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Oxygen Therapy In The New Born


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 GOAL

 

ü     The goal of oxygen therapy is to provide adequate tissue oxygenation without undue risk of oxygen toxicity.

 

ü     An arterial partial pressure of oxygen (Pa02) of 45 torr results in a saturation of fetal hemoglobin  (HbF) of approximately 90%

 

ü     Maintaining the Pa02 above 50 torr should be sufficient for tissue oxygen needs

 

ü     An arbitrary ceiling of 80 torr is set to minimize the risk of retinopathy of prematurity (ROP) in infants weighing  less than 1500 g at birth

 

DEFINITION/DESCRIPTION

Oxygen therapy is the administration of oxygen at concentrations greater than that in ambient air with the intent of treating or preventing the symptoms, and manifestations of hypoxia.

INDICATIONS

§        Documented hypoxemia

 

§        In neonates, PaO2 < 50 torr and/or SaO2 < 88% or capillary oxygen tension (PcO2) < 40 torr

 

§        In adults, children, and infants older than 28 days, arterial oxygen tension (PaO2) of < 60 torr or arterial oxygen saturation (SaO2) of < 90% in subjects breathing room air or with PaO2 and/or SaO2 below desirable range for specific clinical situation

 

§        An acute care situation in which hypoxemia is suspected, substantiation of hypoxemia is required within an appropriate period of time following initiation of therapy

 

§        Severe trauma

 

§        Acute myocardial infarction

 

§        Short-term therapy (eg, post-anesthesia recovery)

 

CONTRAINDICATIONS

No specific contraindications to oxygen therapy exist when indications are judged to be present.

PRECAUTIONS AND / OR POSSIBLE COMPLICATIONS

With PaO2 > or = 60 torr, ventilatory depression may occur in spontaneously breathing patients with elevated PaCO2

 

With FIO2 > or = 0.5, absorption atelectasis, oxygen toxicity, and or depression of ciliary and / or leukocytic function may occur

 

 

§        In premature infants PaO2 of > 80 torr should be avoided because of the possibility of retinopathy of prematurity

 

§        Increased PaO2 can contribute to closure or constriction of the ductus arteriosus a possible concern in infants with ductus dependent heart lesions

 

§        Supplemental oxygen should be administered with caution to patients suffering from paraquat poisoning and to patients receiving bleomycin

 

§        During laser bronchoscopy, minimal levels of supplemental oxygen should be used to avoid intratracheal ignition

 

§        Fire hazard is increased in the presence of increased oxygen concentrations

 

§        Bacterial contamination associated with certain nebulization and humidifications systems is a possible hazard

 

RESOURCES

Low-flow systems

 

ü     deliver 100% (ie, FDO2 = 1.0) oxygen at flows that are less than the patient's inspiratory flowrate (ie, the delivered oxygen is diluted with room air) are classified as variable-performance oxygen delivery systems

 

ü     the oxygen concentration inhaled (FIO2) may be low or high, depending on the specific device and the patient's inspiratory flowrate

 

 

Nasal cannulas

 

Nasal cannulas consist of two soft prongs that arise from oxygen supply tubing. The prongs are inserted into the patient's nares, and the tubing is secured to the patient's face.

 

§        Can provide 24-40% oxygen with flowrates up to 6 L/min in adults (depending on ventilatory pattern)

 

§        In newborns and infants flows should be limited to a maximum of 2 L/min

 

§        Unlike in newborns oxygen supplied to adults via nasal cannula at flowrates less than or equal to 4 L/min need not be humidified

 

Problems

 

o       Nasal cannulas and nasopharyngeal catheters are contraindicated in patients with nasal obstruction (eg, nasal polyps, choanal atresia)

 

o       Skin irritation can result from material used to secure the cannula or from local allergic reaction to polyvinyl chloride

 

o       Inadvertent CPAP may be administered depending upon the size of the nasal cannula, the gas flow, and the infant's anatomy

 

o       Irritation can result if flows are excessive.

 

 

Nasopharyngeal catheters

 

§        Are soft tubes with several distal holes. The catheter should be inserted into the patient's nose to a depth equal to the distance from the ala nasi to the tragus

 

§        Or be gently advanced and then withdrawn until it rests slightly above the uvula

 

§        Oxygen flows from the catheter into the patient's oropharynx, which acts as an anatomic reservoir

 

§         The FIO2 varies with the patient's inspiratory flow at about 20-40%

 

Problems

 

o       Nasopharyngeal catheters are contraindicated in the presence of maxillofacial trauma and in patients in whom a basal skull fracture is present or suspected.

 

o       Excessive flow can produce pain in the frontal sinuses

 

o       Pneumocephalus is a rare but possible complication

 

o       Excessive secretions and/or mucosal inflammation can result

 

o       Skin irritation may result from material used to secure the cannula and / or from local allergic reaction to polyvinyl chloride

 

o       Excessive flow may cause gastric distention

 

 

 

 

 

Tracheostomy oxygen adapters

 

Are devices that attach either directly to a tracheostomy tube or to a heat-moisture exchanger (HME), which is then attached to the tube. (HMEs recycle the heat and moisture of respired air). Work on 'blow on force technique'

 

Simple oxygen masks

 

§        A reservoir effect is produced by the internal capacity of the mask

 

§        Can provide 35-50% oxygen at flowrates from 5-10 L/min

 

§        Flowrates should be maintained at 5 L/min or more in order to avoid rebreathing exhaled CO2 that can be retained in the mask

 

 

Partial-rebreathing masks are similar to simple oxygen masks but contain a reservoir at the base of the mask. The reservoir receives fresh gas plus exhaled gas approximately equal to the volume of the patient's anatomic dead space. The oxygen concentration of the exhaled gases combined with the supply of fresh oxygen, permits the use of flows lower than those necessary for other devices (eg, non-rebreathing masks), and potentially conserves oxygen use.

 

Non-rebreathing masks are similar to partial-rebreathing masks but do not permit the mixing of exhaled gases with the fresh gas supply. A series of one-way valves placed at the reservoir opening and on the side ports, ensures a fresh oxygen supply with minimal dilution from the entrainment of room air. This design provides a higher FIO2 than the simple and partial-rebreathing masks and the nasal devices.

 

 

§        Masks with reservoir bags (partial rebreathers and non-rebreathers) are designed to provide FIO2s of 0.5 or greater

 

 

§        In practice, both partial and non-rebreathers function in a similar manner and provide FIO2 of about 0.6 (depending on mask fit and ventilatory variables) provided the flowrate is sufficient to keep the reservoir bag inflated during inspiration

 

Problems

 

o       Are confining and may not be well tolerated

 

o       Interfere with feeding

 

o       May not be available in sizes appropriate for all patients

 

o       Require a minimum flow to avoid possible rebreathing of CO2

 

High-flow systems

 

ü     deliver a prescribed gas mixture-either high or low FiO2 at flowrates that exceed patient demand and are classified as fixed-performance oxygen delivery systems

 

Jet-mixing masks

 

§        Can accurately deliver predetermined oxygen concentration to the trachea up to 40%

 

Aerosol masks, tracheostomy collars, T-tube adapters, and face tents

 

§        Can be used with high-flow supplemental oxygen systems. The gas flow can be humidified by a continuous aerosol generator or large-reservoir humidifier

 

Mist tents

 

§        May also be used to provide supplemental oxygen to pediatric patients (and occasionally to adults), although FIO2 control and infection control are difficult in such tents

 

Problems

o       Potential exists for electric shock or fire from electrical or battery-operated devices inside the tent

 

o       Large-volume nebulizers used to supply oxygen to tents are susceptible to contamination

 

o       Loss of the air circulation system may result in failure to cool the tent

 

o       Potential exists for asphyxiation if the patient becomes lodged between the mattress and the tent

 

Oygen Hood

 

§        Supplemental oxygen may be administered to newborns and infants by hood, with the high-flow oxygen  at FiO2 close to 1.0

 

Problems

 

o       Prolonged exposure to humidfied oxygen may increase risk for cutaneous fungal infection

 

o       Inadequate or loss of gas flow may result in hypoxia or hypercapnia.

 

o       Temperature within enclosures should be closely monitored to reduce the potential for cold stress or apnea from overheating in neonates

 

o       Use of an improperly sized hood can result in irritation of the infant's skin

 

ASSESSMENT OF NEED

Need is determined by measurement of inadequate oxygen tensions and / or saturations, by invasive or noninvasive methods, and / or the presence of clinical indicators as previously described. Supplemental oxygen flow should be titrated to maintain adequate oxygen saturation as indicated by pulse oximetry (SpO2).

 

Nasal cannulas and nasopharyngeal catheters

 

§        Are used when the need exists to provide low-level supplemental oxygen to the infant or child

 

§        feed the infant without interrupting oxygen delivery;(5,63,64)

 

§        increase mobility

 

 

Simple oxygen masks

 

§        Are used to provide supplemental O2 in the moderate range (0.35-0.50, depending on size and minute ventilation) for short periods of time (eg, during procedures, for transport, in emergency situations)

 

§        Partial rebreathing masks are used to conserve the oxygen supply when higher concentrations (FIO2 > 0.4, < 0.6) are warranted (eg, during transport)

 

§        Non-rebreathing masks are used to deliver concentrations > or = 0.60 or specific concentrations (as from a blender)

 

Hoods are used to provide

 

§        controlled FIO2 and / or increased heated humidity to patients who cannot tolerate other devices

 

§        controlled FIO2 when the chest, abdomen, and extremities must be accessible to caregivers

 

§        the oxygen concentrations necessary for oxygen challenge (hyperoxia) tests in the spontaneously breathing neonate

 

Tents

 

§        are appropriate to deliver supplemental oxygen and / or cool, high-humidity gas mixtures to pediatric patients:

 

§        with laryngotracheobronchitis

 

§        with artificial airways in whom direct attachment of a device to the airway is contraindicated

 

§        who are too big for hoods

 

§        with the need for comfort, without compromising therapy

 

 

Tracheostomy oxygen adapters, which may or may not be coupled with HMEs, are used to deliver oxygen to a tracheostomy

 

MONITORING

Patient

 

ü     Clinical assessment including but not limited to cardiac, pulmonary, and neurologic status

 

ü     Assessment of physiologic para-meters: measurement of oxygen tensions or saturation in any patient treated with oxygen

 

ü     In conjunction with the initiation of therapy; or

 

§        within 12 hours of initiation with FIO2 < 0.40

 

§        within 8 hours, with FIO2 > or = 0.40

 

§        within 1 hour for the neonate

ECMO TECHNOLOGY

INTRODUCTION

extracorporeal Membrane Oxygenation (ECMO) is a new, highly invasive therapy that is being investigated and utilized in newborn and infants  with cardiorespiratory failure.

 

POPULATIONS TO BENEFIT AND INDICATIONS FOR USE

ü     Certain patients with a high risk of morbidity and mortality are appropriate candidates for ECMO when pulmonary function and other studies suggest that mechanical ventilation will be unsuccessful or cause undue harm

 

ü     ECMO should no longer be considered an extraordinary or rescue therapy for moribund infants over 2 kilograms.

Term and Near-Term Newborns

§        Infants born at greater than 35 weeks gestation with the following disease states should be considered candidates:

Meconium Aspiration Syndrome (MAS) and Persistent Pulmonary Hypertension of the Newborn (PPHN)

Congenital Diaphragmatic Hernia (CDH)

§        Mechanical ventilation, general physiologic support, and early surgical repair remain the current standard of care for CDH.

 

§        ECMO may improve survival in infants with CDH who have continued respiratory failure after repair.

 

§        Given the increased vulnerability of the congenitally hypoplastic lung to mechanical ventilation, institution of ECMO should be considered earlier in these infants.

Sepsis

§        ECMO is appropriate for a limited number of infants with respiratory failure due to sepsis who do not respond to other therapy.

Respiratory Distress Syndrome (RDS)

§        Apparent RDS in infants of greater than 2 kilograms birthweight appears in a small number of infants and may include other entitles as yet poorly defined. ECMO is appropriate when optimal ventilatory management fails.

Preterm Infants

§        ECMO is not appropriate for infants under 2 kilograms and 36 weeks gestation except under carefully controlled research protocols.

Postneonatal Pediatric Patients

Respiratory Failure

§        ECMO is currently being used as rescue therapy for severe respiratory failure in pediatric patients (1 month to 16 years) in a small number of centers

Cardiac Support

§        ECMO is also being used as an adjunct to cardiac surgery in a small number of centers.

Patients with Irreversible and Hopeless Conditions

§        ECMO is a temporizing and not a corrective intervention. Repair and recovery is necessary for patients to benefit. There may be some infants with irreversible organ dysfunction or damage with no hope of correction who may be appropriately excluded from ECMO treatment. Each institution should establish a mechanism of review for such infants.

 

ROP: Retinopathy Of Prematurity

§        Excess oxygen produccs a vasoconstriction of immature retinal vessels.

§        This vasoconstriction,  which  is  reversible in  its early stages, occurs first in the termirlal artrioles and in the arteriolar side of the capillary tree.

§        lt is followed by an irreversible vasoobliteration, at which stage the vessel walls are adherent and show degenerative changes.

§        Cytopathic effects are noted first in the endothelium of immature retinal capillaries.

§        Vaso proliferation typically occurs after normalization of oxygen tension.

§        The severity of the vasoobliteration is directly proportional to the duration and concentration of excess oxygen and to the degree of immaturity of the retinal vascular system.

§        The toxic effects of oxygen can be prevented by intermittent breathing.

§        Thus, kittens alternately receiving 1-hour periods of 80% to 90%  ambient oxygen and normal air showed no evidence of vasoobliteration.

§        Completely vascularized retinas of animals and humans are imnmune to the toxic effects of oxgen.

§        The disorder makes its appearance between 10 days and 1 month after birth.

§        Bilateral involvement is nearly invariable.

§        Myopia is present in a great majority to ROPs as a long term sequlae.

Hyperbaric Oxygen Therapy

What difference does extra pressure create?

ü     Hemoglobin (in red blood cells) holds 97% of its maximum amount of oxygen from normal air or holds 100% when breathing pure oxygen.

 

ü     One gram of hemoglobin can only combine with 1.34 ml of oxygen.

 

ü     Therefore, red blood cells can only deliver a limited level of oxygen to tissue cells. This is called oxygen tension (or oxygen partial pressure, "pO2").

 

ü     Injuries, infections and diseases can drop this vital tissue oxygen level down to very low levels.

 

ü     Ischemia, drops the pO2 gravely low, destroys tissue, and slows healing. Research has shown optimal tissue healing occurs if pO2 rises to between 50 and 80 mmHg.

 

ü     Oxygen given in a normal room is not sufficient to raise tissue oxygen levels to that level because red blood cells cannot carry the extra oxygen. The answer is to deliver the oxygen in a pressurized chamber to raise oxygen tension beyond red blood cell saturation

 

Condition In Which HBO Is Helpful

Severe Intestinal Ischemia and Necrotizing Enterocolitis

§        Intestinal pathologies, such as,

ü     radiation necrosis,

ü     intestinal pneumatosis,

ü     intestinal ischemia,

ü     intestinal ischemia/reperfusion injury,

ü     intestinal obstruction,

ü     Crohn's disease,

ü     necrotizirig enterocolitis.

§        Hyperbaric oxygen therapy is  also helpful in disseminated intravascular coagulation (DIC) and shock.

§        Normally, neonates who are treated in the first 6 hours, respond in the first one or two treatments.

 

§        It is rare for these patients to need more than 2 treatment, and it is only in those cases where there are surgical complications that further treatments may be required.

 

§        The effects of HBOT in neonates are visible within the first minutes post-treatment.

 

§        In infants with severe intestinal ischemia and necrotizing enterocolitis there is a significant reduction of abdominal circumference, gut edema and pneumatosis.

 

§        They also have stabilization of the systemic responses (DIC and shock).

 

§        Oral feeding is usually restored in the first 24-h post-HBOT.

 

Ischemic / Anoxic Encephalopathy

§        The rationale for the use of HBOT for this condition is to prevent the development of the primary ischemic/anoxic lesion and secondary ischemic / reperfusion injury.

 

§        It is recommended to treat these patients in the first 6 hours post-delivery

 

Oxygen Toxicity

§        Retinopathy: Presently, the retinopathy of the premature is considered to be like an ischemia/reperfusion injury.

 

§        HBOT has been used to manage, and to prevent ischemia/reperfusion injury.

 

§        Also, short exposures to low pressures (2.0 atmosphere absolute or 202kPa for 45 minutes once or twice a day) will be unlikely to cause this lesion and may even prevent it.

 

§        Toxicity to the CNS is very unlikely to occur at 2.0 atm abs or less, as it usually occurs in compromised patients treated at much higher pressures (3.0 atm abs).

 

§        Pulmonary oxygen toxicity in general, is not seen in HBOT protocols. It is sometimes seen in the treatment of divers when long periods are spent at high pressure -typically 2.8 atm abs on military therapeutic tables.

Probably this type of oxygen toxicity is related to the action of reactive species of oxygen (free radicals) on the lipid part of surfactant.

Fortunately, it responds well to inhaled steroids and/or surfactants.

 

Thank You

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