Printer Friendly

Evaluation of the newborn's blood gas status.

The perinatal period (labor, parturition, and the days following) is one of fundamental change in the cardio-respiratory status of the baby. Nutritional, excretory, and respiratory systems must rapidly assume new responsibilities as the organism changes from a dependent to a free-living individual. Respiratory gas exchange, formerly a placental function, must be established by the lungs within minutes after birth. The cardiovascular system undergoes changes just as dramatic, with conversion from two circulations in parallel to two circulations now in series. Therefore, frequent and serious difficulties in cardio-respiratory adaptation in the perinatal and neonatal periods are not surprising.

Blood gas measurements and complementary, noninvasive monitoring techniques provide the clinician with information essential to patient assessment, therapeutic decision making, and prognostication. Blood gas measurements are as important for ill newborn infants as for other critically ill patients, but unique challenges are provided by rapidly changing physiology, difficult access to arterial and mixed venous sampling sites, and small blood volumes. However, one must not negate the importance of historical and physical findings in the ill newborn. This information must be integrated with the laboratory data to best understand and treat the patient.

Normal values for arterial blood gases are very dependent on postnatal age (Fig. 1). Values of [P.sub.a][o.sub.2], and [P.sub.a][o.sub.2], may also be lower in premature infants, caused by reduced lung function, and at high altitude, caused by reduced inspired oxygen tension. The most accurate method of measuring [P.sub.a][o.sub.2], and [P.sub.a][o.sub.2]. involves placement of an indwelling catheter in either the aorta via an umbilical artery or in a peripheral artery; however, use of such catheters must be restricted to critically ill neonates because of frequent and serious thrombotic and infectious complications [1, 2]. A problem associated with peripheral arterial catheters is hemodilution. For these catheters to remain patent, they are usually perfused with heparinized saline solution. Unless the catheter is cleared of perfusate, diluted samples will have lower [Pco.sub.2], and bicarbonate values [3]. Sampling methods should minimize blood loss and assure an undiluted arterial blood sample [4]. Intermittent sampling of a peripheral artery often changes [P.sub.a][o.sub.2] significantly when the infant responds to pain by crying and can therefore underestimate or overestimate baseline [Pco.sub.2] [5, 6]. The site of arterial access must be considered if the ductus arteriosus, which connects the aorta and pulmonary artery, is still patent because a right-to-left shunt at this level will result in lower oxygen values in the descending aorta than in the blood perfusing the brain and eyes. In patients with chronic lung disease or mild-to-moderate acute cardio-respiratory problems, capillary blood gases are often utilized. Capillary values for pH and [Pco.sub.2] are usually within 0.05 and 7.5 mmHg (1 kPa) of corresponding arterial values; however, [Po.sub.2] underestimates [P.sub.a][o.sub.2] and, therefore, cannot exclude hyperoxemia [7]. Capillary [Po.sub.2] values are no longer useful, having been supplanted by the noninvasive techniques of transcutaneous (tc) [Po.sub.2] and pulse oximetry monitoring that more reliably estimate [P.sub.a][o.sub.2] and [S.sub.a][o.sub.2], respectively. [1] Pulse oximetry or tCP[o.sub.2] monitoring should be combined with capillary blood gases to obtain an accurate and comprehensive evaluation of oxygenation. Capillary blood gases are not reliable for seriously ill patients, or for those with shock, hypotension, or peripheral vasoconstriction. In the first day of life, poor perfusion to the hands and feet ("acrocyanosis") precludes the use of capillary blood gases. In these settings, arterial blood gases are required.

[FIGURE 1 OMITTED]

Precision, measured as the CV for replicate samples, of modern blood gas analyzers should be within 0.2% for pH, 4% for [Pco.sub.2], and 3% for [Po.sub.2] (Table 1). Accuracy, measured as deviation from a known calibrator, for blood gas analyzers must be verified on a regular basis. Total analytic error for [P.sub.a][o.sub.2] and [P.sub.a][co.sub.2] approaches the clinically acceptable error (Table 1).

ASSESSMENT OF OXYGENATION

Blood gas measurements and noninvasive estimations provide important information about oxygenation. Oxygen delivery ([Do.sub.2]) to tissues is the product of cardiac output (c.o.) and blood oxygen content ([C.sub.a][o.sub.2]), Doe = c.o. X [C.sub.a][o.sub.2]. Ignoring the negligible oxygen dissolved in plasma, the equation can be expanded to [Do.sub.2] = (HR X SV) X ([S.sub.a][o.sub.2] X 1.34 X Hgb), where HR = heart rate, SV = stroke volume, [S.sub.a][o.sub.2] = hemoglobin saturation, and Hgb = hemoglobin content. Insufficient oxygen delivery to tissues, hypoxia, can therefore be caused by cardiac failure (decreased HR and (or) SV leading to decreased c.o.), or by low hemoglobin (anemia) or low [S.sub.a][o.sub.2], (hypoxemia) leading to low [C.sub.a][o.sub.2], (Table 2). When insufficient oxygen is provided to tissues, hypoxia leads to metabolic acidosis. Thus, blood gas measurements, specifically [Po.sub.2], [S.sub.a][o.sub.2], pH, and base excess, can help to assess patient oxygenation but must be combined with other clinical and laboratory assessments to provide a comprehensive picture.

The general goals of oxygen therapy in the neonate are to maintain adequate [P.sub.a][o.sub.2] and [S.sub.a][o.sub.2], and to minimize cardiac work and the work of breathing [8]. It is important to realize that "optimal oxygenation" will result in different [P.sub.a][o.sub.2]/[S.sub.a][o.sub.2] goals for different types of neonatal patients. Most commonly, premature infants in respiratory failure should have [P.sub.a][o.sub.2] values between 6.66 and 10.66 kPa (50-80 mm Hg) [9]. These goals minimize the chances of blindness caused by retinopathy of prematurity [10] and lower the inspired [O.sub.2] and airway pressure requirements that, if higher, might increase the likelihood of bronchopulmonary dysplasia (BPD) [11]. By contrast, full-term infants with diaphragmatic hernia or persistent pulmonary hypertension may require [P.sub.a][o.sub.2] values of 10.66-13.33 kPa (80-100 mm Hg) to maintain stability, minimize pulmonary resistance, and avoid worsening pulmonary hypertension [12]. Infants with BPD or chronic lung disease show improved growth and less pulmonary hypertension (cor pulmonale) when [S.sub.a][o.sub.2] is kept >92% during wakefulness, sleep, and feeding [11]. Liberal use of supplemental oxygen may be deleterious by promoting ductus arteriosus closure in some infants with congenital heart disease, such as hypoplastic left heart, by lowering pulmonary vascular resistance in other infants with large left-to-right shunts.

Pulse oximetry and transcutaneous oxygen monitoring are extraordinarily useful techniques of estimating and noninvasively monitoring the neonate's oxygenation. In most settings they complement blood gases by permitting the clinician to noninvasively follow trends in patient oxygenation. However, neither technique can replace arterial blood gas monitoring in the critically ill patient because neither provides comprehensive and exact information on oxygenation, ventilation, acid-base status, and hemoglobin variants. Pulse oximetry has become more widely used because it usually reflects [S.sub.a][o.sub.2] accurately, is easy to use, and very rarely results in complications (Table 3). Neither pulse oximetry nor transcutaneous oxygen monitoring is reliable for severe hypotension or peripheral vasoconstriction [13,14]. A false estimate of [S.sub.a][o.sub.2], can occur if the pulse oximeter probe is applied incorrectly, resulting in poor signal or an optical shunt, or if motion of the patient or probe occurs [14,15]. There has been concern that pulse oximetry monitoring, if not supplemented with intermittent arterial blood gas determinations, will not adequately protect the extremely premature infant from hyperoxia that predisposes to development of retinopathy of prematurity and blindness [10]. For the smallest premature infants, whose retinas are still developing, exclusive reliance on noninvasive pulse oximetry to avoid hyperoxia is not recommended. Instead, keeping pulse oximetry [S.sub.a][o.sub.2], in the 88-92% range and intermittently using arterial blood gases to verify [S.sub.a][o.sub.2], and [P.sub.a][o.sub.2] is preferable [16,17].

ASSESSMENT OF ALVEOLAR VENTILATION

Arterial blood gas determinations of PCO, provide the most accurate determinations of the adequacy of alveolar ventilation. The [P.sub.a][co.sub.2], concentration in a given patient reflects the balance between metabolic production of [CO.sub.2], and excretion by ventilation. Thus, a clinician might respond to an increased [P.sub.a][co.sub.2], by decreasing metabolic rate (sedation, paralysis, or reduction of thermal stress) or by increasing ventilation [increasing ventilator rate or tidal volume, decreasing added dead space, reducing airway resistance, or by surfactant administration in premature infants with respiratory distress syndrome, (RDS) to improve compliance].

The clinician must establish a target or acceptable range for [P.sub.a][co.sub.2], for a given patient. Although the normal range of [P.sub.a][co.sub.2], after the first hours of life can be considered 4.66-6 kPa (35-45 mm Hg), desirable [CO.sub.2], values for a specific situation may be either higher or lower. For instance, in persistent pulmonary hypertension of the newborn, pulmonary artery pressures can be lowered by either respiratory or metabolic alkalosis [18]. Modest respiratory alkalosis can rapidly lower pulmonary vascular resistance in some such patients. Because marked hypocapnea can decrease cerebral blood flow and has been associated with neurologic deficits, most clinicians no longer aim for [Pco.sub.2] values <3.33 kPa (<25 mm Hg) [191. Infants with BPD (chronic lung disease) often tolerate [Pco.sub.2] values of 6.66-8 kPa (50-60 mm Hg) [201, essentially "deciding" that normal blood gas status is not worth the markedly increased work of breathing necessary to achieve it. An approach termed "permissive hypercapnia" or "gentle ventilation" with lower ventilator pressures while tolerating slightly increased [P.sub.a][co.sub.2] resulted in decreased chronic lung disease for premature infants with RDS [21].

For most neonates and small infants, tc[Pco.sub.2] monitoring is usually preferred over end-tidal CO, monitoring ([P.sub.ET][CO.sub.2]) as a means of estimating and "trending" [P.sub.a][co.sub.2], and therefore alveolar ventilation [22,23]. Small tidal volumes, rapid respiratory rates, and inhomogeneous alveolar ventilation/perfusion in neonates with lung disease often preclude [P.sub.ET][CO.sub.2] monitoring in the newborn, especially in small prematures. By contrast, tc[Pco.sub.2] shows good correlation with [P.sub.a][co.sub.2] and provides an excellent trend monitor, accurately reflecting changes in [P.sub.a][co.sub.2]. The tc[Pco.sub.2] monitor, unlike the tc[Po.sub.2] monitor that must be heated to 43-44 [degrees]C, does not cause skin burns. When used at a temperature of 40-42 [degrees]C, the tc[Pco.sub.2]electrode can be left in place for 4 h in neonates and 8 h in infants and older children [24,25]. Because tc[Pco.sub.2] values sometimes are markedly inaccurate, in vivo calibration against an arterial or capillary blood gas is often required. Overestimation errors in hypercarbic patients are particularly frequent.

ASSESSMENT OF ACID--BASE STATUS

Blood gases provide essential information on acid-base status both in critically ill neonates and in chronically or less severely ill patients. One can approach the analysis of simple acid-base disorders by answering three questions. First, is the condition one of acidosis or alkalosis (is the pH less than or greater than 7.4)? Second, is the primary cause metabolic (is bicarbonate high or low) or respiratory (is [Pco.sub.2] high or low)? Third, is the compensation appropriate? Fig. 2 shows a clinically useful approach to blood gas interpretation in the newborn and infant [26].

To properly analyze and describe blood gases, certain terms must be defined. The suffix "emia" refers to the state of blood, for example, acidemia is a condition of excess blood acidity as indicated by pH. The suffix "osis" refers to a pathologic process in which acid or base is gained or lost from the body [27]. Acidosis may not lead to acidemia, depending on the patient's ability to compensate. Compensation is a response to the primary disorder, attempting to bring the pH as close as possible to neutral. Full compensation is often unachieved, and blood gases that appear to have fully compensated for the primary problem are most likely displaying a mixed picture, rather than complete correction.

Table 4 presents some of the most common causes of acid-base disorders in neonates. Metabolic acidosis is most commonly caused by inadequate tissue perfusion (shock) caused by hypovolemia, decreased cardiac output, or sepsis. Hypoxemia caused by lung or heart disease often contributes to the tissue hypoxia and resulting lactic acidosis seen with hypoperfusion states. Sepsis in the newborn, as in older individuals, may cause metabolic acidosis by decreasing perfusion ("cold shock") and by interfering with cellular aerobic metabolism ("warm shock"). To compensate for metabolic acidosis, term neonates and infants will attempt to lower [Pco.sub.2]by hyperventilating; however, compensation is usually not complete, that is, not to a pH of 7.4. A suggested guideline for the desired [Pco.sub.2] is as follows: The last two digits of the pH should equal the expected [Pco.sub.2] [28]. If the actual [Pco.sub.2] is much higher than expected, there may also be a respiratory acidosis. Premature infants are often not able to compensate for a metabolic acidosis by hyperventilation and respiratory alkalosis. After treating the primary underlying problem causing the metabolic acidosis, slow infusions of sodium bicarbonate are often given.

[FIGURE 2 OMITTED]

One common problem in the management of infants with BPD is distinguishing a primary, chronic, respiratory acidosis with metabolic compensation from a diuretic-induced metabolic alkalosis with respiratory compensation. In infants with BPD, lung mechanics, ventilation/ perfusion relations, and work of breathing are abnormal. This results in a chronically high [Pco.sub.2]--a primary respiratory acidosis. Renal compensation causes bicarbonate retention, bringing the pH back towards normal, but compensation is usually not complete, that is, pH remains <7.40. Diuretics are used to improve lung mechanics, to decrease lung water, and to improve gas exchange. Thiazide and especially loop diuretics result in a loss of chloride, potassium, and sodium, and in retention of bicarbonate. When high doses of diuretics are used without salt replacement, metabolic alkalosis can result, with pH values >7.40. Under these circumstances, respiratory drive can be depressed, worsening the hypoventilation. Lowering the dose of diuretics, changing from a loop to a thiazide diuretic, replacement of salt, or use of acetazolamide to lower plasma bicarbonate are strategies that can be used to minimize this problem.

HEMOGLOBIN VARIANTS IN THE NEWBORN

Modern blood gas instruments often include options to measure hemoglobin and its variants such as fetal hemoglobin, carboxyhemoglobin, and methemoglobin. These capabilities can sometimes be used to our advantage in neonatal medicine. Fetal hemoglobin has a left-shifted oxyhemoglobin dissociation curve, with a 50% saturation point ~2.8 kPa vs 3.47-3.6 kPa (21 mm Hg vs 26-27 mm Hg) for adult hemoglobin. Fetal hemoglobin is well designed to facilitate oxygen transport across the placenta. In the neonate, however, fetal hemoglobin releases less oxygen at any given capillary [Po.sub.2]. Pulse oximetry estimates of arterial hemoglobin saturation are as accurate for fetal as for adult hemoglobin. The [Po.sub.2] to achieve "adequate" saturation will be lower for fetal than for adult hemoglobin. In practice, if pulse oximetry is being used to guide oxygen therapy, measurement of adult and fetal hemoglobin percentage adds little to clinical management. It should be realized, however, that [P.sub.a][o.sub.2] values in the 5.5-7 kPa (41-53 mm Hg) range are often high enough to achieve 88-92% [S.sub.a][o.sub.2]. for premature infants with predominantly fetal hemoglobin.

In the neonatal setting, carboxyhemoglobin is of interest primarily in infants of smoking mothers. Carbon monoxide crosses the placenta and binds strongly to fetal hemoglobin, making it unavailable for oxygen transport [29]. Effects of carbon monoxide include the functional anemia of carboxyhemoglobin, a left shift of the hemoglobin dissociation curve making oxygen less available to tissues, and an inhibition of mitochondrial cytochrome oxidase. Pulse oximeters use only two light wavelengths, thereby assuming that only deoxyhemoglobin and oxyhemoglobin are present. A CO-oximeter is required to measure carboxyhemoglobin.

The recent use of inhaled nitric oxide to treat pulmonary hypertension in the newborn and in older patients has refocused attention on methemoglobinemia. Inhaled nitric oxide binds to hemoglobin rapidly in the pulmonary circulation, resulting in selective relaxation of pulmonary vascular smooth muscle. The nitric oxide-hemoglobin complex is converted to methemoglobin, and toxic concentrations of nitric oxide can result in methemoglobinemia. To date, methemoglobinemia has not been a serious problem in neonates receiving 5-80 ppm inhaled nitric oxide. Intermittent CO-oximeter measurements of methemoglobin should be performed in patients receiving inhaled NO, especially at concentrations >40 ppm, to keep methemoglobin concentrations <5% of total hemoglobin [30].

BLOOD GASES IN THE IMMEDIATE PERINATAL PERIOD WITH SPECIAL REFERENCE TO PERINATAL ASPHYXIA

Blood gases can provide important information on patient status even before arterial blood sampling becomes possible after birth (Table 5). Before the onset of labor, the fetus, compared with the normal adult, exists in a hypoxemic, normocarbic, nonacidotic environment. During the stress of normal labor, some tissue hypoxia and placental insufficiency occur, resulting in a mixed respiratory and metabolic acidosis. After birth, as pulmonary gas exchange is established, [Pco.sub.2], pH, and [Po.sub.2]. values move toward normal adult values; the largest changes occur in the first few minutes after birth (Fig. 1). Accordingly, the most important factors to consider when interpreting blood gases are the sampling site, the time of life, and the possible and proven patient diagnoses.

Perinatal asphyxia occurs when there is inadequate placental gas exchange to meet ongoing fetal tissue needs for oxygen consumption and carbon dioxide elimination. The combination of lactic acidosis, the product of anaerobic metabolism, and [CO.sub.2] accumulation results in a mixed acidosis. It is important to note that current work suggests that only 10-20% of cerebral palsy cases is accounted for by perinatal asphyxia [31]. Unfortunately, during labor, there is no noninvasive, simple method of monitoring fetal well-being that is both highly sensitive and highly specific. Fetal heart rate monitoring, either electronic or auscultatory, is reassuring when normal but has a false-positive rate >99%. Measurement of pH from capillary blood samples taken from the presenting part can provide additional information on fetal well-being when there is concern because of an abnormal fetal heart rate pattern. Values >7.24 are reassuring, whereas those <7.2 suggest that obstetric management options should be reevaluated [32].

In summary, although arterial blood gases can provide much useful information about the physiologic state of the patient, a clear and systematic approach is required to give meaning to the values. From procurement to analysis, potential sources of error must be considered and a complete understanding of what blood gases can and cannot tell you is needed to best treat the critically ill newborn.

We thank Pierre Senecal for helpful suggestions and Rosanna Barrafato for preparation of the manuscript.

Received July 30, 1996; revised October 18, 1996; accepted October 18, 1996.

References

[1.] Neal WA et al. Umbilical artery catheterization: demonstration of arterial thrombosis by aortography. Pediatrics 1972;50:6-13.

[2.] Vailas GN, Brouillette RT, Scott JP, Shkolnki A, Conway J, Wiringa K. Neonatal aortic thrombosis: recent experience. J Pediatr 1986; 109:101-8.

[3.] Hansen JE, Simmons DH. A systematic error in the determination of blood [PCO.sub.2]. Am Rev Resp Dis 1977;115:1061-3.

[4.] Thorkelsson T, Hoath SB. Accurate micromethod of neonatal blood sampling from peripheral arterial catheters. J Perinatol 1995:15:43-6.

[5.] Dinwiddie R, Patel BD, Kumar SP, Fox WW. The effects of crying on arterial oxygen tension in infants recovering from respiratory distress. Crit Care Med 1979:7:50-3.

[6.] Graham G, Kenny MA. Changes in transcutenous oxygen tension during capillary blood-gas sampling. Clin Chem 1980;26:1860-3.

[7.] McLain BI, Evans J, Dear PR. Comparison of capillary and arterial blood gas measurements in neonates. Arch Dis Child 1988;63: 743-7.

[8.] Shapiro BA, Peruzzi WT, Templin R. Clinical application of blood gases, 5th edition. St. Louis: Mosby-Year Book, 1994.

[9.] Guidelines for perinatal care, 2nd ed. Washington, DC: American Academy of Pediatrics and American College of Obstetricians and Gynecologists, 1988:246-7.

[10.] Flynn JT, Bancalari E, Synder ES, et al. A cohort study of transcutaneous oxygen tension and the incidence and severity of retinopathy of prematurity. N Engl J Med 1992;326:1050-4.

[11.] Abman SH, Groothius JR. Pathophysiology and treatment of bronhcopulmonary dysplasia. Pediatr Clin North Am 1994;41: 277-315.

[12.] Shochat SJ, Naeye RL, Ford SDA, Whitman VM, Maisels MJ. Congenital diaphragmatic hernia. Ann Surg 1979;190:332-41.

[13.] Hay WW, Thilo E, Brockway Curlander J. Pulse oximetry in neonatal medicine. Clin Perinatol 1991;18:441-72.

[14.] Poets CF, Southall DP. Noninvasive monitoring of oxygenation in infants and children: practical considerations and areas of concern. Pediatrics 1994;93:737-46.

[15.] Lafontaine VM, Ducharme FM, Brouillette RT. Pulse oximetry: accuracy of methods of interpreting graphic summaries. Pediatr Pulmonol 1996;21:121-31.

[16.] Hay WW, Brockway JM, Eyzaguirre M. Neonatal pulse oximetry, accuracy and reliability. Pediatrics 1989;83:717-22.

[17.] Young IH, Le Souef PN. Clinical oximetry. Med J Aust 1993;159: 60-2.

[18.] Schreiber MD, Heymann MA, Soifer SJ. Increased arterial pH, not decreased PaC02, attenuates hypoxia-induced pulmonary vasoconstriction in newborn lambs. Pediatr Res 1986;20:113-7.

[19.] Bifano EM, Pfannenstiel A. Duration of hyperventilation and outcome in infants with persistent pulmonary hypertension. Pediatrics 1988;81:657-61.

[20.] Bancalari E, GerhardtT. Bronchopulmonary dysplasia. Pediatr Clin North Am 1986;33:1-23.

[21.] Wung JT, James LS, Kilchevsky E, James E. Management of infants with severe respiratory failure and persistence of the fetal circulation, without hyperventilation. Pediatrics 1985;76:4889-4.

[22.] Kirpalani H, Kechagias S, Lerman J. Technical and clinical aspects of capnography in neonates. J Med Eng Technol 1991;15:1546-1.

[23.] Binder N, Atherton H, Thorkelsson T, Hoath SB. Measurement of transcutaneous carbon dioxide in low birthweight infants during the first two weeks of life. Am J Perinatol 1994;11:237-41.

[24.] Morielli A, Desjardins D, Brouillette RT. Transcutaneous and end-tidal carbon dioxide pressures should be measured during pediatric polysomnography. Am Rev Respir Dis 1993;148:1599-604.

[25.] Waters KA, Gonzalez A, Jean C, Morielli A, Brouillette RT. Face-straight-down and face near-straight-down positions in healthy, prone-sleeping infants. J Pediatr 1996;128:616-25.

[26.] Nelson W, Adelman RD, Solhung MJ. Nelson textbook of pediatrics, 15th ed. Neslon W, ed. Philadelphia: W.B. Saunders Co., 1996, pp 200-6.

[27.] Gilbert R. Spirometry and blood gases. In: Clinical diagnosis and management by laboratory methods, 18th ed. Henry J, ed. Philadelphia: W.B. Saunders Co., 1991.

[28.] Narins RG, Gardner LB. Simple acid-based disturbances. Med Clin North Am 1984;65:321.

[29.] Longo LID, Hill EP. Carbon monoxide uptake and elimination in fetal and maternal sheep. Am J Physiol 1977;232:H324-30.

[30.] Wessel DL, Adatia I, Thompson JE, Hickey PR. Delivery and monitoring of inhaled nitric oxide in patients with pulmonary hypertension. Crit Care Med 1994;22:930-8.

[31.] Nelson KB, Dambrosia JM, Ting, TY, Grether JK. Uncertain value of electronic fetal monitoring in predicting cerebral palsy. N Engl J Med 1996;334:613-8.

[32.] Huch A, Huch R, Rooth G. Guidelines for blood sampling and measurement of pH and blood gas values in obstetrics. Based upon a workshop held in Zurich, Switzerland, March 19, 1993 by an ad hoc committee. Eur J Obstet Gynecol Reprod Biol 1994;54: 165-75.

[1] Nonstandard abbreviations: c.o., cardiac output; SV, stroke volume; RDS, respiratory distress syndrome; tc, transcutaneous; and BPD, broncho-pulmonary dysplasia.

ROBERT T. BROUILLETTE * and DAVID H. WAXMAN

The Department of Pediatrics, McGill University/Montreal Children's Hospital, Montreal, QC, Canada.

* Address correspondence to this author at: 2300 Tupper St., C-920, Montreal, QC, Canada H3H 1P3. Fax 514-934-4356; e-mail rbronew@newborn. mchis.mcgill.ca.
Table 1. Considerations for interpretation of neonatal blood
gases.

Preanalytic

Sample site (pre/post ductal; capillary/venous/arterial)
Patient status (crying, quiet awake, asleep)
Technique (free-flow of blood, air bubbles, dilution)
Storage time (<15 min at room temp., <1 h on ice)

Analytic

Instrument precision (a)

pH [+ or -] 0.01 unit
[Pco.sub.2] [+ or -] 267-400 Pa (2-3 mm Hg); CV <4%
[Po.sub.2] [+ or -] 267-533 Pa (2-4 mm Hg); CV <3%

Clinical requirements
pH [+ or -] 0.05
[Pco.sub.2] [+ or -] 400 Pa (3 mm Hg)
Pot [+ or -] 666 Pa (5 mm Hg)

Turnaround time
Tertiary neonatal intensive care unit, acute disease <15 min
Longer in other settings

Interpretation
Rapidly changing physiology

a Instrument precision for [Pco.sub.2] and [Po.sub.2] depends on the
[Pco.sub.2] and [Po.sub.2] at which the test is made. Values given
are representative of newer blood gas machines.

Table 2. Some causes of hypoxia in the newborn.

Low cardiac output-shock

Hypovolemia
Fetal-to-maternal transfusion, acute

Sepsis

Group B hemolytic streptococcal infection

Cardiac disorders

Obstructive left heart lesions
Cardiomyopathies
Arrhythmias

Low [S.sub.a][o.sub.2]--Hypoxemia

Lung disease
Respiratory distress syndrome
Sepsis
Persistent pulmonary hypertension
Diaphragmatic hernia

Congenital heart disease with right-to-left shunt

Transposition of the great vessel
Pulmonary atresia

Low hemoglobin--anemia

Fetal-to-maternal transfusion, chronic twin to twin transfusion
Hemolysis

Isoimmunization
Blood drawing

Table 3. Advantages and limitations of pulse oximetry and
transcutaneous monitorinassessment.

 Pulse oximetry Transcutaneous
 [O.sub.2]

Accuracy Excellent (vs Good (vs
 [S.sub.a][O.sub.2]) [P.sub.a][O.sub.2])

Hypoxemia detection Excellent Good

Calibration required No Yes

Ease to use Very easy Moderately difficult

Limitations Hypotension Hypotension
 Poor perfusion Poor perfusion
 Motion Edema
 Skin disorders

Complications Rare Burns

Hyperoxemia detection Good Excellent

Table 4. Common and important causes of acid-base
disorders in neonates.

Metabolic acidosis

Acute, uncompensated
Shock
Sepsis
Intraventricular hemorrhage
Diarrheal dehydration
Hypoxemia
Chronic, compensated

Metabolic alkalosis

Loop diuretics
Thiazide diuretics
Bicarbonate infusion
Pyloric stenosis
Gastric suction/vomiting

Combined metabolic and respiratory acidosis

Perinatal asphyxia
Acute metabolic acidosis superimposed on chronic respiratory
Acidosis

Respiratory acidosis

Lung disease
RIDS
Persistent pulmonary hypertension
Diaphragmatic hernia
Meconium aspiration
Bacterial pneumonia

Upper airway obstruction

Pierre--Robin sequence
Choanal atresia

Neuromuscular disease

Congenital myopathies
Congenital neuropathies

Central nervous system depression

Asphyxia
Narcotic administration
Intracranial hemorrhage

Artificial ventilation

Inadequate rate or tidal volume

Respiratory alkalosis

Artificial ventilation
Excessive rate or tidal volume

Table 5. Comparison of 95% confidence limits * and
decision levels [double dagger] during pregnancy,
during labor, and from the clamped umbilical cord.

Time Pregnancy Labor Capillary
Method Cordocentesis * [double dagger]
Sample site Umbilical vein Presenting part

pH >7.38 >7.2
[PO.sub.2] kPa >2.93
 (mm Hg) >22
[PC0.sub.2] kPa <5.6
 (mm Hg) (42)
Base deficit <3

Adapted from Huch, 1994 [32].

Time Umbilical cord
Method
Sample site

 Artery Vein *
 [double dagger]

pH >7.06 >7.14
[PO.sub.2] kPa >1.33 >1.6
 (mm Hg) (10) (12)
[PC0.sub.2] kPa <9.33 <7.46
 (mm Hg) (70) (56)
Base deficit <15 <13

Adapted from Huch, 1994 [32].
COPYRIGHT 1997 American Association for Clinical Chemistry, Inc.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 1997 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:NACB Symposium
Author:Brouillette, Robert T.; Waxman, David H.
Publication:Clinical Chemistry
Date:Jan 1, 1997
Words:4548
Previous Article:Standards of laboratory practice: evaluation of fetal lung maturity.
Next Article:Therapeutic drug monitoring principles in the neonate.
Topics:

Terms of use | Privacy policy | Copyright © 2020 Farlex, Inc. | Feedback | For webmasters