Acute nephritis
Peer reviewed by Dr Laurence KnottLast updated by Dr Colin Tidy, MRCGPLast updated 21 Mar 2022
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Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Glomerulonephritis article more useful, or one of our other health articles.
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What is nephritis?
Nephritis essentially means inflammation of the kidney. Nephritis may involve the glomerulus, tubule, or the interstitial renal tissue.
When inflammation involves the glomeruli it is called glomerulonephritis.
When kidney disease involves structures in the kidney outside the glomerulus, it is broadly referred to as tubulo-interstitial disease. This disease generally involves the tubules and/or the interstitium of the kidney and spares the glomeruli.
When inflammation affects the area of the kidney between the nephrons (the renal interstitium) it is known as interstitial nephritis, or sometimes tubulo-interstitial nephritis.
Renal disease can present in a number of different ways, including as:
Nephritic syndrome (nephritis).
Renal pain and dysuria.
Glomerulonephritis can present with different clinical syndromes. These include nephrotic and nephritic syndrome. Glomerulonephritis accounts for about 10% of cases of acute kidney injury in adults, mainly related to rapidly progressive glomerulonephritis resulting from granulomatous polyangiitis (GPA, Wegener granulomatosis), microscopic polyangiitis (MPA), and anti-glomerular basement membrane (GBM) disease.1 Glomerulonephritis is discussed in more detail in the separate Glomerulonephritis article.
Interstitial nephritis can be acute or chronic. Acute interstitial nephritis is commonly due to a drug hypersensitivity reaction and presents as sudden-onset acute kidney injury.2 Acute interstitial nephritis is estimated to account for 15-20% of cases of acute kidney injury.3
Granulomatous interstitial nephritis (GIN) is rare, detected in 0.5-0.9% of all renal biopsies.4
So, nephritis and nephrosis are responses to renal disease or injury. There are a number of underlying disease processes that can lead to both nephritic and nephrotic syndromes.5 See also separate articles:
Acute nephritic syndrome
Acute nephritic syndrome is often the most serious and potentially devastating form of the various renal syndromes.
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Clinical features
The key clinical features of acute nephritic syndrome are:
Reduced urine output.
Fluid retention and oedema (including periorbital, peripheral oedema and pulmonary oedema).
Proteinuria (usually <3.5 g/day).
Hypertension.
Uraemic symptoms (including anorexia, pruritus, lethargy, nausea).
Deteriorating renal function.
Acute nephritis causes (aetiology)
Post-infection with nephritogenic strains of Group A beta-haemolytic streptococcus (typically occurs in children).
Any of the other causes of glomerulonephritis:
Other bacterial infections - eg, typhoid, secondary syphilis, meticillin-resistant Staphylococcus aureus (MRSA) infection, pneumococcal pneumonia, infective endocarditis.
Viral infections - eg, hepatitis B, mumps, measles, infectious mononucleosis, varicella, Coxsackievirus.
Parasitic infections - eg, malaria, toxoplasmosis.
Multisystem systemic diseases - eg, systemic lupus erythematosus (SLE), vasculitis, Henoch-Schönlein purpura, Goodpasture's syndrome, granulomatosis with polyangiitis.
Primary glomerular diseases - eg, Berger's disease (IgA nephropathy), membranoproliferative glomerulonephritis.
Diphtheria-pertussis-tetanus vaccine.
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Management
In primary care
Take a history - ask about onset of nephritis symptoms and uraemic symptoms; look for a clue to an underlying cause - eg, recent streptococcal infection, other infection, multisystem disease.
Measure blood pressure.
Assess for peripheral, periorbital and pulmonary oedema.
Perform urine dipstick for protein and blood.
If acute nephritic syndrome is suspected, patients should be referred to secondary care. Acute admission may be required.
In secondary care
Investigations are focused on assessing severity of renal injury and looking for the underlying cause - discussed in detail in the separate Glomerulonephritis article.
Management depends on the underlying cause of acute nephritis and is also discussed in the same article.
Nephritis prognosis
This depends on the underlying cause of nephritis. The prognosis for nephritic syndrome caused by acute post-streptococcal glomerulonephritis in children is generally excellent.
Further reading and references
- KDIGO Clinical Practice Guideline for Glomerulonephritis; International Society of Nephrology (2021).
- Pesce F, Stea ED, Rossini M, et al; Glomerulonephritis in AKI: From Pathogenesis to Therapeutic Intervention. Front Med (Lausanne). 2021 Mar 2;7:582272. doi: 10.3389/fmed.2020.582272. eCollection 2020.
- Moledina DG, Perazella MA; Drug-Induced Acute Interstitial Nephritis. Clin J Am Soc Nephrol. 2017 Dec 7;12(12):2046-2049. doi: 10.2215/CJN.07630717. Epub 2017 Sep 11.
- Raghavan R, Eknoyan G; Acute interstitial nephritis - a reappraisal and update. Clin Nephrol. 2014 Sep;82(3):149-62. doi: 10.5414/cn108386.
- Shah S, Carter-Monroe N, Atta MG; Granulomatous interstitial nephritis. Clin Kidney J. 2015 Oct;8(5):516-23. doi: 10.1093/ckj/sfv053. Epub 2015 Jul 5.
- Moledina DG, Parikh CR; Differentiating Acute Interstitial Nephritis from Acute Tubular Injury: A Challenge for Clinicians. Nephron. 2019;143(3):211-216. doi: 10.1159/000501207. Epub 2019 Jun 14.
Article history
The information on this page is written and peer reviewed by qualified clinicians.
Next review due: 20 Mar 2027
21 Mar 2022 | Latest version
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