Pulmonary embolism in children: causes, symptoms and treatment

A pulmonary embolism (PE) is a medical emergency. One of the arteries (large blood vessels) in the lungs is blocked by a blood clot traveling from the leg or another part of the body.
Although this condition is most common in adults 40 years and older, it can also occur in babies, children, and teenagers.
Here’s how to spot the symptoms of pulmonary embolism in children, how doctors diagnose the condition, and what the outcome may be after treatment.
Any situation that allows a blood clot to form in the body can lead to a pulmonary embolism. clots
They can also form elsewhere, especially in the veins of the abdomen, arms, pelvis or even the brain. Over time, the clot can travel to the lungs, completely or partially blocking the blood supply.
Whereas
Other conditions that put children at risk include:
Age and race can also play a role. A
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If your child has risk factors and also has breathing problems or complains of chest pain, be sure to be very observant.
Symptoms of PE can include:
That said,
As a result, doctors do not always reach a diagnosis quickly. They may misdiagnose it as pneumonia or heart failure.
Seek emergency care
A pulmonary embolism is a medical emergency. Call emergency services or see a doctor right away if your child develops symptoms associated with PE.
Diagnosing PE in children first involves discussing your child’s medical history and risk factors.
A physical exam can help assess problems with breathing, pain, or related symptoms. But the signs of PE can mimic other illnesses, so certain tests can help your doctor make a specific diagnosis.
CT or MRI imaging is considered the most useful diagnostic tool available today. These tests are also non-invasive and relatively safe. MRIs are particularly safe because they do not expose children to high doses of radiation.
A ventilation/perfusion (VQ) analysis is another option your doctor may suggest. This diagnostic tool can measure:
- how air moves through the lungs
- how and where the blood flows
- where blood flow is blocked
The problem with diagnosis is that many children have few or no symptoms. Therefore, some studies have shown that a diagnosis of PE in children can take as long as
Treatment for PE usually involves medications to thin the blood, such as:
Also known as anticoagulant therapy, blood thinners help prevent clots from forming and slow them down.
Other treatment options include:
- Thrombolysis. Also called fibrinolytic therapy, this method involves using drugs to break up existing blood clots.
- Thrombectomy. This minimally invasive surgery physically removes clots from arteries or veins.
- Inferior vena cava (IVC) filter. This device can prevent clots from reaching the lungs. It is generally only used with children weighing more than 22 pounds.
Pediatric patients receive similar treatment as adults with PE. However, your child’s treatment will vary depending on factors including age, medical history, hospital practices and how he responds to each treatment.
Again, since PE is
In a 2020 case study,
With the delay in diagnosis, the mortality rate from pulmonary embolism is around
Follow-up is extremely important after treatment.
Your child’s pediatrician will also use follow-up appointments to monitor any long-term issues that may arise, such as pulmonary hypertension or chronic PE.
Although PE is rare in children, some children may be at higher risk, either due to existing health conditions, their age, or their race.
Classic symptoms may include difficulty breathing or chest pain. But many children have no symptoms or non-specific symptoms, which makes diagnosis difficult.
Fortunately, doctors are becoming more aware of the risks of PE in children so diagnosis can be quicker and treatment can begin earlier, leading to better outcomes.