Table. Summary of Patient, Procedure, and Sedation Characteristicsa.
Characteristic | No. (%) |
---|---|
Age, median (IQR), y | 7.2 (4.5-11.4) |
Sex | |
Male | 31 (72) |
Female | 12 (28) |
Diagnosis (patient may have ≥1) | |
Autism spectrum disorder | 29 (67) |
Developmental delay NOS | 10 (23) |
Epilepsy with associated developmental delay | 7 (16) |
Behavioral disorder NOS | 4 (10) |
Associated genetic or congenital disorder | 8 (19) |
Complex congenital heart disease | 2 (5) |
Chromosome 18q22 anomaly | 1 (2) |
Turner syndrome | 1 (2) |
Creatine-synthesis deficiency | 1 (2) |
MEN2a syndrome | 1 (2) |
Moebius syndrome | 1 (2) |
Tuberous Sclerosis | 1 (2) |
Treated with protocol ≥1 time | |
2 Times | 7 (17) |
3 Times | 1 (2) |
Weight for age, median (IQR), percentile | 75 (31-98) |
Receiving a psychotropic medication (eg, aripiprazole, risperidone, or an amphetamine) | 14 (33) |
Tolerated EMLA placement at home for blood draw, No./total No. with blood draw (%) | 31/38 (82) |
Type of procedure (n = 42) | |
Blood draw | 38 (88) |
Electrocardiogram | 22 (51) |
Immunization or other IM injection | 15 (35) |
Dental examination | 5 (12) |
Abdominal or cardiac ultrasonographic imaging | 3 (7) |
Lumbar puncture | 2 (5) |
Nasofibroscopy | 2 (5) |
Auditory evoked potentials | 2 (5) |
Suture removal | 2 (5) |
Balloon gastrostomy button replacement | 1 (2) |
Optic nerve examination | 1 (2) |
Procedures performed during a sedation, No. | |
1 | 11 (26) |
2 | 15 (36) |
3 | 12 (29) |
4 | 3 (7) |
Indication for procedure (patient may have ≥1) | |
General health maintenance | 29 (68) |
Investigation of symptoms | 13 (30) |
Monitor psychotropic medication effects | 11 (26) |
Prior to starting a psychotropic medication | 2 (5) |
Sedation characteristics, mean (95% CI), min | |
Time from IN dexmedetomidine administration to onset of sedation (RSS 5) | 28 (15-45) |
Duration of n2o administration | 18 (5-35) |
Time from IN dexmedetomidine administration to awakening (RSS 2) | 106 (80-181) |
Time from IN dexmedetomidine administration to readiness for discharge (modified Aldrete of 9-10)a | 132 (93-238) |
Restraint during procedureb | 3 (7) |
Procedure aborted for suboptimal sedation | 1 (2) |
Adverse events | |
During sedation | |
Intermediatec | 0 |
Sentinelc | 0 |
Prolonged sedation (>180 min to RSS 2) | 3 (7) |
Vomiting | 1 (2) |
Seizure not requiring intervention (in a patient known to seize multiple times a day) | 1 (2) |
Reported at 24-hour phone call | |
Slept later than usual the night of sedation | 35 (81) |
Agitation | 1 (2) |
Parental satisfactiond | |
4 | 1 (2) |
5 | 42 (98) |
Abbreviations: EMLA, eutectic mixture of local anesthetics; IM, intramuscular; IN, intranasal; n2o, nitrous oxide; NOS, not otherwise specified; RSS, Ramsay Sedation Scale.
Details on the RSS are provided in eTable 1 in Supplement 1 and details on the Aldrete score are provided in eTable 2 in Supplement 1.
Children requiring restraint were ages 2, 7, and 16 years.
Defined per the International Committee for the Advancement of Procedural Sedation Tracking and Reporting Outcomes of Procedural Sedation.
On a scale of 0, indicating very dissatisfied, to 5, very satisfied.