of 6 or more. Those who were younger than 1 month and older than 24 months, who had a modified Wang respiratory score of less than 6, who had a history of prematurity, recurrent wheeze episodes or were diagnosed with asthma, who had acute or chronic renal insufficiency, a known or newly diagnosed structural cardiac disease, chronic pulmonary disease (such as cystic fibrosis, bronchopulmonary dysplasia), thyroid or pituitary gland disease, neuromuscular disease, and who received recent steroid treatment were excluded from the study. The demographic characteristics, physical examination findings, modified Wang respiratory scores, RSV results in nasopharyngeal swab, vital signs, basal plasma BNP levels, capillary blood gas, complete blood count (CBC), C-reactive protein and biochemical test results, pathological findings on chest X-ray (such as atelectasis, pneumonic infiltration, air leak), echocardiographic measurements, treatments given, length of hospital stay, and outcomes of each patient were recorded. The chest X-rays of all patients were evaluated as single blind by a pediatric radiologist.
Basal plasma BNP levels of the patients were measured. The patients with high (>100 pg/mL) and normal (≤100 pg/mL) serum BNP levels were compared in terms of left ventricular systolic functions, and vital, laboratory, and radiological findings. To compare plasma BNP results, a “BNP control group” was created by using plasma residues of previously healthy 52 children aged between 1 and 24 months, who were admitted to the pediatric outpatient clinics before elective minor surgery and for whom a routine blood test was ordered by the physician. To compare echocardiographic measurement results of patients in the study group, echocardiographic measurement results of 40 healthy children were used; these control subjects were similar in age and were previously referred to the pediatric cardiology outpatient clinic because of innocent murmur and no structural or functional cardiac problems were found.
Sampling and Study Technique for Plasma BNP Level
The blood sample required for the measurement of plasma BNP levels of the patients was obtained at the time of access to the intravenous line and during drawing blood for the tests during the emergency room follow-up without any additional intervention and blood collection. Residues of blood drawn into vacuumed ethylene diamine tetraacetic acid tube for CBC were centrifuged at 4000 rpm/10 min and frozen at -80 °C in the biochemistry laboratory. Plasma samples, collected from 37 patients, and 53 controls, were dissolved and the plasma BNP measurements were performed by the chemiluminescence microparticle immunoassay method by an Abbott architect ci4100 biochemistry autoanalyser using a 100-well Abbot Architect BNP Reagent Kit. 100 pg/mL was accepted to be the plasma BNP threshold value.
Sampling and Study Technique for RSV Antigen
RSV antigen examination of nasopharyngeal swabs was performed at bedside using a BD Directigen EZ RSV kit during emergency room follow-up. The results were obtained within 5-60 minutes.
Echocardiography Examination and Echocardiographic Measurements
Echocardiographic evaluations of the patients were performed by a pediatric cardiologist using a General Electric Vivid model echocardiography device with M mode 2-D Color Doppler method within the first 24 hours following the emergency department admission. Left ventricular end-diastolic diameter (LVEDd) and left ventricular end-systolic diameter (LVISd) were measured using parasternal long axis M mode. The ejection fraction (EF%) and the fractional shortening (Fs%) indicating left ventricular systolic functions were calculated automatically by the Teicholz formulation using the LVEDd and LVISd parameters (16).
Statistical Analysis
Demographic characteristics such as age and sex of the study and control groups were determined and comparison was made between the groups. The mean plasma BNP values in the study group and the healthy control group were determined and compared. The patients in the study group were divided into two subgroups of patients with normal BNP levels (≤100 pg/mL) and patients with high BNP levels (>100 pg/mL), and vital findings, laboratory results, and radiological findings were compared. Echocardiographic measurements (EF%, Fs%) were compared between the study subgroups and the healthy control group. The relationship of plasma BNP level with intensive care need, length of intensive care unit stay, total length of hospital stay, need for noninvasive/invasive mechanical ventilation, and in-hospital mortality were investigated. IBM SPSS Statistics 22 for statistical analysis (SPSS IBM, Turkey) program was used for evaluation of the findings obtained in this study. The normal distribution of parameters was analyzed by the Shapiro-Wilk test when the study data were evaluated. In the comparison of the descriptive statistical methods (mean, standard deviation) as well as the quantitative data, the Kruskal-Wallis test was used for comparison of non-normally distributed parameters between the groups and the Mann-Whitney U test was used for the determination of the group causing the difference. The Student’s t-test was used for the comparison of normally distributed parameters between two groups and the Mann-Whitney U test was used for comparison of two groups with non-normal distribution parameters. Chi-square test, Fisher’s exact test, Fisher-Freeman-Halton test and Continuity (Yates) correction were used for the comparison of qualitative data. Spearman’s rho correlation coefficient was used in the analysis of the relationships between the parameters. Significance was evaluated at the level of p<0.05.
Results
Twenty-three (62.2%) of the 37 patients in the study group were male, 14 (37.8%) were female and the mean age was 6.19±4.94 months. Forty-two cases in the healthy control group (45.7%) were female, 50 (54.3%) were male and the mean age was 7.44±3.85 months. There was no difference between the study and control groups in terms of age and gender (p>0.05).
Although the mean plasma BNP level in the patients was within the normal limits, it was significantly higher than in the control group (p=0.001, p<0.05) (Table 1). There was no clinical evidence of cardiac failure in the patients, and cardiomegaly was not detected on chest X-rays. Electrocardiography examinations showed no rhythm disturbances other than transient sinus tachycardia. Echocardiographic examination showed no left ventricular systolic dysfunction in any of the patients. There was no significant difference in EF% and Fs% mean values between the study and the healthy control groups (p>0.05) (Table 2). Similarly, no significant difference was found in EF% and Fs% values between healthy controls and patients with normal (≤100 pg/mL) and high (>100 pg/mL) BNP levels (p>0.05) (Table 3). There was no correlation between BNP levels and EF% and Fs% measurements of the patients (r=-0,065, p=0,704 and r=-0,002, p=0,989, respectively).
The mean age of the patients with high plasma BNP levels was lower than those with normal BNP levels (p=0.018, p<0.05). However, there was no significant correlation between BNP level and age in the correlation analysis (r=0.083, p=0.439). There was no sex difference between patients with normal and high BNP levels (p>0.05).
There were no differences in respiratory rate, heart rate, oxygen saturation, body temperature, blood pressure, modified Wang respiratory score, chest X-ray findings, RSV positivity in nasal swabs, CBC, and biochemical values between the patients with normal and high plasma BNP levels (p>0.05). However, patients with high BNP levels had lower mean blood pH values and higher mean partial carbon dioxide (pCO2) values in blood gas analysis (Table 4).
There was no difference between the groups in terms of noninvasive and invasive mechanical ventilation requirements and in-hospital mortality when the patients with normal and high plasma BNP levels were compared with regard to disease course. The mean length of hospital stay in patients with higher BNP levels was longer than in patients with normal BNP levels, however, this difference was not statistically significant. Similarly, although the mean length of intensive care unit stay was longer in the group with higher BNP levels, this difference was not statistically significant (Table 5). However, correlation analysis revealed that there was a strong positive correlation between BNP level and length of hospital and intensive care unit stay (r=0.286, p=0.007 and r=0.645, p=0.000, respectively).
Discussion
Studies in the literature on plasma BNP levels in the pediatric population have been conducted mainly on the differential diagnosis of pulmonary diseases and cardiac diseases, monitoring the response of cardiac disease to treatment and prognosis.9,17,18 The number of studies evaluating BNP levels in primary lung diseases, such as bronchiolitis, is very scarce. We evaluated the relationship of basal plasma BNP levels with left ventricular systolic functions and disease prognosis in 37 patients with moderate to severe bronchiolitis who did not have any comorbidity. The mean BNP level in the patients was approximately four and a half times higher than in healthy children. Mild plasma BNP level elevation was found in six of the 37 patients (16.21%). Echocardiography revealed no left ventricular systolic dysfunction in any of the patients. There was no statistically significant difference in EF% and Fs% values between the patients with normal and high BNP levels. This result suggests that an increase in plasma BNP levels may develop without myocardial dysfunction in patients with isolated acute bronchiolitis. Daneshmand et al.12 evaluated how N-terminal-proBNP, which is released from the ventricles in response to increased ventricular end-diastolic volume and pressure, is affected in patients with acute bronchiolitis. It was proposed that in these patients, preload of the left and right atria would be reduced due to systemic venous return associated with pulmonary hyperinflation and low levels of BNP would be found. However, plasma N-terminal-proBNP levels were found to be elevated from the time of admission until the end of the fifth day. Consistent with our results, the mean baseline N-terminal-proBNP values in 27 bronchiolitis patients were significantly (approximately two-fold) higher than in the controls. However, no comment was made about the reasons for this elevation and, the cardiac functions of the patients were not evaluated. In another study, baseline plasma BNP levels in 68 patients who were admitted to emergency unit with respiratory distress, of whom 49 had isolated bronchiolitis and 19 had congenital heart disease and bronchiolitis, were compared with that in controls. Similar to the results of our study, a slight increase in mean the plasma BNP level was found in patients with isolated bronchiolitis. However, the mean BNP level in patients with congenital heart disease and associated bronchiolitis was significantly higher than in those with isolated acute bronchiolitis. There was no correlation between plasma BNP levels of patients and respiratory rate, oxygen saturation, length of hospital stay and respiratory score.11 In our study performed on patients with isolated bronchiolitis only, no relationship of plasma BNP level with respiratory score and vital findings (body temperature, respiratory rate, heart rate, blood pressure, and oxygen saturation) was found. However, it is noteworthy that patients with higher BNP levels had higher mean pCO2 values in the baseline blood gas analysis. Therefore, it is thought that BNP increase without myocardial dysfunction may be related to disease-related pulmonary involvement and impairment in the gas exchange.
In studies comparing the mean plasma BNP levels between healthy children and children who were admitted to the hospital with respiratory distress, BNP levels were slightly higher in children with pulmonary disease than in healthy controls, as in our study. However, the plasma BNP increase in acute cardiac diseases has been found to be much higher than the increase seen in pulmonary diseases.17,18 Evim et al.18 reported that a plasma BNP level of 726 pg/mL was the threshold value for differential diagnosis of heart failure and pulmonary diseases. Nevo et al.19 showed that mean plasma N-terminal proBNP levels in children with noncardiac diseases such as gastroenteritis, dehydration, and infectious diseases were significantly higher than in healthy children, but significantly lower than in children with cardiac diseases. It has been postulated that BNP release from myocytes might be induced as a result of increased cardiac output due to fever, and increased levels of circulating proinflammatory cytokines and stress hormones may stimulate BNP synthesis in these children. In our study, 6 of 37 patients (16%) had fever, but no significant difference was found in body temperature between patients with high and normal plasma BNP level.
There are adult studies showing increased plasma BNP levels without left ventricular systolic dysfunction in patients with systemic inflammatory response, sepsis, and septic shock.20-22 Although unclear, it is believed that lipopolysaccharide and proinflammatory cytokines may increase BNP transcription and translation by direct toxic effect on cardiomyocytes.23 In our study, manifestations of clinical shock were not found in any of the patients. No difference was found between the patients with high and normal plasma BNP levels in terms of blood pressure, heart rate, and plasma lactate levels, which are indicative of hemodynamics and tissue perfusion. However, it is known that many viral agents, such as RSV, can activate proinflammatory cytokines in acute bronchiolitis.22,24-26 Therefore, it is thought that stimulation of cytokines due to viral factors may play a role in the increase of plasma BNP level in our cases.
Another important cause of increased plasma BNP levels involves the conditions where renal clearance is decreased. It has been shown that BNP levels are increased in patients with renal dysfunction.27,28 It was thought that the increase in BNP was not due to renal origin since the children with renal disease had been excluded from our study, and absence of differences in urea and creatinine values between patients with high and normal BNP levels.
It has been shown that plasma BNP levels increased in parallel with disease severity in adult patients with pneumonia in the absence of heart failure. BNP levels were also found to be powerful predictors of death, treatment failure and short- and long-term mortality for adult patients with community-acquired pneumonia.29,30 Knowledge on the effect of BNP on prognosis in children with isolated bronchiolitis without myocardial dysfunction is very limited. In only a recent study on patients who were admitted to emergency room for acute isolated bronchiolitis, it was reported that clinical severity score and plasma BNP levels were independent risk factors for hospital admission, and there was a positive correlation between BNP levels and length of hospital stay.31 Our study included patients who were hospitalized with the diagnosis of moderate-severe isolated bronchiolitis. When the patients were evaluated for prognosis, there was no relationship of plasma BNP level with intensive care unit admission, noninvasive/invasive mechanical ventilation need and duration, and in-hospital mortality. However, there was a strong positive correlation between plasma BNP levels and length of total hospital and intensive care unit stay.
Study Limitations
In our study, serial plasma BNP measurements were not performed. For this reason, no comment was made on the change in BNP levels during the disease course. To compare EF% and Fs% measurement results of the patients, the results of echocardiography were used retrospectively in healthy children who had been addressed by the innocent murmur in the pediatric cardiology department and who did not have any structural or functional cardiac problems. These patients did not have simultaneous plasma BNP measurements. Therefore, for comparison of BNP values, a separate control group had to be formed by using plasma residues of healthy children of similar ages. The patients were evaluated only for left ventricular systolic function and no comment was made on right ventricular function and its relation with plasma BNP level.
Conclusion
Increased plasma levels of BNP can be seen without myocardial dysfunction in patients with acute isolated bronchiolitis. This increase may be related to disease-related pulmonary changes and impaired gas exchange. A positive relationship between plasma BNP levels and length of hospital stay and intensive care unit stay suggests that BNP is a potential prognostic marker in patients with moderate to severe bronchiolitis.