Abstract
Context: There is an ongoing debate on the optimal management of patent ductus arteriosus (PDA) in preterm infants. Identifying subgroup of infants who would benefit from pharmacological treatment might help.
Objective: To investigate the modulating effect of the differences in methodological quality, the rate of open-label treatment, and patient characteristics on relevant outcome measures in randomized controlled trials (RCTs).
Data Sources: Electronic database search between 1950 and May 2020.
Study Selection: RCTs that assessed pharmacological treatment compared to placebo/no treatment.
Data Extraction: Data is extracted following the PRISMA guidelines. Outcome measures were failure to ductal closure, surgical ligation, incidence of necrotizing enterocolitis, bronchopulmonary dysplasia, sepsis, periventricular leukomalacia, intraventricular hemorrhage (IVH) grade ≥3, retinopathy of prematurity and mortality.
Results: Forty-seven studies were eligible. The incidence of IVH grade ≥3 was lower in the treated infants compared to the placebo/no treatment (RR 0.77, 95% CI 0.64–0.94) and in the subgroups of infants with either a gestational age <28 weeks (RR 0.77, 95% CI 0.61–0.98), a birth weight <1,000 g (RR 0.77, 95% CI 0.61–0.97), or if untargeted treatment with indomethacin was started <24 h after birth (RR 0.70, 95% CI 0.54–0.90).
Limitations: Statistical heterogeneity caused by missing data and variable definitions of outcome parameters.
Conclusions: Although the quality of evidence is low, this meta-analysis suggests that pharmacological treatment of PDA reduces severe IVH in extremely preterm, extremely low birth weight infants or if treatment with indomethacin was started <24 h after birth. No other beneficial effects of pharmacological treatment were found.
Introduction
Patent ductus arteriosus (PDA) is common in preterm and very low birth weight infants (). Persistence is associated with a higher risk of morbidities, including bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), and intraventricular hemorrhage (IVH), and mortality (). Nevertheless, pharmacological treatment or surgical closure of PDA is not without adverse effects (, ). After many decades of clinical research, the question remains open if, when, and how PDA should be treated in preterm infants (). Globally, there has been a shift from early pharmacological treatment toward a more expectant management policy (). A uniform definition of a hemodynamic significant PDA does not exist, nor is there clear evidence in favor of or against many of the approaches to treating PDA (7–). Since 1976 we know that pharmacological treatment is an effective way of ductal closure (). A recent meta-analysis, however, showed that neither short-term nor long-term outcomes seem to differ between treated and untreated patients (). This sparked an ongoing debate on the optimal approach to treating PDA, which ranges from expectant management to aggressive treatment with a variety of cyclooxygenase inhibitors or acetaminophen with varying doses and at different intervals (). Although the results of randomized controlled trails (RCTs) on PDA treatment have been reviewed extensively, only a small number of reviews stratified the results according to infant characteristics, methodological quality (, ), timing of treatment (), or to the definitions of a hemodynamic significant PDA ().
To the best of our knowledge this is the first comprehensive systematic review of RCTs to investigate the modulating effect of the methodological quality, the rate of open-label treatment in the placebo/no treatment groups, and several patient characteristics on the benefits, or adverse effects, of pharmacological treatment of PDA in preterm infants. We aim to identify specific subgroups of preterm infants at high risk of adverse outcomes, who would benefit from active closure of PDA.
Methods
Our study is performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines ().
Search Strategy
We searched the following databases: PubMed, the Ovid Embase, and the Cochrane Library. We searched for papers published between 1950 up to and including April 2020. By using the Boolean operators AND and OR, we used all possible combinations of the following search terms: infant, newborn, neonate, preterm, premature, ductus, arteriosus, Botalli. We also used the Mesh terms “Infant, premature,” “Ductus Arteriosus, Patent,” and “Ductus Arteriosus” in the PubMed database. The complete search strategy can be found in Supplement 1. Subsequently, we assessed the publications cited by the selected studies for relevant material eligible for possible additional inclusion.
Study Selection
Three authors (EJ, TH, and WdB) independently screened the publications identified in our initial search for eligibility on the basis of their titles and abstracts. Where disagreement arose, the full text was assessed and then discussed in order to reach consensus. We selected studies with a RCT design and written in either English, Dutch, or German. Generally speaking, we included all studies that assessed pharmacological treatment with either ibuprofen, indomethacin, or acetaminophen vs. placebo/no treatment. We excluded animal studies, studies on antenatal treatment, studies that included patients with a post term age of more than 1 month, and studies concerning patients with a congenital heart defect.
Data Extraction
Two authors (EJ and TH) performed data extraction. The data we extracted from the selected studies were general study parameters, demographic parameters pertaining to the participants, treatment regime(s), and outcomes. We collected the parameters study design, total number of patients, mean gestational age (GA), birth weight (BW), postnatal age (PNA) at the start of treatment, and the rate of open-label treatment in the placebo/no treatment group. The following outcome parameters were collected (if reported in the studies) and analyzed: mortality, failure to close the DA, the need for surgical ligation, the incidence of NEC (any definition), BPD (any definition), sepsis, periventricular leukomalacia (PVL), IVH grade ≥3, retinopathy of prematurity (ROP), oliguria, other respiratory morbidity (e.g., pneumothorax), other gastrointestinal morbidity [e.g., spontaneous intestinal perforation (SIP)], and long-term neurodevelopmental impairment. In case of missing data, we tried to contact the corresponding authors of the studies in question and requested them to kindly provide these data.
Statistical Analysis
As ibuprofen, indomethacin, and acetaminophen are comparable regarding their effectiveness in DA closure (, ), but their side effect profiles may differ (, ), we performed two analyses. In the first analysis we combined all studies reporting either of these three drugs in comparison with placebo/no treatment. In a second analysis we divided the studies according to which drug was used. Subgroups were made, related to known risk factors (GA, BW) and other factors influencing efficacy of treatment, such as PNA. Moreover, the consequences of open label treatment percentage in the control group were analyzed since this is an important methodologic flaw in the RCTs. The following strata were analyzed: BW in five subgroups: <1,000 g, 1,000–1,250 g, 1,251–1,500 g, >1,500 g, and data unknown; GA in four subgroups: <28 weeks, 28–33 weeks, >33 weeks, and data unknown; PNA at the start of treatment in four subgroups: <24 h, 24–72 h, >72 h, and data unknown. Studies with start of treatment <24 h PNA were divided into untargeted (start treatment irrespective whether the ductus is open or closed) and targeted (start treatment only after clinically and/or echocardiographically confirmation of a PDA) treatment. The rate of open-label treatment in the placebo/no treatment arm was expressed as a percentage and divided into four groups: <25%, 25–50%, >50%, and data unknown. For statistical analysis we used Review Manager (RevMan version 5.3 Copenhagen: The Nordic Cochrane Center, The Cochrane Collaboration, 2014). The risk ratio (RR) and risk difference (RD) with a 95% confidence interval (CI) were calculated with the Mantel-Haenszel method. We calculated the number needed to treat (NNT) with a 95% CI for each different outcome in case of statistical significance. We used random-effect meta-analysis if the heterogeneity (I2) was >50% (15) and fixed-effect in case of low heterogeneity.
Risk of Bias
We critically examined the methodological quality of the selected studies and the risk of bias in accordance with the Cochrane guidelines (16). The quality parameters included the type of analysis, random sequence generation, allocation concealment, blinding of participants and personnel, and blinding of outcome assessment. Two authors (EJ and TH) assessed the risk of bias assessment. When disagreement arose, a third author (WdB) assessed the studies in order to reach consensus. The risk of bias was calculated (low risk: 1 point, unclear risk: 2 points, and high risk: 3 points) and the cumulative score was divided into three subgroups: low (7–9 points in total), intermediate (10–12 points), and high (13–21 points). We examined the methodological quality of the studies' outcome parameters with the GRADE method (17). We assessed imprecision as serious if the total number of events was <300 or if the width of the CI of the RR was >0.25. We used the GRADE-pro GDT 2016 software [GRADEpro Guideline Development Tool (Software) McMaster University, 2015] to create a “summary of findings” table to report the quality of evidence. The GRADE approach results in an assessment of the quality of a body of evidence in one of four grades: high, moderate, low, or very low.
Results
Study Selection
Out of the 12,139 articles we identified 10,251 as unique in our initial search. After selection (see Figure 1) a final 47 papers were eligible, comprising a total of 5,242 infants (18–64).
Figure 1
Study Characteristics and Risk of Bias
The relevant characteristics of the 47 papers are described in Table 1 (18–64). Thirty-two (68%) of the studies analyzed the effect of indomethacin (18–44, 46, 47, 55, 60, 61), 12 (26%) studied the effect of ibuprofen (45, 48–54, 56–59), two (4%) studied acetaminophen (62, 64), and one (2%) studied the effect of either indomethacin, ibuprofen, or acetaminophen (63). Thirteen papers (28%) included preterm infants with a mean GA <28 weeks (42, 44, 46–48, 50, 53, 55–58, 61, 63), and 30 (64%) included infants with a mean GA between 28 and 32 weeks (18, 20–24, 26–30, 32–41, 43, 45, 47, 49, 51, 52, 59, 60, 62, 64). Seventeen papers (36%) included preterm infants with a mean BW <1,000 g (33, 35, 39, 41–46, 48, 50, 53, 55, 56, 58, 61, 63), and 19 (40%) included infants weighing between 1,000 and 1,250 g (20, 22–24, 27–30, 34, 36–38, 40, 47, 49, 52, 57, 62, 64). Most studies (62%) investigated treatment that was started within 24 h' PNA (26, 29, 30, 32, 34, 35, 37–53, 55, 58, 60–62, 64). More than two third of the studies reported the rate of open-label treatment, namely 25–50% in 16 (34%) (20, 22, 31, 32, 36, 37, 42, 46, 48, 50, 52, 53, 58, 60, 61, 63), and >50% in 15 (32%) studies (18, 19, 23–25, 27, 33, 34, 40, 43, 45, 47, 51, 55, 56). The median rate of the open-label treatment was 44.5% (range 0–85%). Twenty-one studies (45%) were classified as having a low risk of bias (18, 21–23, 25, 27, 29, 31, 33, 37, 38, 42, 43, 46, 47, 49, 50, 53, 56, 61, 62). Six papers (13%) were assessed as having a high risk of bias (19, 26, 34, 39, 40, 63).
Table 1
| References | Patients (n) | Treatment characteristics | Patient characteristics | Study characteristics | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Intervention | Control | Start at PNA | GA (w) | BW (g) | Open-label treatment | 1 | 2 | 3 | 4 | 5 | 6 | 7 | Risk of bias | ||
| Nestrud et al. (18) | 23 | Indomethacin | Placebo | > 72 h | 28–32 | 1,251–1,500 | > 50% | + | + | + | ? | + | + | ? | Low |
| Merritt et al. (19) | 24 | Indomethacin | No treatment | 24–72 h | unknown | 1,251–1,500 | > 50% | – | – | – | ? | – | + | ? | High |
| Neu et al. (20) | 21 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | 25–50% | ? | + | + | + | – | + | ? | Intermediate |
| Yanagi et al. (21) | 17 | Indomethacin | Placebo | > 72 h | 28–32 | 1,251–1,500 | unknown | + | + | + | ? | + | + | ? | Low |
| Yeh et al. (22) | 55 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | 25–50% | + | ? | + | + | + | + | ? | Low |
| Mahony et al. (23) | 47 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | > 50% | + | + | + | + | + | + | ? | Low |
| Mullett et al. (24) | 47 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | > 50% | ? | + | + | ? | + | – | ? | Intermediate |
| Gersony et al. (25) | 405 | Indomethacin | Placebo | > 72 h | unknown | unknown | > 50% | + | + | + | ? | + | + | ? | Low |
| Kaapa et al. (26) | 27 | Indomethacin | No treatment | <24 h T | 28–32 | >1,500 | unknown | + | ? | – | ? | ? | + | ? | High |
| Rudd et al. (27) | 30 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | > 50% | + | + | + | + | + | + | ? | Low |
| Yeh et al. (28) | 47 | Indomethacin | Placebo | > 72 h | 28–32 | 1,000–1,250 | unknown | + | ? | + | ? | ? | + | ? | Intermediate |
| Mahony et al. (29) | 104 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,000–1,250 | <25% | + | + | + | + | ? | + | ? | Low |
| Ment et al. (30) | 48 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,000–1,250 | unknown | – | ? | + | + | ? | + | ? | Intermediate |
| Hammerman et al. (31) | 24 | Indomethacin | Placebo | > 72 h | unknown | unknown | 25–50% | + | + | + | + | ? | + | ? | Low |
| Rennie et al. (32) | 50 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,251–1,500 | 25–50% | ? | ? | + | + | ? | ? | ? | Intermediate |
| Hammerman et al. (33) | 24 | Indomethacin | Placebo | > 72 h | 28–32 | <1,000 | > 50% | + | + | + | + | + | + | ? | Low |
| Krueger et al. (34) | 32 | Indomethacin | No treatment | <24 h UT | 28–32 | 1,000–1,250 | > 50% | ? | ? | – | ? | ? | + | ? | High |
| Vincer et al. (35) | 30 | Indomethacin | Placebo | <24 h UT | 28–32 | <1,000 | <25% | ? | – | + | ? | + | + | ? | Intermediate |
| Weesner et al. (36) | 26 | Indomethacin | Placebo | 24–72 h | 28–32 | 1,000–1,250 | 25–50% | + | ? | + | + | ? | + | ? | Intermediate |
| Bandstra et al. (37) | 199 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,000–1,250 | 25–50% | + | + | + | + | + | + | ? | Low |
| Hanigan et al. (38) | 111 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,000–1,250 | <25% | + | + | + | + | ? | + | ? | Low |
| Ment et al. (39) | 36 | Indomethacin | Placebo | <24 h UT | 28–32 | <1,000 | unknown | – | ? | + | + | – | + | ? | High |
| Lai et al. (40) | 32 | Indomethacin | Placebo | <24 h UT | 28–32 | 1,000–1,250 | > 50% | – | – | ? | ? | ? | + | ? | High |
| Ment et al. (41) | 431 | Indomethacin | Placebo | <24 h UT | 28–32 | <1,000 | <25% | + | + | ? | + | – | + | ? | Intermediate |
| Couser et al. (42) | 90 | Indomethacin | Placebo | <24 h UT | <28 | <1,000 | 25–50% | + | ? | + | + | + | + | ? | Low |
| Supapannachart et al. (43) | 30 | Indomethacin | Placebo | <24 h UT | 28–32 | <1,000 | > 50% | + | + | + | ? | + | + | ? | Low |
| Couser et al. (44) | 90 | Indomethacin | Placebo | <24 h UT | <28 | <1,000 | unknown | + | ? | + | + | – | + | ? | Intermediate |
| De Carolis et al. (45) | 46 | Ibuprofen | No treatment | <24 h UT | 28–32 | <1,000 | > 50% | + | – | – | + | + | + | ? | Intermediate |
| Schmidt et al. (46) | 1,202 | Indomethacin | Placebo | <24 h UT | <28 | <1,000 | 25–50% | + | + | + | + | ? | + | ? | Low |
| Osborn et al. (47) | 70 | Indomethacin | Placebo | <24 h T | <28 | 1,000–1,250 | > 50% | ? | + | + | + | + | + | ? | Low |
| Gournay et al. (48) | 131 | Ibuprofen | Placebo | <24 h UT | <28 | <1,000 | 25–50% | + | + | + | + | – | + | – | Intermediate |
| van Overmeire et al. (49) | 415 | Ibuprofen | Placebo | <24 h UT | 28–32 | 1,000–1,250 | <25% | + | + | + | + | + | + | ? | Low |
| Dani et al. (50) | 155 | Ibuprofen | Placebo | <24 h UT | <28 | <1,000 | 25–50% | + | + | + | + | ? | + | ? | Low |
| Sangtawesin et al. (51) | 42 | Ibuprofen | Placebo | <24 h T | 28–32 | 1,251–1,500 | > 50% | ? | ? | + | + | + | + | ? | Intermediate |
| Sangtawesin et al. (52) | 62 | Ibuprofen | Placebo | <24 h T | 28–32 | 1,000–1,250 | 25–50% | ? | ? | + | + | + | + | ? | Intermediate |
| Aranda et al. (53) | 136 | Ibuprofen | Placebo | 24–72 h | <28 | <1,000 | 25–50% | + | + | + | + | + | + | ? | Low |
| Amoozgar et al. (54) | 51 | Ibuprofen | Placebo | > 72 h | > 33 | >1,500 | <25% | ? | ? | ? | ? | + | + | ? | Intermediate |
| Maruyama et al. (55) | 19 | Indomethacin | Placebo | <24 h UT | <28 | <1,000 | > 50% | + | + | ? | ? | + | + | ? | Intermediate |
| Sosenko et al. (56) | 105 | Ibuprofen | Placebo | 24–72 h | <28 | <1,000 | > 50% | + | + | + | + | + | + | ? | Low |
| Bagnoli et al. (57) | 134 | Ibuprofen | Placebo | > 72 h | <28 | 1,000–1,250 | Unknown | ? | ? | ? | ? | + | + | ? | Intermediate |
| Kanmaz et al. (58) | 46 | Ibuprofen | No treatment | <24 h UT | <28 | <1,000 | 25–50% | + | + | – | + | – | + | ? | Intermediate |
| Ding et al. (59) | 72 | Ibuprofen | Placebo | Unknown | 28–32 | 1,251–1,500 | Unknown | ? | ? | ? | + | + | + | ? | Intermediate |
| Jannatdoust et al. (60) | 70 | Indomethacin | No treatment | <24 h UT | 28–32 | Unknown | 25–50% | + | + | – | ? | ? | + | ? | Intermediate |
| Kluckow et al. (61) | 92 | Indomethacin | Placebo | <24 h T | <28 | <1,000 | 25–50% | + | + | + | + | + | + | – | Low |
| Harkin et al. (62) | 48 | Acetaminophen | Placebo | <24 h UT | 28–32 | 1,000–1,250 | <25% | + | + | + | + | + | + | ? | Low |
| Clyman et al. (63) | 202 | Any | No treatment | > 72 h | <28 | <1,000 | 25–50% | + | ? | – | ? | + | + | – | High |
| Juujarvi et al. (64) | 44 | Acetaminophen | Placebo | <24 h UT | 28–32 | 1,000–1,250 | Unknown | + | + | + | + | ? | ? | ? | Intermediate |
Treatment, patient and, study characteristics of the RCTs included.
BW, birth weight; GA, gestational age; h, hour; n, number; NA, not available; PNA, postnatal age; any, indomethacin/ibuprofen/acetaminophen; T, targeted treatment, UT, untargeted treatment; risk of bias numbers stand for (1) random sequence generation (selection bias); (2) allocation concealment (selection bias); (3) blinding of participants and personnel (performance bias); (4) blinding of outcome assessment (detection bias); (5) incomplete outcome data (attrition bias); (6) selective reporting (reporting bias), and; (7) other bias.
Outcome Measures
Despite our efforts to contact the corresponding authors and our request to provide missing data, not all data on GA, BW and rate of open-label treatment could be retrieved. Data on GA (19, 25, 31) and/or BW (25, 31, 60) were unavailable in four trials (453 and 499 infants for GA and BW, respectively). The rate of open-label treatment was unavailable for nine trials (21, 26, 28, 30, 39, 44, 57, 59, 64).
RR of outcomes, stratified by the patient characteristics, the quality of the studies, and the rate of open-label treatment in the placebo/no treatment group are described in Table 2. The meta-analyses revealed that in comparison to placebo/no treatment, the administration of indomethacin, ibuprofen, or acetaminophen resulted in a significantly reduced risk of failed ductal closure (RR 0.40, 95% CI 0.33–0.48; RD −0.32, 95% CI −0.38, −0.27; NNT 3.4, 95% CI 3.1–3.7) or risk of surgical ligation (RR 0.61, 95% CI 0.49–0.76; RD −0.04, 95% CI −0.06, −0.02; NNT 22.8, 95% CI 15.8–40.7), irrespective of the used drug. This result was similar for the subcategories based on mean BW, GA, and PNA at the start of treatment. The quality of evidence was graded as very low or very low to low, respectively (Supplement 2).
Table 2
| Failed closure PDA | Need for ligation | NEC | BPD | Sepsis | PVL | IVH (Grade ≥ 3) | ROP | Mortality | |
|---|---|---|---|---|---|---|---|---|---|
| Whole population | 0.40 [0.33–0.48] 40; 4,291 | 0.61 [0.49–0.76] 24; 3,289 | 1.10 [0.89–1.37] 29; 3,686 | 0.97 [0.85–1.10] 26; 3,005 | 1.02 [0.82–1.25] 13; 1,205 | 0.93 [0.65–1.33] 11; 1,619 | 0.76 [0.62–0.93] 19; 3,071 | 0.99 [0.86–1.15] 19; 1,489 | 1.02 [0.89–1.17] 37; 3,987 |
| BW <1,000 g | 0.48 [0.37–0.63] 13; 2,045 | 0.61 [0.46–0.80] 11; 2,102 | 1.07 [0.84–1.37] 14; 2,330 | 0.94 [0.79–1.12] 13; 1,983 | 1.09 [0.84–1.41] 7; 720 | 0.84 [0.55–1.28] 8; 951 | 0.77 [0.61–0.97] 12; 2,251 | 1.18 [0.95–1.47] 9; 864 | 1.08 [0.91–1.28] 15; 2,368 |
| BW 1,000–1,250 g | 0.37 [0.27–0.51] 18; 1,516 | 0.60 [0.41–0.89] 10; 1,088 | 1.21 [0.74–1.97] 13; 1,291 | 1.07 [0.90–1.26] 8; 857 | 0.89 [0.61–1.29] 6; 485 | 1.22 [0.60–2.48] 3; 668 | 0.78 [0.54–1.13] 6; 851 | 0.82 [0.67–1.00] 9; 585 | 0.98 [0.75–1.28] 15; 1,413 |
| BW 1,251–1,500 g | 0.32 [0.16–0.65] 5; 204 | 1.08 [0.08–15.46] 2; 75 | 1.27 [0.54–3.01] 1; 41 | 0.67 [0.10–4.53] 3; 114 | - | - | - | 1.36 [0.25–7.27] 1; 40 | 0.65 [0.33–1.28] 5; 155 |
| BW > 1,500 g | 0.15 [0.02–1.09] 1;27 | - | - | 0.54 [0.06–5.26] 1; 27 | - | - | - | - | 0.27 [0.03–2.11] 1; 27 |
| BW unknown | 0.28 [0.18–0.44] 3; 499 | 0.56 [0.13–2.33] 1; 24 | 0.70 [0.07–6.70] 1; 24 | 1.05 [0.78–1.41] 1; 24 | - | - | 0.69 [0.12–3.85] 1; 69 | - | 1.40 [0.55–3.57] 1; 24 |
| GA <28 w | 0.63 [0.47–0.84] 9; 2,039 | 0.67 [0.52–0.87] 9; 2,130 | 1.20 [0.94–1.54] 12; 2,367 | 0.92 [0.74–1.15] 9; 1,858 | 1.15 [0.89–1.49] 5; 644 | 0.90 [0.59–1.37] 8; 959 | 0.77 [0.61–0.98] 9; 2,008 | 1.17 [0.94–1.46] 7; 809 | 1.05 [0.88–1.25] 12; 2,369 |
| GA 28–32 w | 0.34 [0.28–0.41] 29; 1,823 | 0.45 [0.29–0.71] 13; 1,110 | 0.86 [0.56–1.34] 16; 1,295 | 1.06 [0.92–1.21] 15; 1,100 | 0.83 [0.58–1.18] 8; 561 | 1.02 [0.50–2.04] 3; 660 | 0.77 [0.55–1.09] 10; 1,063 | 0.86 [0.71–1.04] 12; 680 | 0.97 [0.76–1.24] 23; 1,570 |
| GA > 33 w | - | - | - | - | - | - | - | - | - |
| GA unknown | 0.31 [0.22–0.42] 2; 429 | 0.66 [0.19–2.28] 2; 49 | 0.70 [0.07–6.70] 1; 24 | 0.57 [0.08–4.09] 2; 47 | - | - | - | - | 0.88 [0.38–2.04] 2; 48 |
| PNA <24 h (targeted) | 0.59 [0.25–1.35] 3; 159 | 0.22 [0.01–4.41] 1; 92 | 1.56 [0.45–5.42] 3; 224 | 0.68 [0.42–1.09] 3; 177 | 0.85 [0.48–1.49] 1; 92 | 1.70 [0.54–5.37] 2; 146 | - | 0.46 [0.16–1.32] 2; 150 | 0.76 [0.41–1.42] 3; 189 |
| PNA <24 h (untargeted) | 0.39 [0.32–0.48] 21; 2,916 | 0.53 [0.39–0.72] 13; 2,502 | 1.04 [0.79–1.36] 17; 2,677 | 0.96 [0.75–1.22] 14; 2,235 | 0.95 [0.69–1.32] 8; 704 | 0.82 [0.50–1.33] 6; 1,036 | 0.70 [0.57–0.87] 16; 2,630 | 1.02 [0.85–1.21] 9; 706 | 1.04 [0.88–1.21] 20; 2,872 |
| PNA 24–72 h | 0.12 [0.02–0.63] 2; 68 | 0.78 [0.35–1.76] 2; 130 | 1.26 [0.71–2.22] 3; 276 | 0.93 [0.61–1.43] 5; 288 | - | 0.58 [0.18–1.83] 2; 235 | 0.92 [0.50–1.70] 2;239 | 1.20 [0.90–1.61] 4; 294 | 0.77 [0.42–1.42] 5; 289 |
| PNA > 72 h | 0.41 [0.30–0.57] 13;1,076 | 0.75 [0.52–1.07] 8; 565 | 1.33 [0.87–2.04] 7; 907 | [0.86–1.19] 4; 305 | 1.15 [0.84–1.58] 4; 409 | 1.20 [0.57–2.51] 1; 202 | 1.63 [0.82–3.24] 1; 202 | 0.78 [0.48–1.27] 4; 339 | 1.21 [0.81–1.81] 9; 637 |
| PNA unknown | 0.13 [0.02–1.00] 1; 72 | - | - | - | - | - | - | - | - |
| Low risk of bias | 0.39 [0.30–0.50] 18; 3,049 | 0.55 [0.42–0.71] 13; 2,548 | 1.04 [0.80–1.35] 15; 2,767 | 0.97 [0.83–1.14] 13; 2,284 | 0.92 [0.73–1.18] 10; 925 | 0.85 [0.53–1.36] 8; 1,240 | 0.79 [0.63–0.98] 9; 2,393 | [0.86–1.17] 11; 1,029 | 1.03 [0.88–1.21] 19; 2,940 |
| Intermediate risk of bias | 0.37 [0.26–0.53] 17; 927 | 0.74 [0.46–1.20] 8; 483 | 1.61 [0.98–2.64] 11; 655 | 1.03 [0.74–1.44] 8; 408 | [0.07–15.04] 1; 46 | 0.90 [0.36–2.22] 2; 177 | 0.55 [0.32–0.96] 7; 410 | 0.83 [0.48–1.42] 6; 226 | 0.98 [0.70–1.38] 12; 694 |
| High risk of bias | 0.42 [0.19–0.97] 5; 315 | 0.90 [0.45–1.82] 3; 258 | 0.84 [0.47–1.53] 3; 264 | 0.88 [0.68–1.13] 5; 313 | 1.40 [0.89–2.21] 2; 234 | 1.20 [0.57–2.51] 1; 202 | 1.02 [0.57–1.82] 3; 268 | 1.12 [0.68–1.86] 2; 234 | 1.05 [0.62–1.77] 6; 353 |
| Open–label treatment <25% | 0.38 [0.29–0.50] 6; 762 | 0.39 [0.15–0.97] 3; 549 | 0.65 [0.31–1.33] 5; 658 | 1.09 [0.90–1.31] 3; 493 | 0.97 [0.47–1.99] 2; 152 | 2.05 [0.71–5.89] 1; 415 | 1.06 [0.63–1.78] 4; 635 | 0.93 [0.45–1.93] 3; 164 | 1.14 [0.81–1.62] 6; 769 |
| Open–label treatment 25–50% | 0.40 [0.31–0.52] 14; 2,323 | 0.52 [0.39–0.70] 11; 2,226 | 1.09 [0.85–1.39] 12; 2,379 | 0.94 [0.78–1.13] 14; 2,160 | 1.07 [0.82–1.39] 6; 793 | 0.72 [0.47–1.11] 7; 999 | 0.76 [0.61–0.95] 9; 2,152 | [0.87–1.17] 10; 1,036 | 1.05 [0.89–1.24] 14; 2,457 |
| Open–label treatment > 50% | 0.40 [0.25–0.62] 13; 843 | 0.63 [0.40–0.99] 8; 361 | 1.24 [0.68–2.28] 10; 467 | 0.98 [0.76–1.26] 8; 325 | 0.90 [0.61–1.34] 5; 260 | 1.63 [0.58–4.53] 3; 205 | 0.57 [0.25–1.30] 4; 200 | 1.17 [0.64–2.15] 4; 212 | 0.86 [0.55–1.33] 12; 499 |
| Open–label treatment unknown | 0.37 [0.21–0.66] 7; 363 | 1.89 [0.91–3.93] 1; 134 | [0.07–15.08] 1; 48 | 0.54 [0.06–5.26] 1; 27 | - | - | 0.26 [0.05–1.48] 2; 84 | 0.32 [0.07–1.42] 1; 47 | 0.41 [0.15-1.13] 5; 262 |
Risk ratio of outcomes, stratified by the patient characteristics, the quality of the studies, and the rate of open-label treatment in the placebo/no treatment group.
Risk ratio with 95% confidence interval. Number of studies and infants. RR <1 favors treatment; RR > 1 favors placebo/no treatment. In bold the statistically significant differences. BW, birth weight; GA, gestational age; PNA, postnatal age; PDA, patent ductus arteriosus; NEC, necrotizing enterocolitis; BPD, bronchopulmonary dysplasia; PVL, periventricular leukomalacia; IVH, intraventricular hemorrhage; ROP, retinopathy of prematurity. w, weeks; h, hours. - means not estimable.
We found no difference for BPD, NEC, sepsis, PVL, ROP or mortality between the intervention and control group overall, or in any of the subgroups (Table 2), irrespective of the used drug. In most studies BPD was defined as supplemental oxygen requirement at 28 days' PNA or at 36 weeks' postmenstrual age (PMA). Seven RCTs used radiographic criteria (19, 22, 26, 31, 33, 35, 36). Four RCTs did not state their definition of BPD clearly (32, 43, 51, 52). Neither the overall meta-analyses nor the subgroup analyses of the 28 days' PNA and 36 weeks' PMA definition of BPD revealed any differences between the placebo/no treatment and the pharmacological treatment group.
Twenty-eight out of 47 studies started the treatment <24 h PNA. Of these 28 studies, five started treatment only after clinically and/or echocardiographically confirmation of a PDA (targeted treatment) (26, 47, 51, 52, 61). All the other RCTs started irrespective whether the ductus was open or closed within the first 24 h after birth (untargeted treatment).
Compared to the no treatment group, the infants allocated to the pharmacological treatment group had a lower risk of IVH grade ≥3 (RR 0.76, 95% CI 0.62–0.93; RD −0.03, 95% CI −0.05, −0.01; NNT 34, 95% CI 18.9–136.6). This reduced risk of IVH grade ≥3 was also observed in the subgroups GA <28 weeks (RR 0.77, 95% CI 0.61–0.98; RD −0.03, 95% CI −0.06, −0.00; NNT 30.3, 95% CI 16.1–262.9), BW <1,000 g (RR 0.77, 95% CI 0.61–0.97; RD −0.03, 95% CI −0.06, −0.00; NNT 30.2, 95% CI 16.4–199.9), or if treatment was given untargeted <24 h' PNA (RR 0.70; 95% CI 0.57–0.87; RD −0.04, 95% CI −0.06, −0.02; NNT 26, 95% CI 15.7–64.1).
We found a significant reduction in severe IVH only when untargeted treatment with indomethacin was used <24 h PNA compared to no treatment (RR 0.70, 95% CI 0.54–0.90; RD −0.04, 95% CI −0.07, −0.01). Forest plots for the risk of IVH grade ≥3 are depicted for the different subgroups in Figure 2. Furthermore, the incidence of IVH grade ≥3 in the treatment group was significantly lower in the low and intermediate risk of bias groups and if the rate of open-label treatment was 25–50%. The quality of evidence was graded as very low to low (Supplement 2).
Figure 2
Subgroup analyses of the other outcome measurements proved impossible on account of the scarcity of available data. Five RCTs described data on oliguria (37, 40–42, 62). Five studies described the incidence of pneumothorax (30, 32, 37–39), six studies pulmonary hemorrhage (37, 42, 46, 60, 61, 63), and one study reported pulmonary hypertension as outcome measure (60). Five studies described the incidence of gastrointestinal bleeding (24, 27, 32, 40, 61), while two studies reported the incidence of SIP (46, 61). Only three RCTs described the long-term data on neurodevelopmental outcomes regarding motor delay, cognitive delay, the incidence of deafness and blindness, and neurodevelopmental impairment in general (44, 46, 64).
Discussion
Summary of Evidence
The aim of this systematic review was to investigate whether patient characteristics or study characteristics modulate the beneficial or adverse effects of PDA treatment in preterm infants. The main finding of this review was that pharmacologic treatment of PDA is associated with a significantly reduced risk of IVH grade ≥3 in extremely preterm infants (GA <28 weeks), extremely low BW infants (BW <1,000 g), or when untargeted treatment with indomethacin was started <24 h after birth. Moreover, this review revealed no relevant significant differences for the outcome measures NEC, BPD, mortality, sepsis, PVL, and ROP between intervention and control groups in the subgroups BW, GA, risk of bias, and rate of open-label treatment.
Our findings regarding the reduced risk of IVH grade ≥3 is in line with a previous review comprising 2,588 newborns <37 weeks' gestation, which showed that untargeted administration of indomethacin is associated with a decreased risk of IVH (65). In our meta-analysis a total of 2,937 preterm infants were assessed for IVH grade ≥3 and stratified by BW, GA, and PNA. Out of the infants allocated to the treatment group 10% had IVH grade ≥3 compared to 13% of the infants in the placebo/no treatment group. Dividing the included studies who treated the infants <24 h after birth into untargeted treatment or targeted treatment, we found only reduction of severe IVH in the former group if indomethacin was used. The hypothesis is that this reduction of severe IVH is probably not a direct effect of ductal closure itself and therefore limiting cerebral perfusion disturbances, but mediated by prevention of hyperperfusion by a direct drug-induced cerebrovascular vasoconstriction (see Figure 3). This effect has been demonstrated for indomethacin and might prevent the cerebral hypoperfusion-hyperperfusion sequence, which is considered to be an important pathophysiological mechanism associated with IVH (66–69).
Figure 3
Subdividing the studies according to which drug was used, we found no significant differences in the incidences of NEC, BPD, ROP or mortality, which is in line with recently published papers (, ). In contrast to our meta-analysis, these papers used any grade of IVH instead of severe IVH as outcome parameter and observed no significant differences in any of the used drugs vs. placebo/no treatment. Our review selected studies published between 1985 and 2019, whereas currently, as opposed to the previous century, most preterm infants will have received corticosteroids antenatally and surfactants postnatally, if required. We know that this approach reduces the risk of an IVH (70). Including only those studies published in the last 25 years, the significant reduction of severe IVH is still observed in the youngest, smallest and untargeted treated infants.
Although untargeted treatment constitutes the only convincing evidence for active closure of PDA, it is currently seldom provided (). It might, however, be argued that any evidence-based reduction in the risk of IVH grade ≥3 is beneficial to the infant, but sufficient evidence is lacking. In a 2015 meta-analysis about neurodevelopmental impairment after a severe IVH, only observational cohort studies were identified and on the whole the risk of bias was high (71). Moreover, there is also little evidence of improved long-term developmental outcome and mortality after prophylactic treatment (44, 45, 65).
In addition, we stratified by rate of open-label treatment, something that to our knowledge has not been done before. The median rate of the open-label treatment in the studies was 44.5% (calculated from 38 out of 47 studies). Since we reviewed the raw data in our meta-analysis to determine the morbidity and mortality of the different subgroups, we could not analyze whether the original studies performed intention to treat or per protocol analysis. We hypothesized that the potential effects of active treatment of a PDA would be attenuated in RCTs with a high proportion of open label treatment in the control/placebo arm. However, this was not observed. Failure of DA closure and the need for surgical ligation were significantly lower in the treatment group independent of the rate of open-label treatment. To our surprise, however, this subgroup analysis, which stratified the studies according to a high rate vs. a lower rate of open-label treatment in the control group, showed no difference in morbidity and mortality. We found no significant reduction of major clinical outcomes, not even in the subgroup of RCTs with low open-label treatment rates in the no treatment group of patients. This raises the question whether a PDA should be considered as an epiphenomenon as was suggested by recent cohort studies using restrictive treatment policies (72, 73). This should, however, be supported or refuted by well-powered high-quality RCTs targeting the high-risk population (<28 weeks' GA and/or BW <1,000 g) with low-rate open-label treatment of the placebo/no treatment group.
Limitations
The first limitation of this meta-analysis are the missing data in the RCTs. Unfortunately, even though we tried to reduce selection bias by contacting the corresponding authors, not all missing data could be retrieved. As a consequence, we could not include all studies in our subgroup stratification.
Secondly, a meta-analysis has to deal with heterogeneity of the included RCTs. The high statistical heterogeneity in this meta-analysis is comparable with a previously published meta-analyses (74). Heterogeneity leads to lower quality of evidence (, 75). In an attempt to reduce clinical heterogeneity, we stratified the results in several subgroups and subdivided treatment started <24 h after birth in untargeted treatment and targeted treatment. Moreover, the definitions of outcome measures in the included RCTs in a meta-analysis vary. In the current meta-analysis, the outcomes BPD and NEC were not uniformly defined in the selected studies. The possible reason is the large spread in publication years; criteria for short-term morbidities have changed over the years. Nevertheless, neither the overall meta-analyses nor the subgroup analyses of the different BPD definitions revealed any differences. The heterogeneity of studies analyzing NEC was low. Unfortunately, subgroup analyses could not be performed for the outcome measures pneumothorax, pulmonary hemorrhage, pulmonary hypertension, gastro-intestinal bleeding, SIP, and oliguria, because of the scarcity of available data. Last, another important factor that could be a major factor contributing to heterogeneity is the classification of hemodynamic significance of the PDA. Zonnenberg et al. showed that there is substantial variability in the definition of a significant PDA in clinical trials (). In the 47 included RCTs the used definition of a PDA varied much, ranging from clinical, radiographic and echocardiographic parameters.
Future research is required with unambiguously definitions of outcome measures and larger groups of preterm infants. There is a need for well-powered high-quality RCTs with low-rate open-label treatment of the placebo/no treatment group. In addition, more research is needed to investigate which mechanisms might be responsible for the reduction of IVH grade ≥3 in the youngest, the smallest, or in the preterm infants that are treated untargeted with indomethacin within the first 24 h of life.
Conclusions
In this systematic review, in which we investigated the modulating effects of patient characteristics and study characteristics by performing subgroup meta-analyses, the degree of heterogeneity among the included studies and variability in study quality is high. Therefore, the quality of evidence following GRADE assessment is low. Pharmacological treatment of a PDA in extremely preterm infants with either a GA <28 weeks, a BW <1,000 g, or if untargeted treatment with indomethacin is given <24 h PNA is associated with a significantly lower risk of developing IVH grade ≥3. We found no differences in the incidence of other morbidities or in mortality when we stratified the subgroups by BW, GA, and PNA at start of treatment. Important data on long-term consequences of neurodevelopmental impairment are lacking for these studies. More high-quality and low-rate open-label treatment studies are needed to unravel the effects of pharmacological PDA treatment on short-term and long-term morbidity and to elucidate underlying pathophysiologic mechanisms.
Statements
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Author contributions
EJ conceptualized and designed the study, collected the data, drafted the initial manuscript, and analyzed and interpreted the data. TH collected, analyzed and interpreted the data, and reviewed and revised the manuscript. WO, EK, and PA analyzed and interpreted the data, critically reviewed the manuscript, and provided administrative, technical, or material support. WB coordinated and supervised data collection, analyzed data, and critically reviewed the manuscript for important intellectual content. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fped.2021.626262/full#supplementary-material
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Summary
Keywords
ductus botalli, patent ductus arteriosis, premature (babies), ibuprofen, indometacin, acetaminophen
Citation
Jansen EJS, Hundscheid T, Onland W, Kooi EMW, Andriessen P and de Boode WP (2021) Factors Associated With Benefit of Treatment of Patent Ductus Arteriosus in Preterm Infants: A Systematic Review and Meta-Analysis. Front. Pediatr. 9:626262. doi: 10.3389/fped.2021.626262
Received
05 November 2020
Accepted
14 January 2021
Published
09 February 2021
Volume
9 - 2021
Edited by
Yogen Singh, Cambridge University Hospitals NHS Foundation Trust, United Kingdom
Reviewed by
Samir Gupta, Durham University, United Kingdom; Sajeev Job, Cambridge University Hospitals, United Kingdom
Updates
Copyright
© 2021 Jansen, Hundscheid, Onland, Kooi, Andriessen and de Boode.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Esther J. S. Jansen esther.jansen@radboudumc.nl
This article was submitted to Neonatology, a section of the journal Frontiers in Pediatrics
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