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Standardized Classification of Infants With Robin Sequence Using MicroNAPS: The Impact of Syndromes and Comorbidities
Cory M Resnick1, Jody E Heffernan2, Snigdha Jindal1
1From the Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, MA.
Insights
A standardized scoring system for infants with Robin sequence (RS) was developed. This system, MicroNAPS, now includes expert-validated scores for syndromes and comorbidities, improving treatment decision accuracy.
Area of Science:
- Pediatric Surgery
- Genetics
- Clinical Decision Support
Background:
- Robin sequence (RS) management relies on the MicroNAPS classification system.
- The syndromes/comorbidities score (S score) in MicroNAPS lacks objective criteria, introducing subjectivity.
- Reproducibility of MicroNAPS requires a standardized database of RS-associated diagnoses and consensus-based S scores.
Purpose of the Study:
- To develop a consensus-based scoring system for syndromes and comorbidities in infants with Robin sequence.
- To enhance the objectivity and reproducibility of the MicroNAPS classification for guiding treatment decisions.
Main Methods:
- Literature review identified 170 RS-associated syndromes and comorbidities.
- Delphi technique with 35 RS experts achieved >75% consensus on S scores over 4 survey rounds.
- A published cohort of 100 infants was rescored to assess the impact of new S scores.
Main Results:
- Consensus on S scores was reached for 98.2% of 170 diagnoses.
- Rescoring revealed 25% changes in S scores, leading to 5 modifications in R stages.
- The revised scoring system demonstrated improved consistency in classification.
Conclusions:
- A comprehensive, expert-validated list of RS-associated diagnoses with S scores has been established.
- The refined MicroNAPS system enhances objective decision-making for infant RS treatment.
- The updated MicroNAPS calculator is available online for clinical use.
Background:
MicroNAPS, a classification for infants with Robin sequence (RS) intended to guide treatment decisions, consists of 5 elements: micrognathia, nutrition, airway, palatal clefting, and syndromes/comorbidities. Scoring of the first 4 elements is well defined, but the assignment of the syndromes/comorbidities score (S score) introduces subjectivity by necessitating judgment regarding the clinical impact of the diagnosis. A database of comorbid diagnoses associated with RS and consensus-based S scores for each is needed for the MicroNAPS system to be reproducible.
Methods:
Diagnoses known to be associated with RS were identified from existing literature, and preliminary severity grades were applied. A series of electronic surveys were distributed to RS experts seeking agreement or recommendation and explanation for updated scoring, according to the Delphi technique, until at least 75% consensus was achieved for each item. A previously published series of 100 infants was rescored according to the resulting grades, and changes from initial scoring were assessed.
Results:
A total of 170 associated syndromes and comorbidities were identified. Complete responses were received from 20 of the 35 experts (57.1%) surveyed. Consensus on S scores was achieved for all but 3 diagnoses (98.2%) after 4 rounds of surveys. Rescoring of the published series found 25 (25%) changes in S scores resulting in 5 modifications to R stages.
Conclusions:
We have compiled a comprehensive list of syndromes and comorbid diagnoses associated with RS and achieved expert consensus regarding the impact on early treatment decision-making for most. This list, assigned S scores, and a complete MicroNAPS calculator are publicly available at www.prscalculator.com.
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