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Methemoglobinemia in an HIV patient
Author(s)
Riva Raiker, MD
William C. Lippert, MD, MPH
Romil Chadha, MD, MPH, FACP, SFHM

A 45-year-old man with known human immunodeficiency virus infection presented with a 5-day history of dyspnea. When his dyspnea had become symptomatic, he had restarted his home dapsone prophylaxis, but his dyspnea had progressively worsened, and his urine became dark.

Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
On presentation to our institution, he was tachycardic, tachypneic, hypoxic, and cyanotic (Figure 1). Chest radiography revealed multifocal bilateral airspace opacities. He was started on vancomycin and piperacillin-tazobactam for treatment of presumed pneumonia, and his dapsone was continued for prophylaxis against Pneumocystis jirovecii pneumonia.

Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
During the next several hours, his hypoxia worsened, and his peripheral capillary oxygen saturation was 87% despite use of a Venturi mask at a 35% fraction of inspired oxygen. Arterial blood gas testing revealed an elevated partial pressure of oxygen (143 mm Hg) and chocolate-brown colored arterial blood. Due to the low peripheral capillary oxygen saturation, high partial pressure of oxygen, and abnormal color of his blood (Figure 2), serum methemoglobin testing was ordered and revealed a concentration of 22.9% (normal value < 1.5%).

Based on these test results, the patient’s dapsone was stopped and replaced with atovaquone. Intravenous infusion of methylene blue was started, with subsequent improvement of the hypoxia and cyanosis (Figure 1). His urine became green, but it returned to a normal color in a matter of hours. He was ultimately diagnosed with P jirovecii pneumonia and completed a course of atovaquone with total resolution of his symptoms.

THE MECHANISMS BEHIND METHEMOGLOBINEMIA

Heme iron is normally in the ferrous state (Fe2+), which allows for hemoglobin to carry oxygen and release it to tissues.1 Exposure to an oxidative stress can lead to methemoglobinemia from an increase in abnormal hemoglobin that contains iron in a ferric state (Fe3+).1,2

Methemoglobin reduces oxygen-carrying capacity in two ways: it is unable to carry oxygen, and its presence shifts the oxy­gen dissociation curve to the left, causing any remaining normal hemoglobin to be unable to release oxygen to the tissues.1,2

Causes of acquired methemoglobinemia include topical anesthetics (eg, benzocaine, lidocaine) and antibiotics (eg, dapsone).2,3 Signs and symptoms include cyanosis, headache, fatigue, dyspnea, lethargy, respiratory distress, and dark-colored urine.1,2

MANAGEMENT

Treatment consists of intravenous methylene blue, which reduces the hemoglobin from a ferric state to a ferrous state.1–4 Methylene blue is a water-soluble dye excreted primarily in the urine, and common side effects include dizziness, nausea, and green urine.5–7 The blue pigments from methylene blue combine with urobilin (a yellow pigment in the urine), producing a green color.7 This is not pathological and requires no treatment, as the urine returns to normal color after the body fully excretes the dye.5–7

If intravenous methylene blue fails to produce a response, other treatments to consider include hemodialysis, blood transfusion, exchange transfusion, and hyperbaric oxygen therapy.2

References
  1. Umbreit J. Methemoglobin—it’s not just blue: a concise review. Am J Hematol 2007; 82:134–144.
  2. Ash-Bernal R, Wise R, Wright SM. Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore) 2004; 83:265–273.
  3. Coleman MD, Coleman NA. Drug-induced methaemoglobinaemia. Treatment issues. Drug Saf 1996; 14:394–405.
  4. Sikka P, Bindra VK, Kapoor S, Jain V, Saxena KK. Blue cures blue but be cautious. J Pharm Bioallied Sci 2011; 3:543–545.
  5. Stratta P, Barbe MC. Images in clinical medicine. Green urine. N Engl J Med 2008; 358:e12.
  6. Miri-Aliabad G. Green urine secondary to methylene blue. Indian J Pediatr 2014; 81:1255–1256.
  7. Prakash S, Saini S, Mullick P, Pawar M. Green urine: a cause for concern? J Anaesthesiol Clin Pharmacol 2017; 33:128–130.
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Author and Disclosure Information

Riva Raiker, MD
Junior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

William C. Lippert, MD, MPH
Senior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

Romil Chadha, MD, MPH, FACP, SFHM
Assistant Professor of Medicine, University of Kentucky Medical Center, Lexington, KY

Address: William C. Lippert, MD, MPH, University of Kentucky Medical Center, Charles T. Wethington Building, Suite 304B, 900 South Limestone Street, Lexington, KY 40536; [email protected]

Issue
Cleveland Clinic Journal of Medicine - 85(3)
Publications
Cleveland Clinic Journal of Medicine
Topics
Hematology
Infectious Diseases
Dermatology
Drug Therapy
Page Number
186-187
Legacy Keywords
methemoglobinemia, dapsone, human immunodeficiency virus, HIV, methemoglobin, methylene blue, Riva Raiker, William Lippert, Romil Chadha
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The Clinical Picture
Author(s)
Riva Raiker, MD
William C. Lippert, MD, MPH
Romil Chadha, MD, MPH, FACP, SFHM
Author(s)
Riva Raiker, MD
William C. Lippert, MD, MPH
Romil Chadha, MD, MPH, FACP, SFHM
Author and Disclosure Information

Riva Raiker, MD
Junior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

William C. Lippert, MD, MPH
Senior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

Romil Chadha, MD, MPH, FACP, SFHM
Assistant Professor of Medicine, University of Kentucky Medical Center, Lexington, KY

Address: William C. Lippert, MD, MPH, University of Kentucky Medical Center, Charles T. Wethington Building, Suite 304B, 900 South Limestone Street, Lexington, KY 40536; [email protected]

Author and Disclosure Information

Riva Raiker, MD
Junior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

William C. Lippert, MD, MPH
Senior Resident, Department of Internal Medicine, University of Kentucky Medical Center, Lexington, KY

Romil Chadha, MD, MPH, FACP, SFHM
Assistant Professor of Medicine, University of Kentucky Medical Center, Lexington, KY

Address: William C. Lippert, MD, MPH, University of Kentucky Medical Center, Charles T. Wethington Building, Suite 304B, 900 South Limestone Street, Lexington, KY 40536; [email protected]

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raiker_methemoglobinemia.pdf
Article PDF
raiker_methemoglobinemia.pdf
Related Articles
When the dissociation curve shifts to the left

A 45-year-old man with known human immunodeficiency virus infection presented with a 5-day history of dyspnea. When his dyspnea had become symptomatic, he had restarted his home dapsone prophylaxis, but his dyspnea had progressively worsened, and his urine became dark.

Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
On presentation to our institution, he was tachycardic, tachypneic, hypoxic, and cyanotic (Figure 1). Chest radiography revealed multifocal bilateral airspace opacities. He was started on vancomycin and piperacillin-tazobactam for treatment of presumed pneumonia, and his dapsone was continued for prophylaxis against Pneumocystis jirovecii pneumonia.

Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
During the next several hours, his hypoxia worsened, and his peripheral capillary oxygen saturation was 87% despite use of a Venturi mask at a 35% fraction of inspired oxygen. Arterial blood gas testing revealed an elevated partial pressure of oxygen (143 mm Hg) and chocolate-brown colored arterial blood. Due to the low peripheral capillary oxygen saturation, high partial pressure of oxygen, and abnormal color of his blood (Figure 2), serum methemoglobin testing was ordered and revealed a concentration of 22.9% (normal value < 1.5%).

Based on these test results, the patient’s dapsone was stopped and replaced with atovaquone. Intravenous infusion of methylene blue was started, with subsequent improvement of the hypoxia and cyanosis (Figure 1). His urine became green, but it returned to a normal color in a matter of hours. He was ultimately diagnosed with P jirovecii pneumonia and completed a course of atovaquone with total resolution of his symptoms.

THE MECHANISMS BEHIND METHEMOGLOBINEMIA

Heme iron is normally in the ferrous state (Fe2+), which allows for hemoglobin to carry oxygen and release it to tissues.1 Exposure to an oxidative stress can lead to methemoglobinemia from an increase in abnormal hemoglobin that contains iron in a ferric state (Fe3+).1,2

Methemoglobin reduces oxygen-carrying capacity in two ways: it is unable to carry oxygen, and its presence shifts the oxy­gen dissociation curve to the left, causing any remaining normal hemoglobin to be unable to release oxygen to the tissues.1,2

Causes of acquired methemoglobinemia include topical anesthetics (eg, benzocaine, lidocaine) and antibiotics (eg, dapsone).2,3 Signs and symptoms include cyanosis, headache, fatigue, dyspnea, lethargy, respiratory distress, and dark-colored urine.1,2

MANAGEMENT

Treatment consists of intravenous methylene blue, which reduces the hemoglobin from a ferric state to a ferrous state.1–4 Methylene blue is a water-soluble dye excreted primarily in the urine, and common side effects include dizziness, nausea, and green urine.5–7 The blue pigments from methylene blue combine with urobilin (a yellow pigment in the urine), producing a green color.7 This is not pathological and requires no treatment, as the urine returns to normal color after the body fully excretes the dye.5–7

If intravenous methylene blue fails to produce a response, other treatments to consider include hemodialysis, blood transfusion, exchange transfusion, and hyperbaric oxygen therapy.2

A 45-year-old man with known human immunodeficiency virus infection presented with a 5-day history of dyspnea. When his dyspnea had become symptomatic, he had restarted his home dapsone prophylaxis, but his dyspnea had progressively worsened, and his urine became dark.

Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
Figure 1. The patient’s hands on presentation (top) and after treatment with intravenous methylene blue (bottom).
On presentation to our institution, he was tachycardic, tachypneic, hypoxic, and cyanotic (Figure 1). Chest radiography revealed multifocal bilateral airspace opacities. He was started on vancomycin and piperacillin-tazobactam for treatment of presumed pneumonia, and his dapsone was continued for prophylaxis against Pneumocystis jirovecii pneumonia.

Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
Figure 2. The patient’s arterial blood on presentation (left) compared with a sample of normal arterial blood (right).
During the next several hours, his hypoxia worsened, and his peripheral capillary oxygen saturation was 87% despite use of a Venturi mask at a 35% fraction of inspired oxygen. Arterial blood gas testing revealed an elevated partial pressure of oxygen (143 mm Hg) and chocolate-brown colored arterial blood. Due to the low peripheral capillary oxygen saturation, high partial pressure of oxygen, and abnormal color of his blood (Figure 2), serum methemoglobin testing was ordered and revealed a concentration of 22.9% (normal value < 1.5%).

Based on these test results, the patient’s dapsone was stopped and replaced with atovaquone. Intravenous infusion of methylene blue was started, with subsequent improvement of the hypoxia and cyanosis (Figure 1). His urine became green, but it returned to a normal color in a matter of hours. He was ultimately diagnosed with P jirovecii pneumonia and completed a course of atovaquone with total resolution of his symptoms.

THE MECHANISMS BEHIND METHEMOGLOBINEMIA

Heme iron is normally in the ferrous state (Fe2+), which allows for hemoglobin to carry oxygen and release it to tissues.1 Exposure to an oxidative stress can lead to methemoglobinemia from an increase in abnormal hemoglobin that contains iron in a ferric state (Fe3+).1,2

Methemoglobin reduces oxygen-carrying capacity in two ways: it is unable to carry oxygen, and its presence shifts the oxy­gen dissociation curve to the left, causing any remaining normal hemoglobin to be unable to release oxygen to the tissues.1,2

Causes of acquired methemoglobinemia include topical anesthetics (eg, benzocaine, lidocaine) and antibiotics (eg, dapsone).2,3 Signs and symptoms include cyanosis, headache, fatigue, dyspnea, lethargy, respiratory distress, and dark-colored urine.1,2

MANAGEMENT

Treatment consists of intravenous methylene blue, which reduces the hemoglobin from a ferric state to a ferrous state.1–4 Methylene blue is a water-soluble dye excreted primarily in the urine, and common side effects include dizziness, nausea, and green urine.5–7 The blue pigments from methylene blue combine with urobilin (a yellow pigment in the urine), producing a green color.7 This is not pathological and requires no treatment, as the urine returns to normal color after the body fully excretes the dye.5–7

If intravenous methylene blue fails to produce a response, other treatments to consider include hemodialysis, blood transfusion, exchange transfusion, and hyperbaric oxygen therapy.2

References
  1. Umbreit J. Methemoglobin—it’s not just blue: a concise review. Am J Hematol 2007; 82:134–144.
  2. Ash-Bernal R, Wise R, Wright SM. Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore) 2004; 83:265–273.
  3. Coleman MD, Coleman NA. Drug-induced methaemoglobinaemia. Treatment issues. Drug Saf 1996; 14:394–405.
  4. Sikka P, Bindra VK, Kapoor S, Jain V, Saxena KK. Blue cures blue but be cautious. J Pharm Bioallied Sci 2011; 3:543–545.
  5. Stratta P, Barbe MC. Images in clinical medicine. Green urine. N Engl J Med 2008; 358:e12.
  6. Miri-Aliabad G. Green urine secondary to methylene blue. Indian J Pediatr 2014; 81:1255–1256.
  7. Prakash S, Saini S, Mullick P, Pawar M. Green urine: a cause for concern? J Anaesthesiol Clin Pharmacol 2017; 33:128–130.
References
  1. Umbreit J. Methemoglobin—it’s not just blue: a concise review. Am J Hematol 2007; 82:134–144.
  2. Ash-Bernal R, Wise R, Wright SM. Acquired methemoglobinemia: a retrospective series of 138 cases at 2 teaching hospitals. Medicine (Baltimore) 2004; 83:265–273.
  3. Coleman MD, Coleman NA. Drug-induced methaemoglobinaemia. Treatment issues. Drug Saf 1996; 14:394–405.
  4. Sikka P, Bindra VK, Kapoor S, Jain V, Saxena KK. Blue cures blue but be cautious. J Pharm Bioallied Sci 2011; 3:543–545.
  5. Stratta P, Barbe MC. Images in clinical medicine. Green urine. N Engl J Med 2008; 358:e12.
  6. Miri-Aliabad G. Green urine secondary to methylene blue. Indian J Pediatr 2014; 81:1255–1256.
  7. Prakash S, Saini S, Mullick P, Pawar M. Green urine: a cause for concern? J Anaesthesiol Clin Pharmacol 2017; 33:128–130.
Issue
Cleveland Clinic Journal of Medicine - 85(3)
Issue
Cleveland Clinic Journal of Medicine - 85(3)
Page Number
186-187
Page Number
186-187
Publications
Cleveland Clinic Journal of Medicine
Publications
Cleveland Clinic Journal of Medicine
Topics
Hematology
Infectious Diseases
Dermatology
Drug Therapy
Article Type
Article
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Methemoglobinemia in an HIV patient
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Methemoglobinemia in an HIV patient
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methemoglobinemia, dapsone, human immunodeficiency virus, HIV, methemoglobin, methylene blue, Riva Raiker, William Lippert, Romil Chadha
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methemoglobinemia, dapsone, human immunodeficiency virus, HIV, methemoglobin, methylene blue, Riva Raiker, William Lippert, Romil Chadha
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