EUROpean Pain Audit In Neonates

NCT ID: NCT01694745

Last Updated: 2014-01-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

6489 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-10-31

Study Completion Date

2013-06-30

Brief Summary

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EUROPAIN Survey is an epidemiological study aimed at assessing current clinical practices regarding the use of sedative and analgesic drugs in newborns admitted to NICUs or PICUs in different countries in Europe. This study is conducted as part of the NeoOpiod study.

The main objective of this study is to determine the current clinical practices regarding the use of sedative and analgesic drugs in newborns in intensive units in different countries in Europe. The principal criteria are: the frequency of ventilated neonates receiving sedation and analgesia, the medications used for sedation and analgesia in ventilated neonates, the length of use of medications administered for sedation and analgesia in ventilated neonates and similarities and differences in sedation and analgesia practices among European countries.

The secondary objectives are: a) to determine the proportion of neonatal units that have developed and implemented local written guidelines to provide continuous sedation and analgesia in ventilated newborn infants as well as to prevent and treat procedural pain, b) to document the published guidelines for neonatal analgesia and sedation in different European countries and develop consensus for common European standards that can be applied in all medical settings, c) to determine the frequency of use of pain assessment tools in ventilated newborn infants and evaluate their impact on pain management practices and d) to determine practices to assess and prevent withdrawal syndromes.

The EUROPAIN STUDY is observational and therefore it will not interfere with routine practices of participating units. No changes in diagnostic, therapeutic or any managing strategy of patients are imposed by the participation in this study. This epidemiological study will only collect data on clinical practices in each unit. It will include all neonates up to a corrected age of 44 weeks post conception.

The maximum duration of data collection for every included infant is 28 days. Data collection will stop before 28 days if the infant leaves the unit (discharge, death, transfer to another hospital). Data will be entered on a secure web-based questionnaire.

Detailed Description

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1.1 Background and rationale The alleviation of pain is a basic and human right regardless of age. Neonates do feel pain and it has been shown that preterm infants are even more vulnerable to pain than older infants. The more vulnerable preterm neonates are precisely those that are more exposed to pain. Neonates admitted to intensive care units, both neonatal intensive care unit (NICU) and pediatric intensive care unit (PICU), undergo dozens or even hundreds of painful procedures during their stay. These painful procedures include, for many of the ICU neonates, a tracheal intubation followed by mechanical ventilation. The pain and stress that are induced by mechanical ventilation as well as by repetitive procedures or painful diseases has led medical staff to use sedation and analgesia in neonates admitted to intensive care units. The subjectivity and difficulty inherent to pain measurement in neonates have probably contributed to a wide variety of neonatal sedation and analgesia practices. To date, these practices have been rarely studied.

Why would sedation and analgesia be necessary? Mechanical ventilation is a potentially painful intervention. Adults often describe mechanical ventilation as a painful and anxiety-provoking experience. The main objectives of sedation and analgesia are: reduction of pain, stress and irritability, promotion of blood pressure stability, promotion of ventilator synchrony and improvement of oxygenation. In the long term, reduced stress, as well as reduced fluctuations in oxygenation and blood pressure is believed to minimize the risks of neurological injury and death. However, the use of sedation and analgesia is only conceivable in the respect of the principle that must accompany all medical actions: first, do no harm.

Pain and stress undergone during the neonatal period can have deleterious short-term and long-term consequences. Some of these consequences have been reduced with adequate analgesic treatment. Current data show the necessity to give adequate sedation and analgesia to ventilated neonates.

Statements promoting the use of sedation and analgesia The increased awareness that neonates feel pain, the ethical obligation to treat this pain with analgesics, the growing body of evidence demonstrating that untreated neonatal pain can lead to altered reactivity to pain that persists throughout infancy and childhood as well as the need for a humane management of neonates have lead to the development of International and National Guidelines promoting the use of analgesics in the neonatal population. These Guidelines state that units that provide neonatal care should develop and implement guidelines concerning neonatal pain. However, the existing literature is still conflicting regarding the use of sedation and analgesia for ventilated neonates. Current data indicate that there is insufficient evidence to recommend the routine use of opioids in mechanically ventilated newborns and that opioids should be used selectively. Sedation and analgesia in non ventilated babies is extremely rare.

Practices across Europe and USA Data on sedation and analgesia practices in ventilated neonates are very rare. In 1995 the SOPAIN study carried out in the United States showed that factors predicting the use of on-going analgesia and sedation in neonates included: mechanical ventilation, higher gestational age, and male gender. In 2005, the French EPIPPAIN study showed that the rate of continuous sedation and analgesia was 69.6% in ventilated neonates with large variations among centers (16.7% to 90.9%). The most frequently used drugs were midazolam and morphine.

To date, there are no data permitting the comparison of neonatal pain management within the European countries. The availability of these data will enable comparison of practices with state-of-the-art knowledge.

Study Hypothesis

The EUROPAIN study is an epidemiological study that is based on the following hypothesis:

* Most newborn ventilated infants receive continuous sedation and analgesia.
* Non ventilated babies are not sedated.
* Morphine, fentanyl and midazolam are the most frequently drugs used in this setting.
* Infrequent use of validated pain assessment tools to monitor sedation and analgesia occurs in ventilated newborn infants.
* Most units have developed written local guidelines for sedation and analgesia in ventilated neonates, but huge variability exists among practitioners in the same unit, across different units in the same country, and across different countries in Europe.
* Development, dissemination, and regular updates of common European standards will improve the care and clinical outcomes of ventilated newborn infants.

1.2 Main objective • To determine the current clinical practices regarding the use of sedative and analgesic drugs for ventilated newborns in different countries in Europe.

1.3 Principal criteria

* The frequency of ventilated neonates receiving sedation and analgesia in different European units
* The medications used for sedation and analgesia in ventilated neonates across Europe.
* The length of use of medications administered for sedation and analgesia in ventilated neonates
* Similarities and differences in sedation and analgesia practices among European countries

1.4 Secondary objectives and criteria

* To determine the proportion of neonatal units that have developed and implemented local written guidelines to provide continuous sedation and analgesia in ventilated newborn infants as well as to prevent and treat procedural pain.
* To document the published guidelines for neonatal analgesia and sedation in different European countries and develop consensus for common European standards that can be applied in all medical settings.
* To determine the frequency of use of pain assessment tools in ventilated newborn infants and evaluate their impact on pain management practices.
* To determine practices to assess and prevent withdrawal syndromes. Secondary criteria
* Variations across European countries of the proportions of units that have developed and implemented local written guidelines for sedation and analgesia in ventilated neonates
* Identification and description of national guidelines for sedation and analgesia in neonates in all participating countries. Identification of recommended drugs.

1.5 Type of study

• Epidemiological observational study.

1.6 Study plan The EUROPAIN STUDY is observational and therefore it will not interfere with routine practices of participating units. No changes in diagnostic, therapeutic or any managing strategy of patients are imposed by the participation in this study. This epidemiological study will only collect data on clinical practices in each unit.

The inclusion criteria are:

• All neonates up to a corrected age of 44 weeks post conception. That means, for example, that a baby of 40 weeks gestational age can be included up to 28 days (4 weeks) of post natal age or that a baby of 32 weeks gestational age can be included up to 12 weeks of post natal age.

At the unit level

* No modifications of current managing protocols or strategies are required by the participation in the EUROPAIN STUDY. The unit coordinators will only provide data on local protocols to manage procedural pain and sedation and analgesia in neonates as well as on general statistics of the unit. All treatments are authorized for included neonates since this study does not include any intervention
* A nurse and physician coordinator as well as a data quality manager will be designated for each unit.

At the national level

• The country coordinator will provide data on national guidelines to treat or prevent procedural or continuous pain in neonates.

Data collection

* The duration of data collection for every included infant is 28 days. However, data collection will stop before 28 days if the infant leaves the unit (discharge, death, transfer to another hospital).
* Data will be collected on individual data collection forms. These forms include demographic data, modes of respiration, continuous or intermittent sedative, analgesic or neuro-blocking drugs, pain assessment and drug withdrawal practices.
* Paper patient data collection forms are written in English with a subtitled translation in the country language. The web-based databases display questionnaires in the country language.
* The data collection forms will be completed by the unit nurse or physician coordinator or the person that they will designate.
* For each center, the duration of the inclusion period will be one month.
* Data will be entered on a secure web-based questionnaire.

1.7 Justification of number of patients Regarding the number of neonates to include in order to show possible differences in sedation and analgesia practices among the participating European countries, we have considered a scenario where differences are small. Thus, we have chosen an effect size (W) of 0.1. We have also assumed that 15 countries will participate. Using NCSS-PASS 2008 software, we have found that a total sample size of 2303 neonates will achieve 90% power to detect an effect size (W) of 0.1 using a 14 degrees (15 centers) of freedom Chi-Square test with a significance level (alpha) of 0.05. Therefore, we aim at including an average of 154 neonates per participating country.

1.8 Main Actions carried out during the study

* In each country, the National Principal Investigators (NPI) will send invitations to join the study to all level 3 neonatal units of the country. The NPI will then communicate the names, emails and telephone numbers of the units that accept to participate to the EUROPAIN STUDY principal investigators
* The NPI is responsible for the coordination of all units in the country and ensures communication with the EUROPAIN STUDY principal investigators
* The NPI will collect demographic data about the participating country.
* A nurse and physician coordinator as well as a data quality manager will be designated for each unit. The nurse and physician coordinator are responsible for informing all the unit staff about the study.
* The EUROPAIN STUDY principal investigators have prepared a specifically designed web-based database to enter data. Data can be entered directly from the patient's file. A paper copy of this database will be distributed to allow centers that prefer to perform a preliminary entry on paper forms before entering data on the web-based database. The medical coordinator or a person that he (she) will choose will enter the data into these specifically designed databases.
* The physician coordinator will report general statistics of the unit such as number of beds, number of admission, year ventilator-days etc to the Europain study principal investigators.
* Every unit will also report existing local guidelines on sedation and analgesia in ventilated infants, including routines for withdrawal and on the use of pain assessment tools.
* MONITORING PANEL. A monitoring panel will be created to monitor the progress of the study. This panel will ensure communication with all the participating units. This monitoring panel will be constituted by two persons working full-time during the study period. They will be stationed in Paris and working under the responsibility of EUROPAIN STUDY principal investigators.

Conditions

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Pain Analgesia Sedation Intesive Care Intratracheal Ventilation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* • All neonates up to a corrected age of 44 weeks post conceptional. That means, for example, that an infant born at 40 weeks gestational age can be included up to 28 days (4 weeks) of post natal age or that a baby of 32 weeks gestational age can be included up to 12 weeks of post natal age.

NOTE: Since this is an observational epidemiological study, all eligible infants of the unit during the study period should be included.
Maximum Eligible Age

45 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hôpital Armand Trousseau

OTHER

Sponsor Role lead

Responsible Party

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CARBAJAL

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ricardo Carbajal, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Armand Trousseau

Locations

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Universitäts-klinik für Kinder- und Jugendheilkunde Innsbruck

Innsbruck, , Austria

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Landeskran- kenhaus Leoben

Leoben, , Austria

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Universitäts-klinik für Kinder und Jugendheilkunde Salzburg

Salzburg, , Austria

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Universitäts klinik für Kinder-und Jugenheilkunde Wien

Vienna, , Austria

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Universitaire Ziekenhuis Antwerpen

Antwerp, , Belgium

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Hôpital Erasme ULB,

Brussels, , Belgium

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Centre Hospitalier Universitaire Tivoli

La Louvière, , Belgium

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Centre Hospitalier Régional de la Citadelle

Liège, , Belgium

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Neonatal Intensiv Care Unit, Arch. Makarios Hospital

Nicosia, , Cyprus

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Department of Anesthesiology and Intensive Care, Tallinn Children's Hospital

Tallinn, , Estonia

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Paediatric Intensive Care Unit, Clinic of Anaesthesiology and Intensive Care, Tartu University Clinics

Tartu, , Estonia

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Helsinki University Hospital

Helsinki, , Finland

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Kuopio University Hospital

Kuopio, , Finland

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Oulu University Hospital

Oulu, , Finland

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Tampere University Hospital

Tampere, , Finland

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Turku University Hospital

Turku, , Finland

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CHR Félix Guyon

Saint-Denis, La Réunion, France

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CHU Amiens

Amiens, , France

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CHU Angers

Angers, , France

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CH Arras

Arras, , France

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CH Côte Basque

Bayonne, , France

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CHU Besançon

Besançon, , France

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CHU Bordeaux

Bordeaux, , France

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CHU de Brest

Brest, , France

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CHU Caen

Caen, , France

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CH Chambéry

Chambéry, , France

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CH Cherbourg

Cherbourg, , France

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CHU Clermont Ferrand

Clermont-Ferrand, , France

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CHU Dijon

Dijon, , France

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CH Le Havre

Le Havre, , France

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CH Le Mans

Le Mans, , France

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CHU Lyon Croix Rousse

Lyon, , France

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Hôpital Femme,Mère, enfant

Lyon, , France

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Hôpital de la conception - APHM

Marseille, , France

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CHU de Montpellier

Montpellier, , France

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CHU Nancy

Nancy, , France

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CHU Nice

Nice, , France

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CHU de Nîmes

Nîmes, , France

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CHR Orléans

Orléans, , France

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CHU Pau

Pau, , France

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CHU Poitiers

Poitiers, , France

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CHU Reims

Reims, , France

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CHU Rennes

Rennes, , France

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CH Rouen

Rouen, , France

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Ch Saint Etienne

Saint-Etienne, , France

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CHRU de Strasbourg

Strasbourg, , France

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CHU Toulouse

Toulouse, , France

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CHU Tours

Tours, , France

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CH Troyes

Troyes, , France

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CH Bretagne Atlantique

Vannes, , France

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Klinik fUr Kinder und Jugendliche Sozialstiftung Bamberg

Bamberg, , Germany

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Klinikum Coburg

Coburg, , Germany

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Department of Paediatric and Adolescent Medicine University Hospital Erlangen

Erlangen, , Germany

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Cnopf'sche Kinderklinik

Nuremberg, , Germany

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"Gaia" Maternity Hospital

Athens, , Greece

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"Lito" Maternity Hospital

Athens, , Greece

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"Mitera" General Maternity and Pediatric Clinic

Athens, , Greece

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"Rea" Maternity Hospital

Athens, , Greece

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Alexandras Hospital general

Athens, , Greece

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Children's Hospital "Agia Sophia"

Athens, , Greece

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Helena Venilezoy Maternit y Hospital

Athens, , Greece

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University Hospital of Heraklion

Heraklion, , Greece

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University of Ioannina

Ioannina, , Greece

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University of Patras

Pátrai, , Greece

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1st Dept of Neonatalogy, Aristole University of Thessaloniki

Thessaloniki, , Greece

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2nd Dept of Neonatalogy, Aristole University of Thessaloniki

Thessaloniki, , Greece

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Menn Esy, Hippokratio General Hospital

Thessaloniki, , Greece

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TIN Ospedale San Giovanni di Dio

Agrigento, , Italy

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UO TIN Neonatologia AOU Sant'Orsola Malpighi

Bologna, , Italy

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TIN Bolzano

Bolzano, , Italy

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UO TIN e Patologia Neonatale

Camposampiero, , Italy

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TIN Como Valduce

Como, , Italy

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U.O. di Neonatologia e PatNeo con T.I. - Istituti Ospitalieri

Cremona, , Italy

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Ospedale Careggi

Florence, , Italy

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Patologia Neonatale Lodi

Lodi, , Italy

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IN Ospedale Macedonio Melloni Milano-AO Fatebenefratellied Oftalmico

Milan, , Italy

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TIN Centro IRCSS Ca Granda-Policlinico Osp.Maggiore Mangiagalli LI

Milan, , Italy

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TIN Modena

Modena, , Italy

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TIN/Neonatologia- fondazione MBBM- H San Gerardo

Monza, , Italy

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TIN E Patologia Neonatale Dip. di Salute della donna e del bambino- Università di Padova

Padua, , Italy

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UTIN Perugia

Perugia, , Italy

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UO Neonatologia Santa Chiara

Pisa, , Italy

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TIN A.O.Bianchi-Melacrino-Morelli

Reggio Calabria, , Italy

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Azienda Ospedaliera ASMN, Reggio Emilia

Reggio Emilia, , Italy

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NICU Rimini

Rimini, , Italy

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TIN Ospedale Pediatrico Bambino Gesù

Roma, , Italy

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TIN Ospedale San Pietro FBF

Roma, , Italy

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Azienda Ospedaliera Universitaria di Sassari

Sassari, , Italy

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Ospedale Maria Vittoria, Torino

Torino, , Italy

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UO Neonatologia e TIN Ospedale Santa Chiara

Trento, , Italy

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UO TIN e Patologia Neonatale

Treviso, , Italy

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Patologia Neonatale Ospedale S.M.Misericordia

Udine, , Italy

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Terapia Intensiva Neonatale e Pediatrica

Verona, , Italy

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U.O.Patologia e Terapia Intensiva Neonatale AOUI Borgo Roma

Verona, , Italy

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TIN Ospedale San Bortolo

Vicenza, , Italy

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Department of Neonatology Lithuanian University of Health Sciences,

Kaunas, , Lithuania

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Mater Dei Hospital, Triq Dun Karm

Msida, , Malta

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Academic medical Center Amsterdam - Emma Children's Hospital

Amsterdam, , Netherlands

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ErasmusMC - Sophia Childrens Hospital

Rotterdam, , Netherlands

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University Hospital Utrecht - Wilhelmina Children's Hospital

Utrecht, , Netherlands

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Maxima Medical Center Veldhoven

Veldhoven, , Netherlands

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Isala Clinics Zwolle - Amalia Children's Hospital

Zwolle, , Netherlands

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Aalesund Hospital

Ålesund, , Norway

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Haukeland University Hospital

Bergen, , Norway

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Nordland Hospital

Bodø, , Norway

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Vestre Viken Hospital

Drammen, , Norway

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Ostfold Hospital

Fredrikstad, , Norway

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Haugesund Hospital

Haugesund, , Norway

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Sorlandet Hospital

Kristiansand, , Norway

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Sykehuset Innlandet Lillehammer

Lillehammer, , Norway

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Akershus University Hospital

Lørenskog, , Norway

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Oslo University Hospital - Rikshospitalet

Oslo, , Norway

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Oslo University Hospital - Ullevaal

Oslo, , Norway

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Telemark Hospital

Skien, , Norway

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Stavanger University Hospital

Stavanger, , Norway

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University Hospital of North Norway

Tromsø, , Norway

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St. Olavs hospital

Trondheim, , Norway

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Vestfold Hospital

Tønsberg, , Norway

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Oddzial Noworodkow

Bydgoszcz, , Poland

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Szpital Wojewódzki Koszalin

Koszalin, , Poland

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Children's Memorial Health Institute Warsaw

Warsaw, , Poland

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Clinical Hospital Ks.Anna Mazowiecka

Warsaw, , Poland

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Department of obstetric and gynecology, medical University of Warsaw

Warsaw, , Poland

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Hospital Orłowskiego Warsaw

Warsaw, , Poland

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Oddział Neonatologiczny

Warsaw, , Poland

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Departement of Neonato- logy Medical University in Wrocław

Wroclaw, , Poland

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Hospitale Divino Espirito Santo

Açores, , Portugal

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Hospital San Marcos

Braga, , Portugal

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Maternidade Bissaya Barreto

Coimbra, , Portugal

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Maternidade Daniel Matos

Coimbra, , Portugal

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Hospitale Espirito Santa

Evora, , Portugal

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Hospitale Faro

Faro, , Portugal

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Hospitale Vila Nova Gaia

Gaia, , Portugal

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Hospital Dona Estefânia

Lisbon, , Portugal

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Hospital Santa Maria

Lisbon, , Portugal

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Hospitale Amadora Sintra

Lisbon, , Portugal

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Hospitale Sao Francisco Xavier

Lisbon, , Portugal

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Maternity Dr Alfredo da Costa

Lisbon, , Portugal

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Hospitale Funchal

Madeirã, , Portugal

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Hospital San João

Porto, , Portugal

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Complexo Hospitalario Universitario de A Coruña

A Coruña, , Spain

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Hospital Universitario Principe de Asturias

Alcalá de Henares, , Spain

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Hospital General de Alicante

Alicante, , Spain

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Hospital Universitario de Álava

Álava, , Spain

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Hospital Clinic de Barcelona

Barcelona, , Spain

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Hospital de la Santa Creu i Sant Pau

Barcelona, , Spain

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Hospital Sant Joan de Déu

Barcelona, , Spain

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Hospital Vall d´Hebron

Barcelona, , Spain

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Hospital Universitario Puerta del Mar

Cadiz, , Spain

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Hospital General de Castellón

Castellon, , Spain

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Hospital Universitario de Donostia

Donostia / San Sebastian, , Spain

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Hospital Universitari Josep Trueta

Girona, , Spain

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Hospital Universitario Severo Ochoa

Leganés. Madrid, , Spain

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Hospital San Pedro de Logroño

Logroño, , Spain

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Hospital Clínico San Carlos (Madrid)

Madrid, , Spain

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Hospital General Universitario Gregorio Marañón

Madrid, , Spain

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Hospital Infantil Universitario La Paz

Madrid, , Spain

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Hospital Universitario 12 de Octubre

Madrid, , Spain

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Hospital Universitario Central de Asturias

Oviedo, , Spain

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Complejo Hospitalario de Navarra

Pamplona, , Spain

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Complexo Hospitalario de Pontevedra

Pontevedra, , Spain

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Hospital Universitario de Salamanca

Salamanca, , Spain

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Hospital Universitario Marqués de Valdecilla

Santander, , Spain

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Complexo Hospitalario Universitario de Santiago

Santiago de Compostela, , Spain

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Hospital Virgen Macarena

Seville, , Spain

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Hospital Virgen de la Salud (Toledo)

Toledo, , Spain

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Hospital Universitari i Politecnic La Fe

Valencia, , Spain

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Complexo Hospitalario Universitario de Vigo

Vigo, , Spain

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Hospital Clínico Lozano Blesa

Zaragoza, , Spain

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Hospital Universitario Miguel Servet

Zaragoza, , Spain

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Hospital Lasarettet

Falun, , Sweden

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Universitetssjukhuset

Lund, , Sweden

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Universitetssjukhuset

Örebro, , Sweden

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Karolinska University Hospital (Stockholm)

Stockholm, , Sweden

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Sachsska Barnsjukhuset (Stockholm)

Stockholm, , Sweden

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Akademiska Barnsjukhuset

Uppsala, , Sweden

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Aberdeen Maternity Hospital

Aberdeen, , United Kingdom

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Royal United Hospital

Bath, , United Kingdom

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Royal Berkshire NHSFT

Berkshire, , United Kingdom

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Birmingham Children's Hospital

Birmingham, , United Kingdom

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Birmingham Heartlands Hospital

Birmingham, , United Kingdom

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Birmingham Womens Hospital

Birmingham, , United Kingdom

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Sandwell and West Birmingham

Birmingham, , United Kingdom

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Blackpool Teaching Hospital Foundation Trust

Blackpool, , United Kingdom

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Royal Bolton Hospital

Bolton, , United Kingdom

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Bradford Royal Infirmary

Bradford, , United Kingdom

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Royal Alexander Children's Hospital

Brighton, , United Kingdom

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Bristol Royal Infirmary

Bristol, , United Kingdom

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Southmead Hospital

Bristol, , United Kingdom

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St Michael's Hospital, Bristol NICU

Bristol, , United Kingdom

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Royal Brompton Hospital

Brompton, , United Kingdom

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Burnley General Hospital

Burnley, , United Kingdom

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Countess of Chester

Chester, , United Kingdom

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North Tees Hospital

Cleveland, , United Kingdom

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Colchester General Hospital

Colchester, , United Kingdom

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University Hospitals Coventry & Warwick

Coventry, , United Kingdom

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Royal Derby Hospital

Derby, , United Kingdom

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Royal Devon and Exeter NHS Foundation Trust

Devon, , United Kingdom

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Doncaster Royal Infirmary

Doncaster, , United Kingdom

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Edinburgh Royal Infirmary

Edinburgh, , United Kingdom

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Medway Maritime Hospital

Gillingham, , United Kingdom

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Gloucestershire Royal Hospital

Gloucestershire, , United Kingdom

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Royal Gwent Hospital

Gwent, , United Kingdom

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Airedale NHS Foundation Trust

Keighley, , United Kingdom

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Kettering General Hospital

Kettering, , United Kingdom

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Leeds General Infirmary

Leeds, , United Kingdom

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Leicester Royal infirmary NICU

Leicester, , United Kingdom

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Leicester Royal Infirmary PICU

Leicester, , United Kingdom

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Leighton or Mid Cheshire NHS Trust

Leighton, , United Kingdom

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Liverpool Women's Hospital NICU

Liverpool, , United Kingdom

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Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust PICU

London, , United Kingdom

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Great Ormond Street Hospital for Sick Children PICU

London, , United Kingdom

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Imperial College London NICU

London, , United Kingdom

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Royal London Hospital

London, , United Kingdom

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Pennine Acute Hospitals NHS Trust

Manchester, , United Kingdom

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St Mary's Hospital

Manchester, , United Kingdom

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King's Mill Hospital, Mansfield

Mansfield, , United Kingdom

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James Cook University Hospital, Middlesborough

Middlesbrough, , United Kingdom

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West Middlesex University Hospital

Middlesex, , United Kingdom

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Newham University Hospital

Newham, , United Kingdom

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Northampton General Hospital Neonatal Unit

Northampton, , United Kingdom

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Queen's Medical Centre

Nottingham, , United Kingdom

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Southport & Ormskirk & District General Hospital Neonatal Unit

Ormskirk, , United Kingdom

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John Radcliffe Hospital

Oxford, , United Kingdom

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Derriford Hospital, Plymouth

Plymouth, , United Kingdom

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Royal Preston Hospital

Preston, , United Kingdom

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Queen's Hospital, Romford

Romford, , United Kingdom

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Rotherham District General Hospital

Rotherham, , United Kingdom

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Jessop Wing, Sheffield Teaching Hospitals NHS Trust

Sheffield, , United Kingdom

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Royal Shrewsbury Hospital

Shrewsbury, , United Kingdom

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Singleton Hospital

Singleton, , United Kingdom

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University Hospital Of North Staffordshire NHS Trust

Staffordshire, , United Kingdom

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Great Western Hospitals NHS Foundation Trust

Swindon, , United Kingdom

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Musgrove Park Hospital, Taunton

Taunton, , United Kingdom

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Royal Cornwall Hospital

Treliske, , United Kingdom

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Warrington Hospital

Warrington, , United Kingdom

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Calderdale Royal Hospital

West Yorkshire, , United Kingdom

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Pinderfields General Hospital

West Yorkshire, , United Kingdom

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New Cross Hospital, Wolverhampton

Wolverhampton, , United Kingdom

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Worcester Royal Hospital

Worcester, , United Kingdom

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University Hospital of South Manchester, Wythenshawe

Wythenshawe, , United Kingdom

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York Teaching Hospital NHS Foundation Trust

York, , United Kingdom

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Countries

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Austria Belgium Cyprus Estonia Finland France Germany Greece Italy Lithuania Malta Netherlands Norway Poland Portugal Spain Sweden United Kingdom

References

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Lago P, Frigo AC, Baraldi E, Pozzato R, Courtois E, Rambaud J, Anand KJ, Carbajal R. Sedation and analgesia practices at Italian neonatal intensive care units: results from the EUROPAIN study. Ital J Pediatr. 2017 Mar 7;43(1):26. doi: 10.1186/s13052-017-0343-2.

Reference Type DERIVED
PMID: 28270167 (View on PubMed)

Carbajal R, Eriksson M, Courtois E, Boyle E, Avila-Alvarez A, Andersen RD, Sarafidis K, Polkki T, Matos C, Lago P, Papadouri T, Montalto SA, Ilmoja ML, Simons S, Tameliene R, van Overmeire B, Berger A, Dobrzanska A, Schroth M, Bergqvist L, Lagercrantz H, Anand KJ; EUROPAIN Survey Working Group. Sedation and analgesia practices in neonatal intensive care units (EUROPAIN): results from a prospective cohort study. Lancet Respir Med. 2015 Oct;3(10):796-812. doi: 10.1016/S2213-2600(15)00331-8. Epub 2015 Sep 24.

Reference Type DERIVED
PMID: 26420017 (View on PubMed)

Related Links

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Other Identifiers

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EUROPAIN Survey

Identifier Type: -

Identifier Source: org_study_id

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