| Literature DB >> 19847186 |
K Fairchild1, D Sokora, J Scott, S Zanelli.
Abstract
OBJECTIVE: Therapeutic hypothermia instituted within 6 h of birth has been shown to improve neurodevelopmental outcomes in term newborns with moderate-to-severe hypoxic-ischemic encephalopathy (HIE). The majority of infants who would benefit from cooling are born at centers that do not offer the therapy, and adding the time for transport will result in delays in therapy, that may lead to suboptimal or no neuroprotection for some patients. Our objective was to evaluate the effect of our center's experience with therapeutic hypothermia on neonatal transport. STUDYEntities:
Mesh:
Year: 2009 PMID: 19847186 PMCID: PMC2864418 DOI: 10.1038/jp.2009.168
Source DB: PubMed Journal: J Perinatol ISSN: 0743-8346 Impact factor: 2.521
Figure 1Cooling start time and the University of Virginia (UVA) arrival time. A total of 50 infants underwent hypothermia therapy at the UVA Neonatal Intensive Care Unit from March 2005 to February 2009. Cooling start time is shown for inborn infants (hours after birth, n=10, filled squares). Of the 40 outborn infants, 35 were cooled before and during transport, and 5 were not cooled until arrival at UVA (filled triangles). Cooling was classified as passive (no external heat source, filled circles) or active (application of cool gel packs, filled diamonds). Some infants underwent passive followed by active cooling and both start times are included. The arrival time at UVA for all 40 outborn infants is shown (open diamonds). Horizontal lines represent mean hours after birth.
Figure 2Comparison of temperature of 40 outborn neonates with hypoxic–ischemic encephalopathy (HIE) before and after neonatal transport. The rectal temperatures of 40 outborn infants on arrival of the University of Virginia (UVA) transport team to the referring hospital and on arrival of the patients to the UVA Neonatal Intensive Care Unit. Five patients were not cooled until after arrival to UVA, two patients underwent passive cooling only and thirty-three patients underwent active cooling during transport.
Admission characteristics and laboratory values of outborn and inborn infants
| Gestational age (weeks) | 38.8±1.1 | 38.1±2.7 | 38.8±1.1 | 38.0±2.6 | 38.5±1.9 | |
| Birth weight (g) | 2914±415 | 2973±917 | 3284±693 | 3853±971 | 3228±750 | 3197±845 |
| Degree of encephalopathy (moderate/severe) | 2/3 | 3/4 | 16/7 | 3/2 | 24/16 | 4/6 |
| Age at start of cooling, passive or active (h) | 1.9±1.3 | 2.5±1.5 | 3.0±1.6 | 8.1±6.5 | 3.5±3.2 | 0.9±0.7 |
| Age at arrival of transport team (h) | 2.6±1.2 | 2.7±1.5 | 3.0±1.4 | 2.8±1.8 | 2.9±1.4 | N/A |
| Age at arrival to UVA (h) | 6.1±1.0 | 5.8±2.2 | 6.1±2.0 | 5.8±2.9 | 5.9±2.1 | N/A |
| Age when temperature reached <34 °C (h) | 3.2±1.7 | 3.4±0.4 | 4.3±2.0 | 9.8±6.1 | 4.7±3.2 | 2.6±1.8 |
| HR (bpm) | 111±23 | 104±16 | 113±20 | 147±31 | 116±24 | 143±13 |
| Blood pressure (mean, mm Hg) | 55±7 | 49±6 | 50±11 | 53±5 | 51±11 | 43±7 |
| Platelet count (k μl−1) | 136±32 | 146±56 | 193±84 | 234±110 | 183±82 | 207±81 |
| PT (s) | 21.9±5.1 | 27.0±8.9 | 24.9±10.7 | 21.6±8.8 | 24.5±9.7 | 26.0±5.8 |
| INR | 1.8±0.5 | 2.3±0.9 | 2.0±1.2 | 2.0±1.1 | 2.1±1.1 | 2.2±0.5 |
| AST (U l−1) | 121±80 | 398±597 | 575±1082 | 260±209 | 451±866 | 316±391 |
| ALT (U l−1) | 40±22 | 343±714 | 211±273 | 110±165 | 208±423 | 91±108 |
| Creatinine (mg per 100 ml) | 0.8±0.2 | 1.1±0.1 | 0.9±0.3 | 1.3±0.6 | 1.0±0.3 | 0.9±0.1 |
| Glucose (mg per 100 ml) | 191±88 | 188±116 | 139±65 | 73±16 | 142±82 | 143±90 |
Abbreviations: N/A, not applicable; UVA, University of Virginia; HR, heart rate; PT, prothrombin time; INR, international normalized ratio; AST, aspartate aminotransferase; ALT, alanine aminotransferase.
Figure 3The University of Virginia (UVA) admission temperature for 35 outborn infants cooled on transport. The rectal temperatures of 35 outborn infants cooled during transport, recorded on admission to the UVA Neonatal Intensive Care Unit. Gray-shaded area represents target temperature (33 to 34 °C). Two patients with only passive cooling during transport (indicated with an open circle) had admission temperatures of 34.4 and 34.8 °C. All others were transported with active cooling.
Therapeutic hypothermia on neonatal transport
| 1. Decision to implement based on the geographics of the referral base and neonatal transport team capabilities |
| 2. Establish protocols and organize education sessions (including neurological assessment): referring clinicians, transport clinicians and receiving clinicians |
| 3. Equipment: system for continuous rectal temperature monitoring throughout cooling and transport, cool gel packs, receiving blankets and transport incubator |
| 4. Consider passive cooling and/or targeting temperature 34–35 °C in start-up phase to avoid overcooling |
| 5. Maintain flow sheets and database for recording clinical data for quality assessment and improvement |