Skip to main content
Nutrients logoLink to Nutrients
. 2020 Apr 26;12(5):1224. doi: 10.3390/nu12051224

Extrauterine Growth Restriction: Definitions and Predictability of Outcomes in a Cohort of Very Low Birth Weight Infants or Preterm Neonates

Chiara Peila 1,*, Elena Spada 1, Francesca Giuliani 1, Giulia Maiocco 1, Melissa Raia 1,2, Francesco Cresi 1, Enrico Bertino 1, Alessandra Coscia 1
PMCID: PMC7281990  PMID: 32357530

Abstract

Extrauterine Growth Restriction (EUGR) refers to inadequate growth during hospitalization. Current definitions for EUGR are varied and can be classified as cross-sectional (weight at a given t-time <10th centile) or longitudinal (weight loss between birth and a given t-time >1SD). Different t-times are also considered in literature, such as 36 weeks of gestational age (GA) or age at discharge. The aim of this study is to investigate whether EUGR could predict the auxological outcome at 24–30 months, and to evaluate the agreement between cross-sectional and longitudinal definitions. In total, 1589 infants with GA <30 weeks or birthweight ≤ 1500 g and without major congenital anomalies were included in this study. Cross-sectional and longitudinal EUGR were calculated at 36 and 40 weeks of GA, at discharge, and at 28 days. The concordance between the two definitions was estimated by Kappa coefficient. At 24–30 months, 803 infants were measured again. The agreement between the two definitions of EUGR was low. Both EUGR and not-EUGR groups were at lower centiles for weight, but at higher centiles for head circumference at 24–30 months than at birth. Longitudinal EUGR was associated with a poorer growth outcome for weight and height circumference than cross-sectional EUGR. No differences were observed for length. An agreed definition of EUGR is highly desirable in clinical practice to assess medical and nutritional interventions in preterm neonates. Based on the results of this study, we recommend the use of the longitudinal evaluation, that proved to better predict the auxological long-term outcome with respect to the cross-sectional one.

Keywords: extrauterine growth restriction, postnatal growth of preterm neonates, EUGR definition, EUGR and auxological outcomes

1. Introduction

Extrauterine Growth Restriction (EUGR) has often been reported in literature following preterm birth and birth with Very Low Birth Weight (VLBW, i.e., birthweight ≤ 1500 g). The condition of EUGR refers to an inadequate growth that occurs during hospitalization [1]. At discharge, preterm and VLBW infants often fail to gain weight according to expectations based on intrauterine growth charts; their weight is often at lower percentile with respect to birth and below the 10th percentile of expected growth [2,3]. The growth deficit can be observed for weight but also for head circumference and length [4].

EUGR is influenced by a number of factors. It can be partially explained by periods of inadequate nutrition, feeding intolerance (commonly present in preterm infants), and a range of mild to severe morbidities associated with preterm birth [5,6]. Prenatal and postnatal growth rates have been shown to be important for long-term outcomes [7,8,9,10,11,12,13,14,15,16]. There is increasing evidence that children who experienced a transient phase of preterm growth restraint develop a number of sequelae that are independent of whether the restraint occurred in utero (resulting in a small-for-gestational-age (SGA) infant), ex utero (preterm birth followed by poor neonatal growth), or in both phases [17]. It is still unclear to what extent EUGR affects long-term growth, the main reasons being controversial data from literature and the lack of a harmonized EUGR definition.

Current definitions can be classified in two groups: (1) cross-sectional, consisting of having a weight below the 10th centile (or another cut-off) at a given time (t), independently of birthweight; and (2) longitudinal, consisting of a weight loss of more than 1 (or 2) Standard Deviation (SD) between birth and a given t-time. The t-times proposed in literature are three: 36 weeks of GA, age at discharge, and 28 days of postnatal age [18].

The aim of this study was to investigate whether the EUGR (however defined) can predict the auxological outcome at 24–30 months of age, and to evaluate the agreement between cross-sectional and longitudinal definitions at the same t-time.

2. Methods

Clinical and growth data were collected for 1887 infants with GA < 30 weeks or weight ≤ 1500 g (according to the Vermont Oxford Network criteria [19]), born between 1994 and 2010 and admitted to the Neonatal Intensive Care Unit of the University of Turin, Italy. Exclusion criteria were major congenital malformations or genetic syndromes and death prior to discharge. In total, 1589 infants were included in the study. The inclusion threshold indicated by the Vermont Oxford Network (VON) and based on Gestational Age (GA) or on birthweight identifies two clinically different populations. The first one includes all neonates born with GA < 30 weeks (independently of their birth weight), while the second one includes neonates with GA ≥ 30 weeks only if VLBW (Figure 1). As a consequence, a higher percentage of major morbidities related to low GA was expected in the first population, whereas a higher proportion of females, twins (both physiological smaller), and SGA babies (by definition smaller) was expected in the second population. For this reason, the analysis considered separately the two different populations: (1) Population A (newborns with a GA < 30 weeks, n = 695) and (2) Population B (VLBW with GA ≥ 30 weeks, n = 894).

Figure 1.

Figure 1

Inclusion criteria and definition of population study. GA: gestational-age; VLBWi: Very Low Birth Weight infants; VLBW: Very Low Birth Weight.

The weight was expressed in Standard Deviation Score (SDS or z-score) using the INeS charts [20] (at birth, and at the four t-times) and the CDC2000 charts (at 24–30 months) [21] as reference.

Neonates were defined asSGA or Large for GA (LGA) if their birthweight was below the 10th or above the 90th centile of the INeS charts, respectively.

EUGR was defined in the cross-sectional way if weight was below the 10th centile at a given t-time, whereas it was defined in the longitudinal way if the weight loss was more than one SD between birth and a given t-time. Forty weeks of GA was also considered in addition to the t-times typically considered in the literature (i.e., 36 weeks of GA, age at discharge, and 28 days of postnatal age), this being, conventionally, the average duration of a physiological pregnancy.

The agreement between cross-sectional and longitudinal EUGR definitions at the same t-time was estimated by Cohen’s kappa coefficient.

Among 1589 neonates, 803 babies (406 population A, 397 population B) were followed up until 24–30 months; their data were analyzed to assess the auxological outcome with a general linear model that considers as response the difference of weight-, length-, or head circumference-SDS between 24–30 months and birth (∆SDS), and as covariates the EUGR (defined on weight as above), the population (A or B), and the weight by GA (SGA or non-SGA).

3. Results

Table 1 reports the baseline characteristics of the two Populations (A and B). As expected, population B has a higher median GA and a higher proportion of singleton and females. The auxological variables at birth are, on average, higher in Population B than in Population A when the original values are considered. On the contrary, the mean SDSs are close to the expected values in population A (between −0.10 and −0.02, corresponding to 46th and 49th centile), and lower in Population B (between −1.29 and −1.09, corresponding to 10th and 14th centile).

Table 1.

General characteristics of babies by population.

Population A
(N = 695)
Population B
(N = 894)
Females, n (%) 342 (49.2) 492 (55.0)
Singleton, n (%) 527 (75.8) 588 (65.8)
Gestational Age (week), median (IQR) 28 (27–29) 31 (30–33)
Birth weight (g), mean (SD) 991 (255) 1251 (193)
Birth length (mm), mean (SD) 356 (30) 387 (22)
Head circumference (mm), mean (SD) 252 (19) 277 (14)
Birth weight (SDS), mean (SD) −0.02 (0.946) −1.29 (0.845)
Birth length (SDS), mean (SD) −0.10 (0.928) −1.09 (0.976)
Head circumference (SDS), mean (SD) −0.06 (1.046) −1.24 (1.013)
SGA, n (%) 76 (10.9) 459 (51.3)
LGA, n (%) 51 (7.3) 0 (0.0)
Antenatal steroids, n (%) * 534 (86.1) 647 (87.6)

* computed on 620 neonates of population A and 739 of population B. IQR: InterQuartile Range; SD: Standard Deviation; SDS: Standard Deviation Score; SGA: Small for gestational age; LGA: Large for gestational age.

Table 2 shows major morbidities before discharge. GA was the main risk factor for severe morbidities.

Table 2.

Major morbidities during hospital stay.

Population A
(N = 695)
Population B
(N = 894)
Major morbidities, n (%) 621(89.4) 349(39.0)
Late sepsis, n (%) 120(17.3) 34 (1.9)
NEC, n (%) 18(2.6) 17(3.8)
ROP, n (%) 44(6.3) 2(0.2)
BPD, n (%) 24(3.5) 5(0.6)
RDS, n (%) 598(86.0) 299(33.5)
MV, n (%) * 568(83.5) 231(28.9)
HFOV, n (%) ** 67(10.9) 10(1.3)
IVH, n (%) 43(7.4) 6(1.0)
PVL, n (%) 32(5.7) 19(3.2)
PDA, n (%) 292(42.0) 73(8.2)
Age at discharge in days
median (min-max) 65 (24–137) 39 (17–90)

* computed on 680 neonates of population A and 800 of population B. ** computed on 617 neonates of population A and 767 of population B. NEC: necrotizing enterocolitis; ROP: retinopathy of prematurity; BPD: bronchopulmonary dysplasia; RDS: Respiratory Distress Syndrome; MV: Mechanical Ventilation; HFOV: High-frequency oscillatory ventilation; PVL: periventricular leukomalacia; IVH: intraventricular hemorrhage; PDA:patent ductus arteriosus.

Table 3 reports the number of EUGR-babies according to the two definitions (cross-sectional and longitudinal) at the different t-times. In Population A, the proportion of non-SGA infants with longitudinal EUGR was higher than that with cross-sectional EUGR, whereas in Population B an opposite tendency was observed. When considering both populations together, most SGA babies had cross-sectional EUGR; however, when EUGR is defined in a longitudinal way, the percentage of SGA babies with EUGR decreased. This was particularly evident in Population B. It should be noted that the agreement between cross-sectional and longitudinal definition of EUGR at the same t-time was low (−0.07 < Cohen’s kappa coefficient < +0.38).

Table 3.

Infants with EUGR defined in cross-sectional and longitudinal way at the four different t-times.

EUGR Definition Cross-sectional Longitudinal
36 Weeks 40 Weeks 28 Days Discharge 36 Weeks 40 Weeks 28 Days Discharge
Study population
non-SGA,
n (%)
489/561
(87.2)
163/262
(62.2)
335/572
(58.6)
565/732
(77.2)
487/561
(86.8)
179/262
(68.3)
390/572
(68.2)
626/732
(85.5)
SGA, n (%) 340/340
(100.0)
159/167
(95.2)
250/250
(100.0)
331/332
(99.7)
109/340
(32.1)
90/167
(53.9)
62/250
(24.8)
145/332
(43.7)
Population A
non-SGA,
n (%)
268/331
(81.0)
107/170
(62.9)
168/358
(46.9)
318/447
(71.1)
312/331
(94.3)
135/170
(79.4)
260/358
(72.6)
414/447
(92.6)
SGA, n (%) 47/47
(100.0)
43/43
(100.0)
46/46
(100.0)
49/49
(100.0)
36/47
(76.6)
42/43
(97.7)
11/46
(23.9)
43/49
(87.8)
Population B
non-SGA,
n (%)
221/230
(96.1)
56/92
(60.9)
167/214
(78.0)
247/285
(86.7)
175/230
(76.1)
44/92
(47.8)
130/214
(60.8)
212/285
(74.4)
SGA, n (%) 293/293
(100.0)
116/124
(93.6)
204/204
(100.0)
282/283
(99.7)
73/293
(24.9)
48/124
(38.7)
51/204
(25.0)
102/283
(36.0)

Table 4 reports the raw means (SD) of auxological variables at 24–30 months of life. In average, the children are lighter and shorter and have e lower head circumference respect to the CDC-target population.

Table 4.

Raw means of auxological variables at 24–30 months of life.

Study
Population
Population A Population B
Weight (g), mean (SD) 11,146 (1578) 11,261 (1724) 11,029 (1406)
Length (mm), mean (SD) 853 (39) 853 (39) 853 (40)
Head circumference (mm), mean (SD) 477 (18) 477 (19) 477 (17)
Weight (SDS), mean (SD) −1.43 (1.373) −1.39 (1.492) −1.47 (1.240)
Length (SDS), mean (SD) −0.94 (1.060) −1.01 (1.057) −0.86 (1.059)
Head circumference (SDS), mean (SD) −0.41 (1.163) −0.43 (1.231) −0.39 (1.088)

The results of the general linear model estimate the effect of EUGR on growth, is reported in Table 5.

Table 5.

SDS (SDS 24–30 months –SDS at birth) LS means ± Standard Error in EUGR and non-EUGR group. EUGR was defined using weight in cross-sectional and longitudinal way at the four t-times.

TRAIT EVALUATION t EUGR
No Yes No vs. Yes p
WEIGHT Cross-
Sectional
36 weeks of GA −0.32 ± 0.192 −0.67 ± 0.056 +0.36 ± 0.201 0.077
40 weeks of GA −0.57 ± 0.153 −0.86 ± 0.086 +0.29 ± 0.180 0.110
28 days −0.95 ± 0.113 −0.71 ± 0.065 −0.24 ± 0.136 0.076
discharge −0.92 ± 0.121 −0.65 ± 0.051 −0.27 ± 0.133 0.043
Longitudinal 36 weeks of GA −0.23 ± 0.112 −0.82 ± 0.067 +0.59 ± 0.141 <0.001
40 weeks of GA −0.47 ± 0.130 −0.95 ± 0.093 +0.48 ± 0.166 0.004
28 days −0.58 ± 0.087 −0.93 ± 0.074 +0.36 ± 0.120 0.003
discharge −0.38 ± 0.099 −0.80 ± 0.055 +0.42 ± 0.118 <0.001
LENGTH Cross-
Sectional
36 weeks of GA −0.09 ± 0.181 −0.14 ± 0.050 0.05 ± 0.189 0.772
40 weeks of GA −0.30 ± 0.129 −0.27 ± 0.073 −0.02 ± 0.152 0.872
28 days −0.46 ± 0.103 −0.19 ± 0.060 −0.27 ± 0.125 0.030
discharge −0.61 ± 0.108 −0.16 ± 0.046 −0.45 ± 0.120 <0.001
Longitudinal 36 weeks of GA +0.02 ± 0.100 −0.21 ± 0.061 +0.23 ± 0.126 0.072
40 weeks of GA −0.11 ± 0.107 −0.38 ± 0.079 +0.27 ± 0.137 0.053
28 days −0.18 ± 0.078 −0.33 ± 0.069 +0.15 ± 0.109 0.180
discharge −0.11 ± 0.089 −0.29 ± 0.051 +0.18 ± 0.107 0.094
HEAD CIRCUMFERENCE Cross-
Sectional
36 weeks of GA +0.31 ± 0.159 +0.33 ± 0.046 −0.02 ± 0.167 0.924
40 weeks of GA +0.20 ± 0.126 +0.22 ± 0.071 −0.01 ± 0.148 0.939
28 days −0.01 ± 0.094 +0.22 ± 0.053 −0.23 ± 0.113 0.045
discharge +0.07 ± 0.104 +0.32 ± 0.043 −0.25 ± 0.114 0.029
Longitudinal 36 weeks of GA +0.64 ± 0.092 +0.20 ± 0.055 +0.44 ± 0.115 <0.001
40 weeks of GA +0.34 ± 0.108 +0.15 ± 0.077 +0.20 ± 0.138 0.156
28 days +0.33 ± 0.072 +0.03 ± 0.061 +0.30 ± 0.100 0.003
nidischarge +0.52 ± 0.084 +0.20 ± 0.047 +0.32 ± 0.100 0.001

Note: p values in bold are those considered significant.

The LSmeans represents the estimate of the EUGR effect corrected for Population (A or B) and birth weight by GA (SGA or non-SGA).

Both EUGR and non-EUGR groups were, on average, around lower centiles for weight at 24–30 months than at birth (mean ∆SDS < 0). On the contrary, regarding the head circumference, both EUGR and non-EUGR groups were, on average, on higher centiles than at birth (mean ∆SDS > 0).

When EUGR was considered as longitudinal, the worsening of weight-SDS at 24–30 months was greater in EUGR than in non-EUGR group at all four times (p < 0.01). Similarly, the improvement of head circumference-SDS was higher in the non-EUGR than in the EUGR group. There were no differences between the EUGR and the non-EUGR in the cross-sectional evaluation, neither for weight nor for head circumference.

No differences were observed for length.

4. Discussion

In the literature, there is no consensus about the definition of EUGR. For this reason, the results of the available studies are difficult to compare.

Regarding the cross-sectional definition, many studies available in the literature differ for population and time.

Applying the definition of EUGR as weight below the 10th centile at discharge, we estimated a prevalence of 74% of neonates with GA < 30 weeks, and 93% of neonates with GA ≥ 30 weeks and birthweight ≤ 1500 g. Our data are quite different with respect to the previous results described in literature; however, Clark et al. [1], Radmacher et al. [22], and Karagol et al. [23] analyzed significantly different populations. In particular, Clark et al. reported 28% of EUGR in a population of infants with birthweight < 2000 g and GA ≤ 34 weeks, Radmacher et al. [22] found a proportion of 59% in a population of newborns with birthweight < 750 g and GA < 29 weeks, and Karagol et al. reported 17% in population of non-SGA babies with birthweight between 750 g and 1250 g [23].

According to the definition of EUGR as weight below the 10th centile at 36 weeks of GA, we classified as EUGR 83% of infants with GA < 30 weeks, and 98% of newborns with GA≥30 weeks and birthweight ≤ 1500 g. Our results are in agreement with the data reported by Lemons et al. [24], who observed that 97% of VLBW newborns with GA ≤ 30 weeks presented EUGR.

Applying a different definition of EUGR, characterized as weight at 28 days of postnatal life below the 10th centile, we found a prevalence of 53% of EUGR in infants with GA < 30 weeks, and 89% in newborns with GA ≥ 30 weeks and birthweight ≤ 1500 g. Our data agree with the results reported by Martin et al. [25], who estimated a EUGR proportion of 75% in a population of newborns with GA < 28 weeks. On the other hand, Karagol et al. [23] estimated a EUGR prevalence of only 26%, although in a population of non-SGA babies with birthweight between 750 g and 1250 g.

Regarding the longitudinal definition, in the literature, there are many studies that differ not only for population, but also for the choice of ∆SDS threshold.

In our study, we defined the EUGR as the loss of 1SD between birth and discharge and 92% of newborns with GA < 30 weeks, and 55% of babies with GA ≥ 30 weeks and birthweight ≤ 1500 g was classified as EUGR. Franz et al. [26] defined EUGR as loss of 1SD from birth to discharge and estimated 50% of EUGR in a population of VLBW with GA < 26 weeks.

Marks et al. [27], Shlomai et al. [2], and Roggero et al. [28] defined EUGR as loss of 2SD from birth to discharge. They applied it to a population of VLBW newborns [2,27] and to a population of VLBW and AGA newborns [28], observing 10.6%, 5.2%, and 13% of EUGR, respectively.

Concerning the four times considered, each one of them presents advantages and disadvantages. The time of discharge depends on different criteria and often varies among the Neonatal Units and even among physicians of the same Unit. However, this time is often used because it is considered a proxy of the clinical stability of patient. The reliability of times of 36 and 40 weeks of GA depend on the gestational age at birth, and, when the GA at birth is too close to 36 or 40 weeks, the physiologic weight loss could be confused with EUGR. The time of 28 days of postnatal life does not depend on GA at birth and it is equidistant from birth for all neonates; however, the late preterm babies are likely to be discharged before this time.

Using different definitions of EUGR has several clinical implications. The cross-sectional way is an evaluation that does not consider what happened between birth and the t-time. The longitudinal assessment instead reflects changes from birth to a defined t-time. Additionally, for the longitudinal assessment, it is important to choose the right cut-off value to define EUGR (usually, weight loss of 1SD or 2SD) because the probability of exceeding it depends on birthweight: the lower the birthweight centile, the lower the probability to lose 1 or 2 SD. For this reason, and considering the large amount of SGA in our Neonatal Intensive Care Unit, we have chosen weight loss of 1SD as a cut-off of the longitudinal assessment.

The benefit of a harmonized definition of EUGR is of the use of this measure in clinical practice for identifying babies with high risk of long-term auxological or neurological negative outcomes [8,9,10,11,12,13,14,15,16].

The analysis of the auxological outcome at two years shows that, on average, our study population is lighter and shorter and has a lower head circumference with respect to the CDC-target population at the same age. This means that a delay in growth is experienced between birth and 24–30 months. Similar findings are reported in the literature [29,30,31,32].

When Population A (GA at birth < 30 weeks) and Population B (GA at birth ≥ 30 weeks and VLBW) were considered separately, centile crossing down was observed for all three auxological variables in Population A. In population B, weight centile crossing down (lower than in Population A) was observed; however, head centile crossing up and an almost length centile tracking was observed. This is probably due to GA, which is known to affect the postnatal growth more than other conditions [30,31].

The longitudinal definition of EUGR (contrary to the cross-sectional one) was predictive of growth at 24–30 months, showing that the EUGR babies have a higher delay of growth than non-EUGR ones.

Regarding head circumference at 24–30 months, on average, it is of higher centiles than at birth. Additionally, in this case, only the longitudinal assessment of EUGR was predictive of the outcome, showing that, on average, the gain is higher in non-EUGR than in EUGR group. Based on the data reported in our study, we suggest to use the longitudinal definition of EUGR as a better predictor of the auxological long term-outcome. The t-time of choice in our clinical practice is “at discharge” due to the high concordance between operators in the discharge criteria.

The present study has limitations inherent to an observational study with retrospective collected data. For this reason, not all variables are available for all subjects at all the t-times considered. Moreover, even if the sample size is quite large, our study is monocentric. Since this is a single center study, the generalization of results to other centers is limited. On the other hand, the homogeneity of samples from a single center may strengthen the validity of the data. Future research should be designed as prospective, multi-center studies, in order to clarify the discrepancy in results across centers.

5. Conclusions

In conclusion, the low agreement between cross-sectional and longitudinal definitions of EUGR is likely due to the fact that they measure different aspects of the growth. For this reason, it is necessary to have a clear and harmonized definition of EUGR allowing to compare different clinical strategies and nutritional care of preterm infants during hospitalization in Neonatal Intensive Care Unit. This definition should be an indicator useful to clinicians in their everyday practice. Based on the results of this study, we recommend the use of the longitudinal evaluation, which proved to better predict the auxological long-term outcome with respect to the cross-sectional one.

Author Contributions

Conceptualization, C.P. and A.C.; methodology, E.S.; software, E.S.; formal analysis, E.S.; investigation, C.P., M.R.; data curation, C.P., G.M. and M.R.; writing—original draft preparation, C.P., E.S., M.R., F.G., and A.C.; writing—review and editing, C.P., E.S., F.C., F.G., E.B. and A.C.; supervision, E.B. and A.C.; C.P. and E.S. revised the paper according to the reviews requires. All authors have read and agreed to the published version of the manuscript.

Funding

The authors declare that they have not received funding for the paper.

Conflicts of Interest

The authors declare that they have no competing interests.

References

  • 1.Clark R.H., Thomas P., Peabody J. Extrauterine Growth Restriction Remains a Serious Problem in Prematurely Born Neonates. Pediatrics. 2003;111:986–990. doi: 10.1542/peds.111.5.986. [DOI] [PubMed] [Google Scholar]
  • 2.Ofek Shlomai N., Reichman B., Lerner-Geva L., Boyko V., Bar-Oz B. Population-based study shows improved postnatal growth in preterm very-low-birthweight infants between 1995 and 2010. Acta Paediatr. 2014;103:498–503. doi: 10.1111/apa.12569. [DOI] [PubMed] [Google Scholar]
  • 3.Griffin I.J., Tancredi D.J., Bertino E., Lee H.C., Profit J. Postnatal growth failure in very low birthweight infants born between 2005 and 2012. Arch. Dis. Child.-Fetal Neonatal Ed. 2016;101:F50–F55. doi: 10.1136/archdischild-2014-308095. [DOI] [PubMed] [Google Scholar]
  • 4.Shan H.M., Cai W., Cao Y., Fang B.H., Feng Y. Extrauterine growth retardation in premature infants in Shanghai: A multicenter retrospective review. Eur. J. Pediatr. 2009;168:1055–1059. doi: 10.1007/s00431-008-0885-9. [DOI] [PubMed] [Google Scholar]
  • 5.Ruth V.A. Extrauterine growth restriction: A review of the literature. Neonatal Netw. 2008;27:177–184. doi: 10.1891/0730-0832.27.3.177. [DOI] [PubMed] [Google Scholar]
  • 6.Martínez-Jiménez M.D., Gómez-García F.J., Gil-Campos M., Pérez-Navero J.L. Comorbidities in childhood associated with extrauterine growth restriction in preterm infants: A scoping review. Eur. J. Pediatr. 2020 doi: 10.1007/s00431-020-03613-8. [DOI] [PubMed] [Google Scholar]
  • 7.Leppänen M., Lapinleimu H., Lind A., Matomäki J., Lehtonen L., Haataja L., Rautava P., PIPARI Study Group Antenatal and postnatal growth and 5-year cognitive outcome in very preterm infants. Pediatrics. 2014;133:63–70. doi: 10.1542/peds.2013-1187. [DOI] [PubMed] [Google Scholar]
  • 8.Pampanini V., Boiani A., De Marchis C., Giacomozzi C., Navas R., Agostino R., Dini F., Ghirri P., Cianfarani S. Preterm infants with severe extrauterine growth retardation (EUGR) are at high risk of growth impairment during childhood. Eur. J. Pediatr. 2015;174:33–41. doi: 10.1007/s00431-014-2361-z. [DOI] [PubMed] [Google Scholar]
  • 9.Chien H.C., Chen C.H., Wang T.M., Hsu Y.C., Lin M.C. Neurodevelopmental outcomes of infants with very low birth weights are associated with the severity of their extra-uterine growth retardation. Pediatr. Neonatol. 2018;59:168–175. doi: 10.1016/j.pedneo.2017.08.003. [DOI] [PubMed] [Google Scholar]
  • 10.Frondas-Chauty A., Simon L., Branger B., Gascoin G., Flamant C., Ancel P.Y., Darmaun D., Rozé J.C. Early growth and neurodevelopmental outcome in very preterm infants: Impact of gender. Arch. Dis. Child.-Fetal Neonatal Ed. 2014;99:F366–F372. doi: 10.1136/archdischild-2013-305464. [DOI] [PubMed] [Google Scholar]
  • 11.Ramel S.E., Demerath E.W., Gray H.L., Younge N., Boys C., Georgieff M.K. The relationship of poor linear growth velocity with neonatal illness and two-year neurodevelopment in preterm infants. Neonatology. 2012;102:19–24. doi: 10.1159/000336127. [DOI] [PubMed] [Google Scholar]
  • 12.Ehrenkranz R.A., Dusick A.M., Vohr B.R., Wright L.L., Wrage L.A., Poole W.K. Growth in the neonatal intensive care unit influences neurodevelopmental and growth outcomes of extremely low birth weight infants. Pediatrics. 2006;117:1253–1261. doi: 10.1542/peds.2005-1368. [DOI] [PubMed] [Google Scholar]
  • 13.Latal-Hajnal B., von Siebenthal K., Kovari H., Bucher H.U., Largo R.H. Postnatal growth in VLBW infants: Significant association with neurodevelopmental outcome. J. Pediatr. 2003;143:163–170. doi: 10.1067/S0022-3476(03)00243-9. [DOI] [PubMed] [Google Scholar]
  • 14.Casey P.H., Whiteside-Mansell L., Barrett K., Bradley R.H., Gargus R. Impact of prenatal and/or postnatal growth problems in low birth weight preterm infants on school-age outcomes: An 8-year longitudinal evaluation. Pediatrics. 2006;118:1078–1086. doi: 10.1542/peds.2006-0361. [DOI] [PubMed] [Google Scholar]
  • 15.Hsu C.T., Chen C.H., Lin M.C., Wang T.M., Hsu Y.C. Post-discharge body weight and neurodevelopmental outcomes among very low birth weight infants in Taiwan: A nationwide cohort study. PLoS ONE. 2018;13:e0192574. doi: 10.1371/journal.pone.0198310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Li Y., Shah M., Miller M.R., Lee D.S.C., Sharan S. Impact of Early Postnatal Weight Gain on Retinopathy of Prematurity in Very Preterm Infants in Southwestern Ontario. J. Pediatr. Ophthalmol. Strabismus. 2019;56:168–172. doi: 10.3928/01913913-20190208-01. [DOI] [PubMed] [Google Scholar]
  • 17.Finken M.J., Dekker F.W., de Zegher F., Wit J.M. Dutch Project on Preterm and Small-for-Gestational-Age-19 Collaborative Study Group. Long-term height gain of prematurely born children with neonatal growth restraint: Parallellism with the growth pattern of short children born small for gestational age. Pediatrics. 2006;118:640–643. doi: 10.1542/peds.2006-0103. [DOI] [PubMed] [Google Scholar]
  • 18.Bertino E., Di Nicola P., Occhi L., Prandi G., Gilli G. Causes of postnatal growth failure in preterm infants. In: Griffin I.J., editor. Perinatal Growth and Nutrition. CRC Press; New York, NY, USA: 2014. pp. 41–60. [Google Scholar]
  • 19.Vermont Oxford Network Manual of Operations: Part 2. [(accessed on 26 April 2020)]; Available online: https://vtoxford.zendesk.com/hc/en-us/articles/360013115393-2019-Manual-of-Operations-Part-2-Release-23-2-PDF-
  • 20.Bertino E., Spada E., Occhi L., Coscia A., Giuliani F., Gagliardi L., Gilli G., Bona G., Fabris C., De Curtis M., et al. Neonatal anthropometric charts: The Italian neonatal study compared with other European studies. J. Pediatr. Gastroenterol. Nutr. 2010;51:353–361. doi: 10.1097/MPG.0b013e3181da213e. [DOI] [PubMed] [Google Scholar]
  • 21.Kuczmarski R.J., Ogden C.L., Guo S.S., Grummer-Strawn L.M., Flegal K.M., Mei Z., Wei R., Curtin L.R., Roche A.F., Johnson C.L. 2000 CDC growth charts for the United States: Methods and development. National Center for Health Statistics. Vital Health Stat. 2002;11:1–190. [PubMed] [Google Scholar]
  • 22.Radmacher P.G., Looney S.W., Rafail S.T., Adamkin D.H. Prediction of extrauterine growth retardation (EUGR) in VLBW infants. J. Perinatol. 2003;23:392–395. doi: 10.1038/sj.jp.7210947. [DOI] [PubMed] [Google Scholar]
  • 23.Karagol B.S., Zenciroglu A., Okumus N., Polin R.A. Randomized Controlled Trial of Slow vs Rapid Enteral Feeding Advancements on the Clinical Outcomes of Preterm Infants With Birth Weight 750–1250 g. J. Parenter. Enteral Nutr. 2013;37:223–228. doi: 10.1177/0148607112449482. [DOI] [PubMed] [Google Scholar]
  • 24.Lemons J.A., Bauer C.R., Oh W., Korones S.B., Papile L.A., Stoll B.J., Verter J., Temprosa M., Wright L.L., Ehrenkranz R.A., et al. Very low birth weight outcomes of the National Institute of Child health and human development neonatal research network, January 1995 through December 1996. NICHD Neonatal Research Network. Pediatrics. 2001;107:e1–e2. doi: 10.1542/peds.107.1.e1. [DOI] [PubMed] [Google Scholar]
  • 25.Martin C.R., Brown Y.F., Ehrenkranz R.A., O’Shea T.M., Allred E.N., Belfort M.B., McCormick M.C., Leviton A. Extremely Low Gestational Age Newborns Study Investigators. Nutritional practices and growth velocity in the first month of life in extremely premature infants. Pediatrics. 2009;124:649–657. doi: 10.1542/peds.2008-3258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Franz A.R., Pohlandt F., Bode H., Mihatsch W.A., Sander S., Kron M., Steinmacher J. Intrauterine, early neonatal, and postdischarge growth and neurodevelopmental outcome at 5.4 years in extremely preterm infants after intensive neonatal nutritional support. Pediatrics. 2009;123:e101–e109. doi: 10.1542/peds.2008-1352. [DOI] [PubMed] [Google Scholar]
  • 27.Marks K.A., Reichman B., Lusky A., Zmora E. Israel Neonatal Network. Fetal growth and postnatal growth failure in very-low-birthweight infants. Acta Paediatr. 2006;95:236–242. doi: 10.1111/j.1651-2227.2006.tb02213.x. [DOI] [PubMed] [Google Scholar]
  • 28.Roggero P., Gianni M.L., Orsi A., Amato O., Piemontese P., Liotto N., Morlacchi L., Taroni F., Garavaglia E., Bracco B., et al. Implementation of nutritional strategies decreases postnatal growth restriction in preterm infants. PLoS ONE. 2012;7:e51166. doi: 10.1371/journal.pone.0051166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Bertino E., Coscia A., Mombro M., Boni L., Rossetti G., Fabris C., Spada E., Milani S. Postnatal weight increase and growth velocity of very low birthweight infants. Arch. Dis. Child.-Fetal Neonatal Ed. 2006;91:F349–F356. doi: 10.1136/adc.2005.090993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Bertino E., Coscia A., Boni L., Rossi C., Martano C., Giuliani F., Fabris C., Spada E., Zolin A., Milani S. Weight growth velocity of very low birth weight infants: Role of gender, gestational age and major morbidities. Early Hum. Dev. 2009;85:339–347. doi: 10.1016/j.earlhumdev.2008.12.014. [DOI] [PubMed] [Google Scholar]
  • 31.Cole T.J., Statnikov Y., Santhakumaran S., Pan H., Modi N., On behalf of the Neonatal Data Analysis Unit and the Preterm Growth Investigator Group Birth weight and longitudinal growth in infants born below 32 weeks’ gestation: A UK population study. Arch. Dis. Child.-Fetal Neonatal Ed. 2014;99:F34–F40. doi: 10.1136/archdischild-2012-303536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Bonnar K., Fraser D. Extrauterine Growth Restriction in Low Birth Weight Infants. Neonatal Netw. 2019;38:27–33. doi: 10.1891/0730-0832.38.1.27. [DOI] [PubMed] [Google Scholar]

Articles from Nutrients are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES