|Year : 2017 | Volume
| Issue : 5 | Page : 404-409
A randomised comparative study of Miller laryngoscope blade versus Oxiport® Miller laryngoscope blade for neonatal and infant intubations
Raylene Dias, Nandini Dave, Rachana Chhabria, Harick Shah, Madhu Garasia
Department of Anaesthesiology, Seth GS Medical College and KEM Hospital, Mumbai, Maharashtra, India
|Date of Web Publication||9-May-2017|
C 303, Presidential Towers, LBS Marg, Ghatkopar West, Mumbai - 400 086, Maharashtra
Source of Support: None, Conflict of Interest: None
Background and Aims: Neonates and infants are prone to oxygen desaturation during the induction of general anaesthesia. Pharyngeal oxygen insufflation has been shown to delay the onset of desaturation and hypoxaemia during apnoea. We tested the hypothesis that deep laryngeal oxygenation with Oxiport® Miller blade would delay the onset of desaturation compared to laryngoscopy without supplemental oxygen (Miller blade). Methods: One hundred neonates and infants undergoing general anaesthesia with endotracheal intubation for surgery were recruited and randomly assigned to one of the two groups: Miller or Oxiport group (laryngoscopy performed with Miller or Oxiport® blade, respectively). Primary outcome measure was the lowest oxygen saturation (SpO2) attained during intubation. Secondary outcomes were the incidence of severe desaturation (SpO2<85%), correlation between SpO2and time to intubation in each group. Pearson's correlation coefficient was used to measure the correlation between time to intubation and desaturation in each group. P< 0.05 was considered statistically significant. Results: Data from 95 patients were available for the final analysis: Miller group (n = 48) and Oxiport group (n = 47). Mean lowest SpO2was 95.9% ± 5.75% in Miller group and 97.55% ± 2.93% in Oxiport group (P = 0.049). Correlation between time to intubation and SpO2was −0.110; P = 0.459 in Miller group and −0.468; P = 0.001 in Oxiport group. Severe desaturation occurred in 12.5% patients in Miller group and none in Oxiport group. Conclusion: Apnoeic laryngeal oxygen insufflation with Oxiport® laryngoscope blade decreases the incidence of severe desaturation during neonatal and infant intubations.
Keywords: Apnoeic oxygenation, endotracheal intubation, infants, Miller blade, neonates, Oxiport blade
|How to cite this article:|
Dias R, Dave N, Chhabria R, Shah H, Garasia M. A randomised comparative study of Miller laryngoscope blade versus Oxiport® Miller laryngoscope blade for neonatal and infant intubations. Indian J Anaesth 2017;61:404-9
|How to cite this URL:|
Dias R, Dave N, Chhabria R, Shah H, Garasia M. A randomised comparative study of Miller laryngoscope blade versus Oxiport® Miller laryngoscope blade for neonatal and infant intubations. Indian J Anaesth [serial online] 2017 [cited 2021 Mar 2];61:404-9. Available from: https://www.ijaweb.org/text.asp?2017/61/5/404/206003
| Introduction|| |
Neonates and infants are prone to brief periods of oxygen desaturation during laryngoscopy. This is due to lower functional residual capacity (FRC) and high closing volume which falls within tidal ventilation, higher oxygen consumption and immature pulmonary apparatus. Desaturation is more likely in babies having limited respiratory reserve, prolonged apnoea or difficult laryngoscopies. Pre-oxygenation during induction of anaesthesia is intended to prevent or delay onset of hypoxia during subsequent apnoea. Pharyngeal insufflation of oxygen has been shown to delay the onset of desaturation and hypoxaemia during apnoea by enhancing the safe apnoea duration. This technique supplements pre-oxygenation and provides apnoeic diffusion oxygenation during laryngoscopy, significantly delaying the desaturation during subsequent apnoea. Many techniques have been developed in the past for pharyngeal insufflation of oxygen, by fitting a feeding tube to the laryngoscope blade to provide oxygen flow  or incorporating a channel along the side of laryngoscope blade. Neonatal intubations are routinely performed with a Miller blade which has no provision for oxygenation. The Oxiport ® Miller is a modified Miller blade. It consists of a metallic tube incorporated into the blade that has an attachment through which oxygen can be connected and insufflated during laryngoscopy. The blade has been commercially available since 1980's and is used in infants and neonates. Deep laryngeal oxygen insufflation is a method which delivers oxygen closer to the larynx. This can be done with the Oxiport laryngoscope blade through the integrated oxygen delivery channel. Hence, compared to nasal prongs where the inspired oxygen concentration may be variable, oxygen insufflation closer to the larynx provides higher inspired oxygen concentration.
We tested the hypothesis that deep laryngeal oxygenation (with Oxiport ® Miller blade) delays the onset of desaturation compared with laryngoscopy without supplemental oxygen (with Miller blade). Our aim was to compare these two blades for neonatal and infant intubations. Primary outcome measure was to study the lowest level of oxygen saturation (SpO2) attained during intubation with each blade. Secondary outcome measures were to study the incidence of severe desaturation, correlation between SpO2 and time to intubation with each blade and association between the degree of desaturation with type of surgery.
| Methods|| |
This was a prospective, randomised, controlled interventional single-blind study. One hundred neonates/infants in groups of fifty each posted for surgery in paediatric operation theatre (OT) over a period of 6 months were included in the study. The Institutional Ethics Committee approval was obtained for the study. Patients posted for elective surgery were assessed during the pre-anaesthetic check a day prior whereas those taken up for emergency procedures were assessed on the day of surgery by the co-investigators. Participants were enroled during the pre-anaesthetic check on the day of surgery in the pre-operative holding area after reassessment by the principal investigator. Full-term neonates and infants up to 6 months of age of either sex requiring general anaesthesia with endotracheal intubation for elective as well as emergency surgery were included in the study. All broad surgical specialities were included in the study. This comprised three groups: thoracic, abdominal and miscellaneous surgeries. Thoracic surgeries included tracheoesophageal fistula repair, congenital diaphragmatic hernia repair, lobectomies for pulmonary sequestration and congenital lobar emphysema. Abdominal surgeries included intestinal obstruction, duodenal atresia, ileal atresia, colostomy, laparoscopic and open pyloromyotomy, gastroschisis, omphalocele and Kasai procedure for biliary atresia. Miscellaneous surgeries included sacrococcygeal teratoma excision, meningomyelocele repair, ventriculoperitoneal shunt for hydrocephalus, cystoscopy and posterior urethral valve fulguration.
Babies having desaturation before the induction of anaesthesia (SpO2 <94%), known congenital heart disease, hypotension (systolic blood pressure [BP] <60 mmHg), obvious congenital syndromes, anticipated difficult airway and anaemia (haemoglobin <12 g%) were excluded from the study. After obtaining parental consent for the study and confirming fasting status, babies were wheeled into OT in a cradle covered with warm cotton rolls, along with their maintenance fluid. Monitoring used included electrocardiogram and pulse rate on cardioscope, pulse oximetry, capnometry, noninvasive BP, nasopharyngeal and skin temperature. Pulse oximeter probe (Mindray ® pulse oximetry; finger sensor, Mindray DS USA, Inc.) was used in all participants and attached on each participant's toe. This was connected to Mindray ® DPM6 monitor (Mindray DS USA, Inc.). Only waveforms generating a good plethysmographic trace were used for recording SpO2 data. Ringer's lactate was started through an infusion pump at a rate according to the expected losses based on the surgery. Neonates/infants were then randomised into two groups, Miller group or Oxiport group by computer-generated tables. This randomisation was enclosed in opaque-sealed envelope, and then, the randomisation was activated by the co-investigators. The babies were then pre-oxygenated with 100% oxygen at a flow rate of 4 L/min for 3 min on spontaneous ventilation with Jackson–Rees circuit using GE Datex Ohmeda Aestiva ®/5 Anaesthesia Machine. Injection fentanyl 2 μg/kg intravenous (IV) was administered, and anaesthesia was induced with incremental sevoflurane up to 8%. Neuromuscular blockade was achieved with injection rocuronium 1 mg/kg IV. Baseline SpO2 was noted at this point. This was followed by direct laryngoscopy with the designated blade by an anaesthesiology resident (trainee) or a consultant. Laryngoscopy was performed with 0 number blade of Miller laryngoscope in Miller group and 0 number blade of Oxiport ® Miller laryngoscope in Oxiport group followed by endotracheal intubation. In Oxiport group, oxygen insufflation was instituted with oxygen tubing attached to Oxiport blade at a flow rate of 2 L/min (to provide low-flow oxygen during laryngoscopy) through an auxiliary oxygen port. Successful intubation was confirmed by end-tidal carbon dioxide tracing on capnometer and auscultation of bilateral equal air entry on both sides of the chest. This constituted the end-point of the study. The observations noted were intubation time in seconds (interval from the insertion of blade into mouth until successful confirmation of intubation), lowest saturation attained, anaesthesiologist performing laryngoscopy (trainee or consultant) and haemodynamic parameters such as heart rate and systolic BP. For the purpose of this study to quantify desaturation data, it was graded as mild desaturation (lowest SpO2 up to 90%), moderate desaturation (lowest SpO2 between 85% and 89%) and severe desaturation (lowest SpO2 <85%). This grading was selected based on a meta-analysis of SpO2 target range where SpO2, 85%–89% was considered restricted and SpO2, 91%–95% considered liberal oxygen exposure in extremely pre-term infants. The study was terminated when SpO2 decreased to 80% or signs of cardiac instability such as bradycardia appeared. Mask ventilation with 100% oxygen was immediately resumed till SpO2 increased to 98%–100%.
Sample size of 100 was estimated by a study using deep laryngeal oxygen insufflation during laryngoscopy in children. The incidence of desaturation (SpO2 <90%) was 10% in direct laryngoscopy with oxygen cannula group and 49% in standard direct laryngoscopy group. We anticipated a difference of 10% between the two groups. With 99% confidence interval and 90% power, we got a sample size of 42 in each group. Eight patients were added in each group to compensate for the possible loss of data.
Quantitative data are presented with the help of mean and standard deviation. Qualitative data are presented with the help of frequency and percentage table. The incidence of severe desaturation was calculated. Association among study groups was assessed with Pearson's Chi-square test. Pearson's correlation coefficient was used to measure correlation between time to intubation and desaturation in each group. P< 0.05 was considered as statistically significant. Statistics software SPSS version 16 was used (SPSS, Chicago, Illinois, USA).
| Results|| |
Out of the 100 patients enrolled, two were excluded in Miller group and three were excluded in Oxiport group due to unanticipated difficult intubation. Hence, 48 patients in Miller group and 47 patients in Oxiport group were included in the final analysis [Figure 1].
Both groups were comparable with respect to age, sex, weight, mean time to intubation (P = 0.530) and anaesthesiologist performing the laryngoscopy (P = 0.701) [Table 1].
|Table 1: Comparison of demographic profile, intubation time, experience of anaesthesiologist and haemodynamics between the study groups|
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Mean lowest SpO2 recorded was 95.9% ± 5.75% in Miller group and 97.55% ± 2.93% in Oxiport group. This difference was statistically significant (P = 0.049).
The incidence of mild desaturation (SpO2 up to 90%) was 85.4% in Miller group and 95.7% in Oxiport group. The incidence of moderate desaturation (SpO2 between 85% and 89%) was 2.1% in Miller group and 4.3% in Oxiport group. Incidence of severe desaturation (SpO2 <85%) was 12.5% in Miller group and 0 in Oxiport group (Chi-square test P = 0.03).
Correlation between time to intubation and SpO2 in Miller group (Pearson's R2 = −0.110) was statistically not significant at P = 0.459 [Figure 2]. Correlation between time to intubation and SpO2 in Oxiport group (Pearson's R2 = −0.468) was statistically significant at P = 0.001 [Figure 3].
|Figure 2: Correlation between intubation time and lowest oxygen saturation in Miller group. Y axis - Time taken to successful intubation expressed in seconds, X axis - Lowest oxygen saturation recorded (%). Correlation measured using Pearson's (R2) correlation coefficient. P< 0.05 considered statistically significant|
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|Figure 3: Correlation between intubation time and lowest oxygen saturation in Oxiport group. Y axis - Time taken to successful intubation expressed in seconds, X axis - Lowest oxygen saturation recorded (%). Correlation measured using Pearson's (R2) correlation coefficient. P< 0.05 considered statistically significant|
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Both groups were comparable with respect to the type of surgery (abdominal, thoracic, miscellaneous) (P = 0.773). Abdominal surgeries were associated with a higher number of severe desaturations (66.7%) compared to thoracic (16.7%) and miscellaneous (16.7%) surgeries.
| Discussion|| |
Apnoeic oxygenation is based on the principle of passive diffusion of fresh oxygen from the conducting airways into the lungs, and the primary criteria for its use are a patent upper airway. Ever since the introduction of this concept in clinical practice by Holmdahl in 1956, many modifications of the technique have been used., However, these devices were cumbersome and had their own limitations. Since the introduction of Oxiport ® laryngoscope blade in clinical practice, there has been very little published literature on the use of this blade for intubation in vulnerable populations such as neonates and infants. Hence, we conducted this study to compare this blade with Miller size 0 blade which is the current standard of care.
Babies in the Oxiport group had significantly higher saturations compared with those in the Miller group. With Oxiport ® laryngoscope, saturation never fell below 85% during the entire period of apnoea. These results confirmed our hypothesis. Oxygen insufflation closer to the larynx maintains higher SpO2 in neonates and infants by maintaining higher lung oxygen partial pressure and thus delays desaturation. Fresh oxygen continuously replaces the absorbed pulmonary volume by passive diffusion from larynx through the trachea into the lungs. The method increases safe apnoea time by maintaining SpO2 closer to the inflection point of haemoglobin oxygen dissociation curve. Our findings may be extrapolated to use of the Oxiport blade in very sick babies or in emergency situations in the intensive care set up where pre-oxygenation may not be feasible before intubation.
The correlation between time to intubation and incidence of desaturation in Oxiport ® group (Pearson's R2 = −0.468) was not strong, yet it was significant. This is because even as time to intubation increased beyond 60 s, desaturations did not occur in Oxiport group. In Miller group, this correlation was weaker as desaturations occurred irrespective of the time to intubation even in experienced hands. The art of neonatal intubation has a steep learning curve, and there may be significant time taken to successful intubation which can lead to desaturation and/or bradycardia. In this study conducted in a teaching institute where many intubations were performed by novice anaesthesiologists, the Oxiport ® blade helped prevent desaturation in inexperienced hands.
Although not statistically significant, abdominal surgeries had a higher incidence of severe desaturation (66%). Our finding may be attributed to the abdominal distension further reducing FRC and affecting pulmonary compliance. Similar results have been reported by a recent British study  on the use of deep laryngeal oxygen insufflation during laryngoscopy in children between 1 and 17 years of age. The authors measured the time to a 1% decrease in SpO2 from baseline which they considered a harbinger of a more rapid desaturation to come. Three groups were studied: standard direct laryngoscopy, laryngoscopy with TrueView video laryngoscope and laryngoscopy with an oxygen cannula attached to the side of a standard laryngoscope. They concluded that laryngeal oxygen insufflation increases the time to 1% desaturation and reduces the overall rate of desaturation during laryngoscopy in children.
Our study has certain strengths. We have studied the effect of apnoeic oxygenation on a very vulnerable patient population. Only infants up to 6 months of age were included and thus our study subjects comprised very small babies in whom the risk of desaturation is highest. Consequently, the benefit of this device is also substantial to this population. The All India Difficult Airway Association 2016 guidelines strongly recommend apnoeic oxygenation using nasal prongs/catheter during attempts at laryngoscopy in unanticipated difficult tracheal intubation in paediatrics. Authors recommend adjusting flow rate of oxygen targeting SpO2 >95%. The results of our study may change practice in days to come where the Oxiport blade may find a place in the intubation of the difficult paediatric airway.
There were a few limitations to this study. Severe desaturations were used to define desaturation data (SpO2 <85%). This is because on analysis saturations rarely fell below 90%. The British study  had similar issues in data analysis which led the authors to replace their original primary outcome with a coprimary measure; time to a 1% decrease in SpO2 from baseline. Doing this would have been more meaningful in our analysis as well. Superiority testing between the two blades was not possible as our study was not powered for the same. Trainees were allowed to intubate and their experience was not clearly defined. This could be a confounding factor. However, both groups were comparable for the anaesthesiologist performing the intubation (P = 0.701). Trainees were included in an effort to prove the utility of Oxiport blade even in inexperienced hands. No stratified statistical analysis was done for emergency and elective cases. Combining these two groups may not be justifiable as emergency patients tend to be more sick, dehydrated and may have significant abdominal distention making them more prone to rapid desaturation. In addition, site of operation and sickness of the baby are potential confounders.
Our study raises certain controversies in the current practices of oxygen administration based on the increasing understanding of oxygen toxicity in neonates., We used 100% oxygen for pre-oxygenation which is the current standard of care. The oxygen concentration delivered through Oxiport laryngoscope at flows of 2 L/min would be variable based on the amount of air entrained, and this was given for very brief periods. The use of oxygen during neonatal anaesthesia has not been well studied  and further research in essential. It would be reasonable to limit the use of supplemental oxygen only to situations where it is absolutely necessary. We did not use injection atropine or injection glycopyrrolate even though we were dealing with infants up to 6 months of age, who are prone to bradycardia in response to hypoxia. This is in accordance with the 2015 American Heart Association updated paediatric advanced life support recommendations which state that there is no evidence to support the routine use of atropine as a pre-medication to prevent bradycardia during intubation of critically ill infants.
Newer methods of passive diffusion oxygenation by the use of high flow nasal cannula have been gaining attention in recent times as an aid to prevent desaturation during endotracheal intubation in adults. Studying this method of apnoeic oxygenation in children may be a subject for future research.
| Conclusion|| |
In this study, apnoeic laryngeal oxygen insufflation with Oxiport laryngoscope blade decreased the incidence of severe desaturation while intubating neonates and infants. This was easily done as it was non-cumbersome and did not increase the overall cost of anaesthesia.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Steiner JW, Sessler DI, Makarova N, Mascha EJ, Olomu PN, Zhong JW, et al.
Use of deep laryngeal oxygen insufflation during laryngoscopy in children: A randomized clinical trial. Br J Anaesth 2016;117:350-7.
Umesh G, Jasvinder K. Nasopharyngeal airway as a diagnostic and therapeutic tool in difficult airway. Indian J Anaesth 2014;58:508.
] [Full text]
Weingart SD, Levitan RM. Preoxygenation and prevention of desaturation during emergency airway management. Ann Emerg Med 2012;59:165-75.e1.
Hencz P. Modified laryngoscope for endotracheal intubation of neonates. Anesthesiology 1980;53:84.
Muallem M, Baraka A. Pharyngeal oxygen insufflation via the laryngoscope blade. Anaesthesia 2006;61:1015-6.
Manja V, Lakshminrusimha S, Cook DJ. Oxygen saturation target range for extremely preterm infants: A systematic review and meta-analysis. JAMA Pediatr 2015;169:332-40.
Holmdahl MH. Pulmonary uptake of oxygen, acid-base metabolism, and circulation during prolonged apnoea. Acta Chir Scand Suppl 1956;212:1-128.
Todres ID, Crone RK. Experience with a modified laryngoscope in sick infants. Crit Care Med 1981;9:544-5.
Pawar DK, Doctor JR, Raveendra US, Ramesh S, Shetty SR, Divatia JV, et al.
All India Difficult Airway Association 2016 guidelines for the management of unanticipated difficult tracheal intubation in paediatrics. Indian J Anaesth 2016;60:906-14.
] [Full text]
Sola A. Oxygen in neonatal anesthesia: Friend or foe? Curr Opin Anaesthesiol 2008;21:332-9.
Bajaj N, Udani RH, Nanavati RN. Room air vs. 100 per cent oxygen for neonatal resuscitation: A controlled clinical trial. J Trop Pediatr 2005;51:206-11.
van der Walt J. Oxygen - Elixir of life or Trojan horse? Part 2: Oxygen and neonatal anesthesia. Paediatr Anaesth 2006;16:1205-12.
de Caen AR, Berg MD, Chameides L, Gooden CK, Hickey RW, Scott HF, et al.
Part 12: Pediatric advanced life support: 2015 American Heart Association guidelines update for cardiopulmonary resuscitation and emergency cardiovascular care. Circulation 2015;132 18 Suppl 2:S526-42.
Miguel-Montanes R, Hajage D, Messika J, Bertrand F, Gaudry S, Rafat C, et al.
Use of high-flow nasal cannula oxygen therapy to prevent desaturation during tracheal intubation of intensive care patients with mild-to-moderate hypoxemia. Crit Care Med 2015;43:574-83.
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