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Speech Delay in Children — Assessment & ManagementDevelopmental regression red flag · hearing loss mandatory audiology · M-CHAT ASD screen · OME grommets · Hanen parent programme · DLD · EHCP · Bookstart
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The full reasoning pathway β€” always check hearing first, distinguish isolated speech-language delay from global delay or autism features, and refer for early support. Safety-net.StartDecisionInvestigateActionReferStop / Admit
PresentationSpeech / language delay
Receptive vs expressive, milestones, bilingual context, social communication, behaviour. Hearing assessment; check other developmental domains.
Step 1 Β· Safety β€” regression / autism-global red flagsRegression or autism/global red flags?
Loss of language/social skills (regression) Β· no babble/gesture by 12 months, no words by 18 months, no phrases by 2 years Β· poor social communication/eye contact (ASD).
YES
Stop Β· EscalateRefer
Regression β†’ urgent. Autism features/global delay β†’ paediatric/ASD pathway.
NO
AssessBy pattern
History + examination guide management.
Step 3 Β· approach
Isolated speech delay
Common
Often resolves; SALT referral, language-rich environment, reassure if otherwise normal.
Hearing-related
Check first
Glue ear/hearing loss is a common reversible cause β€” audiology.
ASD / global
Refer
Social communication difficulties or global delay β†’ autism/paediatric pathway.
Step 6 Β· ReferEscalation
Audiology + SALT for all speech delay; Community paediatrics / autism pathway if social communication concerns or global delay; urgent if regression.
Step 8 Β· early support & family
Step 8 Β· Early support & familyLanguage-rich environment
Refer to SALT and audiology in parallel with assessment. Coach a language-rich home environment β€” talking, reading, singing, shared play, reducing screen time; reassure that bilingualism does not cause delay. Treat glue ear/hearing loss (a common reversible cause). Support parents, nursery/early-years and any wider developmental needs.
Step 9 Β· review & safety-net
Step 9 Β· Review & safety-netHearing first; watch for regression
Test hearing in every child with speech delay β€” undetected hearing loss (often glue ear) is common and reversible. Urgent re-referral for any loss of language/social skills (regression). Look for autism features (social communication, eye contact, restricted/repetitive behaviour) β†’ autism pathway, and global delay β†’ community paediatrics. Review progress and ensure referrals are actioned.
⚠️ Test hearing in every child with speech delay: undetected hearing loss (often glue ear) is a common and reversible cause β€” and look for autism features alongside the language delay.
1
Safety

Red Flags β€” Regression, Hearing Loss & Neurological Causes

Loss of previously acquired speech or language skills at any age Developmental regression β€” never normal. Consider: Landau-Kleffner syndrome (acquired epileptic aphasia), autism spectrum disorder (regression typically 18-24 months), Rett syndrome (girls β€” stereotyped hand movements, deceleration of head growth), metabolic disorders. β†’ Urgent paediatric neurology. EEG urgently (Landau-Kleffner: continuous spike-wave in sleep).
Speech delay + bilateral profound or severe hearing loss not yet identified Sensorineural hearing loss β€” the most common treatable cause of speech and language delay. Cochlear implant by age 12 months optimises speech outcomes. β†’ Same-day audiology if bilateral profound hearing loss not identified and newborn screen missed/failed. Every child with speech delay: audiogram is mandatory before any other assessment.
Speech delay + autistic features (no pointing by 12 months, no babble by 12 months, no single words by 16 months, no two-word phrases by 24 months, poor eye contact, repetitive behaviours) Autism spectrum disorder (ASD). β†’ Urgent CAMHS/community paediatrics referral for diagnostic assessment. Do not delay referral awaiting speech and language therapy.
Speech delay + global developmental delay + dysmorphic features or microcephaly Genetic syndrome (Down syndrome, fragile X, 22q11 deletion, CHARGE, Williams). β†’ Urgent community paediatrics + genetics referral. Array CGH (chromosomal microarray) if no diagnosis established.
Child with speech delay + parental concern about safeguarding / neglect Severe social deprivation and neglect can cause profound speech delay through absence of language exposure. β†’ MARAC/safeguarding referral if abuse or neglect suspected. Every child with unexplained severe speech delay: consider social circumstances.
Speech delay + new-onset seizures or neurological signs (hypotonia, hyperreflexia, abnormal movements) Neurological cause for speech delay. β†’ Same-day paediatric neurology. MRI brain + EEG + metabolic screen.
Developmental regression β€” the loss of previously acquired skills β€” is a neurological emergency until proved otherwise. A child who was saying 10 words at 18 months and has lost them by 22 months is not 'just a bit slow' β€” this pattern demands urgent investigation. The most important diagnoses not to miss: (1) Landau-Kleffner syndrome (acquired epileptic aphasia) β€” children typically develop normally until 3-8 years, then lose language due to continuous epileptiform discharges in the temporal language areas during sleep. The EEG during sleep is diagnostic; waking EEG may be normal. Treatment with corticosteroids or antiepileptics can restore language if treated early. (2) Autism spectrum disorder β€” language regression in ASD typically occurs between 15-24 months (after a period of apparently normal development), often accompanied by loss of social engagement and the emergence of repetitive behaviours. The RCGP curriculum requires GPs to identify developmental regression as a red flag requiring urgent referral.
2
Diagnose

Normal Speech & Language Milestones β€” Age-Matched Expectations

Prelinguistic (birth to 12 months)
Birth–2 months: startles to sound, calms to familiar voice. 3–4 months: cooing, turns to voice, laughs. 6 months: babbling (consonant-vowel combinations β€” "bababa", "mamama"). 9 months: varied babble with intonation, responds to name. 10–12 months: first words emerging, waves bye-bye, plays peek-a-boo, points (proto-imperative pointing by 12 months).
12–24 months
12 months: 1–3 meaningful words (mama/dada used specifically). 15 months: 5–10 words, proto-declarative pointing (to share interest, not just request). 18 months: 10–50 words, follows simple 1-step commands, identifies body parts. 24 months: 50+ words, 2-word combinations ("more milk", "daddy go"), 50% speech intelligible to strangers. Concern if: no words by 16 months, no two-word phrases by 24 months.
2–5 years
2 years: 2-word sentences, 50% intelligible to strangers. 3 years: 3-word sentences, 75% intelligible, uses pronouns (I, me, you), 200+ words. 4 years: 4+ word sentences, 100% intelligible, tells stories, uses past tense, 1,000+ words. 5 years: complex sentences, can retell stories, rhyming, pre-literacy phonological awareness. Concern if: not using sentences by 3 years, not fully intelligible to strangers by 4 years.
Expressive vs receptive delay
Expressive delay (output only): child understands well, follows commands appropriately, but speaks fewer/less clear words than expected. Often resolves, particularly in boys. Receptive delay (understanding impaired): more serious β€” almost always requires investigation and therapy. Mixed expressive-receptive delay: highest concern β€” usually has an underlying cause (hearing loss, ASD, intellectual disability, neurological).
The distinction between expressive-only delay and receptive-expressive delay is the single most important clinical discriminator in speech delay assessment β€” a child with pure expressive delay who has age-appropriate comprehension (follows two-step commands, understands complex instructions, responds appropriately to questions) has a much more favourable prognosis than a child with impaired comprehension. Pure expressive delay in boys aged 18-30 months with good comprehension and good non-verbal communication (pointing, gesturing, making eye contact) is often described as 'late talking' β€” a benign variant that resolves spontaneously in approximately 50-80% of cases. However, even 'late talkers' with expressive-only delay benefit from early speech and language therapy referral because: (1) the GP cannot reliably distinguish pure expressive delay from early receptive delay or ASD in a 10-minute consultation; (2) early SLT input is safe and beneficial regardless of cause; and (3) approximately 20-30% of late talkers will have persistent language problems without intervention.
3
Diagnose

Assessment β€” History, Examination & Investigations

History (structured)
Prenatal/perinatal: maternal illness in pregnancy (TORCH infections β€” CMV, rubella, toxoplasma, herpes), prematurity (speech delay is common in ex-preterm infants), birth hypoxia (HIE), NICU admission. Past medical history: recurrent otitis media with effusion (OME/glue ear β€” most common cause of fluctuating conductive hearing loss), meningitis, seizures, head injury. Developmental history: age of first words, any regression. Family history: speech delay (heritable), ASD, deafness. Social history: language spoken at home (bilingual children may have smaller vocabulary in each language but total vocabulary is normal β€” reassurance appropriate), screen time (>2-3 hours/day associated with delayed language in under-2s), quality of adult verbal interaction.
Examination
General: dysmorphic features (Down, fragile X, Williams, 22q11). Head circumference (microcephaly β€” Rett, Angelman, congenital infection; macrocephaly β€” fragile X, Sotos). Tympanic membranes (OME β€” dull, retracted, fluid level, no cone of light). Hearing (informal β€” not a substitute for audiology). Orofacial: cleft palate (including submucous cleft β€” examine with a torch, bifid uvula suggests submucosal cleft), tongue tie (significant ankyloglossia impairing articulation β€” but rarely causes language delay). Neurological: tone, reflexes, coordination. Observation of child: eye contact, pointing, joint attention, response to name, social smile.
Investigations
Mandatory: Audiology / pure tone audiogram (every child with speech delay β€” request via audiology or GP direct referral to paediatric audiology). M-CHAT-R/F (Modified Checklist for Autism in Toddlers β€” 16-30 months, screen for ASD). If concerning features: FBC + ferritin (iron deficiency affects brain development), TFTs (congenital hypothyroidism β€” should have been screened at birth but can be missed). Specialist: array CGH (genetic cause suspected), MRI brain (neurological signs), EEG (seizures, regression), metabolic screen (regression + neurological signs).
The M-CHAT-R/F (Modified Checklist for Autism in Toddlers, Revised with Follow-Up) is the validated screening tool for ASD in UK primary care β€” it is a 20-item parent questionnaire designed for children aged 16-30 months that screens for the core features of ASD. The R (revised) version has improved specificity over the original M-CHAT. The F (follow-up) module provides structured follow-up questions for intermediate-risk scores to reduce false positives. The tool is freely available and takes approximately 5 minutes to complete β€” GPs should use it at the 2-year developmental review (or any consultation for speech delay in this age group) for all children, not just those with obvious autistic features. A positive screen (medium or high risk) should prompt immediate referral to the ASD diagnostic pathway (community paediatrics or CAMHS) without waiting for speech therapy assessment results. The key scoring: low risk (score 0-2) = rescreen at next routine check; medium risk (3-7) = complete follow-up interview; high risk (8-20) = refer immediately for ASD assessment.
4
Diagnose

Causes of Speech Delay β€” Diagnostic Framework

Hearing impairment (most common treatable cause)
Conductive: otitis media with effusion (OME / glue ear) β€” most common. Bilateral OME with persistent conductive loss >25 dB for >3 months: refer ENT for consideration of grommets. Grommets typically improve hearing immediately and allow language catch-up. Sensorineural: congenital SNHL (TORCH infection, genetic β€” connexin-26 GJB2 mutation most common). Universal Newborn Hearing Screening (UNHS) detects most bilateral SNHL at birth β€” but mild/moderate or unilateral SNHL may be missed.
Autism spectrum disorder
Speech delay is the most common presenting concern in ASD. Core features: impaired social communication (poor eye contact, reduced joint attention, no pointing or limited pointing, lack of social smile or reduced), repetitive behaviours (hand flapping, spinning, lining up toys), restricted interests, sensory sensitivities. DSM-5 criteria (NICE NG3). Range: highly verbal with subtle social deficits to non-verbal with intellectual disability. CAMHS/community paediatrics diagnostic pathway. NHS Autism Diagnostic Observation Schedule (ADOS-2) and ADI-R gold standard.
Environmental / social causes
Inadequate language exposure: limited adult-directed speech ("serve and return" interaction), excessive screen time, social deprivation, parental mental health difficulties (postnatal depression β€” reduced parent-infant interaction). Bilingual upbringing: code-switching is normal; total vocabulary in both languages combined should meet milestones. These children need SLT support and parental guidance β€” not investigation.
Structural / neurological causes
Cerebral palsy (dysarthria β€” motor speech disorder, not language). Intellectual disability (global developmental delay). Specific language impairment (SLI/DLD β€” developmental language disorder): normal hearing, normal non-verbal intelligence, no ASD, but persistent language disorder. Cleft palate (hypernasality). Childhood apraxia of speech (CAS β€” inconsistent consonant errors, groping oral movements). Selective mutism (speaks at home but not in social settings β€” anxiety-based, not language disorder).
Developmental language disorder (DLD) β€” previously called specific language impairment (SLI) β€” is one of the most common neurodevelopmental conditions in children, affecting approximately 7-10% of school-age children. It is defined as a persistent language disorder in a child with: normal hearing, normal non-verbal intelligence, no ASD, no cerebral palsy, and no known genetic syndrome. Children with DLD have significant difficulty with both understanding and using language β€” grammar, vocabulary, narrative, and phonological processing are all typically impaired. The prognosis is variable: approximately 40% of children with DLD at age 5 have persistent language difficulties at age 15-17. DLD is associated with substantial educational, social, and mental health difficulties in adolescence and adulthood. The RCSLT (Royal College of Speech and Language Therapists) estimates that approximately 1-2 children in every classroom of 30 has DLD. Early identification and intensive SLT input significantly improves outcomes. GPs should be aware that DLD is not a diagnosis of exclusion made in infancy β€” it requires formal SLT assessment, and the diagnosis is typically established around age 4-5 when non-verbal intelligence can be reliably assessed.
5
Refer

Referral Pathways

Same-day / urgent
Any developmental regression (loss of skills) β†’ paediatric neurology same-day Β· Severe bilateral hearing loss not yet identified β†’ audiology same-day Β· Seizures + speech regression β†’ paediatric neurology same-day
Community paediatrics (within 4 weeks)
M-CHAT-R/F positive (ASD screen) β€” do not delay for SLT first Β· Global developmental delay + speech delay Β· Dysmorphic features Β· Suspected genetic syndrome Β· Ex-preterm child with multiple developmental concerns
Speech and Language Therapy (SLT β€” all speech delay)
All children with speech or language delay should be referred to SLT regardless of cause or severity. NHS SLT: request via GP referral. Early referral = better outcomes. Do not delay SLT awaiting audiology results β€” refer both simultaneously.
Audiology
Every child with speech delay β€” mandatory before other investigation. GP can refer directly to paediatric audiology. Automated otoacoustic emission (AOAE) at birth screen + pure tone audiogram (PTA) for children over 3-4 years; visual reinforcement audiometry (VRA) 6 months–3 years.
ENT
Bilateral OME with hearing loss >25 dB for >3 months + speech delay β†’ grommets consideration. Suspected submucous cleft palate β†’ ENT/cleft team. Adenoid hypertrophy causing conductive loss.
CAMHS / paediatric psychology
ASD diagnostic assessment (via community paediatrics or direct CAMHS). Selective mutism (anxiety management + school liaison). Significant behavioural comorbidity with DLD.
The simultaneous referral principle for speech delay is important β€” GPs should refer to both audiology and SLT at the same consultation, rather than waiting for audiology results before referring to SLT. The reason: NHS waiting times for both audiology and SLT are often 4-16 weeks. If the GP waits for audiology before referring to SLT, the total delay to first SLT contact is doubled. Even if hearing loss is found, SLT input is still needed alongside hearing management. The only referral that should be prioritised above the others is audiology β€” hearing loss must be excluded first because it is the most common and most treatable cause. But SLT referral should happen simultaneously, not sequentially. The NICE guideline NG98 (Hearing Loss in Adults) and the NICE pathway for children's speech and language emphasise that early access to SLT is associated with significantly better long-term language outcomes.
6
Treat

Speech & Language Therapy Approaches

SLT interventions for pre-schoolers (1-4 years)
Parent-mediated approaches (most evidence-based for under-3s): Hanen "It Takes Two to Talk" β€” trained SLT delivers group programme to parents teaching techniques to expand child's language in natural interactions. Makaton signing (British Sign Language simplified β€” for children with limited expressive speech, supports communication while speech develops). PECS (Picture Exchange Communication System) for ASD with limited speech. Intensive play-based SLT for late talkers.
SLT for school-age children (5+)
Narrative therapy (story grammar β€” teaching children to structure narratives). Phonological awareness training (preparation for reading β€” phoneme segmentation, blending, rhyming β€” Nuffield Dyspraxia Programme for CAS). Vocabulary enrichment programmes. Social communication groups for ASD (Social Thinking, Lego therapy). Augmentative and alternative communication (AAC β€” PECS, Proloquo2Go iPad app, high-tech voice output devices) for non-verbal or minimally verbal children.
Grommets for OME with hearing loss + speech delay
Bilateral OME + hearing loss >25 dB + speech delay: grommets typically inserted under GA (day case). Immediate restoration of hearing. Average grommet life: 6-12 months (extrude naturally). Post-grommets: language often catches up rapidly. Swimming: grommets without plugs generally safe for surface swimming; avoid diving. Review with SLT post-grommets to assess language catch-up.
Selective mutism treatment
Graduated exposure (CBT-based) β€” systematic desensitisation in school and social settings. School SENCO liaison β€” quiet time, small group activities, non-verbal response initially. Fluoxetine 10-20 mg OD (off-label β€” limited evidence) for severe cases not responding to behavioural therapy. CAMHS psychologist-led treatment. School-home liaison essential.
Parent-mediated early intervention for speech delay has the strongest evidence base for children under 3 β€” multiple RCTs demonstrate that programmes which train parents to modify their communication behaviours (reducing directives, following the child's lead, expanding utterances, using parallel talk and self-talk) are more effective than clinic-based SLT alone for improving language outcomes in pre-schoolers. The reason: children aged 1-3 spend the vast majority of their waking hours with their parents/caregivers, not with SLTs (who typically see them 1 hour per week at most). Changing the quality of every interaction throughout the day β€” which is what parent-mediated intervention achieves β€” produces far more learning opportunities than clinic-based therapy alone. The Hanen 'It Takes Two to Talk' programme is the most widely studied parent-mediated intervention in the UK β€” it involves approximately 8-10 SLT-facilitated group sessions for parents, with in-home video feedback. GPs should be aware that when families are referred to SLT, the most effective intervention may be offered to the parents rather than directly to the child β€” this should be explained proactively to avoid parental disappointment.
7
Treat

Managing Common Underlying Causes

Otitis media with effusion (OME) management
Watchful waiting: OME in a child without significant hearing loss or speech impact β€” observe for 3 months (spontaneous resolution in 50% within 3 months). Hearing loss >25 dB both ears for >3 months: ENT referral + grommets consideration. During watchful waiting: preferential seating in classroom (front, near teacher), face-to-face communication, clear speech at home, reduce background noise. Autoinflation (Otovent balloon) β€” moderate evidence for improving pressure equalisation. Intranasal corticosteroids: limited evidence for OME. Antibiotics: not recommended for OME.
Iron deficiency and speech delay
Iron deficiency (even without frank anaemia) impairs myelination and dopaminergic neurotransmission β€” both critical for language development. Ferritin <12 mcg/L in a child with speech delay: treat with oral ferrous sulphate (3-6 mg/kg/day elemental iron, e.g., ferrous sulphate syrup 1 mg/mL β€” 3-6 mL/kg/day). Dietary sources: red meat, oily fish, fortified cereals, lentils, green leafy vegetables, vitamin C enhances absorption. Avoid excessive cow's milk intake (>500 mL/day in toddlers β€” reduces iron absorption and appetite for iron-rich food).
Screen time reduction
WHO recommends zero screen time for under-2s; maximum 1 hour/day for 2-4 year olds (high-quality interactive content). Passive screen exposure replaces serve-and-return vocal interaction β€” every hour of TV watched by under-2s is associated with a 6-word vocabulary reduction. Replacement activities: shared book reading (30 min/day) is one of the most evidence-based interventions for language development; singing nursery rhymes; floor play.
Bilingual children β€” reassurance and support
Bilingual children may have smaller single-language vocabulary at 18-24 months but total vocabulary across both languages is equivalent to monolingual peers. Both languages should be supported β€” do not advise parents to abandon their home language. SLT referral is appropriate if total vocabulary across both languages is below expected. Schools: bilingual children benefit from high-quality English language exposure in pre-school/nursery. Interpreter for SLT appointments if needed.
The screen time and speech delay relationship deserves explicit clinical communication because it is actionable and reversible β€” multiple prospective studies (Chonchaiya 2008, Zimmerman 2007) and a systematic review demonstrate that background television exposure and heavy screen use in under-2s are associated with reduced parent-child verbal interaction (the primary driver of language development), reduced vocabulary at 24 months, and slower language acquisition. The mechanism is displacement: time spent watching screens is time not spent in face-to-face serve-and-return vocal interaction with adults. The AAP (American Academy of Pediatrics) and NHS guidance recommends zero screen time under 18 months (excluding video calls with family members), and maximum 1 hour per day of high-quality, co-viewed, interactive content for ages 2-5 (not background TV). GPs should ask about screen time at every 12-month and 2-year developmental review and provide concrete alternatives: 'For every 30 minutes of screen time, replace it with 30 minutes of reading books together or singing nursery rhymes β€” this is the single most impactful thing you can do for your child's language development.'
8
Lifestyle

Language-Rich Environment, Reading & Parent Engagement

Serve and return interaction The single most important driver of language development is serve-and-return verbal interaction β€” the adult notices the child's focus, responds with language, and the child responds. "Oh, you're looking at the dog! That's a big brown dog. What sound does the dog make?" Every exchange builds neural connections. Quantity and quality of adult speech directed at the child predicts vocabulary size at age 3 more than any other factor. Encourage parents: narrate daily activities, describe what you see, ask questions, respond to babble as if it's meaningful.
Shared book reading Daily shared book reading is one of the most evidence-based interventions for language development β€” Reading aloud to children from birth (Reach Out and Read programme) increases vocabulary, phonological awareness, and school readiness. Target: 15-30 minutes of shared reading daily. Book Gifting Scheme: Bookstart (UK) provides free books to families at 9 months and 3 years. Choose wordless picture books for non-verbal children β€” commenting on pictures requires no reading ability. Libraries: free; Rhyme Time sessions.
Nursery rhymes and songs Nursery rhymes build phonological awareness (awareness of sound patterns in words) which is the strongest predictor of reading ability. Songs build vocabulary, rhythm, and prosody (speech melody). Singing to and with children from birth. Songs in the home language as well as English. Baby Rhyme Time at local libraries. Singing during daily routines: bath time, getting dressed, car journeys.
Reducing background noise Background TV β€” even when the child is not watching β€” reduces the quantity and quality of parent-child verbal interaction by approximately 20-30%. Turn off the TV and radio as background noise during meal times and play. Create a "language-rich, screen-free" hour each day. Quiet environments allow children to hear speech more clearly, which is especially important for children with mild hearing loss from OME.
Support for parents with postnatal depression Postnatal depression (PND) significantly reduces the quantity and responsiveness of parent-child interaction β€” the "still face" effect of a depressed parent's reduced responsiveness is measurably harmful to infant language development. PHQ-9 screen at every baby review. IAPT referral for PND (CBT or brief counselling). Peer support (PANDAS foundation). Home-Start volunteer support. Treating PND is also treating the child's speech delay.
Makaton and signing support Makaton is a language programme using symbols and signs to support communication β€” it does NOT delay spoken speech development; evidence consistently shows signing support accelerates speech because it reduces communication frustration and provides multi-modal language input. Encourage all parents of pre-verbal or minimally verbal children to learn basic Makaton signs. NHS provides free Makaton workshops in many areas. Mr Tumble (BBC CBeebies) uses Makaton β€” a rare example of beneficial screen content for language-delayed children.
School readiness and EHCP Children with significant speech and language delay may need an Education, Health and Care Plan (EHCP) for additional support in school. GPs can support EHCP applications by providing medical information. EHCP process: local authority; paediatric SLT assessment is a key component. Starting school with unaddressed significant language delay is strongly associated with learning difficulties, reading failure, and mental health problems β€” early identification prevents this.
Support organisations ICAN (ican.org.uk) β€” UK charity for children with speech and language difficulties; free helpline, information for parents and teachers. Talking Point (talkingpoint.org.uk) β€” online resource with milestone information and GP/parent tools. RCSLT (rcslt.org) β€” professional body for SLTs, patient resources. National Deaf Children's Society (ndcs.org.uk) β€” hearing loss support. National Autistic Society (autism.org.uk).
The Bookstart programme (funded by Booktrust, supported by NHS in the UK) is one of the most cost-effective early language interventions available β€” every family in the UK receives a free Bookstart pack at the 9-12 month health visitor review (containing board books, rhyme cards, and reading guidance) and a second pack at age 3. The evidence: families who receive Bookstart packs show higher rates of shared book reading, and children in Bookstart families have measurably better vocabulary and school readiness at age 5. Health visitors and GPs have the opportunity at the 9-12 month review to: (1) ensure the Bookstart pack was received; (2) demonstrate how to read interactively with a board book; (3) signpost to library Rhyme Time sessions; and (4) emphasise the importance of talking to the baby from birth. The investment of 2 minutes in Bookstart discussion at the 9-month review has downstream effects on literacy, language development, and school readiness.
9
Safety

Follow-Up, Monitoring & School Readiness

Follow-up schedule
2-year developmental review (GP or health visitor): use Ages and Stages Questionnaire (ASQ-3) or PEDS (Parents' Evaluation of Developmental Status) β€” standardised screening tools. Record milestones against expected norms. Any concern: SLT referral same day. 3-year review: confirm SLT engaged + assess progress + confirm audiogram done. 4-5 years (pre-school): confirm school readiness β€” can child communicate their needs, follow instructions, engage in group activities?
Response to SLT β€” expected trajectory
Most children with pure expressive delay + good comprehension + early SLT input: significant improvement within 6-12 months. Children with receptive-expressive delay: slower progress, may need EHCP support in school. ASD: language development varies widely; intensive EIBI (early intensive behavioural intervention, e.g., ABA therapy) shown to improve language outcomes in non-verbal ASD. DLD: improvement with therapy but often persistent difficulty β€” needs ongoing school support.
Monitoring for ASD if initial screen negative
A negative M-CHAT-R/F at 18 months does not exclude ASD β€” ASD can present later, or early features may be subtle. Continue monitoring at 2-year and 3-year reviews. Any parental concern about ASD at any age: refer to community paediatrics. ASD diagnosis is not age-limited. Some high-functioning ASD children are not diagnosed until primary or secondary school.
Safeguarding and speech delay
Document: home circumstances, language spoken at home, parent engagement with services. If child is not attending SLT appointments + speech not improving + safeguarding concerns: escalate to HV + social care. Non-engagement with services for a child with significant delay is a safeguarding concern.
Urgent referral today
Developmental regression at any age β†’ paediatric neurology Β· Bilateral profound hearing loss not identified β†’ audiology same-day Β· Seizures + speech loss β†’ paediatric neurology
Within 2 weeks
M-CHAT positive (any score β‰₯3) β†’ community paediatrics Β· No words by 16 months β†’ SLT + audiology Β· No 2-word phrases by 24 months β†’ SLT + audiology + community paediatrics
The age 2 developmental review is the most important speech and language screening opportunity in primary care β€” it is the standardised contact where delayed language development can be identified and early intervention initiated before school entry. In England, the 2-year check is conducted by health visitors using the Ages and Stages Questionnaire (ASQ-3) and the integrated review combining the NHS 2-year check with the Early Years Foundation Stage 2-year progress check from the child's early years setting (nursery/childminder). GPs who see children at the 2-year routine immunisation visit should use this contact proactively to: (1) ask about language development using the 24-month milestones as a guide (50+ words, 2-word combinations); (2) administer the M-CHAT-R/F if any language or social concern; (3) check tympanic membranes; and (4) refer to SLT and audiology simultaneously if any delay identified. The average age of specialist ASD diagnosis in the UK is 5-6 years β€” despite families first raising concerns with GPs at 18-24 months. Reducing this diagnostic delay requires proactive GP screening.
Educational use only. Based on NICE NG3 Autism in Under 19s 2011, RCPCH Development for Safeguarding 2020, RCSLT Speech Language Therapy guidelines, NICE NG98 Hearing Loss, NHS Universal Newborn Hearing Screening Programme, Ages and Stages Questionnaire (ASQ-3).