Clinical Trials Logo

Clinical Trial Summary

Sick or premature neonates are exposed to frequent painful and stressful procedures during their stay in neonatal intensive care units. Although neonates do feel pain and may have long term effects induced by painful experiences, prevention and treatment of neonatal pain is far from optimal in many units. An epidemiological study (EPIPPAIN) conducted in neonatal and pediatric intensive care units in France in 2005 showed that painful procedures were extremely frequent and that analgesics treatments varied a lot among units. Since many guidelines have been issued by international scientific societies to manage neonatal pain, one may expect that the prevention and treatment of neonatal pain has improved over the last 6 years.

Although awake endotracheal intubations are extremely difficult or impossible in older children or adults, such intubations are still frequently performed without sedation/analgesia in neonates. Recent studies have shown that premedications facilitate intubation conditions and greatly improve neonates tolerance of the procedure. Studies aimed at assessing the risks and benefits of different sedations/analgesia strategies are urgently needed in neonates. We also need a tool to assess at the same time the technical conditions of intubations and the tolerance of the neonate to the procedure so that data from different studies can be compared.

The objectives of the present study are:

1. To describe the incidence of painful and stressful procedures performed in the neonate in intensive care units as well as in neonates transported by the medical emergency system (SMUR) of the Ile-de-France region 6 years after the first EPPIPAIN study conducted in the same region and same type of population in order to assess the evolution of practices. The description of painful and stressful procedures will be completed with a real-time around-the-clock assessment of the pain induced by procedures using a validated behavioral pain scale.

2. To link this study with The Epipage study 2 in order to look for associations between the number of painful and stressful procedures and/or analgesic treatments of the neonatal period and the neurological outcome of children that will be followed in the Epipage cohort. The Epipage study is a separate study that will follow for 13 years a cohort of premature neonates recruited in 2011.

3. To describe the incidence of painful or stressful procedures and analgesic treatments in neonates transported by the pediatric emergency system (SMUR) of the Ile-de-France region in France.

4. To obtain initial validity of a tool permitting to assess intubations in neonates. An observational detailed description of endotracheal intubations conditions will be conducted in neonates transported and intubated by SMUR and in neonates intubated in intensive care units

5. To describe continuous sedation and analgesia practices in ventilated neonates in intensive care units. For these neonates, data from medical records will be recovered up to 2 months of admission in intensive care units

6. To describe the frequency of heel sticks for glycemia measurement and blood gazes practices among centers. Relate heel stick practices to the normality or abnormality of glycemia results


Clinical Trial Description

STUDY HYPOTHESIS

Principal hypothesis

- The number of painful and stressful procedures performed in the neonate admitted to intensive care units is still very high but it is lower than in 2005 Pain scores are lower when procedures are performed with a specific analgesia prior to procedure.

Secondary hypothesis

- The frequency of pre-procedural analgesia is higher than in 2005

- Certain common procedures such as heel sticks and endotracheal intubations are carried out with a more frequent analgesia than in 2005

- The use of a continuous sedation and analgesia does not induce a reduction in specific pre-procedural analgesia

- A real-time pain assessment of painful procedures can be carried out in more than 80% of procedures performed in neonates in intensive care units Pain scores show that certain procedures which are apparently not very painful may elicit high pain scores in very sick neonates

- Certain procedures such as nursing care or weighing may induce high pain scores in neonates who have invasive tubes (endotracheal tubes, thoracic drainage)

- A continuous sedation and analgesia is given to more than 50% of ventilated neonates.

- Certain characteristics of neonates may influence the use of analgesics for painful procedures. Ex: gender, age, respiratory support

- Certain contextual characteristics or center may influence the use of analgesics for painful procedures. Ex: day or night, pain referent in the unit, night head nurse, written pain management guidelines.

- More than 80% of semi-urgent or non-urgent intubations are carried out with the use of premedication.

- Opioids are the most commonly drugs used for premedication during endotracheal intubations in neonates

- The assessment of intubating conditions and neonate tolerance show lower scores when intubations are performed with a premedication considered as "recommended" by the American Academy of Pediatrics

- The detailed observation of intubations in SMUR and intensive care units will enable initial validation of a tool assessment

- Too many capillary blood samples by heel sticks are carried out in neonates even in neonates that have normal values throughout repeated sticks.

- The frequency of blood gas assessments is widely variable among centers

- The frequency of capillary blood glycemia is widely variable among centers

LONG-TERM EFFECTS OF PAIN AND ANALGESIC TREATMENTS

This objective will be assessed by matching the data of the current Epippain study and another parallel study (Epipage 2)

Principal hypothesis

- After adjusting for the disease severity, neonates that undergo more painful procedures have a poorer neurological outcome later in infancy.

Secondary hypothesis

- Higher pain scores are associated with a poorer neurological outcome later in infancy

- The use of central analgesics like opioid does not have a negative effect on neurological outcome later in infancy.

- The potential negative effect of numerous painful procedures during the neonatal period can be counteracted by the use of analgesics.

METHODOLOGY

This study will be carried out in neonates cared for in two settings: (i) neonatal or pediatric intensive care units and (ii) the medical regional pediatric transport system (SMUR) In the intensive care units, this study is designed as a prospective observational study to collect around-the-clock bedside data on all painful or stressful procedures performed in neonates admitted to the participating units. All 16 tertiary care centers, Neonatal Intensive Care Units (NICUs) and Pediatric Intensive Care Units (PICUs) in the Paris Region will participate. Since this is an observational study no changes in the standard of care will be carried out. During the first 14 days of admission to the participating units, prospective data will be collected on all neonatal procedures causing pain, stress, or discomfort with the corresponding analgesic therapy. A real-time assessment of pain induced by each procedure will be carried out by unit staff using the DAN scale. A detailed record of conditions of endotracheal intubations will also be carried out.

Demographic data, type and duration of respiratory support, sedative and analgesic drugs administered concomitantly or pre-procedure, and conditions related to each procedure (type, hour of the day, operator, parental presence) will be collected. We'll also record repeat procedure attempts for procedures requiring more than one attempt before successful completion. The use of specific pre-procedural analgesia will be noted for each procedure. If neonates are discharged from the units before 14 days, data collection on painful procedures will be stopped on the day of discharge.

In the medical regional pediatric transport system (SMUR), neonates transported during the 2-months study period, will have all their procedures recorded in a specific data collection form. Demographic data, type of respiratory support, sedative and analgesic drugs administered concomitantly or pre-procedure, and conditions related to each procedure (type, hour of the day, operator, parental presence) will be collected. We'll also record repeat procedure attempts for procedures requiring more than one attempt before successful completion. The use of specific pre-procedural analgesia will be noted for each procedure. A real-time assessment of pain induced by each procedure will be carried out by unit staff using the DAN scale. A detailed record of conditions and neonate tolerance of endotracheal intubations will also be carried out. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01346813
Study type Observational
Source Hôpital Armand Trousseau
Contact
Status Completed
Phase N/A
Start date May 2011
Completion date August 2011

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care