# Congenital anomaly of the circulatory system

- Category: chronic
- Review status: reviewed (every claim checked against a document named on this page)
- Sources: ICPC-3 (WONCA International Classification of Primary Care, 3rd edition) class KD55 - condition scope only, no dose · No dose - referral pathway, no medicine given in primary care · Tetralogy of Fallot - StatPearls (NCBI Bookshelf NBK513288) - https://www.ncbi.nlm.nih.gov/books/NBK513288/
- Verified date: 2026-08

## Verified against

- No dose - referral pathway, no medicine given in primary care
- Congenital anomaly of the circulatory system - disease-level clinical article (congenital-heart-anomaly-full.txt)

## Treatment metadata

- No drug therapy in primary care (Referral & Advice)

## Complete treatment card

```text
CONGENITAL ANOMALY OF THE CIRCULATORY SYSTEM
Sources: ICPC-3 (WONCA International Classification of Primary Care, 3rd edition) class KD55 -
         condition scope only, no dose · No dose - referral pathway, no medicine given in primary
         care · Tetralogy of Fallot - StatPearls (NCBI Bookshelf NBK513288) -
         https://www.ncbi.nlm.nih.gov/books/NBK513288/
Review status: REVIEWED against No dose - referral pathway, no medicine given in primary care,
               Congenital anomaly of the circulatory system - disease-level
               clinical article (congenital-heart-anomaly-full.txt)  (2026-08)

IS IT THIS? - reference only, to read alongside your own examination
  SYMPTOMS - what the patient reports (3)
    - The parent's own observation is a crucial clinical indicator: worsening heart failure, the
      child cannot keep pace with siblings, sweating, tiring quickly, and failure to thrive
      [failure to thrive · sweating]
    - Assess cardiac reserve by asking about age-appropriate activities
    - Ask about past hospitalisations for chest infections, previous surgery and previous
      anaesthetic experience
  SIGNS - what you find (4)
    - The examination points that matter are cyanosis, finger clubbing and signs of congestive
      cardiac failure  [cyanosis · finger clubbing]
    - Record age-specific vital signs, growth charts, weight, height and head circumference
    - About 8% of children with congenital cardiac defects have other congenital abnormalities as
      well
    - Half of children with trisomy 21 have a congenital heart defect, so the examination matters
      particularly there
  TESTS (6)
    - Echocardiography is the essential non-invasive tool, defining both the shape and the function
      of the defect
    - The 12-lead ECG is the gold standard for arrhythmia and for confirming sinus rhythm
    - Chest radiograph is a screening tool for chamber size, great vessel anatomy and pulmonary
      vascularity, but its sensitivity for pulmonary vascularity is only 24% to 68%
    - A child in congestive cardiac failure may have iron-deficiency anaemia; a cyanosed child may
      have erythrocytosis from desaturated haemoglobin
    - Cyanosis can prolong the prothrombin time and partial thromboplastin time
    - MRI quantifies ventricular volumes, valve regurgitation and flow, and shows extracardiac
      vascular anatomy and previous scar tissue
  IF NOT THIS - what else fits (2)
    - Airway abnormalities are more likely in children with congenital heart disease, especially
      those born premature or weighing under 10 kg
    - A high haematocrit needs exchange transfusion before surgery, to prevent the neurological
      consequences of high blood viscosity
  Source  StatPearls "Perioperative Management of Patients With Congenital Heart Disease"
          (NBK585103) - an anaesthesia chapter; this card is scoped to its clinical history,
          physical examination and laboratory sections
  Status  traced to the source above

1. NO DRUG THERAPY IN PRIMARY CARE (REFERRAL & ADVICE)    [1st line]
   Adult    Umbrella category for structural heart defects present at birth (examples given include
            tetralogy of Fallot and patent ductus arteriosus); the GP's role is early recognition
            (murmur, cyanosis, failure to thrive) and referral to paediatric cardiology, which
            manages any medical or surgical treatment. - Refer, with advice
   Peds     Children follow the same pathway: recognise and refer. No primary-care medicine is
            implied.
   Source   No dose - referral pathway, no medicine given in primary care
   Why      Umbrella category for structural heart defects present at birth (examples given include
            tetralogy of Fallot and patent ductus arteriosus); the GP's role is early recognition
            (murmur, cyanosis, failure to thrive) and referral to paediatric cardiology, which
            manages any medical or surgical treatment.
   Caution  Cyanosis, poor feeding, failure to thrive, or a new murmur in an infant needs urgent
            paediatric cardiology referral.
            No medicine is prescribed for this in primary care - this entry is for recognition and
            referral. Anything given is decided by the service it is referred to.
            RED FLAG - Children with Tetralogy of Fallot may develop sudden hypercyanotic (tet)
            spells requiring immediate emergency intervention.

Prices are indicative (dataset snapshot 2026-06); verify with the pharmacy.
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