The
difficult patient. This is the patient I keep seeing lately. This a definite
cohort with many similar features. The
telltale signs of coinfection, Babesia and Bartonella are there. It should be
simple, but it’s not. Every effort to
treat is met with intolerable reactions. Nothing is tolerated.
Patient I
saw today. She is a woman in her 20s who has likely had congenital Lyme. She
had developmental delays and sensory integration problems which were treated
successfully with therapy in childhood. She had cognitive processing issues and
was otherwise GT. This has persisted.
I have been
treating her for 18 months. Before me she saw every Lyme doctor in the
community. She likes me because I treat more things and have helped her the
most. She was bed-ridden and housebound
for years. She is out of bed, out of the house and able to take some classes at
community college.
Fatigue and
collapse. This has improved. She suffers with longstanding POTS secondary to
autonomic dysfunction which was not well managed. I find this to be “low hanging fruit” and
straightforward to manage. Florinef, Midodrine, antidepressant, stimulants and
others as needed. Still discussion of
stimulants below.
I diagnosed
MCAS (mast cell activation syndrome). This was something new. Treatment has
made a big difference. Again, this can be relatively easy to treat (in most
cases). I have discussed treatment elsewhere. Diet is important.
We are
addressing other peripheral issues: mold exposure, methylation defect etc. Not
as helpful as advertised by some.
The real
core issue, I think, is autoimmune encephalitis. The horrific reactions these patients
have when therapies for Babesia and Bartonella are introduced are not
Herxheimer reaction. It is a huge
mistake to keep pushing a particular therapy with the belief there will be a
rainbow on the other side of the mountain. It is not going to happen.
Treating these infections intensely stirs up the underlying autoimmune pathology.
For this
patient and others in a same or similar boat, pushing any Babesia therapy has
led to depression and even suicidal ideation. Pushing Bartonella therapy is
equally disastrous.
Objective
tests may provide clues: GAD-65 aby may
be elevated; Cunningham panel show neuro-autoantibodies, especially against
dopamine receptors and SPECT scans are abnormal with diffuse hypoperfusion of
cortical and deeper areas of the brain.
I don’t
recommend spending a lot of money on these tests if not covered by insurance.
The
collective experience of most patients: alternative therapies including chelation for
ostensible heavy metal toxicity have not helped.
Experience
with hyperbaric oxygen has been disappointing. Somewhat helpful, not amazingly
so.
Steroids may
work but this is a slippery slope.
Moderate doses of Cortef, as in this case, help with: inflammation, POTS
and possible adrenal dysfunction without causing excessive immunosuppression.
This patient
has daily low-grade fevers – about 100.5, night sweats, air hunger, depression,
mood swings, irritability and purple stretch marks. Of course, she also has
malaise, poor sleep, joint pain and a host of other symptoms.
Despite all
this, she is functioning better than she has in years.
This 21-year-old
takes a very long list of meds.
IVIG helps
in some cases. She will never get approved. Some patients have experienced
vast improvement with IVIG. Not always a panacea,
IVIG can be incredibly effective when available. It has to be dosed
appropriately.
IVIG is dose
1.5 – 2 gm/kg. It may take 6-9 months
before improvements are seen.
Generally, I
think treating Babesia before Bartonella is best. But this is not always the
case. Running through an army of Babesia
meds: artemisinin, Mepron, Daraprim and others, we found she tolerates Cryptolepis
best. We are trying this slowly. Daraprim recently caused a severe dip in her
depression. I am promoting Babesia therapy because I think it is behind the
fevers.
Bartonella
could also be causing the fevers. A word about Rifampin, Mycobutin: Reactions
to these meds can be beyond horrible. High fevers are common along with severe
psychiatric symptoms. Stop immediately. I don’t think it’s an allergic reaction.
It happens too often to be a drug reaction. And I don’t think it’s a Herxheimer
reaction. I think the drugs elicit a severe autoimmune response. Sometimes, the potent anti-bartonella drug,
gentamycin, will be well tolerated. I don't know why.
This brings
us around to IV antibiotic therapy. Sometimes IV meds are better tolerated.
Sometimes,
IV Rocephin, hitting Borrelia hard, seems to quiet the entire process down and
allow other therapies to proceed. Rocephin has immunomodulatory effects n the
brain, apart from it germ killing property. I don’t think we know the whole
story but we know the drug reduces the toxic effect of the neurotransmitter, glutamate
which is promoted by an accumulation of brain toxins which are very slow to
exit through the blood brain barrier.
Another
important therapy is addressing neurotransmitter imbalances.
Many
patients have GABA deficits. They may or may not have GAD-65 antibodies. These
patients may benefit from benzodiazepines and gabapentin. Worries about
addiction may be unwarranted. In addition, these drugs are excellent mast cell stabilizers,
if this is part of the equation.
Patients
have antibodies which attack dopamine receptors and become relatively dopamine
deficient. The use of dopamine agonists
such as Ritalin, Adderall can be very helpful. Many, or most patients have
executive function issues ameliorated by these drugs. Crashes described by many
can be managed when the meds are dosed properly.
Patients
have been to specialist al around the east coast, some are Lyme/bartonella
friendly. There is a definite bottleneck
without a clear path. We are all missing something. Be careful before
considering immunosuppressive therapy. IV Rituximab has been very helpful, in
at least one patient, who receives other therapies described above.
For now, we
chip away, celebrate our successes and stay the course.
I live in Maine. I need to find a Lyme clinician that will work me up neurologically and takes Medicare. I have symptoms ranging from seizures to tics and other manifestations. Every neurologist I have seen states they are psychological. My WB was positive ..3 bands strongly positive and 1 IND. The Bart FSH was negative in 2013 and I may repeat this shortly. I need resolution. My family is starting to doubt my diagnosis. Please help me find someone! Thanks
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