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Efficacy of pediatric integrative manual therapy in positional plagiocephaly: a randomized controlled trial

Abstract

Background

Positional plagiocephaly frequently affects healthy babies. It is hypothesized that manual therapy tailored to pediatrics is more effective in improving plagiocephalic cranial asymmetry than just repositioning and sensory and motor stimulation.

Methods

Thirty-four neurologically healthy subjects aged less than 28 weeks old with a difference of at least 5 mm between cranial diagonal diameters were randomly distributed into 2 groups. For 10 weeks, the pediatric integrative manual therapy (PIMT) group received manual therapy plus a caregiver education program, while the controls received the same education program exclusively. Cranial shape was evaluated using anthropometry; cranial index (CI) and cranial vault asymmetry index (CVAI) were calculated. Parental perception of change was assessed using a visual analogue scale (− 10 cm to + 10 cm).

Results

CVAI presented a greater decrease in PIMT group: 3.72 ± 1.40% compared with 0.34 ± 1.72% in the control group (p = 0.000). CI did not present significant differences between groups. Manual therapy led to a more positive parental perception of cranial changes (manual therapy: 6.66 ± 2.07 cm; control: 4.25 ± 2.31 cm; p = 0.004).

Conclusion

Manual therapy plus a caregiver education program improved CVAI and led to parental satisfaction more effectively than solely a caregiver education program.

Trial registration

Trial registration number: NCT03659032; registration date: September 1, 2018. Retrospectively registered.

Background

Head and neck asymmetries are very common in typical healthy newborns [1]. Within these asymmetries, positional plagiocephaly (PP) is a general term describing cranial distortion from pre- or postnatal forces on the infant head [2, 3]. PP features are asymmetrical occipital flattening, accompanied by anterior displacement of the ear on the same side, parietal protuberance on the opposite side, and often ipsilateral frontal protuberance, with fellow frontal flattening. These characteristics make the head look like a parallelogram when viewed from above [4]. Facial findings can be associated with the condition, but PP does not imply or connote this [5].

Prevalence data are limited and depend on the geographic location. However, the prevalence seems to be high as the best estimations of the presence of PP in infants range from 20 to 40% [6,7,8].

Many intrinsic and extrinsic factors can play a role before, during and after childbirth. Besides being associated with lying supine, the development of plagiocephaly is linked to gestational diabetes [9], male sex [10, 11], maternal age [12], skull circumference [12], prematurity [13], primiparity [10, 11], brachiocephaly [9, 10], intra-uterine constraints [14], prolonged labor [14], multiple births [14], improper fetal position during birth [14], use of obstetrical forceps or a suction cup [15], lengthy hospital stay [16], congenital torticollis [6, 17], head positional preference [10,11,12, 18], infant being awake in a prone position less than 3 times a day [10] and delayed motor milestone acquisition [10].

Although many cases of PP improve over time, scientific evidence suggests that conservative management strategies can safely and effectively minimize the degree of cranial asymmetry [19]. The controlled clinical trial carried out by Van Vlimmeren et al. (2008) is one of the highest quality studies. Those researchers compared an intervention group receiving standardized repositioning and physiotherapy treatment with a control group that received the usual care (parents received a leaflet describing basic preventive measures without further education or instructions to intervene). After the intervention, the ratio of babies with severe PP was significantly lower in the treatment group than in the control group. Their findings suggest that, without intervention, some babies with PP and positional preference could develop severe PP [20]. The results also imply an optimal time framework for the treatment, in which the earlier the intervention, the better the outcomes [19].

The main conservative treatment options for PP are parental education [21,22,23,24,25,26,27], repositioning [23,24,25, 28,29,30], physiotherapy [20, 28, 31,32,33] and orthotic helmet therapy [26, 29, 34,35,36].

Only a few studies have analyzed the effect of manual therapy on non-synostosis plagiocephaly [37,38,39]. Most of these studies have been unable to establish a sufficient level of evidence because of the general lack of proper samples sizes, control groups, or randomization.

The objective of this study was to analyze the effectiveness of adding a pediatric manual therapy approach to a caregiver education program in anthropometric cranial measurements and the subjective parental perception of the cranial shape change in infants with PP.

Methods

The Ethics Committee at the Aragon Health Sciences Institute approved recruiting a cohort for this study (Registry No. C.P. - C.I. PI16/0275. Date: October 25, 2017). The study is registered at clinicaltrials.gov, with identification number NCT03659032. Registration date: September 1, 2018.

Subjects

Pediatricians in Section III of the Aragon Health Services referred 34 subjects aged less than 28 weeks having signs of PP. The inclusion criterion was infants with a difference of at least 5 mm between cranial diagonal diameters [40], that is, infants with moderate or severe PP [41]. We excluded infants who had received orthotic treatment, physiotherapy or presented genetic, communicable, metabolic or neurological illness or craniosynostosis.

For the calculation of the sample size, we used non-published data from a previous pilot study with 41 subjects with similar characteristics and who had received a similar manual therapy approach as this present study. This pilot study obtained a decrease of 4,52 ± 2,91% in the cranial vault asymmetry index. The sample size was calculated using the GRANMO calculator (https://www.imim.cat/ofertadeserveis/software-public/granmo/), with the selection of two independent population means, bilateral contrast, with a α risk of 0.05, a ß risk of 0.20 and a ratio of 1 of the number of subjects between the groups. A minimal number of 7 subjects per group was obtained.

Subjects were randomized into 2 groups with a final number of 17 subjects per group. Subjects were randomized following a design generated with the on-line computer application at www.random.org/sequences. The evaluators were blinded to this design.

An informative document about the study was provided to the parents and an informed consent was signed after they had read the document and their questions about the study had been answered. Regulations and guidelines regarding freedom, absence of coercion, disclosure of economic interests, understandable and complete information, confidentiality and acceptance were followed [42].

Measured parameters

Clinical and demographic data were extracted from the medical history and the testimony of the parents: age (weeks), birth weight (gr), sex, prematurity, instrumental delivery, firstborn, multiple birth, head positional preference, pediatrician diagnosis of congenital torticollis, plagiocephaly side, transport type and time that the infant spent in prone position awake and watched at 1 month (min) and at 2 months (min).

The following anthropometric parameters, constituting the dependent study variables, were measured: maximal cranial circumference (MCC) [43], cranial length, cranial width and diagonal cranial diameter taken from the frontozygomatic suture (fz) to the fellow lambdoid suture (lb) [44]. Interrater and intrarater reliability of cranial anthropometric measurements has been previously published [45]. From these data, the next qualifiers were calculated.

Cranial index (CI). The CI was calculated with the formula: “Cranial Width (mm)/Cranial Length (mm) ×100” [24]. Normal range described for CI is between 75 and 85% [44].

Cranial vault asymmetry (CVA). The CVA was calculated with the formula: “Long diagonal cranial diameter (mm) – Short diagonal cranial diameter (mm)” [46]. According to Mortenson & Steinbok, the CVA can be classified into the following categories: normal CVA < 3 mm, mild / moderate CVA ≤ 12 mm, moderate / severe CVA > 12 mm [41].

Cranial vault asymmetry index (CVAI). The CVAI was calculated using the formula “[Long diagonal cranial diameter (mm) – Short diagonal cranial diameter (mm)]/Short diagonal cranial diameter×100” [24]. The classification of the plagiocephaly severity scale (Children’s Healthcare of Atlanta, 2015) [47] is based on the CVAI and it describes the following levels: level 1: < 3.5%; level 2: 3.5 to 6.25%; level 3: 6.25 to 8.75%; level 4: 8.75 to 11.0%; level 5:> 11.0%. CVAI was established as the primary outcome measure.

At the end of the study, the parents were given a visual analogue scale (VAS) to evaluate their perception of head shape change [48]. The parents made a vertical mark on a line graduated from − 10 (much worse) to + 10 (much better) with an intermediate Item 0 (no change).

Intervention

Seventeen subjects received 10 sessions of manual therapy and a caregiver education program, an integrative concept of treatment that will be identified in the manuscript as pediatric integrative manual therapy (PIMT). Each PIMT treatment for remodeling the cranial deformation consisted of:

  • one maneuver to mobilize the neuromeningeal tissue at the lumbosacral level, based on the technique of John E. Upledger [49] but adapted to the pediatric field. Very light traction is induced through the pelvis to stimulate a tissue response. The physiotherapist follows the movements of the baby’s pelvis according to the active movements, trying to move towards increasingly flexed positions.

  • one technique for the cervical spine based on the works of Giammatteo [50]. Very slight traction is applied through the head and the active movement of the head is accompanied to different positions of flexion and extension, lateralization and rotation, stabilizing the atlas gently in a dorsal direction.

  • one technique applying manual pressure to mold the skull base in the opposite direction from the PP torsion on the skull base, based on the work of Arbuckle [51] . The manual pressure was applied to the occipital bone to displace it dorsally, insisting on the flattest area (Fig. 1).

  • two techniques; one to balance the intracranial membranous tension and one molding technique for decompressing coronal suture based on the work of Carreiro [52].

Fig. 1
figure 1

Cranial Base Molding Technique applied in the ;intervention group

This PIMT protocol was applied by several pediatric physical therapists with specialized training and 4 years of experience. The effects of this PIMT treatment in the cervical spine mobility are described in another manuscript previously published [53].

Each manual therapy session was performed once a week with a duration of 20 min.

The caregiver education program consisted of a series of literature-based recommendations [54, 55] that encompassed repositioning, sensory and motor stimulation of the opposite side to the preferred one and prone positions. Parents were instructed with the help of a trained pediatric physiotherapist and an informative booklet about basic recommendations.

The 17 subjects from the control group received solely the same caregiver education program. The control group was convened once during the 10 weeks to monitor the process, listen to their difficulties, resolve their questions and insist on the importance of performing stimulation and repositioning.

Statistical analyses

The Kolmogorov-Smirnov test with the Lilliefors correction was used to test the normality of the distribution of the quantitative variables; the Shapiro-Wilk test was used for this purpose if n < 30. A descriptive analysis of the qualitative variables was carried out, offering the percentages, as well as a descriptive analysis of the quantitative variables, offering the mean ± standard deviation or the median (Q1; Q3) values, depending on whether the distribution of the variables was normal or not, respectively.

If distribution was normal, the Student t-test for independent samples was used for the intergroup comparisons of the dependent pre-intervention variables. The Mann-Whitney U test was used for these comparisons if the distribution was not normal. To compare the intervention effectiveness between the groups, we calculated the improvement indexes of the dependent variables using the difference of the final measurement values minus the baseline measurement values. If the distribution was normal, the improvement indexes were compared using the Student t-test for independent samples; if not, the Mann-Whitney U test was used. The effect size was calculated using Cohen’s d.

Correlation between the improvement index of the CVAI and the VAS reflecting the parental perception of head shape change in the entire sample was analyzed. To do so, the Pearson correlation coefficient was calculated when the variables followed a normal distribution. If the distribution of a variable was not normal, the Spearman Rho coefficient was used.

A confidence interval of 95% was established for the analyses. Statistical significance was set at p < 0.05. The statistical study was performed following the principles of intention-to-treat analysis, without attributing values in the second assessment to the subjects lost to study throughout the intervention.

Results

Study population

A total of 34 subjects were included in the study.Seventeen were assigned to the PIMT group and 17 to the control group (solely caregiver education program). Two subjects were withdrawn from the intervention group, so the final measurement covered 15 subjects in the intervention group and 17 in the control group (Fig. 2). Demographic characteristics were comparable in the 2 groups (Table 1). Anthropometric measurements and head shape were comparable in both groups (Table 2). There were no adverse events with the treatments performed in the study.

Fig. 2
figure 2

Consolidated Standards of Reporting Trial (CONSORT) flow diagram

Table 1 A comparative descriptive analysis of the qualitative variables in the baseline examination.
Table 2 Table describing the homogeneity of the quantitative variables in the baseline examination.

Outcome

The differences between final evaluation and baseline of the anthropometric measurements in the 2 groups are shown in Table 3. The PIMT group showed a statistically significant increase in MCC (2.16 ± 0.69 cm) compared with the control group (1.35 ± 0.75 cm) (p = 0.004). Likewise, there was a significant increase in cranial length in the PIMT group (7.57 ± 2.33 cm) in contrast with the control group (4.25 ± 2.47 cm) (p = 0.001). CVA presented a significantly greater reduction in the PIMT group (− 4.39 ± 1.51 mm) compared with the control group (− 0.11 ± 2,14 mm) (p = 0.000). Our primary outcome, CVAI decreased more in the PIMT group (− 3.72 ± 1.40%) in contrast with the control group (− 0.34 ± 1.72%) (p = 0.000). The CI did not present any statistically significant difference between groups.

Table 3 Table summarizing the variables with descriptive and comparative data on their differences between final values-baseline values.

In the VAS for parental perception of head shape change, the parents of the PIMT group subjects evaluated the change perceived in 6.66 ± 2.07 cm (between − 10 cm and + 10 cm). However, the parents of the control group evaluated the change perceived in 4.25 ± 2.31 cm (p = 0.004).

In the correlation study, the outcomes showed a statistically significant association (Pearson correlation coefficient = − 0.365; p = 0.04) in the entire sample. This association was present between the reduction in CVAI (− 1.92% ± 2.31) and the VAS of head shape change perception (5.38 cm ± 2.49), in the entire sample.

Discussion

In our study, the use of PIMT has been shown to be more effective than solely applying a caregiver education program. The addition of PIMT to a caregiver education program have produced better outcomes in cranial anthropometric values (increased MCC, cranial length and short diagonal cranial diameter and decreased CVA and CVAI) and in parental perception of head shape changes.

The mean gain in MCC, in the 10-week study period, was 2.16 ± 0.69 cm in the PIMT group and 1.35 ± 0.75 cm in the control group. The growth rates observed by Martini et al. (2018) in healthy babies from 4 months to 12 months was an increase of 3.5 ± 8 cm [29]. For Meyer-Marcoti et al. (2018), the total increase of cranial circumference during the first year was 11–13 cm [56]. In their study on a sample of 40 subjects without cranial asymmetry, a mean MCC of 41.38 cm is observed at 4 months, evolving to 43.23 cm at 6 months (1.85 cm of increase). In our 10-week study period, the natural skull growth in both groups is close to physiological values but it is higher in the PIMT group. Consequently, the MCC skull growth data in the PIMT group were closer to the physiological evolution of the skull of a healthy baby in the same time period [56]. The increase in cranial length was also greater in the PIMT group.

The CVA is one of the main cranial indicators to analyze the possible effectiveness of the PIMT protocol used in this population. Kim et al. (2013) found a significant improvement in this parameter using an orthotic treatment. The variable changed from a mean of 13.28 mm ± 3.57 to 6.48 mm ± 1.92 (− 6.8 mm). The control group in this study changed its values to a lesser degree, going from 11.38 mm ± 3.30 to 10.05 mm ± 1.43 (− 1.33 mm) [29]. In our study, the PIMT treatment (with a CVA change of − 4.39 ± 1.51 mm) was significantly better than the control group (− 0.11 ± 2.14) (p = 0.000). The PIMT treatment showed an effectiveness quite similar to orthotic treatments, which are evaluated as the most effective in the literature [29, 57]. Lessard et al. (2011), in a pilot study without a control group on 12 subjects, using a manual intervention, found a significant improvement of − 4.1 mm in the diameter difference [38]. This is close to the outcome in our study.

The cranial index improved in both groups of our study, with no significant differences between them. The predominantly brachiocephalic skull (mainly wide and short) changed towards normal values, without dropping below the limit of 85% that marks the upper limit of the range of normality [24]. In the PIMT group, the CI changed from 88.35 to 87.73%. This was a slightly better improvement than in the control group, which changed from 87.04 to 86.89%. This improvement may be related to the significant improvement in cranial length, a factor needed to balance the CI downwards.

The CVAI improvement was significantly greater in the PIMT group (− 3.72% ± 1.40) than in the control group (− 0.34% ± 1.72) (p = 0.000), with a high size effect (d = 2.16). This variable is the main cranial indicator to analyze the possible effectiveness of the PIMT protocol used in this population. Kim et al. (2013), with a sample of 27 subjects, found a comparable (although somewhat higher) improvement using an orthotic helmet treatment. In this study, the intervention group reduced the CVAI a mean of 5.5%, which was a significant improvement compared with the control group, with a mean reduction of 1.53% [29]. Kluba et al. (2014), with an orthotic helmet intervention, obtained a CVAI reduction of 4.1%, on 128 subjects [57], very close to what we obtained in our study. The studies by di Chiara et al. (2019) [39], Cabrera-Martos et al. (2016) [37] and Lessard et al. (2011) [38], can be considered more similar to our study due to the similarities of the intervention protocol. However, the outcomes in these studies are not comparable with our results because either the CVAI is not measured, or it does not appear with numerical values but with the outcome given in a CVAI severity classification.

Parental perception of head shape change has been one of the variables seen in the literature to assess parents´ satisfaction with the intervention. Naidoo et al. (2015) found that parents whose babies had received helmet treatment were more satisfied than parents whose babies were only indicated repositioning [58]. In our study, the parental perception of improvement in the head shape was better with PIMT in contrast with solely the caregiver education program. In addition, the parental perception of such head shape improvement is related to the CVAI changes in the entire sample.

Our study findings are subject to limitations. The lack of assessments of the skull base asymmetry and of the face constitutes one of them. Including an evaluation of ear position, using a tragus-subnasal measurement with the methodology of Lessard et al. (2011) [38] or Kim et al. (2010) [29], would have made it possible to analyze the change in skull base asymmetry and not just the vault change. Measuring the jaw asymmetry would have increased the evidence available on facial morphology changes obtained using the treatment. Fenton et al. (2018) found a jaw asymmetry in 10% of their sample of subjects with congenital torticollis and PP showing a significant change after 4 months of treatment with physiotherapy [59]. A more exhaustive assessment including facial and skull base measurements is a possible future line of research. It would increase the evidence on the effect of treatments with pediatric manual therapy on cranial base symmetry and on face morphology.

As this study was not a blinded trial, parental perception may have been influenced by the modality of the assigned intervention.

The current lack of a long-term follow-up of our subjects is another limitation. The authors plan to study this in future, by obtaining follow-up data in this research study.

Conclusions

Manual therapy plus a caregiver education program, in a sample of infants with PP, improved CVAI and led to parental satisfaction more effectively than solely a caregiver education program.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

All data generated or analysed during this study are included in this published article.

Abbreviations

CI:

Cranial index

CVA:

Cranial vault asymmetry

CVAI:

Cranial vault asymmetry index

MCC:

Maximal cranial circumference

PIMT:

Pediatric integrative manual therapy

PP:

Positional plagiocephaly

VAS:

Visual analogue scale

References

  1. Stellwagen L, Hubbard E, Chambers C, Jones KL. Torticollis, facial asymmetry and plagiocephaly in normal newborns. Arch Dis Child. 2008;93(10):827–31. https://doi.org/10.1136/adc.2007.124123.

    Article  CAS  PubMed  Google Scholar 

  2. Kalra R, Walker ML. Posterior plagiocephaly. Childs Nerv Syst. 2012;28(9):1389–93. https://doi.org/10.1007/s00381-012-1784-y.

    Article  PubMed  Google Scholar 

  3. Robinson S, Proctor M. Diagnosis and management of deformational plagiocephaly: a review. J Neurosurg Pediatr. 2009;3(4):284–95. https://doi.org/10.3171/2009.1.PEDS08330.

    Article  PubMed  Google Scholar 

  4. Robinson S, Proctor M. Diagnosis and management of deformational plagiocephaly. J Neurosurg Pediatr. 2009;3(4):284–95. https://doi.org/10.3171/2009.1.PEDS08330.

    Article  PubMed  Google Scholar 

  5. Baumler C, Leboucq N, Captier G. Étude de l’asymétrie mandibulaire dans les plagiocéphalies sans synostose. Rev Stomatol Chir Maxillofac. 2007;108(5):424–30. https://doi.org/10.1016/j.stomax.2007.07.005.

    Article  CAS  PubMed  Google Scholar 

  6. Rogers GF. Deformational plagiocephaly, brachycephaly, and scaphocephaly. Part I: terminology, diagnosis, and etiopathogenesis. J Craniofac Surg. 2011;22(1):9–16. https://doi.org/10.1097/SCS.0b013e3181f6c313.

    Article  PubMed  Google Scholar 

  7. Bialocerkowski AE, Vladusic SL, Ng CW, Wei NC. Prevalence, risk factors, and natural history of positional plagiocephaly: a systematic review. Dev Med Child Neurol. 2008;50(8):577–86. https://doi.org/10.1111/j.1469-8749.2008.03029.x.

    Article  PubMed  Google Scholar 

  8. Ahluwalia R, Kiely C, Foster J, Gannon S, Wiseman AL, Shannon CN, et al. Positional posterior plagiocephaly: a single-center review. J Neurosurg Pediatr PED. 2020;25:514–8 Available from: https://thejns.org/pediatrics/view/journals/j-neurosurg-pediatr/25/5/article-p514.xml.

    Article  Google Scholar 

  9. Aarnivala HEI, Valkama AM, Pirttiniemi PM. Cranial shape, size and cervical motion in normal newborns. Early Hum Dev. 2014;90(8):425–30. https://doi.org/10.1016/j.earlhumdev.2014.05.007.

    Article  PubMed  Google Scholar 

  10. van Vlimmeren LA, van der Graaf Y, Boere-Boonekamp MM, L’Hoir MP, Helders PJMM, Engelbert RHHH, et al. Risk factors for deformational Plagiocephaly at birth and at 7 weeks of age: a prospective cohort study. Pediatrics. 2007;119(2):e408–18. https://doi.org/10.1542/peds.2006-2012.

    Article  PubMed  Google Scholar 

  11. De Bock F, Braun V, Renz-Polster H. Deformational plagiocephaly in normal infants: A systematic review of causes and hypotheses. Arch Dis Child. 2017;102:535–42.

    Article  Google Scholar 

  12. Ballardini E, Sisti M, Basaglia N, Benedetto M, Baldan A, Borgna-Pignatti C, et al. Prevalence and characteristics of positional plagiocephaly in healthy full-term infants at 8–12 weeks of life. Eur J Pediatr. 2018;177(10):1547–54. https://doi.org/10.1007/s00431-018-3212-0.

    Article  PubMed  Google Scholar 

  13. Ifflaender S, Rüdiger M, Konstantelos D, Wahls K, Burkhardt W, et al. Prevalence of head deformities in preterm infants at term equivalent age. Early Hum Dev. 2013;89:1041–7.

    Article  Google Scholar 

  14. Peitsch WK, Keefer CH, LaBrie RA, Mulliken JB. Incidence of cranial asymmetry in healthy newborns. Pediatrics. 2002;110:e72.

    Article  Google Scholar 

  15. Sergueef N, Nelson KE, Glonek T. Palpatory diagnosis of plagiocephaly. Complement Ther Clin Pract. 2006;12(2):101–10. https://doi.org/10.1016/j.ctcp.2005.11.001.

    Article  PubMed  Google Scholar 

  16. McKinney CM, Cunningham ML, Holt VL, Leroux B, Starr JR. A case-control study of infant, maternal and perinatal characteristics associated with deformational plagiocephaly. Paediatr Perinat Epidemiol. 2009;23:332–45.

    Article  Google Scholar 

  17. Rogers GF, Oh AK, Mulliken JB. The role of congenital muscular torticollis in the development of deformational plagiocephaly. Plast Reconstr Surg. 2009;123(2):643–52. https://doi.org/10.1097/PRS.0b013e318196b9be.

    Article  CAS  PubMed  Google Scholar 

  18. Boere-Boonekamp MM, van der Linden-Kuiper LT. Positional preference: prevalence in infants and follow-up after two years. Pediatrics. 2001;107(2):339–43. https://doi.org/10.1542/peds.107.2.339.

    Article  CAS  PubMed  Google Scholar 

  19. Flannery ABK, Looman WS, Kemper K. Evidence-based Care of the Child with Deformational Plagiocephaly, part II: management. J Pediatr Heal Care. 2012;26(5):320–31. https://doi.org/10.1016/j.pedhc.2011.10.002.

    Article  Google Scholar 

  20. Van Vlimmeren L, van der Graaf Y, Boere-Boonekamp MM, L’Hoir MP., Helders PJM, Engelbert R, et al. Effect of pediatric physical therapy on deformational plagiocephaly in children with positional preference: A randomized controlled trial. Arch Pediatr Adolesc Med. Department of Physical Therapy, Bernhoven Hospital, PO Box 10.000, 5460 DA Veghel, the Netherlands. l.vanvlimmeren@bernhoven.nl; 2008;162:712–8.

  21. Koren A, Reece SM, Kahn-D’angelo L, Medeiros D. Parental information and behaviors and provider practices related to tummy time and Back to sleep. J Pediatr Heal Care. 2010;24:222–30.

    Article  Google Scholar 

  22. Persing J, James H, Swanson J, Kattwinkel J. American Academy of Pediatrics Committee on practice and ambulatory medicine S on PS and S on NS. Prevention and management of positional skull deformities in infants. Pediatrics. 2011;128:1236–41.

    Article  Google Scholar 

  23. Aarnivala H, Vuollo V, Harila V, Heikkinen T, Pirttiniemi P, Valkama AM. Preventing deformational plagiocephaly through parent guidance: a randomized, controlled trial. Eur J Pediatr. 2015;174(9):1197–208. https://doi.org/10.1007/s00431-015-2520-x.

    Article  PubMed  Google Scholar 

  24. Loveday BPT, de Chalain TB. Active counterpositioning or orthotic device to treat positional plagiocephaly? J Craniofac Surg. 2001;12:308–13.

    Article  CAS  Google Scholar 

  25. Jones MW. Supine and prone infant positioning: a winning combination. J Perinat Educ. 2004;13(1):10–20. https://doi.org/10.1624/105812404826388.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Ditthakasem K, Kolar JC. Deformational plagiocephaly: a review. Pediatr Nurs. 2017;43(2):59–64.

    PubMed  Google Scholar 

  27. Persing J, James H, Swanson J, Kattwinkel J. American Academy of Pediatrics Committee on practice and ambulatory medicine S on PS and S on NS. Prevention and management of positional skull deformities in infants. American Academy of Pediatrics Committee on practice and ambulatory medicine, section on plastic Surgery and section on neurological Surgery. Pediatrics. 2003;112(1 Pt 1):199–202. https://doi.org/10.1542/peds.112.1.199.

    Article  PubMed  Google Scholar 

  28. Bridges SJ, Chambers TL, Pople IK. Plagiocephaly and head binding. Arch Dis Child. Neonatal SpR, Southmead Hospital, Bristol BS10 5NB, UK. Oxford Craniofacial Unit, Radcliffe Infirmary, Oxford OX2 6HE, UK. sarahbridges@hotmail.com; 2002;86:144–5.

  29. Kim SY, Park M-SS, Yang J-II, Yim S-YY. Comparison of helmet therapy and counter positioning for deformational plagiocephaly. Ann Rehabil Med. 2013;37(6):785–95. https://doi.org/10.5535/arm.2013.37.6.785.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Wu Y, Wu ZF, Zhang YP, Zhao CM, Yu XM, Yang W, et al. Efficacy of sleep position correction for treating infants with positional plagiocephaly. Chinese J Contemp Pediatr. 2017;19:688–92.

    Google Scholar 

  31. van Wijk RM, Pelsma M, Groothuis-Oudshoorn CGM, IJzerman MJ, van Vlimmeren LA, Boere-Boonekamp MM, et al. Response to pediatric physical therapy in infants with positional preference and skull deformation. Phys Ther. 2014;94(9):1262–71. https://doi.org/10.2522/ptj.20130304.

    Article  PubMed  Google Scholar 

  32. Tamber MS, Nikas D, Beier A, Baird LC, Bauer DF, Durham S, et al. Guidelines: Congress of Neurological Surgeons systematic review and evidence-based guideline on the role of cranial molding Orthosis (helmet) therapy for patients with positional Plagiocephaly. Neurosurgery. 2016;79(5):E632–3. https://doi.org/10.1227/NEU.0000000000001430.

    Article  PubMed  Google Scholar 

  33. Wilbrand J-F, Schmidtberg K, Bierther U, Streckbein P, Pons-Kuehnemann J, Christophis P, et al. Clinical classification of infant nonsynostotic cranial deformity. J Pediatr. 2012;161(6):1120–5. https://doi.org/10.1016/j.jpeds.2012.05.023.

    Article  PubMed  Google Scholar 

  34. Dörhage KWW, Beck-Broichsitter BE, von Grabe V, Sonntag A, Becker ST, Wiltfang J. Therapy effects of head orthoses in positional plagiocephaly. J Cranio-Maxillofacial Surg. 2016;44(10):1508–14. https://doi.org/10.1016/j.jcms.2016.06.035.

    Article  Google Scholar 

  35. van Wijk RM, Boere-Boonekamp MM, Groothuis-Oudshoorn CGMM, van Vlimmeren LA, IJzerman MJ. HElmet therapy Assessment in infants with Deformed Skulls (HEADS): protocol for a randomised controlled trial. Trials. Department Health Technology and Services Research, Institute of Innovation and Governance Studies, University of Twente, Drienerlolaan 5, 7522 NB, Enschede, Netherlands.: Trials; 2012;Jul 9;13:108.

  36. Goh JL, Bauer DF, Durham SR, Stotland MA, Surgery P. Orthotic (helmet) therapy in the treatment of plagiocephaly. Neurosurg Focus. 2013;35:1–6.

    Article  Google Scholar 

  37. Cabrera-Martos I, Valenza MC, Valenza-Demet G, Benítez-Feliponi A, Robles-Vizcaíno C, Ruiz-Extremera A, et al. Effects of manual therapy on treatment duration and motor development in infants with severe nonsynostotic plagiocephaly: a randomised controlled pilot study. Childs Nerv Syst. 2016;32(11):2211–7. https://doi.org/10.1007/s00381-016-3200-5.

    Article  CAS  PubMed  Google Scholar 

  38. Lessard S, Gagnon I, Trottier N. Exploring the impact of osteopathic treatment on cranial asymmetries associated with nonsynostotic plagiocephaly in infants. Complement Ther Clin Pract. 2011;17(4):193–8. https://doi.org/10.1016/j.ctcp.2011.02.001.

    Article  PubMed  Google Scholar 

  39. Di Chiara A, La Rosa E, Ramieri V, Vellone V, Cascone P, et al. J Craniofac Surg. 2019;30:2008–13.

    Article  Google Scholar 

  40. Graham JM, Gomez M, Halberg A, Earl DL, Kreutzman JT, Cui J, et al. Management of deformational plagiocephaly: repositioning versus orthotic therapy. J Pediatr. 2005;146:258–62.

    Article  Google Scholar 

  41. Mortenson PA, Steinbok P. Quantifying positional plagiocephaly: reliability and validity of anthropometric measurements. J Craniofac Surg. 2006;17:413–9.

    Article  Google Scholar 

  42. Leibson T, Koren G. Informed consent in pediatric research. Pediatr Drugs. 2015;17:5–11.

    Article  Google Scholar 

  43. Martini M, Klausing A, Lüchters G, Heim N, Messing-Jünger M. Head circumference - a useful single parameter for skull volume development in cranial growth analysis? Head Face Med. 2018;14:3.

    Article  Google Scholar 

  44. Wilbrand J-F, Wilbrand M, Pons-Kuehnemann J, Blecher J-C, Christophis P, Howaldt H-P, et al. Value and reliability of anthropometric measurements of cranial deformity in early childhood. J Cranio-Maxillofacial Surg. 2011;39(1):24–9. https://doi.org/10.1016/j.jcms.2010.03.010.

    Article  Google Scholar 

  45. Pastor-Pons I, Lucha-López MO, Barrau-Lalmolda M, Rodes-Pastor I, Rodríguez-Fernández ÁL, Hidalgo-García C, et al. Interrater and intrarater reliability of cranial anthropometric measurements in infants with positional plagiocephaly. Children. 2020;7:306.

    Article  Google Scholar 

  46. Cho IK, Eom JR, Lee JW, Yang JD, Chung HY, Cho BC, Choi KY. A Clinical Photographic Method to Evaluate the Need for Helmet Therapy in Deformational Plagiocephaly. J Craniofac Surg. 2018;29(1):149–52. https://doi.org/10.1097/SCS.0000000000004192.

  47. Holowka MA, Reisner A, Giavedoni B, Lombardo JR, Coulter C. Plagiocephaly severity scale to aid in clinical treatment recommendations. J Craniofac Surg. 2017;28(3):717–22. https://doi.org/10.1097/SCS.0000000000003520.

    Article  PubMed  Google Scholar 

  48. Hoffman C, Yuan M, Boyke AE, O’Connor A, Haussner T, Perera I, et al. Impact of an advanced practice provider–directed plagiocephaly clinic for neurosurgical practices. J Neurosurg Pediatr. 2019:1–4.

  49. Upledger J, Vredevoogd J. Terapia Craneosacra. First ed. Barcelona: Paidotribo; 2004.

    Google Scholar 

  50. Giammatteo T, Giammateeo S. Integrative manual therapy for biomechanics. Application of muscle energy and “beyond” technique. Berkeley: North Atlantic Books; 2003.

    Google Scholar 

  51. Arbuckle BE. Ostéopathie crânienne pour le nouveau-né et l’enfant. Vannes: Sully; 2014.

    Google Scholar 

  52. Carreiro JE. Chapter two - head and neck. In: Carreiro JEBT-PMM, editor. Edinburgh: Churchill Livingstone; 2009. p. 13–97. Available from: http://www.sciencedirect.com/science/article/pii/B9780443103087000028.

    Google Scholar 

  53. Pastor-Pons I, Hidalgo-García C, Lucha-López MO, Barrau-Lalmolda M, Rodes-Pastor I, Rodríguez-Fernández ÁL, et al. Effectiveness of pediatric integrative manual therapy in cervical movement limitation in infants with positional plagiocephaly: a randomized controlled trial. Ital J Pediatr Springer. 2021;47:1–12.

    Article  Google Scholar 

  54. Wittmeier K, Mulder K. Time to revisit tummy time: a commentary on plagiocephaly and development. Paediatr Child Heal. 2017;22(3):159–61. https://doi.org/10.1093/pch/pxx046.

    Article  Google Scholar 

  55. Baird LC, Klimo P, Flannery AM, Lingo PR, Bauer DF, Beier A, et al. Guidelines: congress of neurological surgeons systematic review and evidence-based guideline on the management of patients with positional plagiocephaly: the role of repositioning. Neurosurgery. 2016;79:E627–9.

    Article  Google Scholar 

  56. Meyer-Marcotty P, Kunz F, Schweitzer T, Wachter B, Böhm H, Waßmuth N, et al. Cranial growth in infants─A longitudinal three-dimensional analysis of the first months of life. J Cranio-Maxillofacial Surg. 2018;46:987–93.

    Article  Google Scholar 

  57. Kluba S, Kraut W, Calgeer B, Reinert S, Krimmel M, Bialocerkowski AE, et al. Treatment of positional plagiocephaly--helmet or no helmet? J Craniomaxillofac Surg. 2014;42:683–8.

    Article  Google Scholar 

  58. Naidoo SD, Cheng A-L. Long-term satisfaction and parental decision making about treatment of deformational Plagiocephaly. J Craniofac Surg. 2014;25(1):160–5. https://doi.org/10.1097/SCS.0000000000000383.

    Article  PubMed  Google Scholar 

  59. Fenton R, Gaetani S, MacIsaac Z, Ludwick E, Grunwaldt L. Description of mandibular improvements in a series of infants with congenital muscular torticollis and deformational plagiocephaly treated with physical therapy. Cleft Palate-Craniofacial J. 2018;55:1262–88.

    Article  Google Scholar 

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Acknowledgements

The authors wish to thank the management and pediatricians in Section III of the Aragon Healthcare System (Zaragoza, Spain). Thanks to the Institute of Integrative Therapies (Instituto de Terapias Integrativas) in Zaragoza and its administrative staff. Thanks especially to the children and their families.

Funding

No financial assistance was received in support of the study.

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Contributions

Conceptualization: IPP; Methodology: IPP; Investigation: MBL, IRP; Resources: MBL; Data Curation: IRP; Writing – Original Draft: IPP; Writing – Review – review & editing: OLL, CHG; Formal Analysis: OLL; Visualization: ALRF, JMTM; Supervision: ALRF, JMTM. All authors read and approved the final manuscript.

Corresponding author

Correspondence to María Orosia Lucha-López.

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Ethics approval and consent to participate

An informed consent document with information about the study and in accordance with the requirements established by the “Ethics Committee at the Aragon Health Sciences Institute” was offered to the parents.

The Ethics Committee at the Aragon Health Sciences Institute approved the study (Registry No. C.P. - C.I. PI16/0275).

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The authors declare that they have no competing interests.

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Pastor-Pons, I., Lucha-López, M.O., Barrau-Lalmolda, M. et al. Efficacy of pediatric integrative manual therapy in positional plagiocephaly: a randomized controlled trial. Ital J Pediatr 47, 132 (2021). https://doi.org/10.1186/s13052-021-01079-4

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