Lyme Science Blog
Mar 07

Dental Surgery Pain Flare in Post-Treatment Lyme Disease Syndrome

Comments: 8
Like
Visited 592 Times, 1 Visit today

Dental Surgery Triggers Severe Pain Flare in Post-Treatment Lyme Disease Syndrome

Dental surgery can trigger severe pain flares in patients with post-treatment Lyme disease syndrome (PTLDS). In one reported case, a routine extraction of four molars led to widespread, uncontrolled full-body pain requiring ICU admission.

Lim from the University of California in San Francisco documented this case, highlighting the degree of pain sensitivity that can occur in PTLDS and how poorly understood it remains.


Five Years Bedbound Before Surgery

Before the dental procedure, the patient had been bedbound for approximately five years and required a wheelchair. Her medical history included fibromyalgia, hypothyroidism, anxiety, depression, and insomnia.

She experienced severe skin, spine, bone, and joint pain that was difficult to manage. Despite frequent emergency department visits, opioids were largely ineffective. Her pain responded better to ketamine, suggesting central sensitization rather than a purely peripheral pain process.


What Happened During Surgery

Prior to the extraction, she tapered off methadone. During surgery, physicians used an aggressive multimodal regimen including fentanyl, ketamine, acetaminophen, and ketorolac intravenously, along with local anesthetic in all four quadrants.

Despite this approach, she developed severe, widespread pain after surgery. The oral pain from the extraction itself was minimal. Instead, the procedure triggered a full-body pain flare consistent with her underlying PTLDS.


Pain That Could Not Be Controlled

In the recovery room, additional fentanyl, hydromorphone, lorazepam, gabapentin, and oral ketamine failed to control her symptoms. A ketamine infusion was initiated. When her pain remained severe, she was transferred to the ICU.

For two days, she required around-the-clock multimodal therapy including ketamine infusion, IV acetaminophen, ketorolac, sublingual buprenorphine, oxycodone, and hydromorphone. She was discharged on day three with a structured tapering regimen.

This level of pain following a routine dental extraction underscores the degree of nervous system sensitization that can occur in severe PTLDS.


Why Surgery Can Trigger Pain Flares in PTLDS

The likely mechanism is central sensitization, in which the brain and spinal cord become hyper-responsive to pain signals. In PTLDS, the nervous system may already be operating at an elevated baseline. Additional physiologic stress—such as surgery, infection, sleep disruption, or emotional stress—can trigger widespread pain disproportionate to the initial stimulus.

This process is related to allodynia, where normally non-painful stimuli become painful. In this case, surgical stress amplified an already sensitized system.

Lim notes that persistent symptoms may reflect central sensitization, also referred to as central sensitivity syndrome. Whether this represents a post-infectious process or ongoing infection remains uncertain.


Is PTLDS Post-Infectious or Persistent Infection?

This patient met the IDSA 2006 criteria for PTLDS, including prior Lyme disease, persistent symptoms for more than six months, and functional impairment.

Some clinicians attribute these symptoms to residual inflammatory or neurologic changes after infection. Others consider the possibility of persistent infection, particularly given the lack of tests confirming eradication.

Clinical trials suggesting limited benefit from antibiotics have important limitations, and the underlying biology of persistent Lyme-related symptoms remains incompletely understood.


Clinical Perspective

This case illustrates the vulnerability of PTLDS patients to severe pain flares following routine procedures. Dental surgery, orthopedic interventions, and other stressors may trigger symptoms that are difficult to control with standard protocols.

Pre-procedural planning may need to account for central sensitization, autonomic dysfunction, and the possibility that typical pain management strategies may be insufficient. For patients, this case supports the clinical observation that their pain responses reflect altered nervous system processing rather than exaggeration.


Frequently Asked Questions

Can dental surgery trigger a Lyme disease pain flare?
Yes. In patients with PTLDS, physiologic stress from surgery can trigger widespread pain beyond what is expected from the procedure.

Why didn’t opioids control the pain?
Central sensitization involves altered pain processing in the central nervous system. Opioids may be less effective, while agents such as ketamine may provide more relief.

What is central sensitization?
Central sensitization is a state in which the nervous system becomes hypersensitive to pain signals and contributes to chronic pain conditions.

Should PTLDS patients avoid surgery?
Not necessarily, but careful planning and monitoring are important given the risk of pain flares.

Does this case prove persistent infection?
No. It highlights the severity of symptoms but does not determine whether infection persists.


References

  1. Lim S, Kinjo S. Exacerbation of chronic pain after dental extractions in a patient with post-treatment Lyme disease syndrome. Saudi J Anaesth. 2018;12(1):112–114.
  2. Cameron DJ, Johnson LB, Maloney EL. Evidence assessments and guideline recommendations in Lyme disease. Expert Rev Anti Infect Ther. 2014;12(9):1103–1135.

Dr. Daniel Cameron, MD, MPH
Lyme disease clinician with over 30 years of experience and past president of ILADS.

SymptomsTestingCoinfectionsRecoveryPediatricPrevention

Related Posts

8 thoughts on “Dental Surgery Pain Flare in Post-Treatment Lyme Disease Syndrome”

  1. isn’t it possible that ongoing chronic borreliosis was compounded by the release of dental spirochetal infection into body systems.

  2. Dr. Daniel Cameron
    Kelly-Anne Bryan, RN

    This has happened to me more than once over the 40 years I have had Lyme. The body just can’t handle added insults. I have it now, and due to the current opioid hysteria, I have NO access to pain control, even during the 5 weeks out of the last 6 that I was hospitalized in 2 different hospitals for suicidality because of the intense pain. They simply refused to treat with opiates. Nothing else they tried made any difference. The NSAIDS still have me doubled over in pain. I am home now in agony. Pain specialists in my area that take Medicaid no longer prescribe. I lost my job over my former pain specialist abruptly cutting off my pain meds in January, undoubtedly due to fear of repercussions for prescribing. I can’t possibly work now in this much pain. Now I can’t pay for my Lyme treatment anymore. I fear we are going to see an increase in psychiatric crises and suicides for the poor souls who suffer with chronic pain, including us Lymies.

      1. Diagnosed with RSD in 1996 after a crush accident rt upper limb and that is where it all started. Surgeries that made pain better then quickly worse. Then Fibro in 2003, then severe back problems in 2000, cervical in 2004-5 to presently dealing with a bad pinched nerve ,can’t feel my left hand, and where I broke the head of the humerus is 08′ man it hurts ! I had a rash come and go on left lower leg since after the 2013 bug ? bite incident only to come and stay last Spring 2017. It is still there and was diagnosed as fungal just two weeks ago after several inconclusive biopsies. Cream not clearing it up. I’m at a loss of what to do . I am 52 and in 2013 I had a neg Lyme test but had all the symptoms, then 2017 Sept had a positive test , treated with Doxycycline . I am instructed to stay on it because when I stop the Doxycycline symptoms go crazy bad. Last Saturday despite being on it still I became dizzier than usual, extremely confused, so tired I suddenly had to go to sleep in the middle of the day, so many symptoms, nausea too and my mouth and gums sore, fingers crack open for just carrying a bag up the stairs ??? I’m going to buy some Briggs (mother)Apple Cider Vinegar and what do I have to lose. Arthritis Dr wants to dump me now that he knows I don’t have psoriasis and wants to take me off methotrexate now so my joints are screaming again now from the decrease in that medicine. Sorry if this is hard to understand as I am in between crisis’s

Leave a Comment

Your email address will not be published. Required fields are marked *