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Rescue designs in analgesic trials from 0 to 2 years of age: scoping review
Kyra Haskes1, Carolina Donado1,2, Ricardo Carbajal3,4
1Department of Anesthesiology, Critical Care & Pain Medicine, Boston Children's Hospital, Boston, MA, USA.
Insights
Pediatric analgesic trials for children aged 0-2 years are challenging. Pragmatic designs like add-on or head-to-head with immediate rescue can improve future pediatric pain management research.
Area of Science:
- Pediatric Pharmacology
- Clinical Trial Design
- Pain Management
Background:
- Pediatric analgesic trials, particularly in neonates and infants (0-2 years), present significant design challenges.
- Existing research on analgesic efficacy and safety in this vulnerable population is limited.
- An FDA-academic consensus meeting highlighted the need for improved trial methodologies.
Purpose of the Study:
- To analyze pragmatic rescue designs in postoperative pediatric analgesic trials.
- To assess surgical volumes in children aged 0-2 years to inform trial design.
- To provide evidence-based recommendations for future pediatric analgesic trial design.
Main Methods:
- Conducted a comprehensive literature search across major databases (PubMed, Embase, CINAHL, Cochrane, Web of Science).
- Employed a scoping approach to identify randomized controlled trials (RCTs) using immediate rescue designs for analgesics in children aged 0-2 years.
- Estimated age-specific surgical volumes using French national databases.
Main Results:
- Identified 23 RCTs meeting criteria for study medications and immediate rescue paradigms in children aged 0-2 years out of 3563 studies.
- Add-on and head-to-head designs were frequently utilized, often with rescue medication sparing as a primary outcome.
- French national data indicated inguinal and penile surgeries were most common in ages 1 month to 2 years, while neonates underwent predominantly abdominal and thoracic surgeries.
Conclusions:
- Analgesic trials employing rescue sparing paradigms are currently infrequent in children aged 0-2 years.
- Future pediatric analgesic trials should consider age-specific surgical procedures and pragmatic designs such as add-on or head-to-head approaches.
- These pragmatic designs offer valuable insights into clinical effectiveness, side effects, and safety in young children.
Abstract:
Pediatric analgesic trials are challenging, especially in newborns and infants. Following an FDA-academic consensus meeting, we analyzed pragmatic rescue designs in postoperative trials of local anesthetics, acetaminophen, opioids, and NSAIDs involving children ages 0-2 years and assessed surgical volumes to provide trial design recommendations. Searches of PubMed, Embase, CINAHL, The Cochrane Library, and Web of Science were conducted. A scoping approach identified trends in analgesic trials with an emphasis on randomized controlled trials (RCTs) utilizing immediate rescue designs. Age-specific surgical volumes were estimated from French national databases. Of 3563 studies identified, 23 RCTs used study medication(s) of interest and immediate rescue paradigms in children ages 0-2 years. A total of 270 studies met at least one of these criteria. Add-on and head-to-head designs were common and often used sparing of non-opioid or opioid rescue medication as a primary outcome measure. According to French national data, inguinal and penile surgeries were most frequent in ages 1 month to 2 years; abdominal and thoracic surgeries comprise approximately 75% of newborn surgeries. Analgesic trials with rescue sparing paradigm are currently sparse among children ages 0-2 years. Future trials could consider age-specific surgical procedures and use of add-on or head-to-head designs. IMPACT: Clinical trials of analgesic medications have been challenging in pediatrics, especially in the group from newborns to 2 years of age. Following an FDA-academic workshop, we analyzed features of completed analgesic trials in this age group. Studies using immediate rescue in placebo control, add-on, and head-to-head trial designs are pragmatic approaches that can provide important information regarding clinical effectiveness, side effects, and safety. Using a French national dataset with a granular profile of inpatient, outpatient, and short-stay surgeries, we provide information to future investigators on relative frequencies of different operations in neonates and through the first 2 years of life.
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