Systemic Lupus Erythematosus (SLE) - Medical-Surgical (Immune) | @LevelUpRN

Cathy covers Systemic Lupus Erythematosus (SLE), including pathophysiology, risk factors, signs/symptoms, labs, diagnosis, treatment, nursing care, and patient teaching associated with Lupus.

Our Medical-Surgical video tutorial series is taught by Cathy Parkes BSN, RN, CWCN, PHN and intended to help RN and PN nursing students study for their nursing school exams, including the ATI, HESI and NCLEX.

#NCLEX #Systemiclupus #Erythematosus #SLE #HESI #Kaplan #ATI #NursingSchool #NursingStudent⁠ #Nurse #RN #PN #Education #LVN #LPN

0:00 What to Expect with Systemic Lupus Erythematosus (SLE)
0:10 Systemic Lupus Erythematosus SLE
0:30 Pathophysiology
1:03 Risk Factors
1:21 Signs and Symptoms
1:37 Raynaud’s Syndrome
1:57 Signs and Symptoms
2:09 Lab Values
2:41 Treatment
3:26 Nursing Care
3:35 Patient Teaching
4:04 What’s Next?


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All of the nurses at Level Up RN are here to help! Cathy Parkes started helping her fellow classmates back when she was in nursing school, tutoring so they could pass their exams and graduate. After she got her BSN and started working as an RN at Scripps Encinitas Hospital, she started this YouTube channel to help nursing students around the world. Since then she has built a team of top-notch dedicated nurses and nurse educators who are focused on improving nursing education and supporting career advancement for nurses everywhere. With flashcards, videos, courses, organizational tools and more, we are singularly focused on helping students and nurses Level Up on their exams and nursing careers.

[beyondfamilyentertainment]

Hello nurse Cathy. Thank you for everything, your videos, answering my questions each time I asked you about anything. You're so wonderful. I'm glad to say I passed my Nclex RN yesterday. Your videos helped me alot. I have recommended them for my friends.

[beckyfisher]

I lost daughter in hospital. At the time i was a dialysis nurse RN outpatient. Pulse ox was not used at outpatient dialysis. Difference in hospital nursing & outpatient dialysis. No pain meds given at dialysis center. We gave IV medication & TPN.

[schneed]

Thank you for posting this video - super informative. I was diagnosed with SLE just before Christmas (2021) so doing lots of research on it. Your video was great. :)

[asadkamal]

I'm so much impressed of your lectures, I'm from Pakistan 🇵🇰 I appreciate you, keep it up...

[SuperLoopieWoman]

👏👏Thanks for getting education about SLE out there !

[jamilahadade]

Thank you so much for a very informative video. Stay well God bless you. 🙏

[JustsittingHR]

I have lupus and I’m here for the information but…I must know what camera you use it looks great !

[mattjeffreson]

There could be alternatives. In case of beauty stuff. You could see how hydroxycholoquine deals with malaria people that have similar problem. Through partnerships with certified dermatologists before sending a prescriptions. Something that keeps most users on a safe board. And having tested by VIPPs regularly has helped them achieve reputation.

[melabudhabi]

Sooo glad i clicked ur vid. Suddenly became a big fan.. will be browsing all your vids 💕💟💕💟

[joshuariley]

What do you think about sle causing chronic ischemic colitis? Or colitis in any form?

[seitanbeatsyourmeat]

My rheumatologist just put me on hydroxychloroquine, 200mg 2x a day starting soon; I have to get it filled today. I have ZERO skin symptoms, but all the lab values (we’ve been watching this for about 2 years now, getting steadily worse but I felt “ok”. I don’t feel ok anymore), and this morning I woke up to a painful wrist I couldn’t bend. It’s not swollen but it’s hot. My ankles give me issues on the regular, but everything seems to be in larger joints, no toes or fingers.
I also have hEDS, so I’m extremely “bendy” and always have been until now. I don’t even understand how to operate my body with these joint limitations!! How do regular people operate within such limited movements?

Anyway, I recently had Covid for the first time, which could have contributed to this, as I’ve had Hashimoto’s for 23 years now (another autoimmune condition) and as y’all know, one usually leads to another 😅

I’m just so not looking forward to this, I have plans and this is some grade-A BS to throw into the mix

[heygurl]

Hello Nurse Cathy, I'm still in nursing school; however, I am very interested in wound care nursing and IV infusion therapy. Could you think about incorporating those areas into your youtube channel and flash cards, in the future?

[sakurarosabellmathews]

Dear everyone, I have sle Lupus, so I know how Selena Gomez and everyone else is going through. I had got it in 2018 December. It has been 3 years now. Im 21 now. I got it when I was 18. I have been having headaches 24 seven. Know this not everyone has the same systems, but I love you, Selena Gomez lets fight this together.

[lauriewilson]

I’m late to the video so maybe you can’t respond. Told a few months ago I have Lupus. Told to find my own Rheumatologist also. Not getting any interest from my family Dr.
I live in Michigan. Do you think there’s a shortage of Rheumatologists?

[auroramolina]

Can I ask if it is curable?thank you so much in advance for your reply.

[sithvereosei]

This is what I have, pair that with my RA and my life is fun. Lol

[carriekieler]

I have SLE, i never got any of those medications.

[drei]

Great Vidio Which Stethoskope do you have?

[irenecarislombiso]

May twin A diagnos with SLE he's only 3 years old

[jenn]

I really hate when nurses or professors mention what race has what illness the most. You can always skip it. In the end we are not getting out of life alive.