Short-term complications and long-term morbidities associated with repeated unplanned extubations.

OBJECTIVE: To describe characteristics associated with repeated unplanned extubations, short-term complications and outcomes, and longer-term morbidities including acquired subglottic stenosis. STUDY
DESIGN: Cohort study including neonates admitted to a tertiary care neonatal intensive care unit who experienced an unplanned extubation in a 5-year period.
RESULTS: We reviewed 588 events involving 300 patients. Ten percent had airway trauma with reintubation, 42% required ≥2 reintubation attempts, and 39% led to increased baseline oxygen. Increased odds of repeated events were seen in patients with bronchopulmonary dysplasia and were associated with higher rates of tracheostomy and longer length of stay. The 9% of patients diagnosed with acquired subglottic stenosis had more unplanned extubations, higher rates of airway trauma and tracheitis, and were an older gestational age at birth.
CONCLUSION: Unplanned extubations lead to short- and long-term morbidities. Certain patient characteristics are associated with increased odds of repeated events and the development of acquired subglottic stenosis.

Introduction

An unplanned extubation (UE) is defined as the unintentional dislodgement of an endotracheal tube (ETT) from a patient receiving invasive mechanical ventilation [1]. In North American neonatal intensive care units (NICUs), UE requiring reintubation is the fourth most common adverse safety event [2]. Reported rates of UE in the NICU vary between 0.56 and 5.3 UEs per 100 ETT days [3, 4]. In a review of the adverse events related to intubations in a tertiary care NICU, four out of ten endotracheal intubations were associated with adverse events. A greater than fourfold increased odds of an adverse event was seen if the intubation was performed emergently, with UE found to be the most common reason for an emergent intubation [5]. Other studies demonstrated a 20% rate of cardiovascular collapse following UE in NICU, pediatric ICU, and pediatric cardiac ICU patients [6].

The risk of UE is generally higher in neonates when compared to older patients, likely due to longer duration of intubation, shorter trachea length, low use of routine sedation, use of uncuffed ETTs, and encouragement of skin-to-skin care [1]. Several studies have reported on the specific risk factors for UEs, such as agitation, poor fixation of the tube, and duration of mechanical ventilation. Reported rates of reintubation following UE range from 8.3 to 100%, though there are little data regarding risk factors in neonates for requiring reintubation or the use of sedation and/or restraints [2, 3, 7–9]. A recent single-center cohort study reported that the use of a sedation infusion, high-frequency ventilation, higher mean airway pressure, and need for cardiopulmonary resuscitation were associated with immediate reintubation following UE without a trial of extubation [10]. Despite studies investigating UEs in general, there is little evidence in the literature about the risk factors for repeated UEs or the short- and long-term outcomes associated with these events in the NICU, except for one case-control study of severe acquired subglottic stenosis (SGS) in neonates that reported the incidence of repeated UEs in these patients [11].

In this study, we aim to describe a 5-year cohort of patients who experienced a UE, focusing on risk factors contributing to UE and short-term outcomes and complications. We also will identify risk factors for experiencing repeated UEs in the NICU, describe the outcomes of those patients with more than one UE, and evaluate longer-term outcomes in these infants. To our knowledge, this is the largest cohort study focusing on risk factors and outcomes associated with UEs, and the only study focusing specifically on repeated UEs.

Methods

Study population

We performed a cohort study of all NICU patients who had at least one UE over a 5-year period at Nationwide Children’s Hospital in Columbus, Ohio. Inclusion criteria are all infants admitted to the NICU receiving invasive mechanical ventilation via ETT who experienced a UE between January 1, 2014 and December 31, 2018. The only exclusion criteria was if the patient had an unplanned removal of a tracheostomy tube. This study was approved by the Nationwide Children’s Hospital Institutional Review Board. The NICU at Nationwide Children’s Hospital is a 130-bed, level IV referral center [12]. Our NICU cares for a wide range of patients who might require prolonged mechanical ventilation, including those with extreme prematurity, surgical issues, congenital malformations, and a 24-bed referral center for infants with severe bronchopulmonary dysplasia (BPD). To optimize neurodevelopmental outcomes, routine use of restraints and sedation to prevent UEs is discouraged. The patients were enrolled prospectively and identified by an institutional quality improvement project, in which the Nationwide Children’s NICU has been tracking all UEs since January 2014. Retrospective chart review was used to collect additional clinical and demographic data.

Definitions

We defined a UE as the unintended displacement of the ETT without an order from the provider. Underlying causes identified for UEs include events related to direct provider contact or patient maneuvering, events during holding by family, loose ETT securement device or tape, events related to emesis, and unwitnessed events assumed to be due to patient movement or other unidentified causes. If the ETT was not visibly displaced based on inappropriate depth or loose securement device, a UE was identified by lack of appropriate color change on end-tidal carbon dioxide detector, lack of vital sign improvement with positive-pressure ventilation via ETT, and lack of breath sounds on auscultation. Information about each UE and the reintubation procedure were collected from the medical record and from a UE huddle form completed by bedside providers immediately following the event. Completion of the UE huddle form is the primary method of identification of UE events, and capture of all events is further ensured through multidisciplinary discussion at regular meetings and manual chart review. Reporting of UEs was monitored by the quality improvement committee, and multiple interventions were implemented at the start of the project to optimize identification of all UEs.

Short-term outcomes following UE were selected a priori and were pulled from procedure notes, respiratory therapist documentation, and the medication administration record. Facial or airway trauma was defined as documentation of airway edema or erythema noted during direct laryngoscopy, trauma or bleeding to mucous membranes documented in the intubation procedure note, or nursing notes describing mucous membrane injury following the reintubation. For those patients who remained extubated, stridor or hoarse cry documented in the 6 h following UE was noted. Baseline oxygen requirement is defined as the most frequent fraction of inspired oxygen (FiO2) in the 12 h period before or after the UE. Change in ETT depth is determined by comparing the most recent ETT depth charted before the UE and the depth documented after x-ray confirmation of appropriate depth following reintubation. Appropriateness of the ETT size is determined using the Sherman ratio, which is defined as ETT internal diameter divided by gestational age, with a value less than 0.1 considered acceptable [13]. Flowsheet data were pulled for each patient to determine the total number of different ETTs placed during the NICU stay, the size of each ETT, and the total duration of intubation. Longer-term outcomes at the time of NICU discharge or transfer were defined a priori and were extracted from medical record documentation and problem lists. BPD is defined as the need for supplemental oxygen or respiratory support at 36 weeks postmenstrual age (PMA) in those infants born at less than 32 weeks or at 56 days of life in those born at greater than 32 weeks [14, 15]. A diagnosis of acquired SGS was determined by problem lists and documentation from procedure notes. Acquired SGS severity was classified using the Cotton–Meyer system [16], as documented in the direct laryngoscopy and bronchoscopy procedure note at the time of diagnosis. Data regarding surgical interventions for acquired SGS were extracted from operation notes and procedure codes.

Statistical analysis

Data were analyzed using GraphPad Prism 8.0.0, IBM SPSS Statistics (Version 26), and R (Version 1.3.5033). Categorical variables were compared using χ2 or Fisher’s exact test. Continuous variables were examined using Mann–Whitney U or Kruskal–Wallis test. Multivariable and univariate logistic regression models were used for all outcomes to determine associations between those listed and the odds of having 2 or more UEs and the odds of receiving a diagnosis of acquired SGS. Inverse probability of treatment weighting (IPTW) was utilized as a method to create unbiased comparisons between UE events and diagnosis of acquired SGS. One multivariable logistic regression model was used to assess the odds of having 1 UE vs. 2 or more UEs, while another was created to assess the odds of having a diagnosis of acquired SGS vs. not having a diagnosis of acquired SGS. Variables included in each model to determine propensity scores and gain stabilized weights were determined a priori and included those events that happened prior to UE or receiving a diagnosis of acquired SGS. These variables included sex, gestational age, and birth weight. Standardized mean differences (SMD) with a threshold of >10% were used to determine clinically meaningful differences between covariates and outcomes to include in the model. SMDs were calculated prior to and after weighting. Weighted multivariable logistic regression models were created to determine odds of having 1 UE vs. 2 or more UEs and having a diagnosis of acquired SGS vs. not having a diagnosis of acquired SGS, conditioned on covariates balanced after weighting (SMDs < 10% threshold) and ETT days. A p value of <0.05 was considered statistically significant.

Results

During this study period, our NICU had ~850 admissions per year. Among these patients, we had an average of 5243 ETT days per year. The UE rate in our NICU at the start of this project was 3.3 UE events per 100 ETT days and decreased to 2.0 UE events per 100 ETT days with quality improvement interventions approximately halfway through the study period. Our baseline rates of BPD during this study period ranged between 46 and 69%. During our 5-year study period, there were 588 UEs among 300 patients. At least 2 UEs were experienced by 133 (44.3%) of these patients. Of these 300 patients, 183 (61.0%) are male. Demographic information for these patients is described in Table 1. The majority of patients in this overall cohort were premature, with 217 (72.3%) born at less than 32 weeks gestation. These patients tended to have a long duration of intubation and long length of hospital stay, with 174 (58.0%) having greater than 30 ETT days and 173 (57.7%) having a length of stay in the NICU greater than 120 days. As shown in Table 1, the patients who experienced a single UE and those who experienced repeated events were quite different at baseline.

Table 1

Overall patient demographics and comparison between 1 UE and ≥2 UE groups.

Parameter	Total (n = 300)	1 UE (n = 167)	≥2 UE (n = 133)	P value*
Male sex	183 (61.0%)	96 (57.5%)	87 (65.4%)	0.19
Gestational age at birth (weeks)	26.7 (24.6; 33.1)	28.0 (25.4; 37.0)	25.4 (24.0; 27.9)	<0.0001
Postmenstrual age at first UE (weeks)	34.3 (28.8; 39.8)	36.4 (30.4; 40.1)	32.1 (27.7; 38.6)	0.003
Birth weight (g)	859.0 (615.0; 1964.0)	1069.0 (695.0; 2490.0)	743.0 (583.0; 982.5)	<0.0001
Intrauterine growth restriction	65 (21.7%)	33 (19.8%)	32 (24.1%)	0.40
Weight at first UE (g)	1775.0 (999.8; 2967.5)	2220.0 (1187.5; 3275.0)	1280.0 (885.0; 2640.0)	0.0002
Day of life at first UE	25.4 (8.6; 65.8)	19.3 (6.6; 62.5)	32.9 (13.5; 69.3)	0.01
Day of life at admission to Nationwide Children’s NICU	12.9 (34.6)	7.9 (25.1)	19.1 (43.1)	0.02
Length of stay (days)	147.0 (90.0; 214.0)	107.0 (48.0; 180.0)	191.5 (137.8; 283.0)	<0.0001
ETT days during NICU stay	41.0 (15.0; 85.5)	21.0 (6.0; 56.0)	62.0 (34.0; 118.0)	<0.0001
Number of ETTs during NICU stay	3 (2; 6)	2 (1; 4)	6 (4; 8)	<0.0001

Bold values indicate statistical significance p < 0.05.

Data are expressed as n (%), median (IQR), or mean (SD).

UE unplanned extubation, NICU neonatal intensive care unit, ETT endotracheal tube, IQR interquartile range, SD standard deviation.

*P value compares 1 UE vs. ≥2 UE groups.

Events surrounding UE

Details about the events surrounding each of the 588 UE events and potential causes or contributing factors are listed in Table 2. Of note, 16.3% percent of the UEs occurred during skin-to-skin care or holding by family members and 39.8% were attributed to direct provider contact or maneuvering. Short-term complications and outcomes in the period immediately following the UE are detailed in Table 2. Resuscitation, including bag-mask ventilation, cardiopulmonary resuscitation with chest compressions, and treatment for pulmonary hemorrhage or bronchospasm, was needed following 260 (44.2%) of the UEs. Additionally, two (0.3%) of the UEs resulted in death. Of the 470 events that led to reintubation within 60 min of UE, 166 (35.3%) received sedation or paralytic medications and 196 (41.7%) needed more than one attempt at reintubation. In 183 (38.9%) events, the appropriate position of the new ETT following reintubation was noted to be deeper than the previous tube had been.

Table 2

Events surrounding each UE event and short-term complications.

Parameter (n = 588)	Value
ETT securement method
Standard commercial device	569 (96.8%)
Tape	18 (3.1%)
Nasal intubation	1 (0.2%)
Type of ventilation at time of UE
Conventional	541 (92.0%)
High frequency oscillatory ventilation	47 (8.0%)
Skin-to-skin care or holding at time of UE	96 (16.3%)
Primary cause identified
Direct provider contact	234 (39.8%)
Unwitnessed	23 (3.9%)
Emesis	98 (16.7%)
ETT re-taping	35 (6.0%)
Loose securement device or tape	125 (21.3%)
Unknown	73 (12.4%)
Time of day
Day shift (7 a.m.–7 p.m.)	322 (54.8%)
Night shift (7 p.m.–7 a.m.)	266 (45.2%)
Day of week
Monday	81 (13.8%)
Tuesday	83 (14.1%)
Wednesday	85 (14.5%)
Thursday	87 (14.8%)
Friday	84 (14.3%)
Saturday	84 (14.3%)
Sunday	84 (14.3%)
Feeds held
None/already NPO	516 (87.8%)
1–3 feeds	60 (10.2%)
Made NPO	12 (2.0%)
Resuscitation
None	328 (55.8%)
Bag-mask ventilation to stabilize	242 (41.2%)
Chest compressions	14 (2.4%)
Othera	4 (0.7%)
Death immediately following UE	2 (0.3%)
Airway trauma
None	527 (89.6%)
Mucous membrane bleeding	20 (3.4%)
Airway edema/erythema	33 (5.6%)
Stridor and/or hoarse cry	8 (1.4%)
Reintubated within 60 min of UE	470 (79.9%)
Trial of extubation before reintubation (n = 470)	15 (3.2%)
Medications received for reintubation (n = 470)
None	304 (64.7%)
Opiate alone	26 (5.5%)
Benzodiazepine alone	101 (21.5%)
Opiate and benzodiazepine	10 (2.1%)
Chloral hydrate	4 (0.9%)
Sedation plus neuromuscular blocker	25 (5.3%)
Number of reintubation attempts (n = 470)
1	274 (58.3%)
2	113 (24.0%)
3	50 (10.6%)
≥4	33 (7.0%)
Otolaryngology or anesthesia required for reintubation (n = 470)	8 (1.7%)
Change to baseline oxygen requirement after reintubation (n = 470)
Lower	69 (14.7%)
No change	217 (46.2%)
Increased 1–10%	136 (28.9%)
Increased >10%	48 (10.2%)
Depth of new ETT compared to previous (n = 470)
Less deep	32 (6.8%)
Same depth	230 (48.9%)
0.5–1 cm deeper	173 (36.8%)
>1 cm deeper	10 (2.1%)
Previous depth unknown or not documented	25 (5.3%)
Reintubation alternative (n = 118)
Room air	13 (11.0%)
Low flow nasal cannula	6 (5.1%)
High flow nasal cannula	10 (8.5%)
Continuous positive airway pressure	89 (75.4%)

Data are expressed as n (%).

UE unplanned extubation, ETT endotracheal tube, NPO nil per os.

aIncluding treatment for bronchospasm and pulmonary hemorrhage.

Table 3 compares the number of patients who experienced specific adverse events after at least one UE. A significantly greater number of patients in the ≥2 UE group were exposed to short-term adverse events related to a UE. More patients in the ≥2 UE group had feeds held after a UE, required resuscitation including bag-mask ventilation or chest compressions, had airway trauma associated with a UE, received sedative medications for reintubation, required multiple attempts at intubation, and had an increase in baseline oxygen requirement of >10% following a UE.

Table 3

Number of patients experiencing adverse short-term outcomes following any UE.

Parameter	1 UE (n = 167)	≥2 UE (n = 133)	P value
Being held at time of any UE	27 (16.2%)	50 (37.6%)	<0.0001
Any number of feeds held after a UE	22 (13.2%)	38 (28.6%)	0.001
Made NPO after a UE	7 (4.2%)	4 (3.0%)	0.76
Required any resuscitation	45 (26.9%)	104 (78.2%)	<0.0001
Required bag-mask ventilation	45 (26.9%)	104 (78.2%)	<0.0001
Required chest compressions	3 (1.8%)	11 (8.3%)	0.01
Any documented airway trauma	18 (10.8%)	35 (26.3%)	0.001
Any medication administered for reintubation	28 (16.8%)	60 (45.1%)	<0.0001
Any benzodiazepine given for reintubation	8 (4.8%)	48 (36.1%)	<0.0001
Any opiate given for reintubation	28 (16.8%)	25 (18.8%)	0.65
Any neuromuscular blocker given for reintubation	12 (7.2%)	14 (10.5%)	0.31
Ever reintubated within 60 min of UE	100 (59.9%)	91 (68.4%)	0.15
Ever needed >1 attempt at reintubation	35 (21.0%)	99 (74.4%)	<0.0001
Ever needed >2 attempts at reintubation	15 (9.0%)	55 (41.4%)	<0.0001
Ever needed otolaryngology or anesthesia for reintubation	1 (0.6%)	5 (3.8%)	0.09
Ever had baseline oxygen requirement increased by >10% after UE	33 (19.8%)	44 (33.1%)	0.01

Bold values indicate statistical significance p < 0.05.

Data are expressed as N (%).

UE unplanned extubation, NPO nil per os.

Repeated UE

Repeated UEs were experienced by 133 (44.3%) of patients included in this study. The group that experienced multiple UEs had a lower median gestational age at birth and PMA at the time of UE, but experienced the first UE at a significantly older day of life (DOL). The multiple UE group also had a significantly higher total number of ETT days during the initial NICU admission. Table 4 compares patients who experienced a single UE with those who experienced at least two. Crude, adjusted, and weighted and adjusted odds ratios are shown to compare clinical characteristics between the two groups and identify factors that are associated with a higher odds of experiencing repeat UEs. Longer-term outcomes were also compared between the two groups. Patients who received a diagnosis of BPD had significantly increased odds (weighted and adjusted OR 6.78, p = 0.02) of experiencing more than one UE compared to those with no BPD diagnosis. Significantly increased odds of having a length of stay greater than 90 days (weighted and adjusted OR 3.12, p = 0.04) and having a tracheostomy placed during admission (weighted and adjusted OR 4.16, p = 0.002) were also seen in those with more than one UE.

Table 4

Characteristics and outcomes of those patients with ≥2 UEs compared to those with 1 UE.

Parameter	1 UE (n = 167)	≥2 UE (n = 133)	Crude OR	Adjusted ORa	Weighted and adjusted ORb	P value*
Weight at first UE < 2000 g	75 (44.9%)	86 (64.7%)	2.24 (1.41; 3.60)	1.28 (0.68, 2.38)	1.29 (0.69, 2.40)	0.42
PMA at first UE < 30 weeks	39 (23.4%)	55 (41.4%)	2.31 (1.41; 3.83)	1.74 (0.92, 3.31)	2.01 (1.06, 3.83)	0.03
DOL at first UE < 30 days	89 (53.3%)	72 (54.1%)	1.03 (0.66; 1.64)	0.88 (0.52, 1.48)	0.83 (0.47, 1.44)	0.50
Length of stay >90 days	101 (60.5%)	120 (90.2%)	7.64 (3.87; 16.45)	2.21 (0.92, 5.69)	3.12 (1.08, 9.03)	0.04
Critical airway	6 (3.6%)	3 (2.3%)	0.62 (0.13; 2.39)	2.09 (0.35, 11.17)	1.31 (0.26, 6.68)	0.75
Chromosomal anomaly/genetic syndromec	18 (10.8%)	15 (11.3%)	1.05 (0.51; 2.17)	1.89 (0.66, 5.59)	2.32 (0.72, 7.47)	0.16
Mortality during initial hospitalization	22 (13.2%)	14 (10.5%)	0.81 (0.39; 1.63)	0.41 (0.16, 0.99)	0.41 (0.16, 1.08)	0.07
Bronchopulmonary dysplasia	96 (57.5%)	119 (89.5%)	7.81 (3.96; 16.92)	3.08 (0.88, 11.73)	6.78 (1.42, 32.31)	0.02
Tracheostomy	18 (10.8%)	35 (26.3%)	2.96 (1.59; 5.61)	3.03 (1.38, 6.95)	4.16 (1.68, 10.31)	0.002

Bold values indicate statistical significance p < 0.05.

Data are expressed as N (%) or odds ratio (95% confidence interval).

UE unplanned extubation, OR odds ratio, PMA postmenstrual age, DOL day of life, IPTW inverse probability of treatment weighting.

*P values are displayed from weighted and adjusted models.

aAdjusted odds ratios displayed as adjusted for sex, gestational age, birth weight, and total number of ETT days during initial hospitalization.

bWeighted and adjusted ORs are IPTW weighted for sex, gestational age, and birth weight; and adjusted for sex, gestational age, birth weight, and total number of ETT days during initial hospitalization.

cIncluding Trisomy 21, Stickler syndrome, CHARGE syndrome, Wolff–Hirschhorn syndrome, DiGeorge syndrome, and a chromosome 19 anomaly.

Table 2 shows the respiratory outcomes following UE. Of the 470 events leading to reintubation within 60 min, only 15 (3.2%) were given a trial of extubation. Of the events leading to reintubation within 60 min, 184 (39.1%) led to an increase in oxygen requirement between 1 and 49% above baseline, with a median increase of 5% (interquartile range (IQR) 3–11%). Following the 118 events that did not lead to reintubation within 60 min, the majority required continuous positive airway pressure (CPAP), but 16 (13.6%) only needed nasal cannula and 13 (11.0%) remained stable in room air.

Outcomes at NICU discharge

On assessment of outcomes at the time of NICU discharge or transfer to another facility for these 300 patients, 36 (12.0%) died during their initial NICU stay. Two deaths were directly following the UE; in both cases, the babies had a modified Allow Natural Death order and were not reintubated due to parental preference for comfort care. Of these 300 infants, 215 (71.7%) were diagnosed with BPD and 53 (17.7%) required tracheostomy placement. In addition to those requiring home ventilatory support via tracheostomy, 129 (43.0%) were discharged with nasal cannula oxygen and 3 (1.0%) required CPAP at home.

Acquired subglottic stenosis

Of these 300 patients, 28 (9.3%) were diagnosed with acquired SGS. The severity of acquired SGS was classified as Cotton–Myer grade 1 in 9 patients, grade 2 in 6, the most severe grade 3 in 9, and not graded in the remaining 4 patients. The crude, adjusted, and weighted and adjusted odds ratios comparing those who were diagnosed with acquired SGS and those who were not are detailed in Table 5. Significantly fewer patients in the group diagnosed with acquired SGS were born at less than 25 weeks’ gestational age (3.5% vs 11.3%, p = 0.043). After weighting and adjusting for sex, gestational age at birth, birth weight, and total number of ETT days, characteristics associated with a significantly increased odds of having acquired SGS were having at least four UEs, having documented airway trauma during an intubation attempt, having a history of tracheitis, and having a diagnosis of a major chromosomal anomaly or syndrome. Experiencing the first UE at a weight of <1500 g was associated with a decreased odds of having a diagnosis of acquired SGS. When the subgroup with severe acquired SGS requiring surgical intervention, including balloon dilations and laryngotracheal reconstruction, was compared to the group with no SGS or mild SGS not requiring surgery, no significant differences were seen between the two groups.

Table 5

Characteristics of those patients with acquired SGS compared to those without acquired SGS.

Outcomes	No SGS (n = 272)	SGS (n = 28)	Crude OR	Adjusted ORa	Weighted and adjusted ORb	P value*
Postmenstrual age at first UE < 32 weeks	116 (42.6%)	6 (21.4%)	0.37 (0.13, 0.88)	0.44 (0.15, 1.19)	0.40 (0.15, 1.07)	0.07
Weight at first UE < 1500 g	128 (47.1%)	7 (25.0%)	0.38 (0.14, 0.87)	0.37 (0.13, 0.96)	0.34 (0.13, 0.91)	0.03
DOL at first UE < 21 days	122 (44.9%)	11 (39.3%)	0.80 (0.35, 1.74)	0.77 (0.34, 1.7)	0.73 (0.32,1.67)	0.46
≥ 4 UEs	30 (11.0%)	8 (28.6%)	3.23 (1.25, 7.75)	3.54 (1.19, 10.07)	4.25 (1.35,13.45)	0.01
≥ 3 reintubation attempts following any UE	63 (23.2%)	7 (25.0%)	1.11 (0.42, 2.61)	0.97 (0.36, 2.36)	0.91 (0.36, 2.27)	0.83
≥ 4 ETTs during hospitalization	124 (45.6%)	19 (67.9%)	2.52 (1.13, 6.03)	2.22 (0.77, 6.68)	2.79 (0.98, 7.93)	0.06
Sherman ratio ≥0.1c for any ETT	20 (7.4%)	1 (3.6%)	0.86 (0.05, 4.92)	0.95 (0.05, 5.77)	0.94 (0.15,5.98)	0.95
Airway trauma with reintubation	41 (15.1%)	12 (42.9%)	4.23 (1.83, 9.56)	4.31 (1.81, 10.19)	5.66 (2.15, 14.87)	<0.001
Tracheitis	35 (12.9%)	18 (64.3%)	12.19 (5.31, 29.53)	12.4 (4.99, 32.81)	13.16 (5.04, 34.35)	<0.001
Chromosomal anomaly/genetic syndromed	25 (9.2%)	8 (28.6%)	3.95 (1.51, 9.65)	4.55 (1.44, 14.26)	5.62 (1.49, 21.13)	0.01

Bold values indicate statistical significance p < 0.05.

Data are expressed as N (%) or odds ratio (95% confidence interval).

SGS subglottic stenosis, OR odds ratio, UE unplanned extubation, DOL day of life, ETT endotracheal tube, IPTW inverse probability of treatment weighting.

*P values are displayed from weighted and adjusted models.

aAdjusted odds ratios displayed as adjusted for sex, gestational age, birth weight, and total number of ETT days during initial hospitalization.

bWeighted and adjusted ORs are IPTW weighted for sex, gestational age, and birth weight; and adjusted for sex, gestational age, birth weight, and total number of ETT days during initial hospitalization.

cSherman ratio = ETT size/gestational age.

dTrisomy 21, Stickler syndrome, CHARGE syndrome, Wolff–Hirschhorn syndrome, DiGeorge syndrome, and a chromosome 19 anomaly.

The median age of acquired SGS diagnosis in this cohort was 3.6 months (IQR 2.8–8.5), and all but one case was diagnosed by 14 months of life. The initial presentation leading to diagnosis of SGS was stridor in 10 of the patients and inability to extubate after multiple attempts in 12 of the patients, with the remainder diagnosed incidentally on direct laryngoscopy and bronchoscopy for another clinical indication. Surgical intervention was required in 13 (46.4%) of the patients with acquired SGS, including balloon dilations in 8 (28.6%) patients and laryngotracheal reconstruction in 5 (17.9%) patients. The median age at initial SGS surgery was 4 months (IQR 3–10).

Discussion

UE requiring reintubation is among the most common adverse safety events reported in North American NICUs [2]. In this study spanning 5 years, we describe factors surrounding UEs, short-term outcomes, and longer-term morbidities in a level IV NICU. UEs in general were associated with many short-term complications such as increase in baseline oxygen requirement, missed feeds, airway trauma, and need for cardiopulmonary resuscitation. Repeated UEs were common among this population and were associated with increased odds of longer-term morbidities, including BPD, need for tracheostomy, and a longer length of stay.

Previous studies support the idea that standardizing the ETT securement leads to fewer UEs [1, 17]. In agreement with these studies, the standard practice in our unit is to secure the ETT using a commercial ETT holder, and this device was used in the vast majority of these events. Skin-to-skin care is strongly encouraged in our NICU, and we found that 16% of the events occurred during skin-to-skin care or holding, which higher than rates reported in other studies [18, 19]. This finding prompted further quality improvement interventions to ensure airway safety.

Previous studies have shown mixed results regarding the association of weight and PMA with UE. One study showed that most events happened at <31 weeks PMA, but others showed that most patients were >34 weeks [8, 18, 20]. In our study, the patients had a median birth gestational age of 26.7 weeks, but the UEs happened at a median PMA of 34.3 weeks. Our patients had a median weight of 1775 g at the time of UE, whereas other studies have shown the majority of UEs occurring in smaller babies [3, 21]. Older and larger patients may be more difficult to contain and warrant creative non-pharmacologic interventions to maintain airway safety.

Several short-term complications were noted as a direct result of the UEs, including increased oxygen requirement and discontinued feeds. About 10% had documented airway trauma and almost half of patients who were reintubated required multiple attempts. Notably 14 events led to chest compressions and 41.2% required bag-mask ventilation to stabilize vital signs before a reintubation attempt was made. These short-term complications likely contribute to an increased length of stay and long-term morbidities in these patients, reinforcing the need to focus efforts on UE prevention. Many patients received sedative or paralytic medications for reintubation. In our efforts to improve the potential neurodevelopmental outcome of the patients, our unit discourages the routine use of sedation or restraints to prevent UE. The use of sedation in the setting of reintubation may also negatively impact neurodevelopment. When specifically comparing the single UE group to those patients who experienced multiple UEs, there was greater exposure to many adverse events among the patients with multiple UEs, putting these patients at greater risk for short- and longer-term morbidities.

We documented reintubation within 60 min based on the definitions for UE tracking provided by the Solutions for Patient Safety collaborative. We noted reintubation within 60 min of UE in ~80% of the events. Previous studies have reported reintubation rates within 24 h after UE ranging from 25 to 75% [18, 20–22]. Our higher rate suggests that many of our intubated patients do require invasive mechanical ventilation, but there is still an opportunity to improve identification of extubation readiness, given that 20% did not need to be reintubated. In addition, as shown in Table 2, 25% of these patients did not even require CPAP following UE. Thirty-nine percent of ETTs were replaced deeper than they had previously been taped, indicating a need to continually reassess tube depth, especially in patients who may experience significant growth while intubated due to edema or prolonged duration of intubation.

Although previous studies have reported on risk factors for UEs and subsequent outcomes in the NICU, to our knowledge, none have specifically assessed those patients who experience repeated events. In our study, almost half of the patients had more than one UE. Patients with multiple UEs had a longer duration of intubation on average, so they are already at increased risk for airway and pulmonary morbidities due to prolonged mechanical ventilation. Repeated UEs were seen more often in those patients with BPD, likely due to the prolonged duration of intubation increasing the number of opportunities for UE. In those patients with repeated UEs, higher odds of tracheostomy requirement and home oxygen or ventilator requirement were noted. Care should be taken to prevent UEs in these patients to avoid further increasing the risk for airway trauma and complications.

Previous studies have identified an association between UEs and the development of SGS [11]. In our study population, all but one case of acquired SGS was diagnosed before 14 months of life, with the majority in the first few months of life. The most common clinical presentations leading to this diagnosis were stridor and inability to extubate, so further evaluation for SGS should be considered in this population of patients. Acquired SGS should also be considered in patients following discharge who present with stridor and a history of intubation and UE. Other identified risk factors for acquired SGS in this study include documented airway trauma with reintubation, history of tracheitis, and at least four UEs. We saw a trend toward a greater number of ETTs overall being associated with the development of acquired SGS, which is consistent with previous studies [23-25].

Gestational age has been inconsistently associated with acquired SGS, with some older studies showing no association and a more recent study demonstrating high rates in infants born at 23–24 weeks [11, 23, 26]. Our data actually demonstrated a significantly decreased incidence of acquired SGS in this population of infants born at less than 25 weeks’ gestation, potentially related to permissive air leak in our unit and general avoidance of elective ETT upsizing. The Sherman ratio (ETT internal diameter divided by gestational age) has been used in previous studies to assess the appropriateness of ETT size with a ratio of <0.1 considered acceptable [23]. Unlike in previous studies [23, 27], we found no significant association between Sherman ratio and development of acquired SGS. A recent study reported an overall incidence of 0.93% of severe acquired SGS in intubated neonates, defined as those requiring surgical intervention to manage SGS;[11] our rate in this study of patients with a history of UE is much higher at 4.3%. This higher incidence might be attributable to the airway trauma and multiple intubation attempts seen with reintubation following UE in this population, many of which likely occurred in an urgent or emergent setting.

One limitation of this study is the retrospective nature of some data collection, although the patients were identified prospectively and the forms detailing the situation surrounding the UE are filled out in real-time after the event, which partially mitigates this concern. Similarly, many outcomes of interest listed in this study are taken from documentation in the medical record, which may lead to limited or missing data. This study also represents the experience of a single level IV NICU with an entirely out born population, though patients were admitted relatively early, at 13 days of life on average (median DOL 0; IQR 0–4). It is possible that patients experienced a UE at the birth hospital prior to admission to our NICU. Finally, follow up information is not available for all patients following discharge from the NICU, so there may be a greater number of patients diagnosed with long-term morbidities than identified here.

Conclusions

UEs are a relatively common safety event in the NICU and can lead to serious short- and long-term morbidities, especially when a patient has multiple events. Identification of common clinical scenarios surrounding UEs has helped to identify key areas to target with quality improvement initiatives. Certain patient characteristics were associated with increased rates of repeated UEs and this knowledge may be used to heighten awareness of high-risk patients. Identification of complications associated with UEs can help to reinforce the importance of preventing these events. These patients are at risk for long-term airway morbidities, which may present after the time of NICU discharge. Further initiatives are needed to use these data to decrease overall UE rates and reduce the need for emergent reintubations. Additional research is needed to develop a prediction model to identify those patients at highest risk to experience one or multiple UEs to further improve outcomes.