key: cord-0015892-d8wxw925
authors: Oh, Seong Hee; Lee, Byong Sop; Jung, Euiseok; Oh, Moon Yeon; Do, Hyun-Jeong; Kim, Ellen Ai-Rhan; Kim, Ki-Soo
title: Plasma B-type natriuretic peptide cannot predict treatment response to ibuprofen in preterm infants with patent ductus arteriosus
date: 2020-03-10
journal: Sci Rep
DOI: 10.1038/s41598-020-61291-w
sha: 93919310c6c1ab6024846c9584df92bac5964c58
doc_id: 15892
cord_uid: d8wxw925

Plasma B-type natriuretic peptide (BNP) is a useful marker for diagnosis of hemodynamically significant PDA (hsPDA) and serial BNP measurement is also valuable for monitoring treatment response. This retrospective study was performed to evaluate whether plasma BNP level can predict treatment response to ibuprofen in preterm infants born at <30 weeks of gestation with hsPDA. Plasma BNP was measured before (baseline) and 12 to 24 h after (post-treatment) completion of the first (IBU1) and second (IBU2) course of ibuprofen. We compared the BNP levels of responders (closed or insignificant PDA) with those of non-responders (hsPDA requiring further pharmacologic or surgical closure) to each course of ibuprofen. The treatment response rates for IBU1 (n = 92) and IBU2 (n = 19) were 74% and 26%, respectively. In IBU1, non-responders had lower gestational age and birth weight than responders (both, P = 0.004), while in IBU2, non-responders had lower birth weight (P = 0.014) and platelet counts (P = 0.005) than responders; however, baseline BNP levels did not differ significantly between responders and non-responders in either IBU1 (median 1,434 vs. 1,750 pg/mL) or IBU2 (415 vs. 596 pg/mL). Post-treatment BNP was a useful marker for monitoring treatment efficacy of IBU1 and IBU2 for hsPDA with a cut-off value of 331 pg/mL (P < 0.001) and 423 pg/mL(P < 0.010), respectively. We did not identify a cut-off baseline BNP level that could predict treatment response to ibuprofen in preterm infants with hsPDA.

Among 114 newborns eligible for this study, 22 were excluded based on the exclusion criteria and the remaining 92 were included in the analysis (Fig. 1) . Mean gestational age and birth weight were 27.0 ± 1.8 weeks and 939.9 ± 283.8 g, respectively. Baseline characteristics, treatment, and echocardiographic findings are listed in Table 1 . Response rates to the first (IBU1, n = 92) and second (IBU2, n = 19) ibuprofen courses were 73.9% (n = 68) and 26.3% (n = 5), respectively. Gestational age and birth weight were greater in responders than non-responders in IBU1, while in IBU2, birth weight, but not gestational age, of responders was greater than that of non-responders. There was greater use of inotropic drugs in responders than non-responders to IBU1. In IBU2, baseline pH and platelet count were lower in non-responders than in responders. The incidence of intravenous ibuprofen therapy and the amount of fluid intake did not differ between the study groups. Echocardiographic parameters that reflect transductal shut volume did not differ between responders and non-responders.

Among the echocardiographic parameters available, the ductal diameter indexed to body weight and the left atrium to aorta (LA/Ao) ratio were positively correlated with baseline BNP level of IBU1 ( Table 2 ). The median (range) baseline BNP levels were significantly greater in the patients with large shunt volume (2,167 [82-5,000] pg/mL) than those with moderate shunt volume (1,000 [105-5,000] pg/mL) (P = 0.043) in IBU1. There was no correlation between the echocardiologic parameters and the baseline BNP levels in IBU2.

Baseline BNP levels did not differ between IBU1 or IBU2 responders and non-responders (Table 3) ; however, responders had significantly lower post-treatment BNP levels than non-responders after both courses of ibuprofen. Following IBU1, BNP levels decreased significantly in both responders (P < 0.001) and non-responders (P = 0.002), whereas, after IBU2, BNP levels decreased significantly in responders (P = 0.043), but not in non-responders (P = 0.221) (Fig. 2) .

We performed a receiver operator characteristic (ROC) curve analysis, which revealed a significant association between BNP level and persistent hsPDA after each course of ibuprofen (Fig. 3) . The cut-off post-treatment BNP levels that reflected persistent hsPDA after IBU1 and IBU2 were 331 pg/mL (sensitivity: 75.0%, specificity: 80.9%) and 423 pg/mL (sensitivity: 78.6%, specificity: 100%), respectively.

Among the patients who did not respond to IBU1 (n = 19) and were subsequently subjected to IBU2, neither baseline nor post-treatment BNP levels measured for the previous ibuprofen course (i.e., IBU1) could predict response rate to IBU2 (Table 4 ).

As previously shown 15, 20 , BNP levels of responders to ibuprofen therapy significantly decreased after each course of treatment and thus clearly reflected treatment response, with good sensitivity and specificity. The baseline BNP levels obtained prior to IBU1 were also associated with the transductal shunt volume defined by several echocardiographic parameters including LA/Ao ratio [15] [16] [17] ; however, baseline BNP levels, measured before either IBU1 or IBU2, could not predict treatment response in preterm infants with hsPDA.

To the best of the authors' knowledge, there has only been one previous study of the role of BNP as a predictive marker for response to COX inhibitor therapy against PDA. In contrast to our findings, Hsu et al. reported that baseline BNP levels in preterm infants with large PDA were higher in non-responders than responders to indomethacin therapy 18 . They suggested a cut-off baseline BNP level of >1,805 pg/mL, with relatively high sensitivity and specificity, based on data from a smaller number of patients (n = 31) than that included in the present study. The reason for this discrepancy is unclear. Several antenatal and postnatal factors have been suggested as parameters for predicting poor responsiveness, including gestational age, birth weight, pregnancy-induced hypertension, use of antenatal steroids, respiratory distress syndrome, small for gestational age, and postnatal age at the first www.nature.com/scientificreports www.nature.com/scientificreports/ pharmacologic treatment [21] [22] [23] . In the present study, gestational age was lower and the use of antenatal steroids and surfactant appeared to be greater than in the study reported by Hsu et al. 18 .

In the present study, the transductal shunt volume defined by several echocardiologic parameters including ductal diameter and LA/Ao ratio were not predictive of ibuprofen response. Although these parameters are regarded as good markers for the severity and natural course of PDA 15, 20, 24 , studies of the echocardiographic parameters that predict drug response rate are scarce. In a small study of preterm infants <28 weeks of gestation, the baseline ductal diameter did not differ between responders and non-responders to the first ibuprofen course 25 . By contrast, in a study of relatively mature preterm infants (gestational age <35 weeks), an index of PDA diameter squared/birth weight >9 mm 2 /kg was reported to predict failure of treatment with indomethacin 26 . Similarly, in a multicenter cohort study, ductal diameter >2 mm was suggested as an indicator of ibuprofen treatment response; however, the specificity (0.44) and positive predictive value (0.29) of ductal diameter alone were insufficient 27 . Ductal flow velocity, which reflects higher pulmonary arterial pressure, was suggested as a good predictive marker of response to COX inhibitors in a study of infants of 22-27 weeks' gestation 28 . Hsu et al. reported that neither ductal diameter nor LA/Ao ratio was a predictive factor for responsiveness to COX inhibitors 18 , similar to our findings.

The second course of COX inhibitors usually has a lower treatment response rate than the first course 8-10 , and may harbor a higher risk of complications without therapeutic benefit 5, 8, 10 . We speculated that the degree of change in BNP level before and after IBU1, which may reflect the individual response pattern of ductus to ibuprofen, could predict subsequent treatment response to the same drug. Unfortunately, although both first course pre-and post-treatment BNP levels tended to be higher in non-responders than responders to IBU2, the difference did not reach statistical significance. There has been a limited number of studies regarding predictors Apgar score at 1 min www.nature.com/scientificreports www.nature.com/scientificreports/ of treatment outcomes following a second course of COX inhibitors. Louis et al. suggested that advanced gestational age was a predictor of non-response to a second course of indomethacin therapy 29 . Another retrospective study also reported that persistent ductal Doppler flow within 24 h of completed initial indomethacin course was a significant predictor of failure of the second course 30 ; however, the study did not provide any quantitative data for assessment of ductal shunt flow.

In IBU2, baseline platelet counts were lower in non-responders than in responders. Whether platelet adhesion plays a crucial role in the closure of ductus arteriosus remains controversial, especially in preterm infants 31 . In two recent meta-analyses, a significant relationship was detected between low platelet count in the early days of life and incidence or treatment failure rate of primary COX inhibitors for hsPDA 32, 33 . Another recent large study reached a similar conclusion to the present study; platelet counts after the first course of COX inhibitors and before and after the second course were lower in non-responders than in responders, although initial baseline platelet counts did not differ between the groups 34 . The incidence of pregnancy-induced hypertension did not differ between responders and non-responders.

There are several limitations to this study. First, the sample size, particularly the number of patients who underwent IBU2, was insufficient to address the predictive value of baseline BNP levels. This may have simply resulted in type 2 statistical error, although our population was larger and less heterogenous (in terms of gestational age) than that described in the study of Hsu et al. 18 . Second, the decision of whether or not to administer www.nature.com/scientificreports www.nature.com/scientificreports/ additional ibuprofen or surgically ligate the ductus may have been influenced by baseline BNP levels. That is, surgical closure is more likely to be preferred than ibuprofen treatment in patients with very high baseline BNP levels, which could lead to selection bias for treatment response to the second course of ibuprofen. Third, our retrospective study lacks a well-designed echocardiographic protocol for the assessment of hemodynamic status such as shunt volume. However, quantitation of transductal shunt flow is not always feasible and can only be estimated based on several echocardiographic parameters. We tried to provide the categorized comparative data on the shunt flow by using several echocardiographic indices available. As previously depicted, no difference in the transductal shunt volume was found between the responders and non-responders to both IBU1 and IBU2.

In conclusion, we could not determine a cut-off baseline BNP level able to predict treatment response to ibuprofen in preterm infants with hsPDA. Plasma BNP levels correlated well with PDA hemodynamic status; however, their role as a guide to assist neonatologists in choice of therapeutic modality, particularly for non-responders to an initial standard COX inhibitor course, is questionable. To develop guidelines for optimal treatment for hsPDA, well-designed studies, considering various risk factors that affect ductal patency and response to COX inhibitors, are warranted.

The retrospective review of the medical records of patients hospitalized in the neonatal intensive care unit in Asan Medical Center, Seoul, Korea from 2010 to 2016 was performed. During the study period, data on echocardiography and plasma BNP levels were collected, according to our local protocol for management of hsPDA. The clinical characteristics and BNP levels of responders and non-responders to the IBU1 and IBU2 were compared (see below). The study was approved by the institutional review board of Asan Medical Center (IRB No. 2017-0253), who granted a waiver of informed consent. All methods were performed in accordance with the relevant guidelines and regulations.

Subjects. Eligibility criteria for inclusion of newborn infants in this study were as follows: (1) born at gestational age <30 weeks; (2) diagnosis of hsPDA meeting clinical and echocardiographic criteria (see below); (3) treated with oral and/or intravenous ibuprofen after 24 h of age; and (4) available echocardiography and plasma BNP data before (baseline) and after (post-treatment) each course of ibuprofen treatment. Exclusion criteria were newborns with the following: (1) major congenital anomalies, including congenital heart disease and twin to twin transfusion; (2) unstable medical conditions during the time of ibuprofen treatment that may have affected cardiac function, such as pneumothorax, pleural effusion, and septic shock; (3) incomplete initial course of ibuprofen (<3 doses), due to presentation of ibuprofen contraindications such as oliguria, necrotizing enterocolitis, bowel perforation, or death; or (4) baseline BNP level obtained <24 h after birth. www.nature.com/scientificreports www.nature.com/scientificreports/ bounding pulse, or hypotension; (3) respiratory symptoms, such as tachypnea, apnea, increased PaCO 2 , or increased ventilator needs; and (4) increased pulmonary vascular marking or cardiomegaly on chest radiography. Echocardiographic criteria were as follows: (1) ductal diameter ≥ 1.5 mm with left to right shunt; 35, 36 and/or (2) LA/Ao ratio ≥ 1.4 36 . Echocardiography was performed by attending neonatologists with a Philips IE33 (Philips Ultrasound, Bothell, WA, USA) before (baseline) and between 12 and 24 h after (post-treatment) each course of ibuprofen, or as otherwise indicated. A two-dimensional color flow Doppler was performed to check shunt at the ductus arteriosus. Ductal diameter and transductal peak systolic velocity and systolic-to-diastolic velocity gradient was measured in the parasternal short axis, and LA/Ao ratio was measured using M-mode in the parasternal long axis. To address the impact of hemodynamic status on the ibuprofen responsiveness, transductal shunt volume was categorized into moderate or large according to the classification suggested by de Boode et al. 37 A large transductal shunt volume was defined by the presence of at least 2 of the following parameters: (1) absolute ductal diameter (mm) ≥ 2.0; (2) ductal diameter per body weight (mm/kg) ≥ 1.4; (3) transductal peak systolic velocity (m/s) <1.5; and (4) LA/Ao ratio >2.0.

Measurement of plasma Bnp. According to our local protocol, bedside echocardiography and plasma BNP measurement were indicated for every infant who met the clinical criteria for hsPDA and/or were treated with ibuprofen. Plasma BNP levels were measured at least twice per patient, i.e., pre-(baseline) and post-(between 12 and 24 h after the last ibuprofen dose of each course) ibuprofen treatment. Blood samples were immediately placed in EDTA-treated tubes, transported to the laboratory department of our hospital, and analyzed by sandwich fluorescence immunoassay (Siemens Healthineers, NY, USA). The measurable range of the BNP assay was 2-5,000 pg/mL. BNP values reported as >5,000 pg/mL by our laboratory were counted as 5,000 pg/mL for this study. treatment with ibuprofen. One course of intravenous or oral ibuprofen treatment comprised three doses administered at intervals of 24 h. The doses of ibuprofen were 10 mg/kg/day for the first day, and 5 mg/kg/day for the second and the third days. In the patients. The PDA still fulfilled hsPDA criteria after completion of IBU1, an additional ibuprofen course was started, unless contraindicated. When the PDA was open but did not meet the criteria for hsPDA, follow-up echocardiography was performed 12-24 h later, without an additional course of ibuprofen. PDA ligation was performed when hsPDA remained after two (or three) courses of ibuprofen, or when ibuprofen was contraindicated.

Definition of response to ibuprofen. Patients who completed each course of ibuprofen treatment were categorized as "responders" or "non-responders". "Responders" were defined as infants with (1) closed PDA, or (2) a small PDA that did not meet the diagnostic criteria for hsPDA and thus did not need any further pharmacologic or surgical treatment for PDA within 1 week after previous treatment. "Non-responders" were defined as infants who met the criteria for hsPDA after ibuprofen treatment, and were treated with an additional course of ibuprofen and/or surgical ligation. Statistical analysis. Statistical analyses were performed using SPSS version 24.0 for windows (SPSS Inc., Chicago, IL, USA). Continuous variables were evaluated using the Student's t test or Mann-Whitney U test. Categorical variables were tested by chi-square or Fisher's exact test. The correlations between baseline BNP levels and the echocardiographic parameters were determined using Pearson's correlation coefficient or Spearman's rank correlation test. Changes of BNP levels from baseline to post-treatment were evaluated using the Wilcoxon signed rank test. ROC curve analysis was performed to determine the cut-off BNP level for detection of PDA closure. P < 0.05 was considered statistically significant.

Risk factors for chronic lung disease in the surfactant era: a North Carolina population-based study of very low birth weight infants. North Carolina Neonatologists Association

Patent ductus arteriosus: pathophysiology and management

Ductal shunting, high pulmonary blood flow, and pulmonary hemorrhage

Outcome in neonates with necrotizing enterocolitis and patent ductus arteriosus

A second course of ibuprofen is effective in the closure of a clinically significant PDA in ELBW infants

Repeated courses of ibuprofen are effective in closure of a patent ductus arteriosus

Safety and efficacy of ibuprofen versus indomethacin in preterm infants treated for patent ductus arteriosus: a randomised controlled trial

Comparison of renal effects of ibuprofen versus indomethacin during treatment of patent ductus arteriosus in contiguous historical cohorts

Repeated courses of oral ibuprofen in premature infants with patent ductus arteriosus: efficacy and safety

Multiple courses of indomethacin and neonatal outcomes in premature infants

Intrauterine inflammation as a risk factor for persistent ductus arteriosus patency after cyclooxygenase inhibition in extremely low birth weight infants

Predictors of successful closure of patent ductus arteriosus with indomethacin

Preterm infants who later require duct ligation show different vital signs and pH in early postnatal life

Clinical relevance of measurement of brain natriuretic peptide and N-terminal pro-brain natriuretic peptide in pediatric cardiology

Utility of rapid B-type natriuretic peptide assay for diagnosis of symptomatic patent ductus arteriosus in preterm infants

The use of a bedside assay for plasma B-type natriuretic peptide as a biomarker in the management of patent ductus arteriosus in premature neonates

Can early B-type natriuretic peptide assays predict symptomatic patent ductus arteriosus in extremely low birth weight infants?

B-type natriuretic peptide predicts responses to indomethacin in premature neonates with patent ductus arteriosus

Role of plasma B-type natriuretic peptide in screening for hemodynamically significant patent ductus arteriosus in preterm neonates

Point-of-care testing for B-type natriuretic peptide in premature neonates with patent ductus arteriosus

Early echocardiographic prediction of symptomatic patent ductus arteriosus in preterm infants undergoing mechanical ventilation

Does echocardiography facilitate determination of hemodynamic significance attributable to the ductus arteriosus?

Indomethacin responsiveness of patent ductus arteriosus and renal abnormalities in preterm infants treated with indomethacin

Efficacy of pharmacologic closure of patent ductus arteriosus in small-for-gestational-age extremely preterm infants

Prediction of therapeutic response to cyclooxygenase inhibitors in preterm infants with patent ductus arteriosus

Correlation of B-type natriuretic peptide levels and echocardiographic parameters in preterm infants with patent ductus arteriosus

Echocardiography predicts closure of patent ductus arteriosus in response to ibuprofen in infants less than 28 week gestational age

The effect of ductal diameter on surgical and medical closure of patent ductus arteriosus in preterm neonates: size matters

Echocardiography as a guide for patent ductus arteriosus ibuprofen treatment and efficacy prediction

A high ductal flow velocity is associated with successful pharmacological closure of patent ductus arteriosus in infants 22-27 weeks gestational age

Factors associated with non-response to second course indomethacin for PDA treatment in preterm neonates

Persistent Doppler flow predicts lack of response to multiple courses of indomethacin in premature infants with recurrent patent ductus arteriosus

Vessel remodeling in the newborn: platelets fill the gap

Platelet counts and patent ductus arteriosus in preterm infants: a systematic review and meta-analysis

The association of platelets with failed patent ductus arteriosus closure after a primary course of indomethacin or ibuprofen: a systematic review and meta-analysis

Association between platelet counts before and during pharmacological therapy for patent ductus arteriosus and treatment failure in preterm infants

Role of neonatologist-performed echocardiography in the assessment and management of patent ductus arteriosus physiology in the newborn

Seong Hee Oh and Byong Sop Lee wrote the main manuscript text and Euiseok Jung and Moon Yeon Oh collected the data. Hyun-Jeong Do prepared figures. Byong Sop Lee, Ellen Ai-Rhan Kim and Ki-Soo Kim designed the study and analyzed the data. All authors reviewed the manuscript.

The authors declare no competing interests.

Correspondence and requests for materials should be addressed to B.S.L.

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