1/
How did #endometriosis get labeled a “white woman’s disease”?

Let’s explore a great paper by @DrSonySinghMD in @AJOG

https://www.ncbi.nlm.nih.gov/pubmed/30738028 
2/
First, a quick survey.

Women with endometriosis are most commonly:
3/
If you were to google "endometriosis patient"...this is what you get. ALL. WHITE. WOMEN.

Now why is that? Let's take a deep dive in their article
4/
1921: Sampson describes condition by noting ectopic endometrium

1938: Meigs links #endometriosis to contraceptive use & delayed childbearing
➡️ Fertility pattern more common among the “well to do” he thought

"Endo is a lifestyle disease of white upper middle class women"
5/
Meigs believed & wrote that #endo was more common in his private clinic patients that those in the regular hospital wards

‼️ “The Scourge of the private patient”‼️

BTW ➡️ Ward patient carried (still carries) racial and socioeconomic connotations
6/
Implicit in Meigs’ false belief was the racist assumption that women of color were less “civilized” than their “white” counterparts and thus less susceptible to stress of modern life

Back then: Stress ➡️ Endo
7/
This was also happening in cancer during same time period…

“African-americans rarely develop cancer due to their slow-paced agrarian lifestyles”

😱
8/
Was not until 1976 that African American gynecologist Dr. Donald Chatman published a critique of this racial bias and its neg impact on patient care;

▶️ 1 in 5 of his private black patients had LSC evidence of endo, but 40% had been incorrectly diagnosed with PID
9/
Why?

Pervasive myth that women of color are “immune to endo” and that they were “more promiscuous than their white peers”

Old school pelvic pain differential:
➡️ White = endo
➡️ Black = PID

Again, 😱
10/
Flash forward to the 2000’s, and we are still dealing with paucity of literature on topic of race and endometriosis

Why? Selection bias. Homogenous studies. Access to health care, Variations in socio-cultural acceptance of surgical intervention/diagnosis

etc. etc. etc
11/
Minimal research exists on presentations of endometriosis in various ethinic groups

🔑 Not all pts perceive, report, experience pain symptoms in the same way
🔑 Ethincity & socioeconomic status influences access to care, specialist referral, diagnosis & treatment offered
12/
The take away:

1⃣ Endo can occur in ALL women
2⃣ Pts of various ethnicity may have diff. presenting symptoms & express diff. treatment preferences
3⃣ Research needs to focus on pt symptomatology & disease experience using validated & cultural sensitive pt outcomes measures
13/13

If up to the challenge to contribute meaningfully to endo research...

Involve patients, communities, patience advocacy groups -> don’t go it alone.

Fin.

#endometriosis

Awesome article, @DrSonySinghMD
You can follow @BortolettoMD.
Tip: mention @twtextapp on a Twitter thread with the keyword “unroll” to get a link to it.

Latest Threads Unrolled:

By continuing to use the site, you are consenting to the use of cookies as explained in our Cookie Policy to improve your experience.