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secretion&#44; metabolization&#44; and&#47;or degradation in the immature lung&#46; Its incidence is inversely proportional to gestational age&#44; with a prevalence ranging from 60&#37; to 80&#37; in extremely preterm neonates &#40;&#60;28 weeks&#41; and 15&#37;&#8211;30&#37; in moderate&#47;late preterm neonates &#40;32&#8211;36 weeks&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Nearly 85&#37; of preterm births each year occur are moderate&#47;late preterm births &#40;32&#8211;36 weeks of gestation&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Although preterm survival rates have increased in high-income countries&#44; preterm birth rates have been increasing since 2000&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> As a result&#44; the number of late preterm neonate births is growing&#44; especially in Western countries&#46; Late preterm neonates are at higher risk of immediate mortality and respiratory morbidity&#44; including RDS&#44;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> and at higher risk of disorders in the long term&#44; such as neurodevelopmental disorders&#44; neurobehavioural disorders and educational problems&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#8211;14</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">In preterm neonates&#44; surfactant replacement therapy is essential for RDS management&#46; In spite of this&#44; there are no evidence-based recommendations for surfactant use in late preterm neonates&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15&#44;16</span></a> The aim of the present study was to gather expert opinions on the diagnosis&#44; treatment&#44; potential complications and future trends of RDS with a specific focus on moderate to late preterm neonates&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Study design and participants</span><p id="par0025" class="elsevierStylePara elsevierViewall">The present study involved implementation of a modified Delphi method to obtain consensus in a panel of expert specialists in neonatology&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> It was carried out in several phases&#44; including the creation of the steering committee &#40;SC&#41; creation&#44; the design of the Delphi questionnaire&#44; the definition of the expert panel&#44; administration of the Delphi questionnaire and data analysis and interpretation &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">The functions of the SC included the formulation of the questionnaire&#44; setting the criteria for panel selection&#44; defining the rules of consensus&#44; interpreting the preliminary and final results and collaborating in writing the manuscript&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In regard to panel composition&#44; highly experienced specialists in neonatology from different regions of Spain were invited to participate&#46; The criteria for inclusion in the panel was to be a neonatologist working in a level III B&#47;C neonatology unit in Spain with at least 10 years of experience&#46; The list of participating panellists can be found in <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 1</a>&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Questionnaire</span><p id="par0040" class="elsevierStylePara elsevierViewall">After defining the goals of the study&#44; the SC carried out a literature search and developed the initial questionnaire&#46; It included 53 questions addressing six main areas&#58; &#40;i&#41; prevention&#47;antenatal corticosteroid administration &#40;10 items&#41;&#59; &#40;ii&#41; diagnosis &#40;9 items&#41;&#59; &#40;iii&#41; treatment &#40;72 items&#41;&#59; &#40;iv&#41; sedation for minimally invasive surfactant therapy &#40;MIST&#41; &#40;6 items&#41;&#59; &#40;v&#41; sequelae and follow-up &#40;7 items&#41; and &#40;vi&#41; future trends &#40;5 items&#41;&#46; <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a> presents the final questionnaire&#46; The questionnaire underwent 2 rounds of voting between February 2023 &#40;first round&#41; and April 2023 &#40;second round&#41;&#46; Participants completed the questionnaire through an online platform that ensured data anonymity and confidentiality&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Data analysis and interpretation</span><p id="par0045" class="elsevierStylePara elsevierViewall">All items were rated on a 4-point scale&#58; 1-totally agree&#44; 2-basically agree&#44; 3-basically disagree and 4-totally disagree&#46; In the first round&#44; consensus was defined as at least 70&#37; of panellists selecting the same single rating category&#46; Items for which a consensus was not reached in the first round were subject to a second round of voting&#46; During the second round&#44; the panellists were given the rating they had selected during the first round and the aggregated total panel results for each question&#46; In the second round&#44; consensus for an item was defined as at least 70&#37; of panellists agreeing in giving a rating of 1 or 2 &#40;consensus in agreement&#41; or a rating of 3 or 4 &#40;consensus in disagreement&#41;&#46; When 60&#37;&#8211;69&#37; of panellists agreed in giving ratings of 1&#47;2 or 3&#47;4&#44; the result was considered &#8220;undetermined-majority in agreement&#8221; or &#8220;undetermined-majority in disagreement&#44;&#8221; and if it there was agreement below 60&#37;&#44; the result for the item was categorised as &#8220;no consensus&#46;&#8221; These voting categories were used in both rounds&#46; We conducted a statistical analysis of the responses for each question and made graphical representations of the results using Excel&#46; The results of the Delphi survey were further evaluated and discussed by the SC&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Results</span><p id="par0050" class="elsevierStylePara elsevierViewall">Twenty-nine highly experienced neonatologists distributed throughout Spain were included in the panel and completed the 2 rounds of the Delphi survey&#46; At the end of the Delphi process&#44; consensus was reached on 98 of the 109 items included in the 53 questions of the questionnaire&#58; 76 in &#8220;agreement&#8221; and 22 in &#8220;disagreement&#8221; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Of the 11 remaining items for which panellists did not reach a consensus&#44; 6 were categorised as &#8220;no consensus&#44;&#8221; 2 as &#8220;undetermined-majority in agreement&#44;&#8221; and 3 as &#8220;undetermined-majority in disagreement&#8221; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Prevention and antenatal corticosteroid administration</span><p id="par0055" class="elsevierStylePara elsevierViewall">Regarding antenatal corticosteroid administration&#44; 77&#37; of panellists considered that the current evidence is insufficient to adequately establish the balance of benefits and harms in threatened preterm labour at 34&#8211;36 weeks of gestation&#44; and 73&#37; agreed not to recommend corticosteroid administration from week 34 &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">All panellists agreed not to recommend an additional dose of corticosteroids between 34 and 36 weeks of gestation in women at high risk of preterm delivery if a first course had been administered before 34 weeks&#46; Most panellists agreed that antenatal corticosteroid administration offers respiratory benefits &#40;76&#37;&#41;&#46; The reasons for not recommending corticosteroid administration between 34 and 36 weeks of gestation included an increased risk of hypoglycaemia in the newborn &#40;79&#37;&#41; and a potential deleterious impact on long-term neurodevelopmental outcomes &#40;83&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Diagnosis</span><p id="par0065" class="elsevierStylePara elsevierViewall">Regarding RDS diagnosis&#44; all panellists &#40;100&#37;&#41; considered that the lung ultrasound &#40;LUS&#41; offers advantages over the chest radiograph and that it should be performed within 2 h of birth &#40;100&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0070" class="elsevierStylePara elsevierViewall">Most panellists considered that the differential diagnosis of RDS should include transient tachypnoea of the newborn &#40;TTNB&#41; &#40;97&#37;&#41;&#44; mild respiratory distress &#40;100&#37;&#41;&#44; congenital pneumonia &#40;93&#37;&#41; and primary pulmonary hypertension &#40;PPH&#41; &#40;76&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46; Moreover&#44; cardiologists should evaluate late preterm neonates with suspected RDS and an unfavourable clinical course to rule out PPH &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Treatment</span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Decision to administer surfactant</span><p id="par0075" class="elsevierStylePara elsevierViewall">Most panellists &#40;93&#37;&#41; agreed that studies were needed to determine the benefits and harms&#44; clinical profile and methods of surfactant administration in moderate&#47;late preterm neonates &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; The factors identified as most important in making the decision whether to administer surfactant were&#58; FiO<span class="elsevierStyleInf">2</span> level &#40;100&#37; of panellists&#41;&#44; severity of respiratory distress &#40;100&#37;&#41;&#44; LUS score &#40;100&#37;&#41;&#44; respiratory acidosis &#40;93&#37;&#41;&#44; previous mean airway pressure &#40;93&#37;&#41; and time elapsed from birth to diagnosis &#40;97&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Panellists recommended surfactant administration within 2&#8211;6 h of birth in infants with a diagnosis of RDS &#40;86&#37;&#41; if the previous mean airway pressure was 6 mmH<span class="elsevierStyleInf">2</span>O or greater &#40;83&#37;&#41; and&#47;or the LUS score is 6 or greater &#40;93&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">Most panellists &#40;83&#37;&#41; would recommend surfactant administration in moderate&#47;late preterm neonates with respiratory distress and an unfavourable clinical course&#44; even when the diagnosis of RDS is uncertain &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Moreover&#44; most panellists would administer surfactant for other conditions&#44; including meconium aspiration syndrome &#40;90&#37;&#41; or congenital pneumonia &#40;83&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46; However&#44; most would not administer surfactant in cases of congenital diaphragmatic hernia&#44; pulmonary hypoplasia or TTNB &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Administration technique and potential complications</span><p id="par0085" class="elsevierStylePara elsevierViewall">Regarding the method of surfactant administration&#44; all respondents would use the MIST technique &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Panellists agreed that the recommended initial dose of surfactant for a late preterm neonate is 200 mg&#47;kg &#40;97&#37;&#41;&#46; No consensus was reached on caffeine administration before surfactant administration via MIST &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Benefits and harms of surfactant administration in these patients</span><p id="par0090" class="elsevierStylePara elsevierViewall">All panellists agreed that surfactant administration could reduce the degree of respiratory distress&#44; improve respiratory parameters&#44; reduce the duration and the need for invasive mechanical ventilation &#40;MV&#41; and shorten the length of stay in the intensive care unit &#40;ICU&#41; and&#47;or the hospital&#46; Moreover&#44; most agreed that surfactant administration could lower the risk of mortality &#40;79&#37;&#41;&#44; decrease the need for a referral from a lower-level to a tertiary care hospital &#40;79&#37;&#41; and reduce the incidence of some of the morbidities typically associated with prematurity &#40;83&#37;&#41;&#46; On the other hand&#44; panellists agreed that not administering surfactant to these patients would not increase the risk of necrotizing enterocolitis &#40;97&#37;&#41;&#44; retinopathy of prematurity &#40;100&#37;&#41; or intracranial haemorrhage &#40;93&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Sedation measures for MIST</span><p id="par0095" class="elsevierStylePara elsevierViewall">Regarding sedation&#44; most participants agreed on the use of nonpharmacological methods as the initial approach&#44; such as the administration of sucrose &#40;97&#37;&#41; or breastfeeding &#40;72&#37;&#41; 2 min before the procedure&#44; both accompanied by swaddling &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; In the case that nonpharmacological measures are ineffective&#44; 3 out of 4 respondents agreed on using an opioid as the first-line sedation agent for surfactant administration via MIST &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a>&#41;&#46;</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Sequelae and follow-up</span><p id="par0100" class="elsevierStylePara elsevierViewall">All respondents agreed that moderate&#47;late preterm neonates are at higher risk of neonatal morbidity and mortality compared to term neonates&#44; particularly respiratory problems &#40;<a class="elsevierStyleCrossRef" href="#fig0035">Fig&#46; 7</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Most neonatologists &#40;90&#37;&#41; agreed that all late preterm neonates with perinatal risk factors or complications in the neonatal period need more specialized monitoring in hospital-based follow-up visits&#46; Moreover&#44; there was consensus that the prevalence of immediate and long-term respiratory disease is higher in moderate&#47;late preterm neonates compared to term neonates&#46; Lastly&#44; most respondents agreed that in moderate&#47;late preterm neonates&#44; a history of chorioamnionitis and absence of breastfeeding are risk factors for developing asthma or pulmonary disease in the long term &#40;<a class="elsevierStyleCrossRef" href="#fig0035">Fig&#46; 7</a>&#41;&#46;</p><elsevierMultimedia ident="fig0035"></elsevierMultimedia></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Future trends</span><p id="par0105" class="elsevierStylePara elsevierViewall">All respondents agreed that there was a lack of large-scope longitudinal population-based studies identifying factors associated with an increased risk of adverse outcomes in moderate&#47;late preterm neonates and pre- and postnatal risk factors that increase the likelihood of impaired lung function in school age &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Discussion</span><p id="par0110" class="elsevierStylePara elsevierViewall">Although a significant body of evidence on the management of RDS in preterm neonates has been gathered over the years&#44; guidelines chiefly focus on very preterm infants &#40;&#60;32 weeks of gestation&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> The results of this project address a current gap in the field&#44; providing recommendations for both the diagnosis of RDS and its management in moderate&#47;late preterm infants that can guide decision-making concerning surfactant administration&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">In preterm infants of lower gestational age &#40;&#60;32 weeks of gestation&#41;&#44; antenatal corticosteroid administration provides respiratory benefits and reduces the risk of mortality and other morbidity &#40;intraventricular haemorrhage&#44; necrotising enterocolitis&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> On the other hand&#44; the benefit&#47;harm balance of antenatal corticosteroid administration in late preterm infants is still unclear&#46; In any case&#44; antenatal corticosteroid administration has been associated with an increased risk of hypoglycaemia<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19&#8211;21</span></a> and there are concerns about its long-term effects on neurodevelopment&#46; Several studies have demonstrated an increased risk of neurocognitive and behavioural abnormalities&#46;<a class="elsevierStyleCrossRefs" href="#bib0110"><span class="elsevierStyleSup">22&#44;23</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Furthermore&#44; there is substantial heterogeneity among international recommendations&#59; the American College of Obstetricians and Gynecologists &#40;ACOG&#41; considers its administration in mothers at high risk of preterm delivery within 7 days between 34 and 36 weeks&#44;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> while in Europe the indication is more controversial&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> There was consensus regarding the lack of sufficient evidence to adequately establish the benefit&#47;harm balance in the administration of antenatal corticosteroids&#46; Furthermore&#44; there was consensus among the panellists to not recommend an additional dose of corticosteroids between 34 and 36 weeks of gestation in the case of high risk of premature delivery&#44; nor between 34 and 34<span class="elsevierStyleSup">&#43;6</span> weeks of gestation&#46;</p><p id="par0125" class="elsevierStylePara elsevierViewall">In recent years&#44; the LUS has been integrated as a useful technique in the diagnosis and management of RDS&#46; For diagnosis of RDS&#44; it is preferable to perform a LUS rather than an X-ray because the former is highly sensitive and avoids exposure to radiation&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> When it comes to RDS management&#44; it is important to determine the need for treatment&#44; specifically surfactant administration&#46; When performed shortly after birth&#44; LUS can predict the respiratory support&#47;surfactant treatment needs of late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> In this regard&#44; all panellists agreed on performing a LUS within 2 h of birth&#44; highlighting the importance of early diagnosis to achieve maximum benefit&#46; The lack of evidence regarding the LUS score to guide surfactant administration in late preterm infants led the panellists to establish a cutoff of 6 h during the Delphi process&#46; However&#44; new evidence has emerged since the questionnaire was developed&#44; and De Luca et al demonstrated that a LUS score higher than 8 is associated with the highest global accuracy&#44; supporting its use to guide surfactant administration&#46; The same study showed that a LUS score of 4 or lower is associated with the highest sensitivity&#44; indicating that the need for surfactant is unlikely in this group&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a></p><p id="par0130" class="elsevierStylePara elsevierViewall">No specific guidelines on surfactant administration in late preterm infants are available&#59; however&#44; several studies have shown that it is safe&#44; improves respiratory outcomes and decreases mortality&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">28&#44;29</span></a> Overall&#44; there is a lack of studies on surfactant administration in late preterm infants&#46; However&#44; an ongoing trial&#44; SURFON &#40;SURFactant Or Not&#41;&#44; is investigating the early use of surfactant in late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> In the present study&#44; most panellists recommended surfactant administration in moderate&#47;late neonates&#44; although there were doubts regarding the diagnosis of RDS&#46; In this regard&#44; when panellists were asked about the administration of surfactant for other pathologies&#44; they mostly agreed on its use for conditions such as congenital pneumonia and meconium aspiration syndrome&#46; In contrast&#44; a survey on the use of surfactants in late preterm infants among Belgian neonatologists highlighted the use of surfactants for RDS and meconium aspiration syndrome&#46; Still&#44; there was less unanimity regarding its use in transient tachypnoea of the newborn and congenital pneumonia&#46;<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a></p><p id="par0135" class="elsevierStylePara elsevierViewall">Although surfactant administration is the main treatment for RDS&#44; the method of administration is still under debate&#46; Minimally invasive techniques &#40;less invasive surfactant administration &#91;LISA&#93; or minimally invasive surfactant therapy &#91;MIST&#93;&#41; also offer advantages in moderate&#47;late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> They achieve respiratory improvement with few adverse effects&#44; a significant reduction in exposure to mechanical ventilation&#44; a reduction in the need for transfer to a tertiary care facility&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a> a non-significant reduction in neonatal ICU and hospital lengths of stay<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> and a decrease in the risk of pneumothorax&#46;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> In this Delphi study&#44; there was unanimity in favour of the use of MIST&#44; preferably with devices specifically designed for the purpose&#46; There was broad consensus about the 200 mg&#47;kg dosage&#44; which was consistent with the most recent recommendations&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> There was no consensus regarding the administration of caffeine prior to administration of surfactant&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">There is considerable controversy in the literature regarding the need for pharmacological sedation&#47;analgesia during MIST&#46; There was consensus among panellists in favour of sedation for late preterm infants&#44; with sucrose preferred over breast milk in the case of nonpharmacological sedation&#46; In this regard&#44; in a recent survey conducted in Spain&#44; all participating hospitals &#40;100&#37;&#41; reported the use of sucrose&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> Notably&#44; up to 70&#37; of Spanish hospitals reported using pharmacological sedation&#47;analgesia before the procedure&#44;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> compared to 52&#37; in Europe&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> There is also controversy in the literature regarding the appropriate type of drug and dose in the case of pharmacological sedation&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> In the present consensus&#44; most panellist would prescribe sedation&#44; prioritizing morphine derivatives &#40;76&#37;&#41;&#46; In this line&#44; several surveys have shown that the agents most frequently used for sedation are opioids &#40;23&#37;&#8211;63&#37;&#41;&#44; followed by propofol &#40;5&#37;&#8211;23&#37;&#41;&#44; benzodiazepines &#40;5&#37;&#8211;23&#37;&#41;&#44; ketamine &#40;9&#37;&#41;&#44; and muscle relaxants &#40;9&#37;&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">35&#44;36</span></a></p><p id="par0145" class="elsevierStylePara elsevierViewall">Regarding follow-up&#44; there is evidence that moderate and late preterm infants are at risk of changes in neurodevelopment&#46;<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">38&#8211;40</span></a> In line with this&#44; panellists agreed in recommending long-term follow-up&#46; Studies are needed to determine the risk factors for adverse outcomes to identify children who require specialised follow-up&#46; The long-term sequelae in late preterm infants include impaired pulmonary function in late childhood and adolescence&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> An ongoing longitudinal prospective study &#40;LaPrem&#41; is evaluating the impact of preterm birth &#40;32&#8211;36 weeks of gestation&#41; on neurodevelopment&#44; brain development and respiratory health in late childhood&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> In parallel&#44; the SEN32-36 working group of the Spanish Society of Neonatology is conducting a nationwide study with the same aim&#46;</p><p id="par0150" class="elsevierStylePara elsevierViewall">The &#8220;small&#8221; size of the panel could be considered a limitation&#44; although the ideal number of panellists for a Delphi consensus has not been established&#46; In addition&#44; small panels yield reliable criteria when they are composed of highly qualified experts &#40;as is the case of the present study&#41;&#46; On the other hand&#44; we cannot overlook the intrinsic limitations of the Delphi design&#44; for instance&#44; that the results derive from opinions without the analysis of retrospective or prospective data&#46; Furthermore&#44; studies with statistical power focused specifically on moderate&#47;late infants will help elucidate the best management for these patients and identify prognostic factors&#46; Moreover&#44; in the future&#44; performance of studies to assess the role of antenatal corticosteroids in late preterm infants would be of utmost interest&#44; and further research is needed to identify pre- and postnatal risk factors for lung function impairment in late childhood&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">In the absence of conclusive data regarding prevention&#44; diagnosis&#44; treatment&#44; and follow-up of RDS in moderate&#47;late preterm infants&#44; and given that most clinical decision rules have been extrapolated from studies performed in preterm infants born before 32 weeks&#44; the present study can help guide decision-making&#44; at least until more scientific evidence becomes available&#46;</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Funding</span><p id="par0160" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleGrantSponsor" id="gs0005">Chiesi Espa&#241;a</span>provided financial assistance for the development and performance of the study&#44; methodological support and medical writing&#46;</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Conflicts of interest</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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          "palabras" => array:6 [
            0 => "Neonatos prematuros tard&#237;os"
            1 => "<span class="elsevierStyleItalic">Less Invasive Surfactant Administration</span> &#40;LISA&#41;"
            2 => "<span class="elsevierStyleItalic">Minimally Invasive Surfactant Therapy</span> &#40;MIST&#41;"
            3 => "Neonatos prematuros moderados&#47;tard&#237;os"
            4 => "S&#237;ndrome de distr&#233;s respiratorio"
            5 => "Encuesta Delphi"
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        "titulo" => "Abstract"
        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Introduction</span><p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Respiratory distress syndrome &#40;RDS&#41; is the most frequent cause of respiratory distress in preterm neonates&#46; In the management of RDS&#44; surfactant plays a pivotal role&#44; but there are no evidence-based recommendations for moderate&#47;late preterm neonates &#40;32&#8211;36 weeks&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Methods</span><p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">A scientific committee developed a questionnaire with 53 questions addressing diagnosis&#44; treatment&#44; potential complications and future trends in RDS specifically focused on moderate and late preterm neonates&#46; This was followed by the performance of a Delphi survey of expert neonatologists&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Results</span><p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Consensus was reached on 98 of the 109 items&#46; The recommendations for the diagnosis of RDS included performing a lung ultrasound and including mild respiratory distress&#44; transient tachypnoea of the newborn&#44; congenital pneumonia and primary pulmonary hypertension in the differential diagnosis&#46; Most panellists agreed on the need for studies that determine the benefit&#47;harm balance&#44; clinical profile and methods of surfactant administration in moderate&#47;late preterm neonates&#46; All respondents would use the MIST approach with devices specifically designed for surfactant administration&#46; Regarding sedation measures during MIST&#44; most participants agreed on the use of nonpharmacological interventions and&#44; if these proved ineffective&#44; an opioid&#46; All respondents agreed that moderate&#47;late preterm neonates are at increased risk of neonatal morbidity and mortality&#44; particularly respiratory problems&#44; and considered the need for more specialised monitoring in hospital follow-up visits in neonates with associated risk factors or a history of complications in the neonatal period&#46; Finally&#44; all respondents agreed that there is a lack of studies identifying risk factors and medium-term adverse outcomes in moderate&#47;late preterm neonates&#46;</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conclusion</span><p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">This expert consensus will help with the diagnosis and management of RDS and guide decision-making about surfactant administration in moderate&#47;late preterm neonates&#46;</p></span>"
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        "resumen" => "<span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Introducci&#243;n</span><p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de distr&#233;s respiratorio &#40;SDR&#41; es la causa m&#225;s frecuente de distr&#233;s respiratorio en los reci&#233;n nacidos prematuros&#46; El surfactante desempe&#241;a un papel fundamental en el tratamiento del SDR&#44; pero no existen recomendaciones basadas en la evidencia en neonatos prematuros moderados&#47;tard&#237;os &#40;32-36 semanas&#41;&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">M&#233;todos</span><p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">Un Comit&#233; Cient&#237;fico dise&#241;&#243; un cuestionario con 53 preguntas que abordaban el diagn&#243;stico&#44; el tratamiento&#44; las posibles complicaciones y las tendencias futuras del SDR&#44; espec&#237;ficamente en los reci&#233;n nacidos prematuros moderados y tard&#237;os&#46; Posteriormente&#44; se llev&#243; a cabo una encuesta Delphi entre neonat&#243;logos con experiencia en el campo&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Resultados</span><p id="spar0105" class="elsevierStyleSimplePara elsevierViewall">Se alcanz&#243; consenso en 98 de los 109 &#237;tems incluidos&#46; Se recomend&#243; la realizaci&#243;n de una ecograf&#237;a pulmonar y la consideraci&#243;n de la dificultad respiratoria leve&#44; la taquipnea transitoria del reci&#233;n nacido&#44; la neumon&#237;a cong&#233;nita y la hipertensi&#243;n pulmonar primaria durante el diagn&#243;stico diferencial&#46; La mayor&#237;a de los panelistas coincidieron en la necesidad de realizar estudios para determinar el riesgo&#47;beneficio&#44; el perfil cl&#237;nico y los m&#233;todos de administraci&#243;n de surfactante en neonatos prematuros moderados&#47;tard&#237;os&#46; Se recomend&#243; la t&#233;cnica MIST con dispositivos espec&#237;ficamente dise&#241;ados para la administraci&#243;n de surfactante&#46; La mayor&#237;a de los participantes coincidieron en recomendar el uso de procedimientos no farmacol&#243;gicos de sedaci&#243;n durante el MIST y&#44; en caso de ineficacia&#44; un opi&#225;ceo&#46; Todos los encuestados coincidieron en que los prematuros moderados&#47;tard&#237;os presentan mayor riesgo de morbimortalidad neonatal&#44; en particular de problemas respiratorios&#44; y consideraron necesario m&#225;s monitorizaci&#243;n especializada en el seguimiento hospitalario de neonatos con mayor riesgo y&#47;o complicaciones&#46; Por &#250;ltimo&#44; todos los encuestados coincidieron en la falta de estudios para identificar factores de riesgo y resultados adversos a medio plazo en neonatos prematuros moderados&#47;tard&#237;os&#46;</p></span> <span id="abst0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Conclusiones</span><p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">Este consenso de expertos ser&#225; de ayuda en el diagn&#243;stico y manejo del SDR y en la decisi&#243;n de administrar surfactantes en neonatos prematuros moderados&#47;tard&#237;os&#46;</p></span>"
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Original Article
Management of respiratory distress syndrome in moderate/late preterm neonates: A Delphi consensus
Manejo del síndrome de distrés respiratorio en recién nacidos prematuros moderados/tardíos: consenso Delphi
Segundo Rite Graciaa, Juan José Agüera Arenasb, Gemma Ginovart Galianac, María Jesús Rodríguez Revueltad,
Corresponding author
sriteg@salud.aragon.es

Corresponding author.
a Servicio de Neonatología, Hospital Universitario Miguel Servet, Zaragoza, Spain
b Servicio de Neonatología, Hospital Clínico Universitario Virgen de la Arrixaca, El Palmar, Murcia, Spain
c Servicio de Neonatología, Hospital Universitario Germans Trias i Pujol, Badalona, Spain
d Servicio de Neonatología, Hospital Universitario Virgen Macarena, Sevilla, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Every year&#44; 10&#37; of births worldwide are preterm &#40;&#60;37 weeks&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Preterm birth complications are the leading cause of death among children aged less than 5 years&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Among the common respiratory complications in preterm neonates&#44; respiratory distress syndrome &#40;RDS&#41; is the most frequent cause of respiratory distress&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Respiratory distress syndrome is caused by impaired or delayed surfactant synthesis&#44; secretion&#44; metabolization&#44; and&#47;or degradation in the immature lung&#46; Its incidence is inversely proportional to gestational age&#44; with a prevalence ranging from 60&#37; to 80&#37; in extremely preterm neonates &#40;&#60;28 weeks&#41; and 15&#37;&#8211;30&#37; in moderate&#47;late preterm neonates &#40;32&#8211;36 weeks&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">Nearly 85&#37; of preterm births each year occur are moderate&#47;late preterm births &#40;32&#8211;36 weeks of gestation&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Although preterm survival rates have increased in high-income countries&#44; preterm birth rates have been increasing since 2000&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> As a result&#44; the number of late preterm neonate births is growing&#44; especially in Western countries&#46; Late preterm neonates are at higher risk of immediate mortality and respiratory morbidity&#44; including RDS&#44;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> and at higher risk of disorders in the long term&#44; such as neurodevelopmental disorders&#44; neurobehavioural disorders and educational problems&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#8211;14</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">In preterm neonates&#44; surfactant replacement therapy is essential for RDS management&#46; In spite of this&#44; there are no evidence-based recommendations for surfactant use in late preterm neonates&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15&#44;16</span></a> The aim of the present study was to gather expert opinions on the diagnosis&#44; treatment&#44; potential complications and future trends of RDS with a specific focus on moderate to late preterm neonates&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Study design and participants</span><p id="par0025" class="elsevierStylePara elsevierViewall">The present study involved implementation of a modified Delphi method to obtain consensus in a panel of expert specialists in neonatology&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> It was carried out in several phases&#44; including the creation of the steering committee &#40;SC&#41; creation&#44; the design of the Delphi questionnaire&#44; the definition of the expert panel&#44; administration of the Delphi questionnaire and data analysis and interpretation &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">The functions of the SC included the formulation of the questionnaire&#44; setting the criteria for panel selection&#44; defining the rules of consensus&#44; interpreting the preliminary and final results and collaborating in writing the manuscript&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In regard to panel composition&#44; highly experienced specialists in neonatology from different regions of Spain were invited to participate&#46; The criteria for inclusion in the panel was to be a neonatologist working in a level III B&#47;C neonatology unit in Spain with at least 10 years of experience&#46; The list of participating panellists can be found in <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 1</a>&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Questionnaire</span><p id="par0040" class="elsevierStylePara elsevierViewall">After defining the goals of the study&#44; the SC carried out a literature search and developed the initial questionnaire&#46; It included 53 questions addressing six main areas&#58; &#40;i&#41; prevention&#47;antenatal corticosteroid administration &#40;10 items&#41;&#59; &#40;ii&#41; diagnosis &#40;9 items&#41;&#59; &#40;iii&#41; treatment &#40;72 items&#41;&#59; &#40;iv&#41; sedation for minimally invasive surfactant therapy &#40;MIST&#41; &#40;6 items&#41;&#59; &#40;v&#41; sequelae and follow-up &#40;7 items&#41; and &#40;vi&#41; future trends &#40;5 items&#41;&#46; <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a> presents the final questionnaire&#46; The questionnaire underwent 2 rounds of voting between February 2023 &#40;first round&#41; and April 2023 &#40;second round&#41;&#46; Participants completed the questionnaire through an online platform that ensured data anonymity and confidentiality&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Data analysis and interpretation</span><p id="par0045" class="elsevierStylePara elsevierViewall">All items were rated on a 4-point scale&#58; 1-totally agree&#44; 2-basically agree&#44; 3-basically disagree and 4-totally disagree&#46; In the first round&#44; consensus was defined as at least 70&#37; of panellists selecting the same single rating category&#46; Items for which a consensus was not reached in the first round were subject to a second round of voting&#46; During the second round&#44; the panellists were given the rating they had selected during the first round and the aggregated total panel results for each question&#46; In the second round&#44; consensus for an item was defined as at least 70&#37; of panellists agreeing in giving a rating of 1 or 2 &#40;consensus in agreement&#41; or a rating of 3 or 4 &#40;consensus in disagreement&#41;&#46; When 60&#37;&#8211;69&#37; of panellists agreed in giving ratings of 1&#47;2 or 3&#47;4&#44; the result was considered &#8220;undetermined-majority in agreement&#8221; or &#8220;undetermined-majority in disagreement&#44;&#8221; and if it there was agreement below 60&#37;&#44; the result for the item was categorised as &#8220;no consensus&#46;&#8221; These voting categories were used in both rounds&#46; We conducted a statistical analysis of the responses for each question and made graphical representations of the results using Excel&#46; The results of the Delphi survey were further evaluated and discussed by the SC&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Results</span><p id="par0050" class="elsevierStylePara elsevierViewall">Twenty-nine highly experienced neonatologists distributed throughout Spain were included in the panel and completed the 2 rounds of the Delphi survey&#46; At the end of the Delphi process&#44; consensus was reached on 98 of the 109 items included in the 53 questions of the questionnaire&#58; 76 in &#8220;agreement&#8221; and 22 in &#8220;disagreement&#8221; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Of the 11 remaining items for which panellists did not reach a consensus&#44; 6 were categorised as &#8220;no consensus&#44;&#8221; 2 as &#8220;undetermined-majority in agreement&#44;&#8221; and 3 as &#8220;undetermined-majority in disagreement&#8221; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Prevention and antenatal corticosteroid administration</span><p id="par0055" class="elsevierStylePara elsevierViewall">Regarding antenatal corticosteroid administration&#44; 77&#37; of panellists considered that the current evidence is insufficient to adequately establish the balance of benefits and harms in threatened preterm labour at 34&#8211;36 weeks of gestation&#44; and 73&#37; agreed not to recommend corticosteroid administration from week 34 &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">All panellists agreed not to recommend an additional dose of corticosteroids between 34 and 36 weeks of gestation in women at high risk of preterm delivery if a first course had been administered before 34 weeks&#46; Most panellists agreed that antenatal corticosteroid administration offers respiratory benefits &#40;76&#37;&#41;&#46; The reasons for not recommending corticosteroid administration between 34 and 36 weeks of gestation included an increased risk of hypoglycaemia in the newborn &#40;79&#37;&#41; and a potential deleterious impact on long-term neurodevelopmental outcomes &#40;83&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Diagnosis</span><p id="par0065" class="elsevierStylePara elsevierViewall">Regarding RDS diagnosis&#44; all panellists &#40;100&#37;&#41; considered that the lung ultrasound &#40;LUS&#41; offers advantages over the chest radiograph and that it should be performed within 2 h of birth &#40;100&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0070" class="elsevierStylePara elsevierViewall">Most panellists considered that the differential diagnosis of RDS should include transient tachypnoea of the newborn &#40;TTNB&#41; &#40;97&#37;&#41;&#44; mild respiratory distress &#40;100&#37;&#41;&#44; congenital pneumonia &#40;93&#37;&#41; and primary pulmonary hypertension &#40;PPH&#41; &#40;76&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46; Moreover&#44; cardiologists should evaluate late preterm neonates with suspected RDS and an unfavourable clinical course to rule out PPH &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Treatment</span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Decision to administer surfactant</span><p id="par0075" class="elsevierStylePara elsevierViewall">Most panellists &#40;93&#37;&#41; agreed that studies were needed to determine the benefits and harms&#44; clinical profile and methods of surfactant administration in moderate&#47;late preterm neonates &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; The factors identified as most important in making the decision whether to administer surfactant were&#58; FiO<span class="elsevierStyleInf">2</span> level &#40;100&#37; of panellists&#41;&#44; severity of respiratory distress &#40;100&#37;&#41;&#44; LUS score &#40;100&#37;&#41;&#44; respiratory acidosis &#40;93&#37;&#41;&#44; previous mean airway pressure &#40;93&#37;&#41; and time elapsed from birth to diagnosis &#40;97&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Panellists recommended surfactant administration within 2&#8211;6 h of birth in infants with a diagnosis of RDS &#40;86&#37;&#41; if the previous mean airway pressure was 6 mmH<span class="elsevierStyleInf">2</span>O or greater &#40;83&#37;&#41; and&#47;or the LUS score is 6 or greater &#40;93&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">Most panellists &#40;83&#37;&#41; would recommend surfactant administration in moderate&#47;late preterm neonates with respiratory distress and an unfavourable clinical course&#44; even when the diagnosis of RDS is uncertain &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Moreover&#44; most panellists would administer surfactant for other conditions&#44; including meconium aspiration syndrome &#40;90&#37;&#41; or congenital pneumonia &#40;83&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46; However&#44; most would not administer surfactant in cases of congenital diaphragmatic hernia&#44; pulmonary hypoplasia or TTNB &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Administration technique and potential complications</span><p id="par0085" class="elsevierStylePara elsevierViewall">Regarding the method of surfactant administration&#44; all respondents would use the MIST technique &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Panellists agreed that the recommended initial dose of surfactant for a late preterm neonate is 200 mg&#47;kg &#40;97&#37;&#41;&#46; No consensus was reached on caffeine administration before surfactant administration via MIST &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Benefits and harms of surfactant administration in these patients</span><p id="par0090" class="elsevierStylePara elsevierViewall">All panellists agreed that surfactant administration could reduce the degree of respiratory distress&#44; improve respiratory parameters&#44; reduce the duration and the need for invasive mechanical ventilation &#40;MV&#41; and shorten the length of stay in the intensive care unit &#40;ICU&#41; and&#47;or the hospital&#46; Moreover&#44; most agreed that surfactant administration could lower the risk of mortality &#40;79&#37;&#41;&#44; decrease the need for a referral from a lower-level to a tertiary care hospital &#40;79&#37;&#41; and reduce the incidence of some of the morbidities typically associated with prematurity &#40;83&#37;&#41;&#46; On the other hand&#44; panellists agreed that not administering surfactant to these patients would not increase the risk of necrotizing enterocolitis &#40;97&#37;&#41;&#44; retinopathy of prematurity &#40;100&#37;&#41; or intracranial haemorrhage &#40;93&#37;&#41; &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Sedation measures for MIST</span><p id="par0095" class="elsevierStylePara elsevierViewall">Regarding sedation&#44; most participants agreed on the use of nonpharmacological methods as the initial approach&#44; such as the administration of sucrose &#40;97&#37;&#41; or breastfeeding &#40;72&#37;&#41; 2 min before the procedure&#44; both accompanied by swaddling &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; In the case that nonpharmacological measures are ineffective&#44; 3 out of 4 respondents agreed on using an opioid as the first-line sedation agent for surfactant administration via MIST &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a>&#41;&#46;</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Sequelae and follow-up</span><p id="par0100" class="elsevierStylePara elsevierViewall">All respondents agreed that moderate&#47;late preterm neonates are at higher risk of neonatal morbidity and mortality compared to term neonates&#44; particularly respiratory problems &#40;<a class="elsevierStyleCrossRef" href="#fig0035">Fig&#46; 7</a> and <a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46; Most neonatologists &#40;90&#37;&#41; agreed that all late preterm neonates with perinatal risk factors or complications in the neonatal period need more specialized monitoring in hospital-based follow-up visits&#46; Moreover&#44; there was consensus that the prevalence of immediate and long-term respiratory disease is higher in moderate&#47;late preterm neonates compared to term neonates&#46; Lastly&#44; most respondents agreed that in moderate&#47;late preterm neonates&#44; a history of chorioamnionitis and absence of breastfeeding are risk factors for developing asthma or pulmonary disease in the long term &#40;<a class="elsevierStyleCrossRef" href="#fig0035">Fig&#46; 7</a>&#41;&#46;</p><elsevierMultimedia ident="fig0035"></elsevierMultimedia></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Future trends</span><p id="par0105" class="elsevierStylePara elsevierViewall">All respondents agreed that there was a lack of large-scope longitudinal population-based studies identifying factors associated with an increased risk of adverse outcomes in moderate&#47;late preterm neonates and pre- and postnatal risk factors that increase the likelihood of impaired lung function in school age &#40;<a class="elsevierStyleCrossRef" href="#sec0095">Supplementary Table 2</a>&#41;&#46;</p></span></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Discussion</span><p id="par0110" class="elsevierStylePara elsevierViewall">Although a significant body of evidence on the management of RDS in preterm neonates has been gathered over the years&#44; guidelines chiefly focus on very preterm infants &#40;&#60;32 weeks of gestation&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> The results of this project address a current gap in the field&#44; providing recommendations for both the diagnosis of RDS and its management in moderate&#47;late preterm infants that can guide decision-making concerning surfactant administration&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">In preterm infants of lower gestational age &#40;&#60;32 weeks of gestation&#41;&#44; antenatal corticosteroid administration provides respiratory benefits and reduces the risk of mortality and other morbidity &#40;intraventricular haemorrhage&#44; necrotising enterocolitis&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> On the other hand&#44; the benefit&#47;harm balance of antenatal corticosteroid administration in late preterm infants is still unclear&#46; In any case&#44; antenatal corticosteroid administration has been associated with an increased risk of hypoglycaemia<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19&#8211;21</span></a> and there are concerns about its long-term effects on neurodevelopment&#46; Several studies have demonstrated an increased risk of neurocognitive and behavioural abnormalities&#46;<a class="elsevierStyleCrossRefs" href="#bib0110"><span class="elsevierStyleSup">22&#44;23</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Furthermore&#44; there is substantial heterogeneity among international recommendations&#59; the American College of Obstetricians and Gynecologists &#40;ACOG&#41; considers its administration in mothers at high risk of preterm delivery within 7 days between 34 and 36 weeks&#44;<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> while in Europe the indication is more controversial&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> There was consensus regarding the lack of sufficient evidence to adequately establish the benefit&#47;harm balance in the administration of antenatal corticosteroids&#46; Furthermore&#44; there was consensus among the panellists to not recommend an additional dose of corticosteroids between 34 and 36 weeks of gestation in the case of high risk of premature delivery&#44; nor between 34 and 34<span class="elsevierStyleSup">&#43;6</span> weeks of gestation&#46;</p><p id="par0125" class="elsevierStylePara elsevierViewall">In recent years&#44; the LUS has been integrated as a useful technique in the diagnosis and management of RDS&#46; For diagnosis of RDS&#44; it is preferable to perform a LUS rather than an X-ray because the former is highly sensitive and avoids exposure to radiation&#46;<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> When it comes to RDS management&#44; it is important to determine the need for treatment&#44; specifically surfactant administration&#46; When performed shortly after birth&#44; LUS can predict the respiratory support&#47;surfactant treatment needs of late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> In this regard&#44; all panellists agreed on performing a LUS within 2 h of birth&#44; highlighting the importance of early diagnosis to achieve maximum benefit&#46; The lack of evidence regarding the LUS score to guide surfactant administration in late preterm infants led the panellists to establish a cutoff of 6 h during the Delphi process&#46; However&#44; new evidence has emerged since the questionnaire was developed&#44; and De Luca et al demonstrated that a LUS score higher than 8 is associated with the highest global accuracy&#44; supporting its use to guide surfactant administration&#46; The same study showed that a LUS score of 4 or lower is associated with the highest sensitivity&#44; indicating that the need for surfactant is unlikely in this group&#46;<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a></p><p id="par0130" class="elsevierStylePara elsevierViewall">No specific guidelines on surfactant administration in late preterm infants are available&#59; however&#44; several studies have shown that it is safe&#44; improves respiratory outcomes and decreases mortality&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">28&#44;29</span></a> Overall&#44; there is a lack of studies on surfactant administration in late preterm infants&#46; However&#44; an ongoing trial&#44; SURFON &#40;SURFactant Or Not&#41;&#44; is investigating the early use of surfactant in late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> In the present study&#44; most panellists recommended surfactant administration in moderate&#47;late neonates&#44; although there were doubts regarding the diagnosis of RDS&#46; In this regard&#44; when panellists were asked about the administration of surfactant for other pathologies&#44; they mostly agreed on its use for conditions such as congenital pneumonia and meconium aspiration syndrome&#46; In contrast&#44; a survey on the use of surfactants in late preterm infants among Belgian neonatologists highlighted the use of surfactants for RDS and meconium aspiration syndrome&#46; Still&#44; there was less unanimity regarding its use in transient tachypnoea of the newborn and congenital pneumonia&#46;<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a></p><p id="par0135" class="elsevierStylePara elsevierViewall">Although surfactant administration is the main treatment for RDS&#44; the method of administration is still under debate&#46; Minimally invasive techniques &#40;less invasive surfactant administration &#91;LISA&#93; or minimally invasive surfactant therapy &#91;MIST&#93;&#41; also offer advantages in moderate&#47;late preterm infants&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> They achieve respiratory improvement with few adverse effects&#44; a significant reduction in exposure to mechanical ventilation&#44; a reduction in the need for transfer to a tertiary care facility&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a> a non-significant reduction in neonatal ICU and hospital lengths of stay<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> and a decrease in the risk of pneumothorax&#46;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> In this Delphi study&#44; there was unanimity in favour of the use of MIST&#44; preferably with devices specifically designed for the purpose&#46; There was broad consensus about the 200 mg&#47;kg dosage&#44; which was consistent with the most recent recommendations&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> There was no consensus regarding the administration of caffeine prior to administration of surfactant&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">There is considerable controversy in the literature regarding the need for pharmacological sedation&#47;analgesia during MIST&#46; There was consensus among panellists in favour of sedation for late preterm infants&#44; with sucrose preferred over breast milk in the case of nonpharmacological sedation&#46; In this regard&#44; in a recent survey conducted in Spain&#44; all participating hospitals &#40;100&#37;&#41; reported the use of sucrose&#46;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> Notably&#44; up to 70&#37; of Spanish hospitals reported using pharmacological sedation&#47;analgesia before the procedure&#44;<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> compared to 52&#37; in Europe&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> There is also controversy in the literature regarding the appropriate type of drug and dose in the case of pharmacological sedation&#46;<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> In the present consensus&#44; most panellist would prescribe sedation&#44; prioritizing morphine derivatives &#40;76&#37;&#41;&#46; In this line&#44; several surveys have shown that the agents most frequently used for sedation are opioids &#40;23&#37;&#8211;63&#37;&#41;&#44; followed by propofol &#40;5&#37;&#8211;23&#37;&#41;&#44; benzodiazepines &#40;5&#37;&#8211;23&#37;&#41;&#44; ketamine &#40;9&#37;&#41;&#44; and muscle relaxants &#40;9&#37;&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">35&#44;36</span></a></p><p id="par0145" class="elsevierStylePara elsevierViewall">Regarding follow-up&#44; there is evidence that moderate and late preterm infants are at risk of changes in neurodevelopment&#46;<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">38&#8211;40</span></a> In line with this&#44; panellists agreed in recommending long-term follow-up&#46; Studies are needed to determine the risk factors for adverse outcomes to identify children who require specialised follow-up&#46; The long-term sequelae in late preterm infants include impaired pulmonary function in late childhood and adolescence&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> An ongoing longitudinal prospective study &#40;LaPrem&#41; is evaluating the impact of preterm birth &#40;32&#8211;36 weeks of gestation&#41; on neurodevelopment&#44; brain development and respiratory health in late childhood&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> In parallel&#44; the SEN32-36 working group of the Spanish Society of Neonatology is conducting a nationwide study with the same aim&#46;</p><p id="par0150" class="elsevierStylePara elsevierViewall">The &#8220;small&#8221; size of the panel could be considered a limitation&#44; although the ideal number of panellists for a Delphi consensus has not been established&#46; In addition&#44; small panels yield reliable criteria when they are composed of highly qualified experts &#40;as is the case of the present study&#41;&#46; On the other hand&#44; we cannot overlook the intrinsic limitations of the Delphi design&#44; for instance&#44; that the results derive from opinions without the analysis of retrospective or prospective data&#46; Furthermore&#44; studies with statistical power focused specifically on moderate&#47;late infants will help elucidate the best management for these patients and identify prognostic factors&#46; Moreover&#44; in the future&#44; performance of studies to assess the role of antenatal corticosteroids in late preterm infants would be of utmost interest&#44; and further research is needed to identify pre- and postnatal risk factors for lung function impairment in late childhood&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">In the absence of conclusive data regarding prevention&#44; diagnosis&#44; treatment&#44; and follow-up of RDS in moderate&#47;late preterm infants&#44; and given that most clinical decision rules have been extrapolated from studies performed in preterm infants born before 32 weeks&#44; the present study can help guide decision-making&#44; at least until more scientific evidence becomes available&#46;</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Funding</span><p id="par0160" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleGrantSponsor" id="gs0005">Chiesi Espa&#241;a</span>provided financial assistance for the development and performance of the study&#44; methodological support and medical writing&#46;</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Conflicts of interest</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Introduction</span><p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Respiratory distress syndrome &#40;RDS&#41; is the most frequent cause of respiratory distress in preterm neonates&#46; In the management of RDS&#44; surfactant plays a pivotal role&#44; but there are no evidence-based recommendations for moderate&#47;late preterm neonates &#40;32&#8211;36 weeks&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Methods</span><p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">A scientific committee developed a questionnaire with 53 questions addressing diagnosis&#44; treatment&#44; potential complications and future trends in RDS specifically focused on moderate and late preterm neonates&#46; This was followed by the performance of a Delphi survey of expert neonatologists&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Results</span><p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Consensus was reached on 98 of the 109 items&#46; The recommendations for the diagnosis of RDS included performing a lung ultrasound and including mild respiratory distress&#44; transient tachypnoea of the newborn&#44; congenital pneumonia and primary pulmonary hypertension in the differential diagnosis&#46; Most panellists agreed on the need for studies that determine the benefit&#47;harm balance&#44; clinical profile and methods of surfactant administration in moderate&#47;late preterm neonates&#46; All respondents would use the MIST approach with devices specifically designed for surfactant administration&#46; Regarding sedation measures during MIST&#44; most participants agreed on the use of nonpharmacological interventions and&#44; if these proved ineffective&#44; an opioid&#46; All respondents agreed that moderate&#47;late preterm neonates are at increased risk of neonatal morbidity and mortality&#44; particularly respiratory problems&#44; and considered the need for more specialised monitoring in hospital follow-up visits in neonates with associated risk factors or a history of complications in the neonatal period&#46; Finally&#44; all respondents agreed that there is a lack of studies identifying risk factors and medium-term adverse outcomes in moderate&#47;late preterm neonates&#46;</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conclusion</span><p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">This expert consensus will help with the diagnosis and management of RDS and guide decision-making about surfactant administration in moderate&#47;late preterm neonates&#46;</p></span>"
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        "titulo" => "Resumen"
        "resumen" => "<span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Introducci&#243;n</span><p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de distr&#233;s respiratorio &#40;SDR&#41; es la causa m&#225;s frecuente de distr&#233;s respiratorio en los reci&#233;n nacidos prematuros&#46; El surfactante desempe&#241;a un papel fundamental en el tratamiento del SDR&#44; pero no existen recomendaciones basadas en la evidencia en neonatos prematuros moderados&#47;tard&#237;os &#40;32-36 semanas&#41;&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">M&#233;todos</span><p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">Un Comit&#233; Cient&#237;fico dise&#241;&#243; un cuestionario con 53 preguntas que abordaban el diagn&#243;stico&#44; el tratamiento&#44; las posibles complicaciones y las tendencias futuras del SDR&#44; espec&#237;ficamente en los reci&#233;n nacidos prematuros moderados y tard&#237;os&#46; Posteriormente&#44; se llev&#243; a cabo una encuesta Delphi entre neonat&#243;logos con experiencia en el campo&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Resultados</span><p id="spar0105" class="elsevierStyleSimplePara elsevierViewall">Se alcanz&#243; consenso en 98 de los 109 &#237;tems incluidos&#46; Se recomend&#243; la realizaci&#243;n de una ecograf&#237;a pulmonar y la consideraci&#243;n de la dificultad respiratoria leve&#44; la taquipnea transitoria del reci&#233;n nacido&#44; la neumon&#237;a cong&#233;nita y la hipertensi&#243;n pulmonar primaria durante el diagn&#243;stico diferencial&#46; La mayor&#237;a de los panelistas coincidieron en la necesidad de realizar estudios para determinar el riesgo&#47;beneficio&#44; el perfil cl&#237;nico y los m&#233;todos de administraci&#243;n de surfactante en neonatos prematuros moderados&#47;tard&#237;os&#46; Se recomend&#243; la t&#233;cnica MIST con dispositivos espec&#237;ficamente dise&#241;ados para la administraci&#243;n de surfactante&#46; La mayor&#237;a de los participantes coincidieron en recomendar el uso de procedimientos no farmacol&#243;gicos de sedaci&#243;n durante el MIST y&#44; en caso de ineficacia&#44; un opi&#225;ceo&#46; Todos los encuestados coincidieron en que los prematuros moderados&#47;tard&#237;os presentan mayor riesgo de morbimortalidad neonatal&#44; en particular de problemas respiratorios&#44; y consideraron necesario m&#225;s monitorizaci&#243;n especializada en el seguimiento hospitalario de neonatos con mayor riesgo y&#47;o complicaciones&#46; Por &#250;ltimo&#44; todos los encuestados coincidieron en la falta de estudios para identificar factores de riesgo y resultados adversos a medio plazo en neonatos prematuros moderados&#47;tard&#237;os&#46;</p></span> <span id="abst0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Conclusiones</span><p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">Este consenso de expertos ser&#225; de ayuda en el diagn&#243;stico y manejo del SDR y en la decisi&#243;n de administrar surfactantes en neonatos prematuros moderados&#47;tard&#237;os&#46;</p></span>"
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      "titulo" => "References"
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ISSN: 23412879
Original language: English
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