Peter J. Anderson

Peter J. Anderson

M.B., Ch.B., B.D.S., D.Sc., DDSc, M.D.(Edin), Ph.D.(Adel), M Surg. Ed., M.F.S.T.(Ed), F.D.S.R.C.S.(Eng&Ed), F.R.C.S.(Eng), F.A.C.S., F.R.C.S.(Plast.), F.R.A.C.S.

Pediatrician

36 Years’ Experience Overall

Male📍 Clayton

About of Peter J. Anderson

Peter J. Anderson is a Pediatrician based in Wellington Road, Clayton VIC. He looks after babies, kids, and young people, with a strong focus on the first years of life. That early stage can be full on for families, especially when symptoms show up quickly or need close follow-up.


With 36 years’ experience overall, Dr Anderson has worked with many common childhood health needs, as well as more complex conditions. In many cases, that includes helping newborns and premature babies who need careful monitoring. This can involve breathing problems, feeding and tummy issues, and the sort of concerns that can change from day to day.


He also supports children with sleep and breathing difficulties, including apnoea in babies and obstructive sleep apnoea. Sometimes the issue is linked to growth in the face and airway, and sometimes it is about how the nervous system controls breathing during sleep.


Dr Anderson cares for children with developmental and neurological conditions too. This can include cerebral palsy, spastic diplegia, movement problems, and concerns around communication and behaviour such as ADHD and autism spectrum disorder. He works to make sure families understand what’s happening and what support can help over time.


Another area he deals with is craniofacial and congenital conditions, including conditions like craniosynostosis, Apert syndrome, Pfeiffer syndrome, and Treacher Collins syndrome. Children may also have feeding or growth challenges linked to these conditions, so care often needs to be well coordinated.


Health issues like infections and complications in early life are also within his scope. This may include neonatal sepsis, retinopathy of prematurity, necrotising enterocolitis, and urinary tract infections. He also looks at conditions such as gastro-oesophageal reflux and other gut problems in infants.


In terms of education, Dr Anderson holds qualifications including M.B., Ch.B. and additional degrees listed as M.D. (Edinburgh), Ph.D. (Adelaide), and further medical training. He has also been involved with medical publications. Clinical trial details are not listed here.


If your child needs a paediatrician who can cover newborn health, development, and complex childhood conditions, Peter J. Anderson is based in Clayton and available to provide ongoing care.

Education

  • M.B., Ch.B., B.D.S., M.D.(Edinburgh)
  • Ph.D.(Adelaide)

Services & Conditions Treated

Apnea of PrematurityPremature InfantAcrocephalopolydactylyAcrofacial Dysostosis Rodriguez TypeAcrofrontofacionasal Dysostosis SyndromeApert SyndromeCerebral PalsyCraniosynostosisCrouzon SyndromeGoldenhar DiseaseInfantile ApneaMetopic RidgePfeiffer SyndromePlagiocephalySaethre-Chotzen SyndromeSyndactylyTreacher Collins SyndromeAcromicric DysplasiaAttention Deficit Hyperactivity Disorder (ADHD)Binder's SyndromeBronchopulmonary DysplasiaCraniofrontonasal DysplasiaFetal Alcohol Syndrome (FAS)Intraventricular Hemorrhage of the NewbornLacrimo-Auriculo-Dento-Digital SyndromeMicrognathiaMuenke SyndromeSpastic Diplegia Infantile TypeVan Der Woude SyndromeAcrofacial Dysostosis Catania TypeAcrofacial Dysostosis Nager TypeAdenoidectomyAmblyopiaAutism Spectrum DisorderCleidocranial DysplasiaCorpus Callosum AgenesisCraniectomyDehydrationDevelopmental Dysphasia FamilialEncephaloceleEsophageal AtresiaFibrodysplasia Ossificans ProgressivaGastroesophageal Reflux in InfantsGastroschisisHearing LossHerniaHigh Blood Pressure in InfantsHIV/AIDSIntrauterine Growth RestrictionLung MetastasesMemory LossMovement DisordersNecrotizing EnterocolitisNeonatal SepsisObstructive Sleep ApneaOmphaloceleOsteomyelitis in ChildrenPierre Robin SequencePlacental InsufficiencyRetinopathy of PrematuritySepsisTissue BiopsyUmbilical HerniaUrinary Tract Infection (UTI)

Publications

5 total
Low to Moderate Prenatal Alcohol Exposure and Facial Shape of Children at Age 6 to 8 Years.

JAMA pediatrics • February 10, 2025

Evelyne Muggli, Harold Matthews, Michael Suttie, Jane Halliday, Anthony Penington, Elizabeth Elliott, Deanne Thompson, Alicia Spittle, Stephen Hearps, Peter Anderson, Peter Claes

In addition to confirmed prenatal alcohol exposure and severe neurodevelopmental deficits, three cardinal facial features are included in the diagnostic criteria for fetal alcohol spectrum disorder. It is not understood whether subtle facial characteristics occur in children without a diagnosis but who were exposed to a range of common pregnancy drinking patterns and, if so, whether these persist throughout childhood. To determine whether subtle changes in facial shape with prenatal alcohol exposure found in 12-month-old children were evident at age 6 to 8 years using extended phenotyping methods and, if so, whether facial characteristics were similar to those seen in fetal alcohol spectrum disorder. In a prospective cohort study in Melbourne, Victoria, Australia, commencing in July 2011 with follow-up through April 2021, pregnant women were recruited in the first trimester from low-risk, metropolitan, public maternity clinics over a period of 12 months. Three-dimensional craniofacial images from 549 children of European descent taken at age 12 months (n = 421 images) and 6 to 8 years (n = 363) were included. Data analysis was performed from May 2021 to October 2024. Predominantly low to moderate prenatal alcohol exposure in the first trimester or throughout pregnancy compared with controls without prenatal alcohol exposure. Following hierarchical facial segmentation, phenotype descriptors were computed. Hypothesis testing was performed for 63 facial modules to analyze different facial parts independently using principal component analysis and response-based imputed predictor (RIP) scores. Comparison was made with a clinical discovery sample of facial images of children with a confirmed diagnosis of partial or full fetal alcohol syndrome. A total of 549 children took part in the 3-dimensional craniofacial image analysis, of whom 235 (42.8%) contributed an image at both time points. Time 1 included 421 children, comprising 336 children (159 [47.3%] female) with any prenatal alcohol exposure and 85 control children (45 [52.9%] female); time 2 included 363 children, comprising 260 children with any prenatal alcohol exposure (125 [48.1%] female; mean [SD] age, 6.9 [0.7] years) and 103 control children (53 [51.5%] female; mean [SD] age, 6.8 [0.7] years). At both time points, there was consistent evidence for an association between prenatal alcohol exposure and the shape of the eyes (eg, module 15: RIP partial Spearman ρ, 0.19 [95% CI, 0.10-0.29; P < .001] at 6-8 years) and nose (eg, module 5: RIP partial Spearman ρ, 0.19 [95% CI, 0.09-0.27; P < .001] at 6-8 years), whether exposure occurred only in trimester 1 or throughout pregnancy. Facial variations observed differed from those in the clinical discovery sample. Low to moderate prenatal alcohol exposure was associated with characteristic changes in the face, which persisted until at least 6 to 8 years of age. A linear association between alcohol exposure levels and facial shape was not supported.

Elevated scaled scores when using the digital version of the WISC-V coding subtest.

Child Neuropsychology : A Journal On Normal And Abnormal Development In Childhood And Adolescence • February 03, 2025

Stephanie Malarbi, Rachel Ellis, Elisha Josev, Kristina Haebich, Thi-nhu-ngoc Nguyen, Kristal Lau, Alice Burnett, Natalie Pride, Jonathan Payne, Peter Anderson

This study investigated the digital version of the Wechsler Intelligence Scale for Children, Fifth Edition (WISC-V) Coding subtest in a large Australian clinical and non-clinical sample of 6-11 year old children (N = 794). Data was retrospectively pooled from several studies. Results showed the digital Coding scaled score was significantly elevated compared with all other subtests (M difference = 2.01, 95% CI. 1.74-2.27). Overall FSIQ was higher when calculated using Coding compared with Symbol Search (M difference = 2.067, 95% CI. 1.79-2.34). The Coding and Symbol Search discrepancy in digital administration did not vary according to age and was unrelated to general intelligence. Girls scored higher on average than boys on the digital Coding subtest, but there was no sex effect for the digital Symbol Search subtest (girls: M = 10.76, 95% CI 10.41-11.12; boys: M = 10.27, 95% CI 9.92-10.63). Inflated digital Coding scaled scores were observed across our subsamples of clinical and non-clinical cases, without any significant group differences. Overall, our findings support the notion that the digital WISC-V Coding subtest is inflated, particularly for girls, supporting cessation in the digital administration of this subtest.

Descriptive epidemiology of orofacial clefts in South Australia.

Journal Of Cranio-Maxillo-Facial Surgery • January 22, 2025

Objective: There is wide variability in the prevalence of orofacial clefts at birth across geographic locations. The study aimed to quantify the prevalence of orofacial clefts and provide demographic details of the individuals identified with an orofacial cleft in South Australia. Methods: The South Australian Birth Defects Register (SABDR) data was used to identify individuals born in South Australia with any orofacial cleft including cleft lip (CL), cleft lip and palate (CL + P), cleft palate (CP), cleft uvula (CU) and facial clefts (FC) between 1986 and 2019. The proportion of orofacial clefts for livebirths was calculated by sex, Indigenous status, geographic location, socioeconomic status, maternal age, plurality, gestation, birthweight and family history of orofacial clefts. Results: A total of 1127 individuals were identified as having an orofacial cleft and livebirth: with a combined prevalence of 17.1 in 10,000 or 1 in 580 livebirths for all orofacial clefts. The prevalence for CL was 3.3 per 10,000, CL + P was 5.4 per 10,000, CP was 8.1 per 10,000, CU was 0.2 per 10,000 and FC was 0.1 in 10,000. A greater proportion of orofacial cleft diagnoses were male, born in major cities, non-Indigenous, higher SES, lower maternal age, normal gestational age and birthweight, non-syndromic diagnoses, with no family history of orofacial clefts. Conclusions: Prevalence data provides an understanding of individuals born with orofacial clefts in South Australia since 1986 which are comparative to national and international birth registries. The quality of the SABDR is high and provides a reference for comparison to published prevalence reports.

The association between gestation at birth and maternal sensitivity: An individual participant data (IPD) meta-analysis.

Early Human Development • February 05, 2025

Julia Jaekel, Peter Anderson, Dieter Wolke, Günter Esser, Gorm Greisen, Alicia Spittle, Jeanie Cheong, Anneloes Van Baar, Marjolein Verhoeven, Noa Gueron Sela, Naama Atzaba Poria, Lianne Woodward, Erica Neri, Francesca Agostini, Ayten Bilgin, Riikka Korja, Elizabeth Loi, Karli Treyvaud

Objective: Studies have documented differences in dyadic sensitivity between mothers of preterm (<37 weeks' gestation) and term born children, but findings are inconsistent and studies often include small and heterogeneous samples. It is not known to what extent variations in maternal sensitivity are associated with preterm birth across the full spectrum of gestational age. Objective: To perform a systematic review and individual participant data (IPD) meta-analysis assessing variations in observed dyadic maternal sensitivity according to child gestational age at birth, while adjusting for known confounders correlated with maternal sensitivity. Methods: We harmonised data from 12 birth cohorts from ten countries and carried out one-stage IPD meta-analyses (N = 3951) using mixed effects linear regression. Maternal sensitivity was z-standardised according to the scores of contemporary term-born controls within each respective cohort. All models were adjusted for child sex, age at assessment, neurodevelopmental impairment, small for gestational age birth, and maternal education. Results: The fixed linear effect of the association between gestation at birth and maternal sensitivity across all 12 cohorts was small but stable (0.02 per week [95 % CI = 0.01, 0.02], p < .001). The binary effects of maternal education (0.32 [0.24, 0.40], p < .001) and child neurodevelopmental impairment (-0.33 [-0.50, -0.17], p < .001) were associated with maternal sensitivity. Conclusions: Gestational age at birth is positively associated with dyadic maternal sensitivity, however, the size of the effect is small. Over and above gestation, maternal education and child neurodevelopmental impairment appear to affect sensitivity, highlighting the importance of considering these factors in future research and intervention designs.

Socioeconomic outcomes in very preterm/very low birth weight adults: individual participant data meta-analysis.

Pediatric Research • December 21, 2024

Yanlin Zhou, Marina Mendonça, Nicole Tsalacopoulos, Peter Bartmann, Brian Darlow, Sarah Harris, John Horwood, Lianne Woodward, Peter Anderson, Lex Doyle, Jeanie L Cheong, Eero Kajantie, Marjaana Tikanmäki, Samantha Johnson, Neil Marlow, Chiara Nosarti, Marit Indredavik, Kari Anne Evensen, Katri Räikkönen, Kati Heinonen, Sylvia Van Der Pal, Dieter Wolke

Background: Very preterm (VPT; <32 weeks) or very low birth weight (VLBW; <1500 g) birth is associated with socioeconomic disadvantages in adulthood; however, the predictors of these outcomes remain underexplored. This study examined socioeconomic disparities and identified neonatal and sociodemographic risk factors among VPT/VLBW individuals. Methods: A one-stage individual participant data meta-analysis was conducted using 11 birth cohorts from eight countries, comprising 1695 VPT/VLBW and 1620 term-born adults aged 18-30 years. Results: VPT/VLBW adults had lower odds of higher educational attainment (0.40[0.26-0.59]), remaining in education (0.63[0.47-0.84]) or paid work (0.76[0.59-0.97]), and higher odds of receiving social benefits (3.93[2.63-5.68]) than term-borns. Disparities in education and social benefits persisted after adjusting for age, sex, and maternal education, even among those without neurosensory impairments (NSI). Among VPT/VLBW adults, NSI significantly impacted all socioeconomic outcomes, increasing the odds of receiving social benefits 6.7-fold. Additional risk factors included medical complications, lower gestational age and birth weight, lower maternal education, younger maternal age, and non-white ethnicity. Conclusions: NSI is the strongest risk factor for adulthood socioeconomic challenges in the VPT/VLBW population. Mitigating these disparities may require improved neonatal care to reduce NSI prevalence and targeted social and educational support for VPT/VLBW individuals. Conclusions: Very preterm or very low birth weight (VPT/VLBW) birth is associated with socioeconomic disadvantages in adulthood, including lower educational attainment, lower employment rates, and a higher need for social benefits compared with individuals born at term. Neurosensory impairments are strongly associated with adverse socioeconomic outcomes among VPT/VLBW adults, while lower gestational age, lower birth weight, and sociodemographic disadvantages serve as additional risk factors. Early interventions in the NICU that reduce medical complications, along with enhanced educational support throughout childhood, may help mitigate long-term socioeconomic disparities for individuals born VPT/VLBW.

Clinical Trials

1 total

Novel Approaches for Quantitative Assessment of Adherence

Completed

Approximately 12 adults subjects will be enrolled. Participants will be randomized to one of two directly observed dosing regimens with 2mg adenine 5+ (five stable-labeled nitrogens) as follows: 1 dose/week followed by 4 doses/week OR 3 doses/week followed by 7 doses/week. Each dose regimen will have a duration of approximately 12 weeks and will be separated by a 12-week washout period for a total study duration of approximately 36 weeks. Dried blood spots (DBS) and whole blood will be collect weekly. Urine will be collected less frequently, about every 2 weeks. The ratio of ATP 5+ to naturally occurring ATP 2+ is dried blood spots will be the primary outcome, as adenine is phosphorylated to ATP in red blood cells. Breakdown products will be measured in urine. Investigators will allow flexibility in terms of which days are used for dosing for the 1, 3, and 4 dose(s)/week regimens. This is scientifically justified as investigators expect a 20-30 day half-life of ATP 5+ in DBS.

Participants: 15

Frequently Asked Questions

What services does Dr Peter J. Anderson offer for newborns and infants?
Dr Anderson provides care for a range of neonatal and paediatric conditions, including apnea of prematurity, prematuro infant care, and issues such as gastroesophageal reflux in infants, sepsis, and dehydration. He also treats conditions seen in newborns and infants that may require specialist input.
Which conditions in children does he regularly manage?
He has experience with developmental and congenital conditions such as craniosynostosis, various craniofacial syndromes (for example Treacher Collins and Apert syndrome), cerebral palsy, ADHD, autism spectrum disorder, and paediatric airway or facial development concerns. He also sees general paediatric issues like infections and growth concerns.
Where is Dr Anderson's clinic located and how can I book an appointment?
Appointments are available at the Clayton practice on Wellington Road, Clayton, VIC 3800, Australia. For booking specifics, please contact the clinic directly to arrange a suitable time.
What ages does he treat?
Dr Anderson is a paediatrician with extensive experience, focusing on infants, children, and their developmental needs. He has treated patients from newborns through the paediatric years.
What kinds of conditions related to craniofacial development does he handle?
He has expertise in a range of craniofacial and syndromic conditions, including craniosynostosis, various craniofacial dysostoses, Pfeiffer syndrome, Apert syndrome, Crouzon syndrome, Saethre-Chotzen syndrome, and related developmental concerns.
Does he treat sleep-related or breathing problems in children?
Yes. He addresses issues such as obstructive sleep apnea in paediatric patients and related respiratory concerns that can affect children’s health and development.
What is his experience level and background?
Dr Peter J. Anderson has around 36 years of experience in paediatrics. His qualifications include multiple degrees and fellowships across paediatrics and related specialties, reflecting a broad and deep background in child health.

Contact Information

Wellington Road, Clayton, VIC 3800, Australia

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Memberships

  • Asia Pacific Craniofacial Association
  • The Australia and New Zealand Craniomaxillofacial Society