You are on page 1of 8

Macrosomic births in the United States: Determinants,

outcomes, and proposed grades of risk


Sheree L. Boulet, MPH, Greg R. Alexander, RS, MPH, ScD, Hamisu M. Salihu, MD, PhD, and
MaryAnn Pass, MD, MPH
Birmingham, Ala

OBJECTIVE: We describe maternal risk factors for macrosomia and assess birth weight categories to deter-
mine predictive thresholds of adverse outcomes.
STUDY DESIGN: We analyzed linked live birth and infant death cohort files from 1995 to 1997 for the United
States with the use of selected term (37-44 weeks of gestation) single live births to mothers who were US
residents. We compared macrosomic infants (4000-4499 g, 4500-4999 g, and >5000 g infants) with a normo-
somic control group of infants who weighed 3000 to 3999 g.
RESULTS: Maternal risk factors for macrosomia included nonsmoking, advanced age, married, diabetes
mellitus, hypertension, and previous macrosomic infant or pregnancy loss. The risks of labor complications,
birth injuries, and newborn morbidity rose with each gradation of macrosomic birth weight. Infant mortality
rates increased significantly among infants weighing >5000 g.
CONCLUSION: Although a definition of macrosomia as >4000 g (grade 1) may be useful for the identifica-
tion of increased risks of labor and newborn complications, >4500 g (grade 2) may be more predictive of
neonatal morbidity, and >5000 g (grade 3) may be a better indicator of infant mortality risk. (Am J Obstet Gy-
necol 2003;188:1372-8.)

Key words: Macrosomia, birth weight, infant death, cesarean delivery, diabetes mellitus, prenatal
care, birth injury

Fetal macrosomia, varyingly characterized as birth Risk characteristics that increase the probability of the
weight of >4000, >4500, or >5000 g, is associated with nu- delivery of a macrosomic infant include maternal obesity,
merous perinatal and maternal complications. 1-7 Past re- multiparity, previous macrosomic infant, male fetus, ma-
search indicates that the incidence of macrosomia in the ternal birth weight, paternal birth weight, maternal dia-
United States has been increasing over time, most likely betes mellitus, postdatism, prepregnancy weight/height,
because of the rising rates of maternal diabetes mellitus body mass index, advanced maternal age, ethnicity, ex-
and/or obesity.8-13 Macrosomic infants are at elevated cessive maternal weight gain, gestational hypertension,
risk of shoulder dystocia, brachial plexus injury, skeletal preeclampsia, prolonged labor, increased interpregnancy
injuries, meconium aspiration, perinatal asphyxia, hypo- interval, and marital status.1-3,9-11,15-20 There is substantial
glycemia, and fetal death.1-5,7,9 Maternal complications variation in the literature regarding the strength of the
are often related to cephalopelvic disproportion and in- association between these risk characteristics and macro-
clude prolonged labor, labor augmentation with oxy- somia. In fact, few pregnancies with these risk factors will
tocin, cesarean delivery, postpartum hemorrhage, actually result in a large baby, even when several risk fac-
infection, third- and fourth-degree lacerations, throm- tors are present in a single patient.15
boembolic events, and anesthetic accidents.1-6,9,14 The establishment of a widely accepted, standard defi-
nition for macrosomia has been problematic. Fetal macro-
From the Department of Maternal and Child Health, School of Public somia is defined by the American College of Obstetricians
Health, University of Alabama at Birmingham. and Gynecologists as infants with an absolute birth weight
Supported in part by the Department of Health and Human Services, the of >4500 g, irrespective of gestational age or other demo-
Health Resources and Services Administration, and the Maternal and
Child Health Bureau (grant No. 5T76MC00008). graphic variables.9 Nevertheless, considerable variation
Received for publication August 14, 2002; revised November 6, 2002; in the definition (eg, 4000, 4100, 4500, and 4536 g) per-
accepted January 23, 2003. sists in the literature, with some researchers using differ-
Reprint requests: Greg R. Alexander, RS, MPH, ScD, Department of Ma-
ternal and Child Health, School of Public Health, University of Al- ent cutoffs for diabetic and nondiabetic patients.11 In
abama at Birmingham, 320-A Ryals Bldg, 1665 University Blvd, addition to hindering comparisons among studies, the
Birmingham, AL 35294-0022. E-mail: alexandg@uab.edu use of prophylactic cesarean delivery for suspected
© 2003, Mosby, Inc. All rights reserved.
0002-9378/2003 $30.00 + 0 macrosomia has been questioned because of the lack of a
doi:10.1067/mob.2003.302 universally accepted definition for macrosomia, along

1372
Volume 188, Number 5 Boulet et al 1373
Am J Obstet Gynecol

Table I. Maternal characteristics by birth weight category for single live births to mothers who were US residents
(1995-1997)
Category (%)

Control, Grade 1, Grade 2, Grade 3,


Characteristic 3000-3999 g (No.) 4000-4499 g (No.) 4500-4999 g (No.) >5000 g (No.)

Race of mother
White 62.6 (44,614,159) 71.9 (691,207) 73.4 (116,141) 69.7 (11,896)
Black 12.9 (917,258) 7.6 (73,389) 7.0 (11,019) 8.5 (1,447)
Hispanic 18.1 (1,288,253) 15.4 (147,940) 14.7 (23,211) 16.1 (2,748)
American Indian 1.0 (67,435) 1.1 (10,708) 1.3 (2,095) 1.7 (283)
Samoan 0.05 (2,646) 0.07 (627) 0.08 (133) 0.2 (29)
Other 5.5 (390,478) 3.9 (37,596) 1.3 (5,648) 3.9 (662)
Married 70.1 (4,994,417) 78.1 (751,176) 80.1 (126,793) 79.0 (13,486)
Maternal age (y)
10-17 4.6 (330,293) 2.5 (23,975) 1.7 (2,660) 1.2 (199)
18-34 83.6 (5,958,498) 82.8 (796,571) 81.2 (128,511) 78.4 (13,375)
35-49 11.8 (838,697) 14.7 (140,914) 7.1 (27,074) 20.5 (3,490)
Educational attainment
High 46.0 (3,235,791) 52.4 (498,254) 53.2 (83,201) 50.8 (8,547)
Average 35.2 (2,474,116) 32.9 (312,326) 32.8 (51,253) 33.6 (5,660)
Low 18.8 (1,324,654) 14.7 (139,610) 14.0 (21,947) 15.6 (2,629)
Parity
Primiparous 41.4 (2,936,922) 34.0 (324,830) 29.9 (47,052) 26.5 (4,499)
High parity for age 2.5 (179,584) 2.8 (26,477) 3.7 (5,851) 5.6 (947)
Previous macrosomic birth 0.9 (60,528) 3.7 (35,575) 7.3 (11,524) 11.6 (1,972)
Previous pregnancy loss 2.5 (177,347) 2.7 (25,639) 2.9 (4,596) 3.2 (552)
Maternal complications
Diabetes mellitus 2.3 (162,300) 3.7 (35,322) 6.2 (9,727) 11.8 (2016)
Hypertension 3.3 (232,551) 3.3 (31,721) 3.9 (6,207) 4.9 (838)
Smoking during pregnancy 9.6 (682,147) 5.5 (52,821) 4.5 (7,072) 4.0 (689)

All maternal characteristics differed significantly (P < .05, 2) by birth weight categories.

with the relative inaccuracy of fetal weight estimates at cause of the large sample size, group comparisons can be
higher birth weights and the controversy regarding the anticipated to reveal statistically significant differences,
efficacy of interventions in reducing adverse outcomes even for very modest differences that may not be of clini-
that are associated with macrosomia.4,15,20-27 cal importance.
The purpose of this investigation, which used recent Maternal risk factors that were selected for this study
national birth data, is to describe maternal risk factors for included marital status, maternal age, educational attain-
macrosomia and to assess birth weight categories to de- ment, parity, previous macrosomic birth, previous preg-
termine thresholds that are most predictive of adverse nancy loss, diabetes mellitus, hypertension, and smoking
outcomes, including labor and delivery complications, while pregnant. Maternal educational attainment was
neonatal morbidity, and infant death. Although it is classified as high if the mother reported S12 years of ed-
widely accepted that high birth weights are associated ucation and as low if the mother reported <12 years of
with increased neonatal mortality rates, the birth weight education. Adolescents were classified as having high ed-
cutoffs that signal significant increases in general mor- ucational attainment if they were S2 years above their
bidity and death have yet to be determined. grade level for age. Conversely, low educational attain-
ment for adolescents was considered to be S2 years
Material and methods below expected grade level for age. High parity for age
The data used for this study were derived from the Na- was considered to be 1 births for adolescents, S3 previ-
tional Center for Health Statistics 1995 through 1997 US ous births for mothers 18 to 21 years old, S4 previous
linked live birth/infant death files.28 Term (37-44 weeks births for mothers 22 to 24 years old, and S5 previous
of gestation), single live births to mothers who were resi- births for mothers S25 years old. The Revised-Graduated
dents of the United States were selected for analysis. We Index of Prenatal Care Utilization (R-GINDEX) was used
further selected birth weights that were >3000 g. After to measure adequacy of prenatal care use. 29 This index
these selections, the sample included 7,127,529 normo- assesses the adequacy of prenatal care use on the basis of
somic births (3000-3999 g) and three groups of macro- three variables (the trimester that prenatal care began,
somic births (961,467 births [4000-4499 g], 158,247 the number of visits, and the gestational age of the infant
births [4500-4999 g], and 17,065 births [>5000 g]). Be- at birth) and is recommended for use in the assessment
1374 Boulet et al May 2003
Am J Obstet Gynecol

Table II. Prenatal care, obstetric procedure, obstetric complication, birth outcome, and mortality rate by birth weight
category
Category (%)

Control, Grade 1, Grade 2, Grade 3,


Variable 3000-3999 g (No.) 4000-4499 g (No.) 4500-4999 g (No.) >5000 g (No.)

Prenatal intensive care 5.9 (417,051) 6.4 (61,313) 7.2 (11,462) 9.1 (1,554)
Obstetric complication
Meconium staining 6.1 (432,503) 7.1 (67,740) 7.4 (11,627) 8.2 (1,404)
Excessive bleeding 0.5 (34,850) 0.7 (6,888) 0.9 (1,402) 1.1 (184)
Prolonged labor 0.9 (64,325) 1.2 (11,641) 1.3 (2,111) 1.5 (251)
Dysfunctional labor 2.8 (201,492) 4.3 (41,289) 5.2 (8,174) 5.6 (947)
Cephalopelvic disproportion 2.3 (166,533) 5.3 (50,723) 8.3 (13,118) 11.1 (1897)
Breech presentation 2.7 (189,084) 2.6 (24,912) 3.2 (5,007) 4.0 (674)
Obstetric procedure
Fetal monitoring 82.1 (5,853,780) 81.8 (786,298) 80.5 (127,424) 78.3 (13,364)
Ultrasound scan 98.6 (7,026,355) 98.8 (950,132) 98.9 (156,531) 99.0 (16,899)
Induced labor 17.5 (1,249,384) 22.4 (215,265) 23.4 (36,991) 20.3 (3,456)
Cesarean delivery 18.0 (1,279,370) 25.5 (245,166) 35.6 (56,406) 50.6 (8,629)
Birth outcome
Apgar score S6 (5 min) 0.6 (35,590) 0.7 (5,592) 1.0 (1,257) 2.2 (285)
Apgar score S3 (5 min) 0.1 (5,767) 0.1 (968) 0.2 (246) 0.5 (71)
Assisted ventilation <30 min 1.7 (121,307) 2.1 (19,888) 2.5 (4,027) 3.3 (556)
Assisted ventilation S30 min 0.3 (20,026) 0.3 (3,173) 0.5 (850) 1.3 (215)
Birth injuries 0.3 (18,347) 0.5 (5,004) 0.8 (1,337) 1.3 (218)
Hyaline membrane disease 0.2 (12,974) 0.2 (2,004) 0.4 (551) 0.8 (133)
Meconium aspiration 0.2 (16,736) 0.3 (2861) 0.4 (603) 0.6 (105)
Mortality rate
Hebdomadal (<7 d) 0.40 (2,863) 0.37 (360) 0.44 (70) 1.41 (24)
Neonatal (<28 d) 0.71 (5,044) 0.60 (579) 0.71 (113) 1.93 (33)
Postneonatal (S28 d) 1.44 (10,312) 1.00 (961) 1.08 (171) 2.05 (35)
Infant (<1 y) 2.16 (15,356) 1.60 (1,540) 1.80 (284) 3.98 (68)

All outcome variables differed significantly (P < .05, 2) by birth weight categories; Cochran-Armitage O2 trend test was significant for
all comparisons at P < .01 (trend tests for mortality rates were limited to 4000 g to >5000 g birth weight categories).

of birth weight– and gestational age–related birth out- care use, parity, previous macrosomic birth, previous
comes.29 Gestational age in completed weeks was com- pregnancy loss, maternal diabetes mellitus, hypertension,
puted from the interval between the date of the last smoking, alcohol use, and gestational age). Macrosomic
menstrual period (LMP) and the date of birth. For birth weight categories (4000-4499 g, 4500-4999 g, >5000 g)
records that were missing the day of LMP, a gestational were entered into the logistic models as dummy variables,
age value was input when there was valid data for month and normal weight infants (3000-3999 g) were used as the
and year of LMP. Where the LMP was unknown or in- reference group.
compatible with birth weight, the clinical estimate of ges-
tation was used if it was consistent with birth weight.30 Results
The 2 test was used to test for significant differences in Table I shows maternal characteristics by birth weight
the proportions of maternal demographic risk character- category. A number of maternal risk factors occurred
istics, prenatal care use, obstetric complications and pro- with higher frequency among the macrosomic categories
cedures, birth outcomes, and infant death among the compared with the normosomic categories. Among race
birth weight categories. Positive monotonic relationships of mother categories, white, American Indian, and
between advancing birth weight categories and increas- Samoan mothers were disproportionately overrepre-
ing risks of adverse birth outcomes were tested with the sented in the macrosomic groups. Mothers of macro-
use of the Cochran-Armitage 2 trend test. Multiple lo- somic infants were significantly more likely than those of
gistic regression was then used to calculate odds ratios normal birth weight infants to be married and older
and 95% CIs for the independent association of macro- (S35 years old), and less likely to be <18 years old and
somic birth weight categories on an array of outcome primiparous. Significantly higher proportions of mothers
measures that included obstetric complications, obstetric with a higher educational level, a high parity for age, a pre-
procedures, intensive use of prenatal care, and infant vious pregnancy loss, or a previous macrosomic birth were
death and morbidity, after controlling for maternal risk found in the macrosomic groups. Mothers of macrosomic
factors (such as age, marital status, education, prenatal infants were more likely than mothers of normosomic in-
Volume 188, Number 5 Boulet et al 1375
Am J Obstet Gynecol

fants to have diabetes mellitus and hypertension and less


likely to have smoked during the index pregnancy.
Table II shows prenatal care, obstetric procedures, ob-
stetric complications, birth outcomes, and mortality rates
by birth weight category and reveals that, although in-
creasing birth weight is associated with unfavorable birth
outcomes, the vast majority of macrosomic infants (even
those >5000 g) are not reported to experience an adverse
outcome or death. Mothers in all categories of macroso-
mia were more likely to report intensive use of prenatal
care than the nonmacrosomic mothers. The proportion
of all obstetric complications (meconium staining, exces-
sive bleeding, prolonged labor, dysfunctional labor,
cephalopelvic disproportion, breech presentation)
showed a progressive and significant increase among the
macrosomic birth weight categories. The frequency of
cephalopelvic disproportion demonstrated the most dra-
matic increase with the complication being reported for
2.3% of infants who weighed 3000 to 3999 g and 11.1% of Figure. Increased risk of adverse outcomes by macrosomia
infants who weighed >5000 g. Among the obstetric proce- grade. Open bars, Grade 1 (4000-4499 g); gray bars, grade 2 (4500-
dures, the proportion of cesarean deliveries increased 4999 g); black bars, grade 3 (5000+ g).
substantially across birth weight categories, with more
than one half of all infants weighing >5000 g delivered by
cesarean section, compared with only 18% of normo-
somic infants. Labor induction increased among the among all macrosomic groups, with the 4000- to 4499-g
4000- to 4499-g and 4500- to 4999-g groups and then de- group having an almost 2-fold risk compared with nor-
creased slightly among the >5000-g group yet still re- mosomic infants. The risk of other adverse birth out-
mained higher than the normosomic infants. The comes (such as hyaline membrane disease, meconium
frequency of adverse birth outcomes increased slightly aspiration, birth asphyxia, and poor Apgar scores) were
over the birth weight categories, with the >4500-g infants elevated moderately among the 4000- to 4499-g category
showing the most significant differences. For example, yet were increased substantially among the higher birth
the proportion of infants who were affected by hyaline weight categories. Increased risk of death, compared with
membrane disease was 0.4% in the 4500- to 4999-g cate- normal-birth-weight infants, was only evident in the
gory and 0.8% in the S5000-g category compared with >5000-g category. Infants in this category were 2.69 times
0.2% for the 3000- to 3999-g and 4000- to 4499-g cate- as likely as nonmacrosomic infants to die during the
gories. Finally, the mortality rates either declined or neonatal period.
showed very little change for the 4000- to 4499-g and The Figure shows the stepwise increase in risk of ad-
4500- to 4999-g categories compared with the 3000- to verse outcomes by macrosomic categories defined as
3999-g category. However, all mortality rates increased grade 1 (4000-4499 g), grade 2 (4500-4999 g), and grade
substantially for the >5000-g category, as evidenced by the 3 (>5000 g). Over this 3-year study period, macrosomic
change in the infant mortality rate from 2.16 (3000-3999 births (if defined by the above birth weight categories,
g) to 3.98 (>5000 g). without regard to their gestational age) represented ap-
Table III shows the results of the logistic regression proximately 10.5% of the reported single live births to
analysis of obstetric procedures, obstetric complications, mothers who were US residents (approximately 8.7%
birth outcomes, and deaths. The normosomic group was grade 1, 1.5% grade 2, and 0.2% grade 3).
used as the reference group. After maternal sociodemo-
graphic risk factors were controlled, macrosomic infants Comment
were far more likely to have cephalopelvic disproportion Many of the risk factors for fetal macrosomia that were
compared with normosomic infants (4000- to 4499-g in- identified in this investigation (eg, white race of mother,
fants: odds ratio, 2.42 [95% CI, 2.40, 2.45]; 4500- to 4999- advanced maternal age, previous macrosomic birth, high
g infants: odds ratio, 4.07 [95% CI, 3.99, 4.15]; and educational attainment, married, maternal diabetes mel-
>5000-g infants: odds ratio, 5.79 [95% CI: 5.50, 6.08]). All litus, hypertension, multiparity, and nonsmoker) have
categories of macrosomic infants were at greater risk of been recognized in the literature.1-3,9-11 In this study, pre-
being delivered by cesarean delivery compared with the vious macrosomic birth and diabetes mellitus were the
reference group. Birth injuries were also more likely strongest risk factors for macrosomia, with the magnitude
1376 Boulet et al May 2003
Am J Obstet Gynecol

Table III. Logistic regression analyses of obstetric procedure, obstetric complication, birth outcome, and death by birth
weight category
Category

Grade I, 4000-4499 g Grade II, 4500-4999 g Grade III, >5000 g

Variable Odds ratio 95% CI Odds ratio 95% CI Odds ratio 95% CI

Prenatal intensive care 1.04 1.03-1.05* 1.15 1.12-1.17* 1.38 1.30-1.46*


Obstetric complication
Meconium staining 1.18 1.17-1.19* 1.22 1.21-1.25* 1.35 1.28-1.42*
Excessive bleeding 1.41 1.37-1.45* 1.65 1.56-1.74* 1.86 1.61-2.16*
Prolonged labor 1.38 1.35-1.41* 1.55 1.48-1.62* 1.76 1.55-1.99*
Dysfunctional labor 1.56 1.54-1.58* 1.89 1.85-1.93* 1.99 1.86-2.13*
Cephalopelvic disproportion 2.42 2.40-2.45* 4.07 3.99-4.15* 5.79 5.50-6.08*
Breech presentation 1.02 1.01-1.04† 1.26 1.23-1.30* 1.55 1.43-1.67*
Obstetric procedure
Induced labor 1.20 1.20-1.21* 1.19 1.17-1.20* 0.93 0.89-0.96*
Cesarean delivery 1.62 1.61-1.63* 2.61 2.58-2.64* 4.68 4.54-4.83*
Birth outcome
5-min Apgar score S6 1.21 1.17-1.24* 1.65 1.56-1.75* 3.49 3.10-3.94*
5-min Apgar score S3 1.30 1.21-1.39* 2.01 1.76-2.29* 5.20 4.09-6.62*
Assisted ventilation S30 min 1.19 1.14-1.23* 1.85 1.73-1.99* 3.96 3.45-4.55*
Assisted ventilation <30 min 1.21 1.19-1.23* 1.46 1.43-1.51* 1.81 1.66-1.97*
Birth injuries 1.99 1.92-2.05* 3.14 2.96-3.32* 4.53 3.95-5.19*
Hyaline membrane disease 1.16 1.10-1.22* 1.84 1.68-2.01* 3.70 3.11-4.40*
Meconium aspiration 1.28 1.23-1.34* 1.65 1.52-1.79* 2.61 2.15-3.16*
Deaths
Neonatal 0.87 0.80-0.96† 1.00 0.83-1.21 2.69 1.91-3.80*
Postneonatal 0.79 0.74-0.85* 0.86 0.74-1.00 1.62 1.16-2.26†
Infant 0.82 0.78-0.86* 0.91 0.80-1.02 2.01 1.58-2.55*

All logistic regression models include measures of maternal race, age, education, marital status, prenatal care use, parity, previous
macrosomic birth, previous pregnancy loss, maternal diabetes mellitus, hypertension, smoking, alcohol use, and gestational age; the ref-
erence group was 3000-3999 g.
*P <.0001.
†P < .005.

of risk rising as the grade of macrosomia increased. This mine whether the prevalence of these risk factors ade-
study demonstrated that mothers of macrosomic infants quately explains the rising incidence rates. The effective-
were more likely than mothers of normosomic infants to ness of clinical interventions for the treatment of
have a previous pregnancy loss and to receive intensive suspected macrosomia among mothers who have specific
prenatal care and a cesarean delivery. The likelihood of risk factors (such as diabetes mellitus, excessive weight
obstetric complications and the occurrence of poor birth gain, and obesity) should also be assessed.
outcomes increased markedly with heavy birth weight. The limitations of this study include the finite set of
Grade 3 macrosomic infants had significantly higher risk factors that were available on vital records for investi-
mortality rates compared with normosomic infants, yet gation. Furthermore, vital record data have been well
grades 1 and 2 exhibited a lower risk of infant death, noted for possible miscoding and/or misclassification
which possibly reflects the role of nutrition, weight gain, problems and, in particular, for a lack of precision in the
or other uncontrolled factors that influence both heavier reported diagnoses of medical conditions and morbidi-
birth weights and lower mortality risk. ties. There is little evidence to suggest that these prob-
The findings of this study are in general agreement lems vary by the birth weight categories used in this study
with numerous others that have found macrosomia to be and would bias severely the relationships that were ob-
associated with maternal and neonatal morbidity and served between the grades of macrosomia and birth out-
death.1-7,9,18 It has been reported that the incidence of comes. Nevertheless, the interpretation of these results
macrosomia has been increasing across the United States should incorporate an understanding of the limits of the
and in other developed countries.8-13 Subsequent analysis data set and should explore the potential validity of atyp-
of national data is needed to confirm the continuation of ical findings. For example, hyaline membrane disease is a
this trend. Further investigation of the relationship be- neonatal complication that is associated strongly with
tween the prevalence of documented risk factors (such as preterm birth as a consequence of immature lungs. In
maternal obesity and diabetes mellitus) and changes in this study of term births, the occurrence of hyaline mem-
the incidence of macrosomia is also warranted to deter- brane disease and its increasing prevalence with higher
Volume 188, Number 5 Boulet et al 1377
Am J Obstet Gynecol

grades of macrosomia may more likely be attributable to complications, a definition of >4500 g (grade 2) may be
medical conditions other than prematurity. Diabetic ba- more predictive of neonatal morbidity, and >5000 g
bies may be born with an appropriate birth weight or (grade 3) may be a better indicator of infant death risk.
even macrosomia and also have hyaline membrane dis- The proposed three-step definition for macrosomia in-
ease because of immature lung functions. Further analy- corporates easily remembered birth weight cutoff values
sis of our data showed a strong correlation between that may facilitate both the assessment of risk and the pre-
maternal diabetes mellitus and the presence of hyaline diction of outcome.
membrane disease. Hence, the occurrence of hyaline
membrane disease among macrosomic babies in the
study population is probably due to morbidities (such as
REFERENCES
diabetic condition) in the mother.
1. Boyd ME, Usher RH, McClean FH. Fetal macrosomia: predic-
To our knowledge, there are no similar published stud- tion, risks, and proposed management. Obstet Gynecol 1983;
ies that use recent national data to examine adverse out- 61:715-22.
comes that are associated with macrosomia across a 2. Spellacy WN, Miller S, Winegar A, Petersen PQ. Macrosomia:
maternal characteristics and infant complications. Obstet Gy-
number of different birth weight thresholds. This study necol 1985;66:158-61.
provides a conceptual framework for the establishment of 3. Meshari AA, DeSilva S, Rahman I. Fetal macrosomia: maternal
progressive birth weight categories of macrosomia that risks and fetal outcome. Int J Gynecol Obstet 1990;32:215-22.
4. Lipscomb KR, Gregory K, Shaw K. The outcome of macrosomic
are based on the risk of increased health care use, mor- infants weighing at least 4500 grams: Los Angeles County + Uni-
bidity, and death. Our data suggest that the incorporation versity of Southern California experience. Obstet Gynecol
of a three-step definition for fetal macrosomia may be 1995;85:558-64.
5. Wollschlaeger K, Nieder J, Köppe I, Härtlein K. A study of fetal
more clinically useful than a single birth weight cutoff macrosomia. Arch Gynecol Obstet 1999;263:51-5.
value. Thus, grade 1 macrosomia may be viewed as a 6. Ferber A. Maternal complications of fetal macrosomia. Clin Ob-
threshold indicator for an increased risk of delivery com- stet Gynecol 2000;43:335-9.
7. Grassi AE, Giuliano MA. The neonate with macrosomia. Clin
plications and can alert the clinician to the need for more Obstet Gynecol 2000;43:340-8.
intensive intrapartum treatment. Along with represent- 8. Johar R, Rayburn W, Weir D, Eggert L. Birth weights in term in-
ing a further increment in the risk of labor and delivery fants: a 50-year perspective. J Reprod Med 1988;33:813-6.
9. ACOG practice bulletin No. 22. Washington (DC): American
complications, grade 2 infants often have a greater num- College of Obstetricians and Gynecologists; 2000.
ber of obstetric procedures and a greater likelihood of 10. Brunskill AJ, Rossing MA, Connell FA, Daling J. Antecedents of
adverse morbidity outcomes. Women at risk for delivery macrosomia. Paediatr Perinat Epidemiol 1991;5:392-401.
11. Langer O. Fetal macrosomia: etiologic factors. Clin Obstet Gy-
of a grade 2 macrosomic infant may require enhanced necol 2000;43:283-97.
prenatal treatment. Finally, grade 3 macrosomia repre- 12. Baker P, Lever P, Gorton E. An increasing incidence of fetal
sents significant newborn mortality risks. macrosomia. J Obstet Gynecol 1992;12:281.
13. Ørskou J, Kesmodel U, Henriksen TB, Secher NJ. An increasing
It should be noted that these broadly aggregated 500-g proportion of infants weighing more than 4000 grams at birth.
birth weight categories or “grades” of macrosomia are Acta Obstet Gynecol Scand 2001;80:931-6.
based on considerations of practicality and ease of use in 14. Yawn BP, Wollan P, McKeon K, Field CS. Temporal changes in
rates and reasons for medical induction of term labor, 1980-
clinical, research, and policy situations rather than on a 1986. Am J Obstet Gynecol 2001;184:611-9.
more detailed analysis of the specific birth weight values 15. Sacks DA, Chen W. Estimating fetal weight in the management
that would demark changing levels of risk optimally. This of macrosomia. Obstet Gynecol Surv 2000;55:229-39.
16. Parks DG, Ziel HK. Macrosomia: a proposed indication for pri-
study’s more easily recollected classification strategy was mary cesarean section. Obstet Gynecol 1978;52:407-9.
selected therefore as a heuristic approach to facilitate 17. Davis R, Woelk G, Mueller BA, Daling J. The role of previous
standard reporting and to promote the conceptualization birth weight on risk for macrosomia in a subsequent birth. Epi-
demiology 1995;6:607-11.
of macrosomia as a multilevel condition, with distinctive 18. Bérard J, Dufour D, Vinatier D, Subtil D, Vanderstichèle S, Mon-
variations in its degree of risk with specific adverse health nier JC, et al. Fetal macrosomia: risk factors and outcome: a
care use, morbidity, and mortality outcomes. Neverthe- study of the outcome concerning 100 cases >4500g. Eur J Obstet
Gynecol Reprod Biol 1998;77:51-9.
less, further research toward the generation of a macro- 19. Mocanu EV, Greene RA, Byrne BM, Turner MJ. Obstetric and
somia risk score for a variety of adverse outcomes is neonatal outcome of babies weighing more than 4.5 kg: an analy-
warranted. sis by parity. Eur J Obstet Gynecol Reprod Biol 2000;92:229-33.
20. Xiong X, Demianczuk NN, Buekens P, Saunders L, Duncan MB.
In summary, the risk factors for macrosomia that are re- Association of preeclampsia with high birth weight for gesta-
ported in this study are largely consistent with the current tional age. Am J Obstet Gynecol 2000;183:148-55.
literature. We demonstrated that adverse outcomes (such 21. Rouse DJ, Owen J. Sonography, suspected macrosomia, and pro-
phylactic cesarean: a limited partnership. Clin Obstet Gynecol
as labor complications, use of obstetric procedures, 2000;43:326-34.
neonatal morbidity, and infant death) differ across vary- 22. O’Reilly-Green C, Divon M. Sonographic and clinical methods
ing birth weight thresholds. Thus, although defining in the diagnosis of macrosomia. Clin Obstet Gynecol 2000;
43:309-20.
macrosomia as >4000 g (grade 1) may be useful for the 23. Sokol RJ, Chik L, Dombrowski MP, Zador IE. Correctly identifying
identification of the increased risks of labor and newborn the macrosomic fetus. Am J Obstet Gynecol 2000;182:1489-95.
1378 Boulet et al May 2003
Am J Obstet Gynecol

24. Öçer F, Kaleli S, Budak E, Oral E. Fetal weight estimation and 28. National Center for Health Statistics. 1995, 1996, 1997 Birth Co-
prediction of fetal macrosomia in non-diabetic pregnant hort Linked Birth/Infant Death Data Sets, NCHS CD-ROM Se-
women. Eur J Obstet Gynecol Reprod Biol 1999;83:47-52. ries 20, Numbers 12a, 14a, 15a, ASCII Version, US Dept Health
25. Weeks JW, Pitman T, Spinnato JA II. Fetal macrosomia: does an- and Human Services, Centers for Disease Control and Preven-
tenatal prediction affect delivery route and outcome? Am J Ob- tion. Available from: www.cdc.gov/nchs.
stet Gynecol 1995;173:1215-9. 29. Alexander GR, Kotelchuck M. Quantifying the adequacy of pre-
26. Kolderup LB, Laros RK, Musci TJ. Incidence of persistent birth natal care: a comparison of indices. Public Health Rep 1996;
injury in macrosomic infants: association with mode of delivery. 111:408-18.
Am J Obstet Gynecol 1997;177:37-41. 30. Ventura SJ, Martin JA, Curtin SC, Mathews TJ. Report of the na-
27. Rouse DJ, Owen J, Goldenberg RL, Cliver SP. The effectiveness tality statistics, 1995 (monthly vital statistics report: vol 45, no
and costs of elective cesarean delivery for fetal macrosomia di- 11, supp 2). Hyattsville (MD): National Center for Health Sta-
agnosed by ultrasound. JAMA 1996;276:1480-6. tistics; 1997.

Correction
In the letter by Sharma and El-Refaey, the second author’s name was misspelled. The cor-
rect citation is Sharma S, El-Refaey H. The use of misoprostol as a cervical ripening agent in
operative hysteroscopy. Am J Obstet Gynecol 2003;188:297-8.

You might also like