Milk-alkali syndrome classification: Difference between revisions

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{{Milk-alkali syndrome}}
==Overview==
There is no established system for the classification of [disease name].
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].
OR
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3].
[Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features:
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
==Classification==
==Classification==


There is no established system for the classification of [disease name].
Milk- alkali syndrome  may be classified as 


OR
==== Acute or toxemic form ====
*The acute or toxemic form occurred after approximately one week of treatment
*The symptoms are  acute hypercalcemia
*Nausea and vomiting
*weakness
*Mental changes with psychosis
*Depressed sensorium
*Severe metabolic alkalosis
*Normal to elevated plasma phosphate concentration
*Acute renal insufficiency
*Withdrawal of milk and alkali led to rapid relief of symptoms and the return of normal renal function.


[Disease name] may be classified according to [classification method] into [number] subtypes/groups:
===== Subacute or  Cope's syndrome =====
*[Group1]
*Patients were usually seen during therapy with milk and alkali that had been taken intermittently for years.
*[Group2]
*Affected patients had symptoms of both acute and chronic hypercalcemia and responded to medication withdrawal with gradual improvement. Renal function remained mildly impaired in some cases.
*[Group3]
*[Group4]


OR
===== Chronic  or Burnett's syndrome =====
*Long history of high milk-alkali intake with symptoms of chronic hypercalcemia such as
*Polyuria
*polydipsia
*Muscle aches, and pruritus
*Evidence of metastatic calcifications, including band keratopathy and nephrocalcinosis
*Laboratory abnormalities were similar to those in the acute syndrome, but the response to withdrawal of milk and alkali was quite different
*The muscle aches and pruritus improved slowly as the plasma calcium concentration slowly normalized
*There is usually minimal or no improvement in renal function, as many patients continued to have chronic renal failure.<ref name="pmid18126919">{{cite journal |vauthors=BURNETT CH, COMMONS RR |title=Hypercalcemia without hypercalcuria or hypophosphatemia, calcinosis and renal insufficiency; a syndrome following prolonged intake of milk and alkali |journal=N. Engl. J. Med. |volume=240 |issue=20 |pages=787–94 |date=May 1949 |pmid=18126919 |doi=10.1056/NEJM194905192402001 |url=}}</ref>


[Disease name] may be classified into [large number > 6] subtypes based on:  
[Disease name] may be classified into [large number > 6] subtypes based on:  

Revision as of 16:49, 21 April 2019

Classification

Milk- alkali syndrome may be classified as

Acute or toxemic form

  • The acute or toxemic form occurred after approximately one week of treatment
  • The symptoms are acute hypercalcemia
  • Nausea and vomiting
  • weakness
  • Mental changes with psychosis
  • Depressed sensorium
  • Severe metabolic alkalosis
  • Normal to elevated plasma phosphate concentration
  • Acute renal insufficiency
  • Withdrawal of milk and alkali led to rapid relief of symptoms and the return of normal renal function.
Subacute or Cope's syndrome
  • Patients were usually seen during therapy with milk and alkali that had been taken intermittently for years.
  • Affected patients had symptoms of both acute and chronic hypercalcemia and responded to medication withdrawal with gradual improvement. Renal function remained mildly impaired in some cases.
Chronic or Burnett's syndrome
  • Long history of high milk-alkali intake with symptoms of chronic hypercalcemia such as
  • Polyuria
  • polydipsia
  • Muscle aches, and pruritus
  • Evidence of metastatic calcifications, including band keratopathy and nephrocalcinosis
  • Laboratory abnormalities were similar to those in the acute syndrome, but the response to withdrawal of milk and alkali was quite different
  • The muscle aches and pruritus improved slowly as the plasma calcium concentration slowly normalized
  • There is usually minimal or no improvement in renal function, as many patients continued to have chronic renal failure.[1]

[Disease name] may be classified into [large number > 6] subtypes based on:

  • [Classification method 1]
  • [Classification method 2]
  • [Classification method 3]

[Disease name] may be classified into several subtypes based on:

  • [Classification method 1]
  • [Classification method 2]
  • [Classification method 3]

OR

Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.

OR

If the staging system involves specific and characteristic findings and features:

According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].

OR

The staging of [malignancy name] is based on the [staging system].

OR

There is no established system for the staging of [malignancy name].==References==

  1. BURNETT CH, COMMONS RR (May 1949). "Hypercalcemia without hypercalcuria or hypophosphatemia, calcinosis and renal insufficiency; a syndrome following prolonged intake of milk and alkali". N. Engl. J. Med. 240 (20): 787–94. doi:10.1056/NEJM194905192402001. PMID 18126919.

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