minimally invasive surfactant therapy in preterm

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BMJ– FETAL & NEONATAL MEDICINE MARCH 2013

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Page 1: Minimally invasive  surfactant therapy in preterm

BMJ– FETAL & NEONATAL MEDICINEMARCH 2013

Page 2: Minimally invasive  surfactant therapy in preterm

Ojective : to evaluate the applicability & potential effectiveness of a technique of minimal invasive surfactant therapy in preterm infants on cpap

Page 3: Minimally invasive  surfactant therapy in preterm

Already known on this topic

Preterm infants managed intially on cpap will go on to require intubation because of respiratory distress related to surfactant defeciency

Page 4: Minimally invasive  surfactant therapy in preterm

What this study addsA technique of MIST using narrow bore

vascular catheter inserted into trachea was successfully applied by neonatal physicians at two sites

Administration of surfactantb via MIST resulted in sustained reduction in o2 requirement &decrease in the need in intubation for 25-28 weeks gestation

Page 5: Minimally invasive  surfactant therapy in preterm

Outcomes for infants commencing on CPAP coud be further improved if those with significant RDS were to receive exogenous surfactant at an early stage

Page 6: Minimally invasive  surfactant therapy in preterm

INSURE limitations has prompted the pursuit of alternative less invasive means of giving surfactant therapy to preterm infants on CPAP

Page 7: Minimally invasive  surfactant therapy in preterm

MISTDirect tracheal catherizationFlexible feeding tube positioned in trachea

with Magills forceps

Page 8: Minimally invasive  surfactant therapy in preterm

A new alternative method of surfactant delivery via tracheal catherization using a semirigid vascular catheter

Which was found to be practicable with no significant procedural complication s

Page 9: Minimally invasive  surfactant therapy in preterm

aiimsTo evaluate the applicability & apparent

safety of the technique

Document the physiologic response to surfactant administration

Comare outcomes of infants receiving MIST with like gestation historical controls

Page 10: Minimally invasive  surfactant therapy in preterm

MethodsSite

NICU of ROYAL HOBART HOSPITAL&NICU OF ROYAL WOMEN HOSPITAL

BOTH UNITS USED cpap as initial respiratory support

Page 11: Minimally invasive  surfactant therapy in preterm

Study groupsInfants receiving MISTSTUDY conducted b/w june 2009-2011 may Preterm infants b/w 25 &32 completed weeks

of gestation were eligible for inclusion with CPAP &,24 hrs age required cpap pressure of ≥7

Page 12: Minimally invasive  surfactant therapy in preterm

Control Data were collected frm infants managed on

CPAP in time period immediately before beginning the study (2006-2009)

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Mist procedureSurfactant instilled via tracheal

catheterization On stable babies with HR>120 SPO2>85%A 16 gauge vascular catheter was marked to

indicate desired depth of ninsedtion (25-26 – 1cm )(27-28 wks 1.5 cm)

Direct larygoscopy performed tracheal catheter was inserted beyond vocal cords surfactant given at dose of 100 or 200 mg/kg

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Catheter withdrawn CPAP recommenced

Care after MIST included monitoring &treatment of PDA &screening of IVH &ROP

Page 15: Minimally invasive  surfactant therapy in preterm

RESULTSTOTAL 61 infants were enrolledInfants at 25-28 weeks gestation received

surfactant via MIST at early age (3hrs)Those at 29 32 weeks gestation (9hrs)

A modest decrease in CPAP pressure was notedafter MIST sustained at least 24 hrs of life

Oxygenation improved after MIST in both gestational ages with reduction in Fio2

Page 16: Minimally invasive  surfactant therapy in preterm

Comparedb with historical controls the need for intubation before 72h was considerably reduced after MIST in 25-28 wks

In this study the narrow bore semirigid design of catheter means that, unlike a standard endotracheal tube

Page 17: Minimally invasive  surfactant therapy in preterm

It can be passed down the eyeline without obscuring the view of the glottis , with an external diameter less than half that of a 2.5 mm endotracheal tube

Mist catheter passes easily through vocal cords

Page 18: Minimally invasive  surfactant therapy in preterm

MIST well tolerated by infants on CPAP , despite receiving no premedication

Surfactant administration via MIST was associated witha more rapid and pronounced improvement in oxygenation

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Based on these results large scale RCT OF MIST IS REQUIRED

Page 20: Minimally invasive  surfactant therapy in preterm

SURFACTANT REPLACEMENTONE OF THE BEST STUDIED THERAPIES

IN NEONATESurfactants of human,bovine or porcine

origin have been studied

Page 21: Minimally invasive  surfactant therapy in preterm

TimingProphylactic treatment of deficiency before

lung injury occurs ,results in better distributon and less lung injury than supplementation once respiratory failureb is severe

Page 22: Minimally invasive  surfactant therapy in preterm

ResponseResponse variesThe reasons include timing of treatment &

patient factors such as concurrent illness & degree of of lung maturity

Delayed resuscitationExcessive fluid administrationImproper ventilator stratagies

Page 23: Minimally invasive  surfactant therapy in preterm

Combined use of antenatal steroids& post natal surfactant therapy improves neonatal outcome

In established RDS repeated surfactant treatment results in greater improvement in oxygenation& ventilation decreased risk of pneumothorax & improve d survival when compared to single dose therapy

Page 24: Minimally invasive  surfactant therapy in preterm

retreatment infants on mechanical ventilation&Pressure >7 Fio2>0.3

Page 25: Minimally invasive  surfactant therapy in preterm

administrationSurvanta-beractant bovine dose 4ml/kg(100m/kg) divided in 4 quater

doses

Prophylaxis : give with in 15 min of birth in infats at risk

4 doses can be given no more frequently than every 6hrs

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Infasurf (calfactant)3 ml/kg for prophylaxis or rescue therapyMax 3 doses

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Curosurf (poractant) Intial dose 2.5 ml/kg 2 susequent doses 1.25ml/kg administered

12hrs apart

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complicationsPulmonary hemorrage Occurs in extremely LBW babies MalesWho have clinical evidence of PDA