Primary Immunodeficiency (PID)
Introduction
PID disorders are inherited conditions sometimes caused by single-gene mutations, or more often by an unknown genetic susceptibility combined with environmental factors1.
In Scope
Patients suspected of having Primary Immunodeficiency (PID)
Not in scope
Secondary or ‘acquired’ Immunodeficiency. e.g. HIV, malnutrition, immunodeficiency secondary to chemotherapy*
*this list is not exhaustive.
Referral Criteria
- Adults or children with unusually frequent or severe infections, or infections with unusual organisms. For further information see Immunodeficiency UK website. Secondary causes should be excluded (e.g. drugs, underlying malignancy, structural defects)
Referral Instructions
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Referrals for PID are via referral letter in the usual way. (The Allergy referral form cannot be used)
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Please include the following in your referral
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Results of any microbiology (e.g. sputum/swabs)
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Full immunisation history (vaccine names and date administered)
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Relevant Radiology (if done outside Derriford)
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Details of family history (especially infections)
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FBC (with differential, immunoglobulin levels (if bacterial infections), sputum cultures. If history strongly suggested of immunodeficiency, referral should not be delayed pending blood results
- If history suggestive of hereditary angioedema (angioedema, no urticaria, often involving recurrent abdominal pain, family history) check C4 and follow advice on angioedema RMS page.
Supporting Information
Patients
Professionals
- Immunodeficiency (Primary and Secondary) | Doctor
- https://www.immunodeficiencyuk.org/wp-content/uploads/2021/05/GuideforGPs.pdf
- Symptoms & diagnosis - Immunodeficiency UK
References
Page Review Information
Review Date 03 June 2025
Next Review Date 03 June 2027
Speciality Lead GP Dr Kate Northridge
Contributors Dr Catherine Elliott, Specialist Doctor in Allergy, University Hospital Plymouth