Cerebral hypoxia occurs when the brain doesn’t get enough oxygen. Because the brain needs a constant supply of oxygen to function, cerebral hypoxia is a medical emergency. It can be fatal or cause severe, irreversible brain damage.

amount of time before oxygen-deprived brain cells start to die
blood oxygen saturation is the point at which brain damage risk begins
the amount of the body’s oxygen is required for the brain, despite it being only 2% of total body weight
Cerebral hypoxia technically refers to the brain’s cerebral hemispheres, but the term is often used to refer to a reduced supply of oxygen to the entire brain or any part of it. (When there is a complete lack of oxygen reaching the brain, this effect is called cerebral anoxia.) The word “cerebral” also differentiates this type of hypoxia from other forms that can occur and affect other tissues in the body.
There are many possible causes for cerebral hypoxia, relating to the respiratory, circulatory, or nervous systems. It can be caused by a temporary but sustained interruption in breathing or issues that prevent blood (which carries oxygen) from reaching the brain. The nervous system requires oxygen to send nerve signals and messages through the body for voluntary and involuntary processes. Cerebral hypoxia is a life-threating emergency, and anyone experiencing it needs immediate medical care to restore the flow of oxygen to the brain. Brain cells are extremely sensitive to a lack of oxygen, and they begin to die less than four minutes after losing their supply of oxygen.
Healthy adults typically have a blood oxygen saturation (abbreviated SpO2) between 95% and 100%, reflecting the percentage of hemoglobin in the blood that carries oxygen. The risk of brain damage begins when blood oxygen saturation drops below 80%, and it becomes severe when this measurement falls below 60%.
Cerebral hypoxia can happen to anyone, and it can occur any time something interrupts the flow of oxygen to the brain. It can be caused by any of the following issues:
It is possible to experience mild hypoxia, where oxygen flow to the brain is only slightly below a healthy level. For example, this can occur when a person is visiting a high-altitude location, experiencing sleep apnea, or when there is inadequate ventilation in a room. This leads to mild symptoms, which might be difficult to recognize:
In these cases, the condition often can be counteracted by getting more breathable air, for example by returning to a lower elevation, getting treatment for sleep apnea, or improving indoor ventilation.
Moderate to severe cerebral hypoxia is extremely dangerous, however. Symptoms vary depending on how long the brain goes without sufficient oxygen. Within a few minutes, the initial symptoms may include the following:
As hypoxia continues, the symptoms become more obvious and increasingly serious:
However, prolonged cerebral hypoxia of more than a few minutes can lead to coma. Permanent brain damage can lead to post-coma unresponsiveness (also known as unresponsive wakefulness syndrome, defined by complete unawareness and unresponsiveness). The most severe potential complication of cerebral hypoxia is death.
Cerebral hypoxia can usually be diagnosed based on a physical exam and the consideration of a patient’s medical history. To determine the cause, a healthcare provider can perform various tests:
Cerebral hypoxia is an emergency condition that needs to be treated immediately. The sooner that healthcare providers can identify the cause and restore the flow of oxygen and/or oxygen-rich blood to the brain, the lower the patient’s risk for severe brain damage and/or death. Basic life support is the top priority.
Depending on the cause of the hypoxia, one or more of these treatments will be the first course of action to restore oxygen supply:
The outlook for patients depends on the extent of brain injury, based on how long the brain lacked oxygen and additionally whether blood flow (containing necessary nutrients) to the brain was also affected. Brain damage begins within four minutes of the start of cerebral hypoxia. The longer the brain lacks oxygen, the more likely it is that a person will experience brain damage.
Most people who make a full recovery are those who only briefly lose consciousness. If the brain lacks oxygen only for a few minutes, a person is more likely to be able to regain full or partial brain function. Sometimes individuals who recover from cerebral hypoxia have some lasting effects such as twitching or jerking muscle movements or seizures. The longer a person remains unconscious, the lower the chances of recovery.
Individuals who experience cerebral hypoxia and remain unconscious for an extended period have a high risk of death or severe brain damage that leaves them completely unresponsive and lacking awareness. Many in this state pass away within a year, but those who survive will not regain brain function and will require caretaking for the rest of their lives. They also face potential risks such as bed sores, deep vein thrombosis, pneumonia, and malnutrition.
Given the seriousness of these outcomes, it is imperative to call 911 or your region’s emergency number immediately if someone is experiencing the symptoms of cerebral hypoxia.
Cleveland Clinic: Cerebral Hypoxia
MedlinePlus Medical Encyclopedia: Cerebral Hypoxia
NeuroLaunch: Oxygen Levels and Brain Damage: Critical Thresholds and Consequences

We need your help to continue to fund brain research projects and find cures. Stand with us in the fight against brain diseases and disorders.
Explore more brain disease information, research, and stories.
Discover the latest news in brain disease research, hear stories from people affected by brain disease and their caregivers, read up on brain disease-specific information, and more.
Orlena was driving with her young daughter in the car when she suffered a stroke because of a rare brain vessel disorder called Moyamoya. After two brain surgeries and six months unable to care for her daughter, Orlena began to reclaim her independence and became a Moyamoya advocate.
Read More of Orlena’s Story

At 15 years old, Zoe has been navigating her Tourette syndrome diagnosis for eight years. “I had to figure out at a young age how my emotions affect my tics, from good to awful ways. It has been frustrating to figure out on my own and learn to deal with. This was the first moment in my life where my parents couldn’t fix something for me.”
Read More of Zoe’s Story

Sasha was diagnosed with epilepsy after sustaining a soccer-related brain injury in high school. Since then, Sasha has worked to find both a treatment that controlled her seizures and a career that fulfilled her desire to care for others. “Life isn’t meant to be lived taking multiple medications and having seizures you can’t control.”
Read More of Sasha’s Story

Before frontotemporal lobe dementia, sometimes called Pick’s disease, Ken Keene Sr. was a respected community member and a handyman who could fix anything. For his oldest son and namesake Ken Keene Jr., there was nothing his father couldn’t do: “To my family, he was just that super dad. Then all of a sudden he’s reaching out for help.”
Read More of Ken’s Story

It started with a twinge. After a simple surgery and some physical therapy, Morgan wasn’t getting better. It took two more surgeries before she was diagnosed with Complex Regional Pain Syndrome (CRPS) type II.
Read More of Morgan’s Story

In 2018, Kelly was diagnosed with glioblastoma after an MRI confirmed that a golf-ball-sized tumor above her right ear was affecting the left side of her body. After surgery to remove the tumor, Kelly was able to get through her darkest days with a healthy dose of humor. Now she is an advocate for other patients living with strokes and brain tumors.
Read More of Kelly’s Story

When her father was diagnosed with vascular dementia in 2005, Nancy quickly shifted into the role of his caregiver. Nancy and her sisters drew from their individual strengths to provide their father with medical assistance and emotional support until his passing in 2012. At that time, he was diagnosed again with Lewy body dementia. “No matter what your financial situation, there’s probably going to be help out there… Just don’t do it alone, because burning yourself out is not going to help anybody.”
Read More of Nancy’s Story

Maureen worked as a high school English teacher until she started experiencing a confusing array of symptoms that affected her ability to work, along with her relationships with family and friends. After visiting numerous specialists for years, Maureen received a delayed diagnosis of Lewy body dementia. Now Maureen wants to raise awareness about what life is like with living with this disease. “I felt that I just wanted to offer something to this community that I hadn’t been able to find really.”
Read More of Maureen’s Story

For the first 32 years of his life, Joey experienced seizures from epilepsy. For several years, Joey worked hard in his career as a pipe welder and in construction until his seizures started happening more frequently and intensely. Brain surgery became Joey’s only viable option for treatment. Doctors were unsure if Joey would be able to survive after finding more brain damage than expected, but he surprised everyone by thriving during his post-surgery recovery.
Read More of Joey’s Story

At age 40, Ben was perfectly healthy and active until he started noticing the early symptoms of a neurological condition that weakened his physical movements. After a 2-year search for his diagnosis of X-linked adrenoleukodystrophy, he began his journey as an advocate for others living with rare diseases. Last year, Ben joined the board of the American Brain Foundation to further his impact.
Read More of Ben’s Story

In 2002, while her young daughter battled a fatal diagnosis of pons glioma, Michele experienced a life-threatening brain hemorrhage when a brain malformation she likely had since birth ruptured. She experienced drastic changes in the way her brain functioned, especially in regard to memory and spatial awareness. Today, Michele is still learning to adjust. “When someone’s brain is not functioning correctly it impacts everything in their life. It impacts how they think, how they feel about themselves, it’s a very hopeless space to be in as a person.”
Read More of Michele’s Story

Matt is a husband, father, and professional photographer. Over the past 11 years, he has had surgeries and radiation to remove five benign brain tumors. Following the third surgery, he began to experience more struggles in his daily life. “I think the biggest loss is my relationship to my family. They saw me as the dad and strong. Now they can’t count on me as much. It’s important to support people with brain disease ‘cause it can happen to anybody.’”
Read More of Matt’s Story

When she was in her early 30’s, Mary Jo’s relationship with her parents was forever altered by brain disease. Her father suffered a subdural hematoma, was diagnosed with diabetic neuropathy, and experienced a stroke while her mother was diagnosed with Alzheimer’s and dementia. “They’re a responsibility that I have to take care of as they have taken care of me.”
Read More of Mary Jo’s Story

Tom suffers from dystonia, a painful neurological movement disorder with no known cure. When he first started experiencing strange pains and cramps in his neck muscles, he saw chiropractors and physical therapists—but when this didn’t help, Tom started down a long and painful road to an eventual diagnosis. Before his diagnosis at 30 years old, Tom was an athlete and an entrepreneur, but as his symptoms worsened, even performing everyday tasks became a challenge. Before long, the pain became debilitating. Over time, Tom learned to accept his new limitations and focus on his physical and mental health.
Read More of Tom’s Story
