Pain and the Brain

brain
As a clinician who works with patients who experience chronic pain and who recognizes the importance of this topic, I take great pride blogging about the fact that September is Pain Awareness Month.  More than fifty percent of individuals who experience chronic pain also develop depression.  In fact, both chronic pain and depression activate the same areas in the brain.

 

Not all pains are created equal.  In fact, there are many different types of pain.  Chronic pain is subdivided into nociceptive pain, which is pain caused by inflammation or damaged tissue, and neuropathic pain, which is nerve related pain.

 

Nociceptive pain can be further divided into superficial and deep pain. The superficial pain pathway is stimulated is by nociceptors (sensory pain receptors) in the skin or superficial tissues.  Deep pain is further subdivided into somatic and visceral pain. Deep somatic pain is felt when nociceptors in ligaments, tendons, bones, blood vessels, fascia, and muscles are stimulated.  It is often described as dull, aching, and poorly-localized pain. Deep visceral pain, on the other hand, originates in the organs. While the location of visceral pain may at times be easy to identify, it is often extremely difficult to pinpoint its location.

 

As opposed to nociceptive pain, neuropathic pain is divided into peripheral and central pain. Peripheral pain originates in the peripheral nervous system (the portion of the nervous system that exists outside of the brain and spinal cord), and it is often described as burning, tingling, stabbing, or pins and needles.  Central pain is pain that originates in the brain or spinal cord.

 

 

Pain breeds pain.  What this means is that as an individual chronically experiences pain, the threshold decreases for pain signals to be transmitted via C-fibers to the brain.  In other words, the same signal that previously would be perceived as non-noxious (non-painful) will be perceived as painful.  The cortical somatotropic organization of the brain is different than previously in this case of neuroplasticity gone awry. This is referred to as the pain wind up phenomenon or central sensitization.  In fact, MRI studies have revealed that pain processing centers of the brain appear different, including abnormal grey matter loss (especially in the prefrontal cortex and right thalamus) in individuals experiencing chronic pain compared to individuals who do not.  These brain changes are reversible if the state of chronic pain is terminated.

 

For those who are curious to learn more about pain and how it affects the brain, I refer you to Explain Pain, by David S. Butler and G. Lorimer Moseley.  This book, which is appropriate for clinicians and patient alike, explains what occurs when an individual experiences pain and explores pathways to resolve pain.

Pondering Preeclampsia


In honor of May being Preeclampsia Awareness Month, I have decided to blog about gestational hypertensive disorders. A wide spectrum of blood pressure related issues may develop during pregnancy. The mildest condition that may occur is gestational hypertension, which is development of elevated blood pressure after twenty weeks of gestation. Majority of women will experience spontaneous resolution of symptoms following delivery. However, according to Saudan et al in British Journal of Obstetrics and Gynaecology (1998), 15-25% of women who experience gestational hypertension will proceed to develop preeclampsia.

Preeclampsia, the next condition along the severity spectrum, is classified as elevated blood pressure (140/90 and higher) in women who had normal blood pressure levels within the first twenty weeks of pregnancy, proteinuria (excess protein in one’s urine), and edema (swelling). Full on eclampsia occurs if the symptoms worsen to the point that it interferes with brain function and causes coma and/or seizure. Vision difficulty, upper right abdominal pain, severe headache, or severe nausea and/or vomiting may be indicative of eclampsia, and immediate medical attention should be sought if one experiences these symptoms.

Women experiencing either preeclampsia or eclampsia may sustain what is known as the HELLP syndrome. HELLP is an acronym for the complications experienced:

• H – Hemolysis, breakdown of red blood cells, which play a crucial role in oxygen transport throughout the body
• EL – Elevated Liver enzymes, indicative of liver damage
• LP – Low Platelet count, which interferes with normal clotting

The etiology of these blood pressure disorders are unknown. Researchers are investigating many factors that may affect development of these conditions, including genetic, environmental, maternal nutrition, immunologic, cardiovascular, and hormonal factors. Scientists have suggested that globally, 5-10% of pregnancies are accompanied with preeclampsia (vs. 3-5% in the United States). 40-60% of maternal deaths in developing countries are due to preeclampsia. Risk factors associated with development of preeclampsia include hypertension or kidney disease prior to pregnancy, obesity, age (women younger than twenty and older than thirty five have a greater risk), known family history of preeclampsia, and multiple pregnancy.

Delivery of the fetus is the only cure for preeclampsia. Most health care providers view 37 weeks and beyond as a safe time to deliver the baby, however any sooner than 37 weeks is generally considered grey territory. On the one hand, delivery will be beneficial for the mother, but on the other hand, delivery will be detrimental for the fetus from a growth and development perspective. Women experiencing preeclampsia should discuss options and make these important decisions with their health care provider.

 

Hopefully, increased knowledge about these disorders can enable faster intervention and medical attention.  I encourage you to spread the word about preeclampsia this May (and beyond)- you never know who you can help with a single conversation.

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732-595-1DPT (1378) | riva@revitalizephysicaltherapy.com

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