Methemoglobinemia: Difference between revisions

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{{SI}}
{{Infobox medical condition
| name            = Methemoglobinemia
| image          = [[File:ChocolateBrownBlood_(cropped).jpg|250px]]
| caption        = Chocolate brown blood, a characteristic of methemoglobinemia
| field          = [[Hematology]]
| symptoms        = [[Cyanosis]], [[headache]], [[fatigue (medical)|fatigue]], [[shortness of breath]], [[tachycardia]]
| complications  = [[Seizures]], [[coma]], [[death]]
| onset          = Can be [[congenital]] or [[acquired]]
| duration        = Varies depending on cause
| causes          = [[Genetic mutation]], [[exposure]] to certain [[drugs]] or [[chemicals]]
| risks          = [[Anesthetics]], [[antibiotics]], [[nitrates]], [[nitrites]]
| diagnosis      = [[Blood test]] showing elevated [[methemoglobin]] levels
| differential    = [[Sulfhemoglobinemia]], [[carboxyhemoglobinemia]], [[anemia]]
| treatment      = [[Methylene blue]], [[ascorbic acid]], [[hyperbaric oxygen therapy]]
| prognosis      = Good with treatment, potentially fatal if untreated
| frequency      = Rare
}}
'''Methemoglobinemia''' is a blood disorder characterized by an increased level of methemoglobin, a form of hemoglobin that contains iron in an oxidized state. Unlike normal hemoglobin, methemoglobin is unable to bind oxygen and carry it to body tissues, leading to tissue hypoxia.
'''Methemoglobinemia''' is a blood disorder characterized by an increased level of methemoglobin, a form of hemoglobin that contains iron in an oxidized state. Unlike normal hemoglobin, methemoglobin is unable to bind oxygen and carry it to body tissues, leading to tissue hypoxia.
[[File:ChocolateBrownBlood (cropped).jpg|thumb|ChocolateBrownBlood (cropped)]]
== Etiology ==
== Etiology ==
*Methemoglobinemia can be either acquired or congenital:
*Methemoglobinemia can be either acquired or congenital:
*'''Acquired Methemoglobinemia''': This is the most common type and is usually caused by exposure to certain drugs (such as dapsone, local anesthetics like benzocaine, and some antibiotics) and chemicals (like nitrates and nitrites).
*'''Acquired Methemoglobinemia''': This is the most common type and is usually caused by exposure to certain drugs (such as dapsone, local anesthetics like benzocaine, and some antibiotics) and chemicals (like nitrates and nitrites).
*'''Congenital Methemoglobinemia''': This type is less common and is caused by a genetic deficiency of the enzyme methemoglobin reductase (also known as cytochrome b5 reductase), which is responsible for converting methemoglobin back to hemoglobin.
*'''Congenital Methemoglobinemia''': This type is less common and is caused by a genetic deficiency of the enzyme methemoglobin reductase (also known as cytochrome b5 reductase), which is responsible for converting methemoglobin back to hemoglobin.
== Pathophysiology ==
== Pathophysiology ==
Under normal conditions, a small amount of methemoglobin is produced in the body but is quickly reduced back to hemoglobin by methemoglobin reductase. However, when this enzyme is deficient or overwhelmed by the presence of certain drugs or chemicals, methemoglobin can accumulate, leading to methemoglobinemia.
Under normal conditions, a small amount of methemoglobin is produced in the body but is quickly reduced back to hemoglobin by methemoglobin reductase. However, when this enzyme is deficient or overwhelmed by the presence of certain drugs or chemicals, methemoglobin can accumulate, leading to methemoglobinemia.
== Clinical Features ==
== Clinical Features ==
The primary symptom of methemoglobinemia is cyanosis, a bluish discoloration of the skin and mucous membranes, that does not improve with oxygen administration. Other symptoms can include headache, fatigue, shortness of breath, and at higher levels, confusion, seizures, and loss of consciousness.
The primary symptom of methemoglobinemia is cyanosis, a bluish discoloration of the skin and mucous membranes, that does not improve with oxygen administration. Other symptoms can include headache, fatigue, shortness of breath, and at higher levels, confusion, seizures, and loss of consciousness.
== Diagnosis ==
== Diagnosis ==
Methemoglobinemia is diagnosed through blood tests that measure the level of methemoglobin in the blood. In cases of congenital methemoglobinemia, genetic testing may be performed to identify the specific enzyme deficiency.
Methemoglobinemia is diagnosed through blood tests that measure the level of methemoglobin in the blood. In cases of congenital methemoglobinemia, genetic testing may be performed to identify the specific enzyme deficiency.
== Treatment ==
== Treatment ==
Treatment for methemoglobinemia aims to reduce the level of methemoglobin and treat any underlying causes. In severe cases, treatment may include the administration of methylene blue, a medication that accelerates the conversion of methemoglobin back to hemoglobin. In cases of drug-induced methemoglobinemia, the offending drug must be discontinued.
Treatment for methemoglobinemia aims to reduce the level of methemoglobin and treat any underlying causes. In severe cases, treatment may include the administration of methylene blue, a medication that accelerates the conversion of methemoglobin back to hemoglobin. In cases of drug-induced methemoglobinemia, the offending drug must be discontinued.
== Prognosis ==
== Prognosis ==
With appropriate treatment, the prognosis for individuals with methemoglobinemia is generally good. However, repeated or prolonged exposure to methemoglobin-inducing agents should be avoided to prevent recurring episodes.
With appropriate treatment, the prognosis for individuals with methemoglobinemia is generally good. However, repeated or prolonged exposure to methemoglobin-inducing agents should be avoided to prevent recurring episodes.
== See Also ==
== See Also ==
* [[Hemoglobin]]
* [[Hemoglobin]]
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* [[Oxygen transport]]
* [[Oxygen transport]]
* [[Methylene blue]]
* [[Methylene blue]]
== References ==
== References ==
*Ash-Bernal R, Wise R, Wright SM. (2004). Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore), 83(5), 265-273.
*Ash-Bernal R, Wise R, Wright SM. (2004). Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore), 83(5), 265-273.

Latest revision as of 04:25, 8 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Methemoglobinemia
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Cyanosis, headache, fatigue, shortness of breath, tachycardia
Complications Seizures, coma, death
Onset Can be congenital or acquired
Duration Varies depending on cause
Types N/A
Causes Genetic mutation, exposure to certain drugs or chemicals
Risks Anesthetics, antibiotics, nitrates, nitrites
Diagnosis Blood test showing elevated methemoglobin levels
Differential diagnosis Sulfhemoglobinemia, carboxyhemoglobinemia, anemia
Prevention N/A
Treatment Methylene blue, ascorbic acid, hyperbaric oxygen therapy
Medication N/A
Prognosis Good with treatment, potentially fatal if untreated
Frequency Rare
Deaths N/A


Methemoglobinemia is a blood disorder characterized by an increased level of methemoglobin, a form of hemoglobin that contains iron in an oxidized state. Unlike normal hemoglobin, methemoglobin is unable to bind oxygen and carry it to body tissues, leading to tissue hypoxia.

Etiology[edit]

  • Methemoglobinemia can be either acquired or congenital:
  • Acquired Methemoglobinemia: This is the most common type and is usually caused by exposure to certain drugs (such as dapsone, local anesthetics like benzocaine, and some antibiotics) and chemicals (like nitrates and nitrites).
  • Congenital Methemoglobinemia: This type is less common and is caused by a genetic deficiency of the enzyme methemoglobin reductase (also known as cytochrome b5 reductase), which is responsible for converting methemoglobin back to hemoglobin.

Pathophysiology[edit]

Under normal conditions, a small amount of methemoglobin is produced in the body but is quickly reduced back to hemoglobin by methemoglobin reductase. However, when this enzyme is deficient or overwhelmed by the presence of certain drugs or chemicals, methemoglobin can accumulate, leading to methemoglobinemia.

Clinical Features[edit]

The primary symptom of methemoglobinemia is cyanosis, a bluish discoloration of the skin and mucous membranes, that does not improve with oxygen administration. Other symptoms can include headache, fatigue, shortness of breath, and at higher levels, confusion, seizures, and loss of consciousness.

Diagnosis[edit]

Methemoglobinemia is diagnosed through blood tests that measure the level of methemoglobin in the blood. In cases of congenital methemoglobinemia, genetic testing may be performed to identify the specific enzyme deficiency.

Treatment[edit]

Treatment for methemoglobinemia aims to reduce the level of methemoglobin and treat any underlying causes. In severe cases, treatment may include the administration of methylene blue, a medication that accelerates the conversion of methemoglobin back to hemoglobin. In cases of drug-induced methemoglobinemia, the offending drug must be discontinued.

Prognosis[edit]

With appropriate treatment, the prognosis for individuals with methemoglobinemia is generally good. However, repeated or prolonged exposure to methemoglobin-inducing agents should be avoided to prevent recurring episodes.

See Also[edit]

References[edit]

  • Ash-Bernal R, Wise R, Wright SM. (2004). Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore), 83(5), 265-273.
  • Coleman MD, Coleman NA. (1996). Drug-induced methaemoglobinaemia. Treatment issues. Drug Saf, 14(6), 394-405.
  • Mansouri A, Lurie AA. (1993). Concise review: methemoglobinemia. Am J Hematol, 42(1), 7-12.
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