| Literature DB >> 34069996 |
Ariann Lenihan1, Vannessa Ramos1, Nichole Nemec2, Joseph Lukowski3, Junghyae Lee4, K M Kendall1,5, Sidharth Mahapatra1,5.
Abstract
Limited data exist regarding feeding pediatric patients managed on non-invasive respiratory support (NRS) modes that augment oxygenation and ventilation in the setting of acute respiratory failure. We conducted a retrospective cohort study to explore the safety of feeding patients managed on NRS with acute respiratory failure secondary to bronchiolitis. Children up to two years old with critical bronchiolitis managed on continuous positive airway pressure, bilevel positive airway pressure, or RAM cannula were included. Of the 178 eligible patients, 64 were reportedly nil per os (NPO), while 114 received enteral nutrition (EN). Overall equivalent in severity of illness, younger patients populated the EN group, while the NPO group experienced a higher incidence of intubation. Duration of stay in the pediatric intensive care unit and non-invasive respiratory support were shorter in the NPO group, though intubation eliminated the former difference. Within the EN group, ninety percent had feeds initiated within 48 h and 94% reached full feeds within 7 days of NRS initiation, with an 8% complication and <1% aspiration rate. Reported complications did not result in escalation of respiratory support. Notably, a significant improvement in heart rate and respiratory rate was noted after feeds initiation. Taken together, our study supports the practice of early enteral nutrition in patients with critical bronchiolitis requiring NRS.Entities:
Keywords: acute respiratory failure; critical bronchiolitis; early enteral nutrition; non-invasive respiratory support
Year: 2021 PMID: 34069996 PMCID: PMC8157845 DOI: 10.3390/children8050410
Source DB: PubMed Journal: Children (Basel) ISSN: 2227-9067
Figure 1Flow diagram of patient enrollment. CGA = corrected gestational age, EN = enteral nutrition, NPO = nil per os (nothing by mouth), NRS = non-invasive respiratory support.
Demographic Data for Entire Cohort (n = 178).
| NPO | EN |
| |
|---|---|---|---|
| Sex, | |||
| Male | 39 (61%) | 70 (61%) | 1.0 |
| Weight (kg), median (IQR) | 8.4 (5.4–10.5) | 5.7 (4.7–7.4) | <0.001 |
| Age (months), median (IQR) | 10 (3–16) | 3 (2–6) | <0.001 |
| Age, | |||
| ≤1 month | 7 (11) | 13 (11) | <0.001 |
| 2–12 months | 31 (48) | 94 (82) | |
| 13–24 months | 26 (41) | 7 (6) | |
| Maturity, | |||
| Full-term at birth | 41 (64) | 68 (60) | 0.56 |
| Pre-term at birth | 23 (36) | 46 (40) | |
| Late (33 to <37 weeks) | 15 (23) | 33 (29) | 0.79 |
| Very (28 to <32 weeks) | 5 (8) | 7 (6) | |
| Extreme (<28 weeks) | 3 (5) | 6 (5) | |
| Genetic abnormalities, | 12 (19) | 12 (11) | 0.12 |
| Neurology abnormalities, | 7 (11) | 9 (8) | 0.50 |
| PRISM-III ROM, % (IQR) | 0.5 (0.5–0.8) | 0.5 (0.3–0.6) | 0.57 |
| Mortality, | 0 (0) | 0 (0) | - |
IQR = interquartile range, PRISM-III ROM= risk of mortality based on Pediatric Risk of Mortality-III score. Wilcoxon rank-sum test used to compare continuous variables presented as median (interquartile range); Chi-square test of independence used to compare categorical variables presented as n (%).
Clinical Characteristics of Entire Cohort (n = 178).
| NPO | EN |
| |
|---|---|---|---|
| NRS duration (days), median (IQR) | 1 (0.8–2) | 3 (2–4) | <0.001 |
| Type of NRS, | |||
| RAM | 52 (95) | 108 (99) | 0.34 |
| CPAP | 0 (0) | 1 (1) | |
| BiPAP | 3 (5) | 2 (2) | |
| Intubation #, | 9 (14) | 5 (4) | 0.016 |
| Pathogen | 1 (1–2) | 1 (1–1) | 0.21 |
| Pathogen positive, | 57 (89) | 105 (92) | 0.5 |
| Single | 41 (72) | 81 (77) | 0.53 |
| Multiple | 16 (28) | 25 (24) | |
| Virus only | 53 (93) | 99 (94) | 0.74 |
| Virus + Bacteria | 4 (7) | 6 (6) | |
| PICU LOS (days), median (IQR) | 2 (1–3) | 3 (2–5) | <0.001 |
# Refer to Table S1 for details; refer to Table S2 for details; NRS = non-invasive respiratory support, IQR = interquartile range, CPAP = continuous positive airway pressure, BiPAP = bilevel positive airway pressure, PICU LOS = pediatric intensive care unit length of stay, Wilcoxon rank-sum test used to compare continuous variables presented as median (interquartile range); Chi-square test of independence used to compare categorical variables presented as n (%).
Nutrition Details for Non-Intubated EN Group (n = 109).
| EN | |
|---|---|
| Route, | |
| PO | 11 (10) |
| NG | 69 (63) |
| NJ | 14 (13) |
| GT/JT | 15 (14) |
| Mode, | |
| Bolus | 24 (22) |
| Continuous | 85 (78) |
| Time to initiation (h) *, median (IQR) | 19 (11–37) |
| | |
| ≤48 h | 98 (90) |
| >48 h | 11 (10) |
| Reached full EN (h) *, median (IQR) | 40 (24–58) |
| | |
| ≤7 days | 103 (94) |
| >7 days | 6 (6) |
| Complications #, | |
| Yes | 9 (8) |
| No | 100 (92) |
| Evidence of aspiration, | |
| Yes | 1 (1) |
| No | 108 (99) |
* Hours after NRS; # refer to Table S3 for details; PO = per os (by mouth), NG = nasogastric, NJ = nasojejunal, GT/JT = gastrostomy tube/jejunostomy tube, EN = enteral nutrition, h = hours.
Figure 2Physiometric parameters for the enteral nutrition (EN) group demonstrating (A) heart rate and (B) respiratory rate trends prior to (2 h pre-) and after (12 h post-) EN initiation. Data presented as mean standard error of mean. *** p < 0.001 by paired two-tailed Student’s t-test. Avg = average, bpm = beats/breaths per minute, resp = respiratory.