LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » New! Dr H Dapsone Combination Therapy

 - UBBFriend: Email this page to someone!    
Author Topic: New! Dr H Dapsone Combination Therapy
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's here folks!
Thank you to Dr H 💚

"Precision medicine: retrospective chart review and data analysis of 200 patients on dapsone combination therapy for chronic Lyme disease/post-treatment Lyme disease syndrome : Part 1

Combo treatment 1 was a tetracycline, rifampin, dapsone.
Combo treatment 2 was a tetracycline, rifampin, dapsone and either cephalospom or a macrolide.

The choice of treatment was based on their prior clinical response to these medications and co-infection status. All patients were placed on atleast 3 different probiotics. Plaquenil, grape seed extract, stevia, and oregano oil was also noted.

All patients had complete CBC's, CMP's, and methemoglobin levels tested every 3 weeks. More than 1 laboratory was used to assess each patient. Galaxy Lab was not used as iit is unavailable in N.Y. State.

Both treatment protocols were effective in decreasing symptoms, there was no difference in outcomes.

Purpose:
Collected data from 200 patients for the efficacy of dapsone combo therapy and agents that disrupt biofilms for the treatment of chronic Lyme disease/PTLDS. Also performed labs for co-infections. We evaluated the efficacy of newer persister drug regimens like dapsone. We evaluated how other TBI's may be contributing to the burden of chronic illness leading to resistant symptomatology.

Patients:
Over 200 patients recruited from a specialized Lyme disease medical practice who have been ill for 1 year completed a patient symptom severity questionare, before beginning treatment, during, and after 6 months of dapsone combo therapy.
Excluded from trial:
No patients under 18 years old.
No patients who were allergic to dapsone combo therapy.
No pre-trial abnormal labs/anemia

All patients met criteria for Lyme disease. These patients had either failed or had inadequate response to prior antibiotic therapy or had relapsed with persistent symptoms after stopping anti-infective treatments.

Patients symptoms were monitored every 6 -8 weeks. Rigorous patient safeguards were in place.
Must get blood labs every 3 weeks.
Dietary guidelines.
Name and phone number of medical center staff for medical issues.

Survey Symptoms measured were:
1. Fatigue
2. Muscle/joint pain
3. Headache
4. Tingling, numbness, burning
5. Sleep problems
6. Forgetfulness/brain fog
7. Difficultly with speech or writing
8. Day/night sweats
Patients indicated the severity of each symptom using a 5 point scale, 1 being no symptom and 5 being the most severe.

Results:
53% of patients took dapsone therapy atleast 6 months.
46% no longer take dapsone therapy.
Dosages used were 25mg (12% of patients), 50mg (23.5%), 75mg (12%), and 100mg (51.5%).
20% of patients used pulsed therapy.

Side Effects:
66.7% of patients experienced herxs.
48.3% anemia.
7% mild rashes
18% elevated methemoglobin levels
3.5% blue hands or lips
21% shortness of breath
These were reversed by stopping meds, using higher doses of folic acid, Glutethoine, and N-acetyl-cysteine..
No C-diff was reported.

Co-Infections of Patients
Anaplasma (13.5%).
Babesia (32%).
Bartonella (46.5%).
Brucellosis (10%).
C.pneumoniae (51%).
Cytomegalovirus (37%).
Coxsackle (7.5%).
EVB (80%).
Ehrlichiosis (14.5%).
Helicobacter (7.5%).
Herpes HHVS (31%).
Herpes HSVI (23%).
Mycroplasmas (82%).
Parvovirus (11.5%).
Q-Fever (8.5%).
RMSF (10%).
Toxoplasmosis (11.5%).
Tularemia (16.5).
Typhus (10.5%).
West Nike Virus (6.5%).

64% of patients had exposure between 5 - 8 co-infections.
45% had positive IgM blots showing active infections,

Borrelia, Bartonella, Babesia, and Mycroplasmas species were all shown to persist despite commonly prescribed courses of antibiotics or anti malarial/Babesia therapy.

Clindamycin and quinine as well as atovaquone and azithromycin for Babesia were shown to be inadequate. Research into more effective treatments for Babesia are urgently needed.

Part 2 will address abnormalities found on the MSIDS maps and optimal treatments. Coming soon.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590688/pdf/ijgm-10-249.pdf

[ 02-22-2019, 11:37 PM: Message edited by: Bartenderbonnie ]

Posts: 2977 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
t9im
Frequent Contributor (1K+ posts)
Member # 25489

Icon 1 posted      Profile for t9im   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi BTB:

Thanks for posting this. I know he has been cutting edge with Dapsone and he has kept trying to help his patients.

If I remember this right his wife also has had a persistent borrelia infection and the dapsone treatment has worked which is why he expanded it to many more patients.

I do know one does need L/T meds to successfully treat tick borne diseases.

[ 02-25-2019, 07:21 PM: Message edited by: Robin123 ]

--------------------
Tim

Posts: 1111 | From Glastonbury, CT | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi folks - I have just edited this thread to remove any LLMD bashing - we do not bash LLMDs here. Also we discuss treatment options without putting other options down, since we're all different.

The issue was recognition of mold toxicity in Lyme patients. I agree this is a major issue, as I have recently watched the online mold summit.

But we need to discuss mold issues without attacking doctors, so I will be private messaging the person whose posts I removed. We would like to hear info about mold, but not attack doctors.

Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

Icon 1 posted      Profile for Tincup         Edit/Delete Post   Reply With Quote 
Thanks Robin4927459573!!

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691

Icon 1 posted      Profile for kidsgotlyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
These doctors are true warriors and I love every single one of them!!!

--------------------
symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections.

Posts: 1470 | From Tennessee | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.