Namieta Janssen MD

Namieta Janssen MD Dr. Janssen is a board certified Rheumatologist in practice for over 20 years. Call for your consultation!

Dr. Janssen aims to provide compassionate, state of the art care to her patients with rheumatic diseases. She has been in practice for over 20 years, and is a Clinical Associate Professor at Baylor College of Medicine. She is a board member of the Lupus Foundation Gulf Coast Chapter and the Arthritis Foundation Community Advisory Board. In addition, she conducts clinical trials in Rheumatology at the Houston Institute for Clinical Research. She is honored to be the Medical Honoree for the Arthritis Foundation Bone Bash 2015, and the 2016 Medical Honoree for the Lupus Foundation. She believes in one-on-one, responsive, caring and hands on compassionate care to help her patients manage their condition and achieve well-being.

07/10/2024

Thankful our power was restored! Our clinic is open !

07/09/2024

We hope you're all safe through the effects of Beryl! Unfortunately the power to our office building and the adjacent hospital (as well as power for our doctors and staff) is OUT!! And like everyone else, we are not sure when power will be back. If you have a medical emergency, please call 911. Please see our website: drnjanssen.com for updates!

07/08/2024

Our office is closed today! Please stay safe and we will regroup on Tuesday!

07/05/2024

Our office is closed July 3 and 4 to observe Independence Day! Happy 4th!

04/06/2022

We are very excited to announce we have a limited amount of Evusheld available for our established patients. Please read the medication guide and call us if you think you qualify for it!

All virtual this year!
10/12/2021

All virtual this year!

Only TWO days left to purchase a VIP ticket for the Virtual Houston Bone Bash event!! VIP ticket holders will receive a delightful wine & cheese basket from Harry & David. Regular tickets for $35 will still be available until October 21st. Don't miss out on our fun, magical event! đź’š

Grab VIP tickets by October 13th!
➡️ arthritis.org/bonebashhouston ⬅️

09/13/2021

Our office will be closed tomorrow, Tuesday Sept. 14th. We'll be monitoring our phones and portal remotely. Please stay safe!

Good news!! The FDA has just approved a booster COVID vaccine for certain people with conditions or medication use that ...
08/13/2021

Good news!! The FDA has just approved a booster COVID vaccine for certain people with conditions or medication use that make them less likely to make a protective antibody response to the original vaccine. We still don’t know exactly who that would be, but suspect that some of our patients would qualify. The FDA meets again this weekend and we will have more information soon but based on the press release below it seems patients on Rituxan or mycophenolate would qualify. Others on higher doses of methotrexate, steroids, and those on Xeljanz or Rinvoq should too. Dr. Janssen is definitely in favor of booster shots!! Stay tuned.

The FDA authorized the use of an additional dose of the Pfizer-BioNTech or Moderna COVID-19 Vaccines in certain immunocompromised individuals.

This is a nice review of where we are right now on booster shots.  Stay tuned!  Things seem to change moment by moment.
07/13/2021

This is a nice review of where we are right now on booster shots. Stay tuned! Things seem to change moment by moment.

A third shot?

There’s been a pretty dramatic run of events in the past week re: booster shots in the US. For those of you who have not closely followed, this is what’s happened thus far:

-June 25: During an ACIP meeting, Dr. Sara Oliver delivered a fantastic presentation (as per usual) stating that the CDC will not suggest a booster until one of two things happen:
1. Evidence of declining protection against illness, such as declines in vaccine effectiveness. NOT only waning antibody response
2. An escape variant (variant of concern substantially impacting vaccine protection)

-July 8 (Thursday): Pfizer announced it will seek emergency use authorization (EUA) for a booster shot due to new evidence regarding reduced vaccine effectiveness

-July 8 (Thursday): The CDC and FDA quickly released a counter statement saying there is no evidence for a third shot at this time

-July 12 (today): Key players from both sides had a closed door meeting to discuss Pfizer and FDA/CDC’s differing opinions.

***So, what did they discuss during the meeting today?***
I’m guessing three topics came up…

First, Pfizer said there was evidence for waning antibodies. They cited an Israeli study showing a decrease in vaccine effectiveness (specifically against symptomatic disease) 6-months post inoculation. Further, they said an internal Pfizer study showed that a booster could give us “5 to 10 times higher response than two doses”. These two studies are not publicly available yet. But even without them, we know that antibodies (COVID19 or not) naturally decrease over time. And the rate in which they decrease is highly dependent on the initial efficacy rate. Because Pfizer started with such a high efficacy (94%), it will take longer for antibodies to wane compared to less efficacious shots. Also, antibodies are important but they are not the whole story. Two other types of cells, T-cells and memory B-cells, hold the key to long-term immunity. Unfortunately, they are a lot more difficult to study.

Second, Pfizer referenced the Delta variant for the need of a booster shot. I’ll be honest, though, I’m not entirely sure why. We have pretty solid evidence that our mRNA vaccines work against Delta. It’s protecting decently against symptomatic disease but, more importantly, protecting against severe disease.

Third, I assume the discussion then turned to an even more important debate: Do specific populations need a booster?

Since April, France has handed out boosters to cancer patients and others with immune system impairments. Israel also started three-dose regimens this week. Other countries, like the UK, are planning to administer booster shots in September to older populations (70+), healthcare workers, and 16+ that are immunocompromised.

There is plenty of scientific evidence demonstrating that some immunocompromised groups don’t get full protection from the COVID19 vaccines. This is especially true among organ transplant patients, some cancer patients, and some patients using immunosuppressive drugs.

So, several research groups have studied the impact of a third shot among specific immunocompromised groups:
-A French study found that the number of organ transplant recipients who had antibodies increased from 40% (after two doses) to 68% (after 3rd dose). Out of 59 patients, 33 (56%) remained without antibodies after the third dose.

-An American study among organ transplant patients found that among 24 patients with no antibodies after the second vaccine dose, 6 (25%) patients had high levels of antibodies after the third dose. 16 (67%) patients had no antibodies after the third dose.

So, a third dose helps a little but not a lot. It could also help on a population-level. Emerging evidence (here, here, and here) suggest that immunocompromised individuals act as incubators for mutations. For example, the first documented case of B.1.526 was found in a patient with advanced AIDS.

***So, do we get a third shot?***
The scientific evidence says we don’t need one right now. At least for the general population. As we know, scientists continually reevaluate the situation, so this may change tomorrow or this may never change. Today, we don’t need it. The need for a booster for specific populations is another question.

Other important considerations into this policy debate include:
-Global vaccine equity. In other words, could that third dose be better used in other countries so we stop this virus from spreading quickly (and thus mutating)?
-Time. The application takes a while and, in a month or so, we may have more data or a new variant. So, one might argue that this is a proactive approach.
-Profits. One also can’t help but think that big pharma will financially benefit from a third dose.

Nonetheless, Pfizer can apply for a booster EUA. This certainly doesn’t mean that the FDA and/or CDC will approve it. It would be beneficial for everyone to get on the same page though. And hopefully that was the result from the meeting today. Only time will tell.

Love, YLE

Newsletter with sources is here: https://yourlocalepidemiologist.substack.com/p/a-third-dose

06/27/2021

Online courses designed to help you live and cope with lupus.

Address

1327 Lake Pointe Pkwy, Ste 315
Sugar Land, TX
77478

Opening Hours

Monday 8:30am - 4:30pm
Tuesday 8:30am - 4:30pm
Wednesday 8:30am - 4:30pm
Thursday 8:30am - 4:30pm
Friday 8:30am - 3:30pm

Telephone

+18325005002

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