Childs Nerv Syst (2015) 31:2333–2340 DOI 10.1007/s00381-015-2905-1 ORIGINAL PAPER Posture and movement in very preterm infants at term age in and outside the nest M. Zahed 1 & J. Berbis 1 & V. Brevaut-Malaty 1 & M. Busuttil 1 & B. Tosello 1 & C. Gire 1 Received: 24 August 2015 / Accepted: 1 September 2015 / Published online: 5 October 2015 # Springer-Verlag Berlin Heidelberg 2015 Abstract Objective The objective of this study is to evaluate the use of nests on general movements (GM) and posture in very preterm infants at term age. Method Seventeen high-risk preterm infants—less than 30 weeks of gestation (GA)—underwent a video recording, lying in supine position, with or without nest. Posture, GM quality, and movements made around the child’s midline, as well as abrupt movements and frozen postures—in extension or flexion of the four limbs—were analyzed. Results Nest did not modify quality of GM. Children significantly adopted a curled-up position. The nest system was associated with an increase in movements toward or across the midline, as well as reduction of the hyperextension posture and head rotation movements. Frozen postures in flexion or extension, as well as abrupt movements of the four limbs, were reduced but not significantly. * M. Zahed [email protected] J. Berbis [email protected] V. Brevaut-Malaty [email protected] M. Busuttil [email protected] B. Tosello [email protected] C. Gire [email protected] 1 Aix Marseille University, Hospital Nord, Department of Neonatology, Chemin des Bourrely, Marseille 13015, France Conclusions Nest helps very preterm infants to adopt semiflexed posture and facilitates movements across the midline and reduces movements of spine hyperextension, without GM global quality modifications. Keywords Preterm infants . Installation . Nest . Posture . Spontaneous motor activity Introduction Very preterm infants are at risk of developing cognitive, motor, and behavioral impairments [1]. A recent Cochrane review [2], focused on quite heterogeneous intervention programs, has reported a positive influence on cognitive and motor development up to preschool age. Children are generally placed in nests with their four limbs semi-flexed, adducted in intensive care units (ICUs), to limit environmental stimuli and stress and also to reduce orthopedic malformations as part of an individualized program of developmental care (Newborn Individualized Developmental Care and Assessment Program (NIDCAP)) [3]. Several studies have focused on preterm infants’ motor behavior and posture in nests—in ICUs—and have demonstrated that posture improvement, in the nest, has beneficial effects on the preterm infants’ motor behavior [4, 5]. There is only one study analyzing nest’s effect on healthy very preterm infants’ spontaneous motricity and posture [6]. The aim is to put forward the efficiency of nests, recommended by neonatology units during hospitalization, and, depending on the team, on very preterm (under 30 WA) motor risks and the association of added comorbidity. The first hypothesis was that, apart from endogenous spontaneous motor activity, some aspects of the preterm infants’ motor behavior could be improved when these children were 2334 placed in a nest after they have left the hospital. By removing passive constraints, the nest should favor a midline children’s head position, four-limb flexed posture, and limit abrupt arm extension movements and movements triggering the Moro reflex. If motor behavior is improved, we could implement this system for discharge from hospital until voluntary movements appear, especially in high-risk preterm infants, in order to assure a global posture support [7, 8]. But, the question about which rhythm, and in addition to which support, is still open; another study, to evaluate the after checkout, is required. Thus, this study sought to evaluate the effect of a preformed nest called BCocoonababy^ on the posture and motor behavior of very preterm infants (<30 GA, before leaving hospital). What we add, with this article, is that being placed in a nest reduces abrupt movements, facilitates elegant wrist movements and movements toward and across the midline, and promotes a flexed and adducted posture of the limbs, for healthy and none healthy preterm infant. Material and methods Material The preterm infants included were children whose term age was strictly 30 GA, or under, but over 24 GA; this is a highrisk population. They were out of the incubator; aged at least 37 GA at the time of video recording; had neither gene syndrome, progressive neurologic disease, nor malformative pathology; and whose parents or legal guardians had agreed to the children’s participation in this study and had signed an informed consent. The non-inclusion criteria were as follows: children born at a term age strictly over 30 GA, with a gene syndrome, progressive neurological disease, or malformative pathology; who did not undergo a brain MRI; who were aged under 37 GA at the time of video recording; and whose parents or legal guardians had refused to let their children take part in the study. This data helps us to describe the population and shows that there are some infants with high risk. Perinatal morbidity items described in the spreadsheet 1 are the following: CLD item was associated to all children in need of a ventilatory support at 36 GA (corrected age). Patent ductus arteriosus (PDA) was defined by a significant arterial canal persistence, in terms of hemodynamics, after 1 week of life. Necrotizing enterocolitis (NEC) was defined by an enterocolitis appearance, with a clinical symptomatology and a radiological image suggestive of pneumatosis. Childs Nerv Syst (2015) 31:2333–2340 The MRI examination was performed as usual, as we proceed in the current care unit with all the preterm infant under 30 GA, without sedation (after bottle-feeding), between 36 and 41 WG, by means of conventional T1-and T2-weighted sequences, T2 gradient echo sequence, and diffusion sequence (b 0, 500, 1000). The preterm infants’ lesions were classified based on Paneth’s model, according to their anatomical distribution. MRI results were divided into two severity stages: group I with normal MRI or moderate abnormalities (types 1, 2, 3, and 4) and group II with severe abnormalities (types 5 and 6) [9]. Methods This was a prospective single-center study, during which each child acted as his own control (when placed or not in the Cocoonababy). The children were recruited in the study by the neonatology department. The physician in charge of recruitment was responsible for explaining to the newborn’s parents or legal guardians the study. The study was granted authorization by the Comité de protection des personnes Sud Méditerranée, regional research ethics committee. The cocoon is a shell-shaped or circle foam device, depending on each units, which will be placed in the child’s incubator or bed; it is very often used in neonatal units for the comfort of the newborn (NIDCAP). In our study, each nest system was then adapted to the child, by adjusting the height of the wedge and position of the top of the child’s head, which should be placed three fingerbreadths from the top of the nest. Two sizes were available: a small and medium one (sizes 1 and 2, respectively) depending on the size of the child about to be filmed (Fig. 1). Video recordings for each patient were taken at term age, 20 min in the Cocoonababy nest, and then 20 min outside the nest. The camera was placed on a stand, directly above the child’s bed, and recordings were carried out without touching the baby or seeking to catch the baby’s attention. Each video recording was performed with quiet children, with no soother, and outside periods of crying or eating. Preterm infants were filmed in supine position, undressed, but in a room with pleasant temperature. An observer was present, though hidden, in order to ensure the children’s safety, as well as compliance with the above-mentioned conditions. These recordings were viewed by two separate operators, both trained in Prechtl’s method [10]. GM was assessed on a qualitative and semi-quantitative basis [11]. The Bwrithing movements^ (WM) were qualitatively classified as Bnormal, ^ Bcramped synchronized,^ Bhypokinetic,^ Bpoor repertoire,^ or Bchaotic.^ They were then classified on a semi-quantitative basis, the analyzed parameters being movement fluidity and amplitude, time and space variation, and movement speed [12]. Interoperator agreement was 0.90. There is no order for random with nest or without. Childs Nerv Syst (2015) 31:2333–2340 2335 was also assessed. The outcome was evaluated by an age and stage questionnaire. Statistics Fig. 1 Cocoonababy® Posture was defined as a cessation of movement for at least 10 s. Posture was analyzed at rest, before, or after a spontaneous movement. Out of four postures determined for each child, we kept the most physiological or natural one. The rating grid used ranged from 0 to 17 (Table 5) [6]. The following joints were observed: neck, shoulders, elbows, hips, and knees. Depending on their location in space (flexion, semi-flexion, extension, abduction, adduction, or neutral), these joints were assigned 0, 1, or 2 points. The closer the posture score was to 0, the more the child was in a physiological fetal position. Finally, we analyzed whether there were normal or abnormal movements when the children were placed in supine position, flat on their backs, and then when placed in the Cocoonababy. Its aim was to observe whether there were more movements around the children’s midline inside the nest system (head rotation, hand-to-mouth contact, hand-to-head contact, hand-to-foot contact, and foot-to-foot contact), as well as whether abnormal movements, such as abrupt movements and four-limb frozen postures in extension and flexion, were reduced inside the nest (Tables 5 and 6) [6]. This assessment was qualitative. We regrouped the total of different normal and abnormal movements noted at the time of assessment and assessed them on a semi-quantitative basis. The Cocoonababy’s effect on the pattern of spine hyperextension Data analysis was performed using SPSS software (Version 17.0). A descriptive analysis of the clinical variables, available with the inclusion of the whole sample, was carried out. Qualitative variables were expressed as proportions, while quantitative variables were given using the central tendency characteristics (mean and standard deviation). A comparative analysis was performed between both groups with and without the Cocoonababy nest, using non-parametric tests for paired samples: McNemar’s chi-squared test for qualitative variables or Wilcoxon’s test for quantitative variable. The test significance threshold was set at 0.05. To help interpret the differences in the quantitative variable mean scores’ clinical significance (WM score; mean posture; movement around the midline; four-limb abrupt movements; four-limb frozen flexion-extension), effect sizes were calculated in absolute value by dividing the difference between the mean score of the Bwith nest^ group and the mean score of the Bwithout nest^ group, by the without nest group’s standard deviation. We considered an effect size of 0.2 to 0.49 as Bsmall,^ 0.5 to 0.79 as Bmedium,^ and 0.8 or higher as Blarge.^ Results Population: Table 1 The study population comprised 17 very preterm infants, who were treated in the neonatology department and whose mean hospitalization length was 104.7 days (±63.1). Mean age was 27 GA + 5 days (±1.75), and mean weight was 1024.9 g (±237.1). Of the 17 children, five (30 %) displayed a development delayed and ten (60 %) had MRI grade II. Population characteristics are provided in Table 1. Spontaneous motor activity analysis inside and outside the nest When observed lying flat on their bed, 3 out of the 17 babies from the group showed a chaotic repertoire (17 %), 1 cramped synchronized movement (6 %), 2 a poor repertoire (12 %), and 11 babies displayed a normal repertoire (65 %). When the Cocoonababy nest was used, five babies from the group showed a poor repertoire (29 %) and 12 a normal one (71 %). 2336 Table 1 Childs Nerv Syst (2015) 31:2333–2340 Characteristics of the study population Baby number GA BW (g) Number of NI CLD NEC PDA MRI Length of hospitalization (days) DD Baby 1 29+2 days 1005 5 Yes No Yes II 140 Yes Baby 2 29+5 days 1130 0 No No No I 330 No Baby 3 Baby 4 27+4 days 26+4 days 1100 965 3 2 Yes Yes Yes No Yes Yes II I 103 113 Yes No Baby 5 Baby 6 25+1 day 28+1 day 880 1010 1 0 Yes No No No Yes No II I 113 70 No No Baby 7 27+0 day 850 3 Yes Yes No I 85 No Baby 8 Baby 9 24+4 day 28+1 day 650 1000 2 1 Yes Yes No No Yes No II I 119 49 Yes No Baby 10 Baby 11 29+4 days 24+0 day 1284 750 0 3 No No No No No No II II 97 119 Yes Yes Baby 12 30+0 day 1330 0 No No No I 32 No Baby 13 Baby 14 29+2 days 27+6 days 1550 1120 2 1 Yes No No No Yes Yes I II 96 81 No No Baby 15 Baby 16 28+0 day 27+6 days 720 1230 3 1 Yes Yes Yes No No Yes II II 94 91 No No Baby 17 26+4 days 850 1 Yes Yes No II 111 No GA gestational age, BW birth weight, NI nosocomial infection, CLD bronchopulmonary dysplasia at 36 WG, NEC necrotizing enterocolitis, PDA patent ductus arteriosus, MRI magnetic resonance imaging, severity stage, DD delayed walking or delayed development at 2 years The chaotic repertoire or cramped synchronized movements which were observed outside the nest in four preterm infants from this population disappeared inside the nest system. The mean spontaneous motor activity’s semi-quantitative score of the 17 preterm infants inside the nest was 14.94 (±3.61), as against 14.12 (±3.72) outside the nest, which means it had slightly improved by 0.8 points but without significant (p=0.008). The Cocoonababy did not significantly affect the overall interpretation of GM, whether the analysis was qualitative or semi-quantitative (Table 2). system, 14 babies from the cohort (82 %) obtained a score higher than 5, while with the nest, only 1 had such a score (5.9 %) (p < 0.001). With the nest, the mean score was 2.47 (±2.21) as against 8.12 (±4.03) without it (p<0.001). The nest system enabled the children to adopt a curled-up position (score close to 0). Their shoulders and hips were more flexed, adducted, and their elbows and knees more bent. Posture analysis inside and outside the nest: Table 2 There was an increase in movements toward or across the midline when the child was placed in the nest system. Children made a mean of four movements when placed outside the nest, as against 5.6 inside of The Cocoonababy nest had a significant effect on the children’s postural behavior values. Without the nest Table 2 Posture analysis inside and outside the nest Analysis of normal and abnormal movements inside and outside the nest: Table 3 Writhing movements Without the nest (n=17) With the nest (n=17) Abnormal repertoire Chaotic repertoire Cramped synchronized Poor repertoire Mean WM score Mean posture 6 (35 %) 3 1 2 14.94 (±3.61) 8.12 (±4.03) 5 (29 %) 0 0 5 14.12 (±3.72) 2.47 (±2.21) Z value (Wilcoxon’s test) p value 1 −2.585 −3.520 0.008 <0.001 Childs Nerv Syst (2015) 31:2333–2340 Table 3 2337 Analysis of normal and abnormal movements inside and outside the nest Without the nest (n=17) With the nest (n=17) Z value (Wilcoxon’s test) p value Movement around the midline [10] 4.00 (±1.94) 5.65 (±1.46) −3.336 <0.001 Abrupt movements of the four limbs [4] 0.88 (±1.22) 0.65 (±0.86) −1.100 0.08 Frozen flexion-extension of the four limbs [4] 0.59 (±0.80) 0.18 (±0.39) −2.333 0.03 Effect size: WM 0.22, posture 2.56, midline 0.85, abrupt 0.19, frozen 0.5 it, the difference being statistically significant (p < 0.001). Furthermore, without the nest, nine babies adopted a pattern of spine hyperextension (53 %), while only two babies displayed such a pattern (12 %) once they were placed in the nest system. The Cocoonababy nest, therefore, significantly enabled seven children not to adopt the hyperextension posture (p=0.016). It also promoted a reduction in frozen postures, in flexion or extension (0.18 inside vs. 0.59 outside the nest; p=0.031). The test was at the threshold of significance. Four-limb abrupt movements decreased by 0.15 points, though the difference was not significant. Description of the most frequently observed normal movements when using Cocoonababy (Table 4) The proportion of children exhibiting hand-to-leg or foot-to-foot contact was significantly increased inside the cocoon. Placement in the nest also resulted in more hand-to-head contact movements; the difference is approaching significancy. On the other hand, movements of 180° head rotation appeared to be significantly limited by the nest (p=0.05). Discussion Nest and posture Although already demonstrated in other research work [6, 7], this study showed that the nest significantly imTable 4 Influence of the nest on normal movements Normal movements Hand-to-leg contact Foot-to-foot contact Hand-to-head contact 180° head rotation *Significant; p<0.05 proves posture. Children placed in the Cocoonababy nest adopted a more curled-up position and were less subject to the gravity force. Their joints were bent, so muscle, tendon, and bone structures could develop more harmoniously. Hyperextension patterns were also less frequent inside the nest, which enabled an overall balance between extensor and flexor muscles. The Cocoonababy nest, therefore, makes it possible for children, who are in a more physiological position, to promote some movements around the midline. Nest and GM General movement did not seem to be improved by the nest system, but only modified. The cramped synchronized and chaotic movements were no longer observed in the nest but transformed into poor repertoire. This change in the neurological examination could also be accounted for by the fact that some movements were enabled around the midline, as well as by the decreased number of four-limb abrupt movements, spine hyperextension, and frozen postures in flexion or extension. Head rotation, however, seemed to be reduced by the Cocoonababy system, contrary to other systems. Only few studies which have focused on the nest’s direct effects on the spontaneous motor activity of preterm infants, who are close to term age, or on its potential consequences for the children’s future development are available. Slevin et al. [14] investigated the effect of the placement in a nest on reducing retinopathy in children lying in a nest during their ICU stay. De Graff [7] evaluated Without the nest [13] With the nest [13] p value 3/17 (18 %) 15/17 (88 %) <0.001 8/17 (47 %) 11/17 (65 %) 8/17 (47 %) 14/17 (82 %) 16/17 (94 %) 2/17 (12 %) 0.03* 0.063 0.07 2338 the immediate effects of identical Bnest^ systems at 1 and 5 months post-term in term newborns. The author found that the nest support did not affect movement quality but could promote some movements, especially in the event of minor abnormalities. This was so in our study during which movements made around the midline were allowed. It should be noted that our study population was high-risk preterm infants with 41 % brain MRI considered grade II. Overall, five children exhibited a delayed development. In our study, there were fewer abrupt movements at term age, but the decrease was not significant, except for spine hyperextension. On the other hand, frozen postures were almost significantly reduced, while movements made around the midline were promoted. In this curled-up position, it therefore appeared that the children were able to touch their head, legs, and feet more significantly. The nest system, therefore, improved movement complexity. Similarly, some stressful movements, such as abrupt movements and frozen postures in flexion or extension, seemed to be reduced. Nest and abnormal movement It seems that placing infants in the nest promotes complexity and variation in spontaneous motor activity, while reducing some abnormal movements at term age. In this way, the nest could have an impact on future motor and cognitive development at least up to 2 months of corrected age, as suggested by previous studies [13, 15–19]. It is interesting to observe this positive change, toward more physiological pattern, before the hospital checkout, especially with high-risk children, because it is a sensitive sensorimotor period and probably very conducive to early rehabilitation one. In order to reduce some postural and motor deviances, wich sometimes can become permanent failures? Since its present design requires further studies, focuses on the impact of these cocoons’ long-term use after leaving the hospital and probably not as the only support system [7, 8]. Several recent studies have shown that, apart from the analysis of GM at 3 months of corrected age, the automatic assessment, in particular, the stereotypy score of arm movements, was an excellent predictor of CP, whereas stereotyped repetitive movements of the legs predicted no neurodevelopment impairment [17]. Similarly, at 3 months of corrected age, persistence of immature movements like startle response, lateral decumbent position, predominant shoulder rotation, and maintaining hip adduction was more frequently observed in Childs Nerv Syst (2015) 31:2333–2340 case of intellectual disability. Such mature movements like hand sucking, maintaining shoulder abduction, shoulder adduction, elbow flexion, isolated hip adduction, hip abduction, and leg lift were less frequently seen than in the normal preterm [13]. Two other studies, conducted in preterm infants at term age, demonstrated that jerkiness of spontaneous movements at term age provides additional information for prediction of CP [18]. Likewise, spontaneous movements, less active with intermittent occurrences of limbs abrupt and synchronized movements, were associated with psychomotor delays at 3 years [19]. Thus, the improvement of posture and of certain movements affects neurological examination findings, especially in high-risk preterm infants, as in our study population. This improvement of motor behavior could play a role in sensory and nociceptive stimulation with improved central nervous feedback. Movement that promotes sensory exploration can permit the development of synaptic connections, and a functional improvement could, therefore, be favored by this nest system [20, 21]. It was noted that Cocoonababy reduced head rotation movements in our patient population. This result was at the significance threshold (p=0.057). The consequences of such a limitation could lead to an increased rate of plagiocephaly and inhibit eye exploration, which is required to ensure a good future development for the child, as well as being responsible for a delayed development of isolated mature movement of the neck, this being correlated with later psychomotor development, especially when the child remains placed in the nest system for a prolonged period without any other postural guidance [6, 7]. Study limitations All the babies from the neonatology department were placed in a cot system while being moved from the incubator (Bhome nest^) to the bed (Cocoonababy nest). The 20-min recording outside the nest constituted an abrupt, new change for the children to which they had to adapt so as to regain their balance. But, the question about which rhythm, and in addition to which support, is still open; another study, to evaluate the after checkout, is required. Furthermore, the observers were not blinded during the study, which may have led to a subjective bias for the nest effect. Conflict of interest The authors declare no conflict of interest. Childs Nerv Syst (2015) 31:2333–2340 2339 Table 6 (continued) Appendix 1 Table 5 3. Abrupt abduction-extension of the four limbs 4. Abrupt rolling to side frozen postures of the limbs (= abnormal movements) 1. Arms frozen in extension 2. Arms frozen in flexion 3. Legs frozen in extension Items of posture assessment -Shoulder: 0 = adduction (0–20°) 1 = neutral (21–90°) 2 = abduction (>90°) -Elbow: Yes/no Yes/no Yes/no Yes/no Yes/no References 0 = flexion (0–30°) 1 = semi-flexion (31–150°) 1. 2 = extension (>150°) -Hip: 0 = flexion (0–80°) 1 = semi-flexion (81–150°) 2. 2 =extension (>150°) 3. -Knee: 0 = flexion (0–60°) 1 = semi-flexion (61–150°) 2 = extension (>150°) 4. -Asymmetrical neck posture: Absent Present -Head position: 5. 6. 0 = head in the midline (rotation <20°) 1 =head to side (rotation 20–70°) 7. Score from 0 to 17 (the closer the score is to 0, the more the child is in a physiological position) 8. Appendix 2 9. 10. Table 6 Detailed items of general and spontaneous movement assessment Movements around the midline (= normal movements) 1. Head rotation from side to midline 2. Head rotation from side to side 3. Hand-to-mouth contact 4. Hand-to-head contact 5. Opening of the hands 6. Hand-to-hand contact 7. Hand touching contralateral shoulder and trunk 8. Hand-to-leg contact 9. Foot-to-foot contact wrist movements (= normal movements) 1. Rotational movements of the wrists abrupt limb movements (= abnormal movements) 1. Abrupt opening of fingers 2. Abrupt abduction-extension of the arms Yes/no Yes/no Yes/no Yes/no Yes/no Yes/no Yes/no Yes/no Yes/no 11. 12. 13. 14. 15. Yes/no Yes/no Yes/no 16. Larroque B, Breart G, Kaminski M, Dehan M et al (2004) Survival of very preterm infants: Epipage, a population based cohort study. Arch Dis Child Fetal Neonatal Ed 89:F139–F144 Spittle A, Orton J, Anderson P, Boyd R, Doyle LW (2012) Early developmental intervention programmes; The Cochrane Library Issue 12 Westrup B, Von Kleberg A, Eichwald K et al (2000) A randomized controlled trial to evaluate the effects of the newborn individualized developmental care and assessment program in a Swedish setting. Pediatrics 105:66–72 Monterosso L, Kritjanson LJ, Cole J et al (2003) Effect of postural supports on neuromotor function in very preterm infants to term equivalent age. J Pediatr Child Health 39:197–205 Provasi J, Lequien P (1993) Effect of non-rigid reclining infant seat on preterm behavioral states and motor activity. Early Hum Dev 35: 129–140 Ferrari F, Bertoncelli N, Gallo C et al (2007) Posture and movement in healthy preterm infants in supine position in and outside the nest. Arch Dis Child Fetal Neonatal Ed 92:386–390 De Graaf-Peters VB, de Groot–Hornstra AH, Dirks T (2006) Specific postural support promotes variation in motor behaviour of infants with minor neurological dysfunction. Dev Med Child Neurol 48:966–972 Vaivre-douret L, Golse B, Thomas N, Janaud J-C (2009) Favoriser la prévention posturale du nouveau-né prématuré. Soins Pédiatr Puéric 250:35–39 Paneth N, Chair MPH (1999) Classifying brain damage in preterm infants. J Pediatr 134:527–529 Prechtl HFR (1990) Qualitative change of spontaneous movements in fetus and preterm infants are a marker of neurological dysfunction. Early Hum Dev 23:151–158 Ferrari F, Cioni G, Prechtl HFR (1990) Qualitative changes of general movement in preterm infants with brain lesions. Early Hum Dev 23:193–231 Einspieler C, Prechtl HFR, Ferrari F, Cioni G, Arend FBOS (1997) The qualitative assessment of general movements in preterm, term and young infants – review of the methodology. Early Hum Dev 50: 47–60 Kouwaki M, Yokochi M, Togawa Y et al (2014) Spontaneous movements in the supine position of preterm infants with intellectual disability. Brain Dev 36:572–577 Slevin M, Murphy JFA, Daly et al (1997) Retinopathy of prematurity screening, stress related responses, the role of nesting. Br J Ophtalmol 81:762–764 Butcher PR, van Braeckel K, Bouma A et al (2009) The quality of preterm infant’s spontaneous movements: an early indicator of intelligence and behaviour at school age. J Child Psychol Psychiatry 50:920–930 Kodric J, Susteric B, Paro-panjan D (2010) Assessment of general movements and 2,5 year developmental outcomes: pilot results in a diverse preterm group. Eur J Pediatr Neurol 2340 17. 18. 19. Childs Nerv Syst (2015) 31:2333–2340 Philippi H, Karch D, Kang KS, et al (2014) Computer –based analysis of general movements reveals strereotypies predict cerebral palsy. Dev Med Child Neurol 1–7 Kanemaru N, Watanabe H, Kihara H et al (2014) Jerky spontaneous movements at term age in preterm infants who later developed cerebral palsy. Early Hum Dev 90:387–392 Kanemaru N, Watanabe H, Kihara H, et al (2013) Specific characteristics of spontaneous movements in preterm infants at term age are associated with developmental delay at age 3 years. Dev Med Child Neurol 713–721 20. 21. Woollacott M, Sveistrup H, Swinne SP, Massion J, Heur H et al (1994) The development of sensorimotor integration underlying posture control in infants during the transition to independence stance. Interlimb coordination neural dynamical and cognitive constraints. Academic, San Diego, pp 371–389 Inguaggiato E, Sgandurra G, Perazza S, Guzzetta A, Cioni G (2013) Brain reorganization following intervention in children with congenital hemiplegia: a systematic review. Neural Plast 1–8
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