Musculoskeletal presentations (chronic) in babies and children

Many thanks to the Paediatric Physiotherapy team at University Hospitals Dorset for developing these resources. 

Developmental Dysplasia of the Hip (DDH)

DDH describes a spectrum of conditions related to the development of the hip in infants and young children. It encompasses abnormal development of the acetabulum and proximal femur, and mechanical instability of the hip joint.

Key Assessment points

  • Lower limb symmetry; check leg length and skin / gluteal creases
  • Barlows/Ortolani test
  • Restricted or asymmetrical hip abduction (should be > 80 degrees, and equal right and left)
  • Check for Waddling gait/limp (when walking age)

 

Referral not indicated

  • Child has full hip range of motion, no instability or asymmetry
  • Baby has had a normal hip USS

Refer for a Hip Ultrasound scan if:

 

Baby is under 10 months of age and has...

  • A positive Barlow or Ortolani indicating a clinically unstable hip, obvious asymmetry or reduced hip abduction
  • A risk factor for hip screening including family history (1st Degree: Siblings or parents), breech presentation (from 36 weeks gestation), oligohydramnios , intrauterine moulding (torticollis / SMT / windswept / calcaneovalgus feet / metatarsus adductus)
  • A risk factor that has been identified in a twin/ multiple pregnancy – all babies should be scanned

NB:  if baby is less than 12 weeks old, US referral should be urgent, as conservative treatment (Pavlik harness) cannot be commenced over this age.

 

Refer for Pelvis X-ray if:

 

Baby is over 10 months of age and has…

  • Leg length asymmetry  and skin / gluteal crease asymmetry
  • Restricted or asymmetrical hip abduction (over 80 degrees, and symmetrical)
  • A waddling gait or mobilises with a limp

Refer to Paediatric Orthopaedics

 

  • USS or XR is abnormal and baby falls outside of window of treatment for Pavlik harness application (usually over 12 weeks)

Information leaflets

 

  • STEPS charity leaflet ‘Baby Hip Health’. StepsCharity.org

International Hip Dysplasia Institute https://hipdysplasia.org/Baby Feet positional issues

 

 

Baby Feet positional issues

It is common for newborn babies to have moulded feet due to Intra-uterine positioning. This is usually fully correctable, and will improve within the first few months after birth.

Positional talipes equinovarus

 The foot rests inwards and downwards

Calcaneovalgus

The foot rests upwards and outwards

Metatarsus adductus

The forefoot curves inward

Does not require a routine hip ultrasound scan OR PHYSIO

Hip ultrasound scan at 6 weeks, PHYSIO IF TIGHT/STIFF

Hip ultrasound scan at 6 weeks, PHYSIO IF TIGHT/STIFF

 

Congenital talipes equinovarus CTEV (clubfoot) is a true, rigid fixed foot, with a smaller leg and calf, and a high riding small heel. This is usually identified on antenatal scans and is treated with Ponseti casting at Southampton Hospital.

 

Key assessment points

  • Assess ankle and foot range of movement (passive and active)
  • Examine hips for DDH (see Developmental Hip Dysplasia guidelines)
  • Quick check of neck range of movement and head shape

 

Referral not indicated

 

Refer to Paediatric Physiotherapy

  • The foot has persisting tightness / stiffness (not fully passively correctable)

Refer to Southampton Paediatric Orthopaedics

  • Refer all CTEV (clubfoot) or  rigid / fixed foot postures; to Mr Barry and Julia Judd at Southampton for the Foot Casting Clinic

Refer to ultrasound for a hip scan

  • Calcaneovalgus or metatarsus adductus, if the baby has not been referred directly from maternity
  • If clinically indicated ( please see Developmental Hip Dysplasia guidelines)

 

 

Torticollis / head turning preference / plagiocephaly

Intra-uterine positioning and a prolonged or difficult labour can cause newborn babies to have a misshapen head.

This is common and will usually improve within the first few weeks after birth. However, if associated with a loss of range of movement in the neck (torticollis), and/or a strong preferential head turn, the problem may persist and the head shape may worsen.

  • Positional plagiocephaly is an asymmetrical distortion of the skull caused by uneven external pressures
  • A sternomastoid mass (Fibromatosis Coli) is a haematoma in the sternocleidomastoid muscle due to birth trauma. This is replaced with fibrous scar tissue and can cause progressive muscle shortening and restriction of movement. A palpable lump can appear up to 2-6 weeks after birth.
  • Craniosynostosis is a rare condition and is defined as the premature fusion of one or more of the cranial sutures. It can cause cranial and facial asymmetry.​

Key assessment points

  • Assess neck range of movement (passive and active) checking both neck rotation and side flexion.     
  • Palpate neck for lumps/ swelling indicating a Sternomastoid tumour (SMT)
  • Observe head shape and palpate fontanelles and sutures, for signs of plagiocephaly or craniosynostosis.

 

Referral not indicated

 

  • Mild plagiocephaly with full neck range of movement

Educate re) encouraging equal movement to right and left when awake,  and repositioning baby’s head when asleep, to less preferred side. Encourage regular supervised tummy time. Give appropriate leaflet; “APCP leaflet on Head Turning Preference and Plagiocephaly

 

Refer to Paediatric Physiotherapy

 

  • Decreased neck range of movement / congenital torticollis
  • Palpable lump in neck; Sternomastoid mass (Fibromatosis Coli)
  • Significant head turning preference
  • Mod- severe plagiocephaly

Refer to Paediatrician

  • Craniosynostosis
  • Abnormal fontanelle / cranial sutures
  • Dysmorphic features
  • Abnormal neurology

Refer to Community Paediatrician

  • Abnormal neurology
  • Developmental delay
  • Dysmorphic features

 

 

 

Childhood Growing Pains

Growing pains are described as acute muscular pain in the legs which can cause nocturnal waking. This condition occurs in about 15% of children as early as 1 year old. The child does not limp and symptoms are relieved by massage and simple analgesics.

Typical features;

•       Usually non-articular, in 2/3 of children its located in the shin, calves, thighs or popliteal fossa and is almost always bilateral

•       Pain usually appears late in the day, and often wakes the child at night

•       Duration ranges from minutes to hours, severity can be mild to severe

•       By morning the child is almost always pain-free

•       Often parents can predict when the child will have pain on days of increased activity

 

Key Assessment points

•   Perform The paediatric gait, arms, legs and spine examination  (pGALS), check for limp, check joints for restriction/swelling

•   Rule out systemic features

•   Check skin for a rash, bruising

•   Review developmental milestones

•   Ensure normal growth (height and weight percentiles)

Referral not indicated

•   Typical growing pain presentation with no indications for concern (fits typical features listed above)

•    Reassure parent/guardian. Explain the natural benign course of growing pains, reducing parental anxiety. Advice leaflet  Childhood growing pains

Investigations that may be indicated in Primary Care

•    Full blood count

•    Acute phase reactants (ESR, CRP)

•    Biochemistry (bone biochemistry and vitamin D)

•    Thyroid function

•    Creatine kinase (CK)

•    Growth chart (height and weight)

•    XR of legs (hips with frog views)

IMPORTANT NEGATIVES: (normal FBC/ESR, joints normal, no CV features)

Refer to Paediatric Physiotherapy

•    There is associated muscle tightness and/or weakness with pain

Refer to Paediatric Orthopaedics

 

•     A limp with positive Pelvic XR findings

•     Concern about bony pathology

•     Palpable lump in muscle (bakers cyst, semimembranosis bursitis)

Refer to Paediatrician

•     Poor appetite and/or weight loss

•     Poor growth

•     Systemic symptoms

•     Pain not relieved by massage or analgesics

•     Muscle weakness, extreme fatigue

Refer to Paediatric Rheumatologist

•     Joint swelling, pain and morning stiffness indicating inflammatory pathology

•     Positive pGALS with restricted joint range of motion

Curly toes 

Congenital curly toes are a common condition that tend to affect the 3rd, 4th and 5th toes of one or both feet, usually present at birth but can become more noticeable when a child starts walking.

Curly toes are a normal variant and generally don’t require treatment unless they are symptomatic. They generally do not cause any problems. Occasionally the tendons can become tight and pull the tip of the toe underneath the next toe and towards the sole of the foot. Children complain of rubbing or pain and may have problems with finding suitable shoes that fit properly.

Key Assessment points

•    Check passive range of motion of the toes, will they fully correct to a neutral position and is there any tightness in the toe flexor tendons?

•    Check for generalised muscle tightness particularly in toe flexor tendons and calf complex (silfverskiold test)

•    Check for ‘clawing’ toes or cavus feet

Referral not indicated

 

•    Overriding toes are flexible/correctable

•    Advise on silicone toe spacers and foot wear with a wide toe box

Reassure the parent/guardian that curly toes are entirely normal and give advice leaflet titled "curly toes” and if indicated APCP advice leaflet titled “Choosing Footwear for Children”

Refer to Paediatric Physiotherapy

  • There is associated muscle tightness and/or weakness that is exacerbating the problem   

Refer to Paediatric Orthopaedics

  • Refer curly toes that are not passively correctable to a neutral position and causing painful blisters or rubbing, callouses or ingrowing infected toe nails possibly requiring surgical intervention.

 

Refer to Community Paediatrician or Neurologist

 

  • If all of the toes of one or both feet are clawed, resulting in a cavus foot this requires further investigation

Refer to Community Podiatry Service

 

  • If curly toes are significant refer for consideration of toe props/wedges

Flat Feet (pes planus) 

Most children under the age of three have flat feet and rolling ankles. The arch on the inside of the foot does not begin to develop until after this age. The arches may be visible when a child is sitting, when the big toe is bent backwards or if the child stands on tiptoe. Full development of an arch is usually between the ages of 5-7 years old. In most children flat feet do not cause any problems.

Key Assessment points

•    Ask the child to stand on tip toes. If the arch lifts, the foot is flexible

•    Passively lift (extend) the big toe, to see the child’s arch lifts

Referral not indicated

 

•    Child is asymptomatic

•    Flat feet are fully flexible

Reassure the parent/guardian and give APCP advice leaflet titled “Flat Feet in Young Children” and if indicated APCP advice leaflet titled “Choosing Footwear for Children”

 

Refer to Paediatric Physiotherapy

 

  • There is pain in the lower limbs
  • There is associated muscle tightness and/or weakness
  • Referrals for children under the age of 3 with flat feet will not be accepted
  • Referrals for pain free flat feet will not be accepted      

Refer to Paediatric Orthopaedics

  • Rigid / stiff flat feet (arch of the foot doesn’t correct on tip toes in over 5’s)
  • Structural asymmetrical flat feet (especially with heel valgus)
  • Painful flat feet that have not improved with orthotics and physio

Refer to Podiatry/Orthotics

 

 

 

  • Flat feet are causing pain, rubbing or uneven shoe wear

Intoeing

Intoeing

In-toeing gait (walking with feet facing inwards) is a common, normal variance of developing gait and usually does not require intervention or onward referral.  In most cases it resolves over time. Occasionally it will persist into adolescence or be a sign of more serious pathology.

Common causes:

  • Femoral ante-version (excessive range of internal rotation compared to external rotation of the hips) is a normal variant up to 10 years of age.
  • Metatarsus adductus/ searching big toe is a normal variant up to 5 years of ag
  • Internal tibial torsion (In sitting: knee flexed to 90˚, foot points inwards relative to the thigh) is a normal variant up to 7 years of age
​​​

Key Assessment points

•   Observe gait pattern and ensure symmetrical

•   Check for full range of movement in the lower limb joints, especially the hips.

•   Check for abnormal neurology in both the upper and lower limbs

Referral not indicated

 

•   Child is asymptomatic and up to 9 years of age

Physiotherapy cannot prevent tripping often associated with intoeing. Please DO NOT refer asymptomatic patients, or on parental concern alone. Reassure the parent/guardian and give APCP Advice leaflet titled “Intoeing gait”

                                                                 

Refer to Paediatric Physiotherapy

 

  • Metatarsus adductus with true tightening of the medial structures of the foot and a medial crease.
  • Intoeing associated with hip/knee/ankle pain
  • There is associated muscle tightness and/or weakness

 

Refer to Paediatric Orthopaedics

  • Asymmetrical hip range of motion (you may wish to request AP Pelvis first)
  • Child is over 8/9 years of age with pain, tripping over, significant deformity causing psychological distress

 

Refer to Community Paediatrician

  • Abnormal neurology
  • Regression of acquired motor skills

Refer to Podiatry or Orthotics

  • Flat feet are causing pain, rubbing or uneven shoe wear

 

Outoeing

Out-toeing is a common, normal variance of gait and usually does not require intervention or onward referral. It usually improves as a child grows. Out-toeing often runs in families, and can persist into adult life but rarely causes problems. It is commonly seen in later walkers and may be associated with knock knees (genu valgus) and flat feet.

Common causes:

  • External femoral torsion
  • External tibial torsion
  • Marked flat feet/ calcaneo-valgus foot posture

Less Common causes:

·       Legg-Calve Perthes Disease /Slipped Capital Femoral Epiphysis, especially when unilateral – due to decreased hip rotation and abduction

​​​​​​

Key Assessment points

 

•       Observe gait pattern and ensure symmetrical

•       Check for full range of movement in the lower limb joints, especially hips

•       Check for abnormal neurology in both the upper and lower limbs

Referral not indicated

•       Symmetrical asymptomatic out-toeing

•       Please DO NOT refer patients on parental concern alone. Reassure the parent/guardian

•       If indicated give APCP advice leaflet titled “Choosing Footwear for Children”

Refer to Paediatric Physiotherapy

 

·      Out-toeing associated with hip/knee/ankle pain

·       There is associated muscle tightness and/or weakness 

Refer to Paediatric Orthopaedics

 

·      Asymmetrical hip range of motion (you may wish to request AP/frog lateral Pelvis first)

·      Child is over 8/9 years of age with pain and/or significant deformity causing psychological distress

·       Persistent pain assocaited with out-toeing that has not improved with physiotherapy/orthotics

Refer to ED/CAU

 

·       Sudden onset of out-toeing following trauma, particularly if asymmetrical and associated with a limp – may suggest Perthes/SCFE

                                                                                                

Refer to Podiatry or Orthotics

 

·       Flat feet/calcaneo-valgus foot posture is causing pain, rubbing or uneven shoe wear

Toe walking

It is common for children to walk intermittently on their tip toes when they are learning to walk. Idiopathic toe walking (ITW) is an exclusionary diagnosis given to healthy children who persistently walk on their toes after they should typically have achieved a heel‐toe gait.

Common causes:

  • Toe-walking is usually idiopathic and resolves with age. It may simply be a preference and/or a habit. Suspended walkers and door bouncers should be discouraged as they exacerbate the problem.
  • Children may have tight, shortened calf muscles and limited ankle dorsiflexion
  • Toe-walking may be seen in children with neurodevelopmental conditions, such as autism spectrum disorders and is related to sensory differences these children have.
  • Toe walking may be due to an underlying neurological or neuromuscular impairment (e.g. cerebral palsy or muscular dystrophy)​​​​​

Key assessment points

 

•    Observe gait and ensure symmetrical pattern

•    Functional checks; Can the child stand with their heels down and trunk straight, can they squat keeping their heels down, can they walk on their heels?

•    Check ankle dorsiflexion and calf muscle length and size

•    Check for abnormal neurology in both the upper and lower limbs, including Gowers Sign and muscle tone / clonus.

Referral not indicated

 

•     Child is under 3 years of age (with no neurological signs and no muscle tightness)

•     Educate/reassure parent/guardian re) it is likely to resolve with age.

•     Give appropriate leaflet;  ‘Toe walking in children’

Refer to Paediatric Physiotherapy

  • Reduced ankle dorsiflexion with calf muscle tightness
  • If associated with pain
  • If there are associated functional difficulties

 

Refer to

Paediatric Orthopaedics

  • Not improved with physiotherapy input (stretches / serial casting etc)
  • Unilateral toe-walking, with no abnormal neurology
  • Inability to dorsiflex foot beyond neutral or stand with heels down despite conservate intervention

 

Refer to Community Paediatrician/ Neurologist

 

  • Abnormal neurology
  • Signs of cerebral palsy eg) asymmetry, increased tone / clonus
  • Signs of muscular dystrophy: calf hypertrophy, positive Gowers and/or regression of milestones

Genu Varum (Bow legs)

Physiological bowing is the most common cause of genu varum. It is a normal variant and usually corrects by the age of 2-3. It can be associated with overweight babies/toddlers as well as early walkers and can also be associated with in-toeing gait.
 

Be aware of pathological causes e.g. Rickets and Blount’s disease, indicated by swellings at the wrist and ankles, a poor dietary history and marked, progressive or asymmetrical bowing. 

 

Key Assessment points

•    Observe the child in supine, standing and observe gait

•    Check for symmetry and leg length discrepancy

 

Referral not indicated

•    Symmetrical asymptomatic genu varum

•    Reassure parents. Physiological bow legs will begin to resolve by age two with normal development. No specific treatment is required.

•    Consider completing bloods for Vitamin D and recommend supplements if indicated 

•    Reassure the parent/guardian and if indicated give advice leaflet titled “Bow legs and knock knees in Children”

•    Provide information on healthy weight management

 

Refer to Paediatric Physiotherapy

  • There is associated muscle tightness and/or weakness with associated pain

Refer to Paediatric Orthopaedics

 

  • Significant genu varum persists after 2 years or progressively worsens from 12-18 months (Rickets and Blount’s need to be excluded)
  • Asymmetrical knee varus
  • Inter-condylar distance with feet together of over 6 cm in standing

 

Refer to Podiatry or Orthotics

  • Flat feet/calcaneo-valgus foot posture is causing pain, rubbing or uneven shoe wear

 

 

 

Genu Valgum (Knock knees)

Physiological knock knees are seen from three to five years of age; it normally resolves by the age of eight. It may be familial and/ or associated with obesity.

 

Key Assessment points

•    Observe the child in supine, standing and observe gait

•    Check for symmetry and leg length discrepancy

•    Determine the patient’s height and weight percentiles

•    If concerned, measure the inter-malleolar distance every six months and document progression or resolution

NB: A child who is significantly overweight with increased adipose tissue around the inner thighs may appear knock kneed.

Referral not indicated

•    Symmetrical asymptomatic genu valgum

•    Reassure. The majority of physiological knock knees will resolve with normal development by the age of eight; no specific treatment is required

•    If indicated give advice leaflet titled “Bowlegs and knock knees in Children”

•    Provide information on healthy weight management

 

Refer to Paediatric Physiotherapy

  • There is associated muscle tightness and/or weakness with pain

Refer to Paediatric Orthopaedics

 

  • Asymmetrical knee valgus
  • Excessive or worsening valgus knees after 6 years of age
  •  Inter-malleolar distance of over 8 cm in standing

 

Refer to Podiatry or Orthotics

  • Flat feet/calcaneo-valgus foot posture is accentuating lower limb position, causing pain, rubbing or uneven shoe wear

Heel / foot / ankle pain

Heel pain is common in children, especially during puberty when there is an accelerated rate of bone growth and significant changes in hormone levels

  • Severs Disease is a common cause of heel pain in growing children; the Achilles tendon pulls on the active growth plate at the back of the heel.
  • The vast majority of growth related pain is not serious and will resolve quickly with muscle stretches.
  • Some children may also benefit from strengthening exercises.

Key assessment points

  •  Observe gait
  •  Check range of movement of hips, knees, ankles and feet, including subtalar joint is full and symmetrical
  •   Heel squeeze test and palpate around heel growth plate to ascertain area of pain
  •   Check lower limb muscle flexibility, especially calf muscle length
  •   Painful, stiff or rigid flat feet may indicate tarsal coalition

 

Referral not indicated

 

  • Mild pain with no muscle tightness
  • Educate and reassure parents/guardians. The majority of heel pain will resolve with improved flexibility
  • Give ‘Heel pain in Children’ leaflet and advice, advise patient to try exercises prior to referring to physiotherapy

 

Refer to Paediatric Physiotherapy

  • Tight/Weak muscles despite trying exercises in ‘heel pain leaflet’ and/or poor core stability
  • Persisting/ chronic pain
  • Difficulty in functional activities or reduced activity levels due to pain e.g.  running, jumping, PE
  • Reduced / non weight bearing

 

Refer to Paediatric Orthopaedics

  • Indication of serious orthopaedic pathology / red flags
  • Limping child with no trauma / mechanism of injury
  • Stiff / rigid painful feet
  • Pain that has not resolved despite Physiotherapy

Knee pain

Knee pain is common in children, most symptoms are caused by growth, overuse or muscle imbalance.

Common causes of knee pain;

1.     Osgood-Schlatter (OS) and Sinding-Larsen-Johansson (SLJ) syndrome are traction apophysitis conditions in growing adolescents. With OS pain is located at the tibial tuberosity and with SLJ at the apex of the patella

2.     Anterior knee pain is a dull, aching or sharp pain that can be felt behind, below or to the sides of the patella

3.     Patella instability/ dislocation

​​​​​​

Key assessment points

 

  • Assess gait and function
  • Check posture, leg length, symmetry / limb alignment
  • Check range of movement of hips and knees and muscle flexibility
  • Palpate knee to check for swelling and to ascertain area of pain
  • Perform special tests to ligaments and menisci as indicated

 

Referral not indicated

 

  • Mild pain with no muscle tightness
  • Educate and reassure parents/guardians.
  • The majority of knee pain will resolve with improved flexibility and strength
  • Go to ’Knee advice and exercises’ on our website and give info leaflet
  • If acute knee injury and referral not required, go to provide family with “acute knee injury” leaflet

 

Refer to Paediatric Physiotherapy

  • Tight muscles/Weak muscles / poor core stability/ persisting or chronic pain
  • Reduced function/activity  due to knee pain e.g. NWB,  running, jumping, PE
  • Knee rehabilitation following patella dislocation, ligament, meniscal damage

Refer to ED/CAU

 

  • Large haemarthrosis
  • First time patella dislocation (to follow protocol)
  • Suspected fracture
  • Severe pain, reduced peripheral pulses or muscle weakness

 

Investigations

 

X-rays: Following trauma, suspicion of OCD: weight-bearing X-ray (AP, lateral)

Bloods: Inflammatory/infective/sinister pathology suspected

 

Refer to Paediatric Orthopaedics

  • Suspicion of meniscal tear or ACL tear or other acute ligament injury
  • Bony knee pathology
  • Knee pain/functional limitation that is not resolving with physiotherapy
  • Excessive or asymmetric deformity

 

Refer to Acute Paediatrician

 

  • A fever and/or red flags suggesting serious pathology
  • Suspicion of non-accidental injury
  • Abnormal neurology

 

Refer to Podiatry or Orthotics

  • Flat feet/calcaneo-valgus foot posture  accentuating lower limb position, causing knee/foot pain, rubbing or uneven shoe wear

 

Paediatric Red Flags

 

Children presenting with red flags, indicating the possibility of more serious underlying pathology, warrant urgent assessment, with some cases requiring referral directly to the Emergency Department or CAU.

 

  • Unremitting pain
  • Night pain (Pain that awakens the child from sleep)
  • Systemic symptoms; fever, malaise, unexplained weight loss, sickness
  • Changes in bladder and bowel habit
  • Hot, swollen and inflamed joint(s)
  • Early morning stiffness (may indicate JIA) with persistent swelling
  • Painful guarded movement/ muscle spasm/ significant loss of range of motion, in absence of trauma
  • Regression of development / loss or deterioration of function
  • Antalgic gait / inability to weight bear / gait disturbance / lower limb asymmetry
  • Sensation changes (pins and needles/ numbness), absent or exaggerated reflexes, unexplained muscle weakness 

This list is not exhaustive nor a diagnostic tool, but areas to consider        

 

 

Limp / hip pain

Hip pain is common in children and adolescents and has a broad range of causes, ranging from the benign to the potentially devastating. Transient synovitis, one of the most common causes of hip pain in children, must be differentiated from septic arthritis. Hip pain may be caused by conditions unique to the growing paediatric skeleton including Perthes, slipped capital femoral epiphysis and apophyseal avulsion fractures of the pelvis as well as growth related disorders.

Key Assessment points

•       Assess gait and function

•       Check posture, leg length, symmetry

•       Check hip range of movement; hip rotation and abduction should be full and symmetrical if there is no pathology

•       pGALS:  Check spine

•       Temperature / observations

 

Initial GP management

•       Exclude serious pathology

·      Exclude inflammatory cause (Bloods – if inflammatory processes suspected)

·      Direct to Paediatric Physio Website for appropriate information leaflets link

 

Refer to Paediatric Physiotherapy

 

•       Tight/Weak muscles / poor core stability/ Persisting or chronic pain

•       Reduced weight bearing or gait changes

•       Lateral hip pain / ‘snapping hip’ syndrome

•       Reduced function/activity levels due to pain, e.g.  running, jumping, PE

·       Rehab following a period of inactivity/post-surgery

 

Refer to ED/Acute Paediatricians urgently via the Children’s Assessment Unit (CAU)

·      Acute limp or obviously painful or restricted hip movements

·      Unable to weight bear

•       A fever and/or red flags suggesting serious pathology

•       Severe pain, agitated, reduced peripheral pulses or muscle weakness which may indicate neurovascular compromise/ compartment syndrome

•       Suspicion of accidental injury

 

Refer for x-ray

•       Urgent X-ray for a limping child, history of trauma or reduced hip ROM

•       Routine x-ray for patients with mildly reduced hip range of motion, leg length difference or hip pain indicating pathology such as DDH

 

Refer to Paediatric  Orthopaedics

•       A well child with a working diagnosis of transient synovitis but the symptoms fail to resolve within 1 week of onset or for follow-up

·      A child presents with limp on multiple different occasions

·      There is uncertainty about the diagnosis

·      Diagnosis of Perthes/Avascular necrosis/DDH  confirmed on x-ray

 

Refer to Podiatry/Orthotics

•       Flat feet/calcaneo-valgus foot posture is accentuating lower limb position, causing hip pain, rubbing or uneven shoe wear

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

PAEDIATRIC RED FLAGS 

 

Children presenting with red flags, indicating the possibility of more serious underlying pathology, warrant urgent assessment, with some cases requiring referral directly to the Emergency Department or CAU.

  • Unremitting pain
  • Night pain (Pain that awakens the child from sleep)
  • Systemic symptoms; fever, malaise, unexplained weight loss, sickness
  • Changes in bladder and bowel habit
  • Hot, swollen and inflamed joint(s)
  • Early morning stiffness (may indicate JIA) with persistent swelling
  • Painful guarded movement/ muscle spasm/ significant loss of range of motion, in absence of trauma
  • Regression of development / loss or deterioration of function
  • Antalgic gait / inability to weight bear / gait disturbance / lower limb asymmetry
  • Sensation changes (pins and needles/ numbness), absent or exaggerated reflexes, unexplained muscle weakness 

This list is not exhaustive nor a diagnostic tool, but areas to consider        

Back Pain

Back pain in children is becoming increasing common, more so in girls than boys; but is rarely a serious problem. In younger children back pain may be growth related or may indicate more serious pathology such as infection or tumours.  In older children back pain is commonly musculo-skeletal; overuse, carrying heavy backpacks, and sprains and fractures may cause pain. Less common conditions include slipped discs and inflammatory diseases. Congenital disorders such as scoliosis may present at any age.

Key Assessment points

•       Subjective:

•       Red flags, particularly night pain

•       Age of menarche in girls, spine ceases growth 2 years after onset

•       Activity levels / sports/school attendance / school bags

•       Screen time / posture

 

•       Objective:

•       Undress, to see the spine check  posture / symmetry - kyphosis/scoliosis

•       Observe spinal range of movement, gait and function

•       Palpate for areas of vertebral tenderness or muscle spasm

•       Neurological examination if indicated

•       pGALS

Initial GP management

•       Exclude serious pathology

•       Exclude inflammatory cause (bloods – if inflammatory processes suspected)

•       Provide advice on healthy active lifestyle / diet / fitness and posture

•       Give info leaflet:- “Your Healthy Back”

Refer to Paediatric Physiotherapy

 

•       Mechanical or postural back pain

•       Tight/Weak muscles / poor core stability/chronic pain

•       Reduced function/activity levels due to pain e.g.  running, jumping, PE

•       Rehab following a period of inactivity/post-surgery

•       Back pain associated with obesity

•       Postural scoliosis with pain

Refer to Acute Paediatricians via the Children’s Assessment Unit

•       Under 5 years old

•       A fever and/or red flags suggesting serious pathology

•       In severe pain, agitated or has significant muscle weakness

•       Acute onset painful or restricted spinal movements, without trauma

Refer for x-ray

•       Suspected spondylolysis/ spondylolysthesis/ structural scoliosis

Refer to Paediatric  Orthopaedics/Spinal Team at SGH

•       Spondylolysis / spondylolisthesis

•       Structural scoliosis/ kyphosis

•       Scheurmanns disease

•       Disc pathology

•       Trauma

Refer to

Paediatric  Rheumatology

•       AM stiffness

•       Guarded movement / muscle spasm

•       FH of AS/RA

•       Increased ESR/ CRP/ Rheum facto

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Paediatric Red Flags

 

Children presenting with red flags, indicating the possibility of more serious underlying pathology, warrant urgent assessment, with some cases requiring referral directly to the Emergency Department or CAU.

 

  • Unremitting pain
  • Night pain (Pain that awakens the child from sleep)
  • Back pain < 5 years old
  • Systemic symptoms; fever, malaise, unexplained weight loss, sickness
  • Changes in bladder and bowel habit
  • Hot, swollen and inflamed joint(s)
  • Early morning stiffness (may indicate JIA) with persistent swelling
  • Painful guarded movement/ muscle spasm/ significant loss of range of motion, in absence of trauma
  • Acute torticollis persisting over 7 days with an inability to achieve midline head and neck position
  • Regression of development / loss or deterioration of function
  • Antalgic gait / inability to weight bear / gait disturbance / lower limb asymmetry
  • Sensation changes (pins and needles/ numbness), absent or exaggerated reflexes, unexplained muscle weakness  

             

This list is not exhaustive nor a diagnostic tool, but areas to consider        

Complex Regional Pain Syndrome (CRPS) / complex / chronic pain

CRPS / complex or chronic pain can present in varied ways; including reduced function and hypersensitivity with a pain response disproportionate to the movement or action. Minor injuries precipitate 80% of cases of CRPS eg) an ankle sprain.

 

Key Assessment points

•   Check for hypersensitivity to touch

•   Pain response that is disproportionate to the injury

•   Check joint range of movement

•   Check gait / weight-bearing

•   Check for autonomic changes including:  allodynia, swelling, colour changes, skin changes, shiny skin, hair growth, temperature changes

Initial GP management

 

•    Education to parents/guardian and child, to explain pain.

For example: “Unlike the useful warning signal of acute pain, persistent or chronic pain messages no longer serve a useful purpose. These messages are not protecting our bodies from further damage. The nerves continue to respond with pain signals, because they have been so over active - like they are stuck on repeat, or amplified.”

Explain importance of regaining normal movement and sensation. Advice that weight bearing, gentle exercise and normal ADL’s should be maintained and encouraged

Give ‘Understanding and overcoming long term pain’ leaflet.

My pain toolkit: www.paintoolkit.org

Understanding pain: www.Retrainpain.org

Refer to Paediatric Physiotherapy

 

•    Non, or reduced, weight-bearing

•    Reduced function / gait changes

•    Reduced / painful range of movement

•    Autonomic changes / hypersensitivity

•    Muscle weakness / tightness

Refer to Paediatricians

•    Limited progress with physiotherapy

•    Indication for referral to a Specialist Pain Centre/ Rehabilitation facility/ clinical psychology

•    Exclude serious  organic pathology / red flags

Refer to

Paediatric Orthopaedics

•    Exclude serious orthopaedic pathology / red flags

Refer for Investigations

•    X-ray/MRI to exclude pathology/used as a reassurance tool

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Paediatric Red Flags

 

Children presenting with red flags, indicating the possibility of more serious underlying pathology, warrant urgent assessment, with some cases requiring referral directly to the Emergency Department or CAU.

  • Unremitting pain
  • Night pain (Pain that awakens the child from sleep)
  • Back pain < 6 years old
  • Systemic symptoms; fever, malaise, unexplained weight loss, sickness
  • Changes in bladder and bowel habit
  • Hot, swollen and inflamed joint(s)
  • Early morning stiffness (may indicate JIA) with persistent swelling
  • Painful guarded movement/ muscle spasm/ significant loss of range of motion, in absence of trauma
  • Regression of development / loss or deterioration of function
  • Antalgic gait / inability to weight bear / gait disturbance / lower limb asymmetry
  • Sensation changes (pins and needles/ numbness), absent or exaggerated reflexes, unexplained muscle weakness  

This list is not exhaustive nor a diagnostic tool, but areas to consider        

 

 

Hypermobility

Joint flexibility is normal. It is important not to over-medicalise hypermobility, or create unnecessary fear, as   around 10 % of our population is hypermobile, but most have no symptoms of difficulties. Most children are flexible, some more so than others. The majority of children will become less supple as they get older but a small percentage will remain very flexible. This is more common if their parents have remained flexible. Hypermobility should not be diagnosed under the age of 6 years. 
 

A diagnosis of hypermobile Ehlers-Danos should only be made by a paediatric rheumatologist. Joint hypermobility is now classified using the idea of a spectrum However, it is not validated in children. Use this as a guide:

Key Assessment points

  • Beighton score for children over 6 years of age  (see table below)
  • Check skin for elasticity, scaring, stretch marks
  • pGALS screen (to rule out inflammatory arthropathy)

 

Initial GP management

 

  • Reassure parents. Hypermobility is common and normal in childhood. Must not be diagnosed <6 years
  • Provide APCP advice sheet on ‘Hypermobility’
  • Give exercise advice – it is important for flexible children to have good muscle strength, to provide stability around their joints. Good core stability is essential. Start with low-impact sports (e.g. swimming, cycling etc.)
  • Young children may not wish to walk far and may want to be carried or use a push chair. Provide advice about encouraging regular and varied chunks of activity. Recommend limiting the use of a push chair.

 

Refer to Paediatric Physiotherapy

 

  • Reduced mobility / function
  • Weakness or tightness in muscle groups
  • Persistent muscle or joint pain
  • Back Pain (consider spondylosis, spondylolisthesis)
  • Recurrent joint subluxations / dislocations

 

Refer to Paediatricians

  • Limited progress with physiotherapy
  • Indication for referral to a Specialist Pain Centre/ Rehabilitation facility/ clinical psychology
  • Exclude serious organic pathology / red flags

 

Refer to Community Paediatricians

  • Abnormal neurology
  • Regression or delay of developmental milestones / motor skills
  • Motor Co-ordination Problems / DCD

 

Refer to

Paediatric Orthopaedics

  • 1st  joint dislocation (if not previously seen via ED)
  • Recurrent painful joint dislocations
  • Exclude serious orthopaedic pathology / red flags

 

 

 

 

 

         

    

Rest palm and forearm flat.

Elbow flexed at 90°.

Extend the metacarpal-phalangeal joint of the 5th finger.

Positive if over 90° 

Score 1 point for each side

Arm outstretched forward, with hand pronated.

Passively move thumb to touch the ipsilateral forearm. Check both arms.

 

If positive score 1 point each side

Arm outstretched. Hand supine.

Elbow extension over 10°.

 

If positive score 1 point each side

Standing. Knees locked straight. Knee extension over 10°.

 

If positive score 1 point each side

Knees locked straight and feet together.

Bend forward to place the whole palm of both hands flat on the floor, just in front of the feet.

 

If positive score 1 point

 

 

 

         

    

Rest palm and forearm flat.

Elbow flexed at 90°.

Extend the metacarpal-phalangeal joint of the 5th finger.

Positive if over 90°

 

Score 1 point for each side

Arm outstretched forward, with hand pronated.

Passively move thumb to touch the ipsilateral forearm. Check both arms.

 

If positive score 1 point each side

Arm outstretched. Hand supine.

Elbow extension over 10°.

 

If positive score 1 point each side

Standing. Knees locked straight. Knee extension over 10°.

 

If positive score 1 point each side

Knees locked straight and feet together.

Bend forward to place the whole palm of both hands flat on the floor, just in front of the feet.

 

If positive score 1 point

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