PRACTICE VARIABILITIES DURING PRETERM NEONATAL RESUSCITATION BY THE DEDICATED RESUSCITATION STABILIZATION TEAM

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OBJECTIVES: To evaluate the current practice variabilities during resuscitation of preterm infants by the dedicated Resuscitation Stabilization Team (RST) using videos and respiratory function recordings of the delivery room management. DESIGN/METHODS: At our center, neonatal stabilization rooms are equipped with video recording and respiratory function monitor. We analyzed the first 10 minutes of delivery room stabilization of preterm infants at birth. The RST performance was evaluated and compared against the Canadian and regional Neonatal Resuscitation Guidelines. RESULTS: Thirty infants were video recorded over 8 months, with mean gestational age (GA) 26 (±2) weeks and birth weight 960 (±315)g. There was 100% compliance with using the plastic drape for infants less than 28 weeks GA. EKG leads and Pulse Oximetry were applied to all 30 patients. The median time[IQR] for application of the pulse oximetry was 47 seconds [35- 65] from the time of arrival at the table. Only 9/30 infants were suctioned prior to starting the respiratory support. There were inconsistencies in drying and stimulation within first minute for infants less than 28 weeks GA. There was a trend of initiating mask Continuous Positive Airway Pressure (CPAP) prior to completing initial assessment for adequacy of spontaneous breathing. 14 infants were apneic when placed on the table. The median [IQR] time to initiate positive pressure ventilation (PPV) in these apneic babies was 26 seconds [12-37.5]. 5/9 apneic babies didn’t have clinical assessment of heart rate as a part of initial assessment or to establish effectiveness of the ventilation. There were 10 events in 7 patients where PPV was interrupted by the PPV provider for purposes other than ventilation corrective steps. Early initiation of nasal CPAP i.e., less than 10 minutes was noted in 8 babies. CONCLUSION: The results of the RST performance are comparable to available literature. The results represent efficient neonatal stabilizations by a well-trained stabilization team. The variability of sequence in accomplishing each step of resuscitation could indicate resuscitator’s training and experience for individual skill set or judgement on rapidly changing clinical situation. There is a need of ongoing resuscitation training with special focus on situational awareness to prepare the NRP providers for timely strategized performance. Resuscitation videos can be a useful tool for educational and training of NRP providers.The results of the RST performance are comparable to available literature. The results represent efficient neonatal stabilizations by a well-trained stabilization team. The variability of sequence in accomplishing each step of resuscitation could indicate resuscitator’s training and experience for individual skill set or judgement on rapidly changing clinical situation. There is a need of ongoing resuscitation training with special focus on situational awareness to prepare the NRP providers for timely strategized performance. Resuscitation videos can be a useful tool for educational and training of NRP providers.The results of the RST performance are comparable to available literature. The results represent efficient neonatal stabilizations by a well-trained stabilization team. The variability of sequence in accomplishing each step of resuscitation could indicate resuscitator’s training and experience for individual skill set or judgement on rapidly changing clinical situation. There is a need of ongoing resuscitation training with special focus on situational awareness to prepare the NRP providers for timely strategized performance. Resuscitation videos can be a useful tool for educational and training of NRP providers.

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Positive airway pressure (PAP) devices are used to treat patients with sleep related breathing disorders (SRBDs), including obstructive sleep apnea (OSA). After a patient is diagnosed with OSA, the current standard of practice involves performing attended polysomnography (PSG), during which positive airway pressure is adjusted throughout the recording period to determine the optimal pressure for maintaining upper airway patency. Continuous positive airway pressure (CPAP) and bilevel positive airway pressure (BPAP) represent the two forms of PAP that are manually titrated during PSG to determine the single fixed pressure of CPAP or the fixed inspiratory and expiratory positive airway pressures (IPAP and EPAP, respectively) of BPAP for subsequent nightly usage. A PAP Titration Task Force of the American Academy of Sleep Medicine reviewed the available literature. Based on this review, the Task Force developed these recommendations for conducting CPAP and BPAP titrations. Major recommendations are as follows: (1) All potential PAP titration candidates should receive adequate PAP education, hands-on demonstration, careful mask fitting, and acclimatization prior to titration. (2) CPAP (IPAP and/or EPAP for patients on BPAP) should be increased until the following obstructive respiratory events are eliminated (no specific order) or the recommended maximum CPAP (IPAP for patients on BPAP) is reached: apneas, hypopneas, respiratory effort-related arousals (RERAs), and snoring. (3) The recommended minimum starting CPAP should be 4 cm H2O for pediatric and adult patients, and the recommended minimum starting IPAP and EPAP should be 8 cm H2O and 4 cm H2O, respectively, for pediatric and adult patients on BPAP. (4) The recommended maximum CPAP should be 15 cm H2O (or recommended maximum IPAP of 20 cm H2O if on BPAP) for patients or = 12 years. (5) The recommended minimum IPAP-EPAP differential is 4 cm H2O and the recommended maximum IPAP-EPAP differential is 10 cm H2O (6) CPAP (IPAP and/or EPAP for patients on BPAP depending on the type of event) should be increased by at least 1 cm H2O with an interval no shorter than 5 min, with the goal of eliminating obstructive respiratory events. (7) CPAP (IPAP and EPAP for patients on BPAP) should be increased from any CPAP (or IPAP) level if at least 1 obstructive apnea is observed for patients or = 12 years. (8) CPAP (IPAP for patients on BPAP) should be increased from any CPAP (or IPAP) level if at least 1 hypopnea is observed for patients or = 12 years. (9) CPAP (IPAP for patients on BPAP) should be increased from any CPAP (or IPAP) level if at least 3 RERAs are observed for patients or = 12 years. (10) CPAP (IPAP for patients on BPAP) may be increased from any CPAP (or IPAP) level if at least 1 min of loud or unambiguous snoring is observed for patients or = 12 years. (11) The titration algorithm for split-night CPAP or BPAP titration studies should be identical to that of full-night CPAP or BPAP titration studies, respectively. (12) If the patient is uncomfortable or intolerant of high pressures on CPAP, the patient may be tried on BPAP. If there are continued obstructive respiratory events at 15 cm H2O of CPAP during the titration study, the patient may be switched to BPAP. (13) The pressure of CPAP or BPAP selected for patient use following the titration study should reflect control of the patient's obstructive respiration by a low (preferably 3 hr).

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Study of factors affecting compliance of continuous positive airway pressure (CPAP) in obstructive sleep apnea-hypopnea syndrome (OSAHS)
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Background: Poor adherence (30-60%) to CPAP is a recognized limiting factor in treating OSAHS, leaving patients at risk for co-morbid conditions and impaired quality of life. Aims and Objectives: To study patient9s compliance to CPAP in OSAHS, evaluate effect of regular follow-up on compliance and establish causes for noncompliance. Method: 42 patients with OSAHS on polysomnography and symptoms of excessive daytime sleepiness were randomised in 2 equal groups. All were counseled on CPAP initiation. Follow up was at regular intervals over six months in group 1 and directly at end of 6 months in group 2. The groups were compared for a co-relation between frequency of follow up and CPAP compliance. Effect of age, sex, AHI, Epworth Sleepiness Scale (ESS) Score, hours of first night use of CPAP and type of CPAP machine was also studied. Results: Good compliance to CPAP was seen in 52% and poor compliance in 48%. Regular follow up had no statistically significant change in compliance amongst the group 1 patients. Epworth Sleepiness Scale (ESS) Score >12 [p 4 hours [p=0.003] and usage of auto CPAP unit [p=0.007] were statistically significant predictors of compliance. No significance was established with factors like age, gender and AHI. Causes of poor compliance were, mask related (60%), patient related (25%) and machine related (15%). Conclusion: Counseling at CPAP initiation is important in improving long term CPAP compliance. Addressing factors like mask size, fitting or type of machine on CPAP initiation itself will increase adherence to CPAP therapy and may obviate the need for frequent follow up.

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