COVERS THE ENTIRETY OF THE CLASS) UNIVERSITY OF TEXAS,
ARLINGTON | LATEST 2025 UPDATE
UTA – NURS 5432 – FNP 1 – Exam Study Notes
This document covers the entirety of the class – consisting of a midterm and the comprehensive final. Don’t waste
your time watching all those videos, they are horribly low yield. By following this document, I just saved you a
dozen or so hours of studying – you’re welcome. All highlighted, red, italicized text are those focused questions that
appear in those outlined summaries of each module. Double check these against your current semester taking this
course. That said, I can’t really make any of these modules high yield as anything could be on the exams from
these modules; and in all honesty, that was the case for me. However, think about it this way - since you are
only going to get 150 questions (between the midterm and the final) and there’s over 100 pages in this
document summarizing the entirety of the course, comprised of I-don’t-know-how-many-data-points, focus
on that topics/categories that you are most likely to be tested on; or, to put it another way, what do you think
you are going to be absolutely, 100% be tested on? That answers I’m going for are – pharmacology, diagnostics,
physical assessment, patho, etc. I would tackle each topic in this manner. I highly recommend to focus on these
categories of each topic first – as it is basically impossible to simply review everything covered in the course and
properly retain everything. For instance, focus on (and memorize) all the pharmacology for each topic covered in
the course (anki maybe); then do the same for diagnostics, and so on. Doing this, you may not cover every possible
question you could get, but you would at least ace the questions you are for sure going to be asked in each of those
categories. Trust me, you will be. Any italicized text is my own note/addition/snarky comment and did not come from
lecture material. I would suggest cross-referencing all these topics w/ Osmosis videos (if you have time) and chatgpt
(ask your question, followed by the prompt “please explain in advanced medical terminology.” Be cognizant of
possible AI hallucinations). Also, you must get 100% on everything else in the course. Good luck.
I won’t be making another one of these for FNP2 or FNP3 – so don’t bother looking for it. This took too much time to create.
Recommend your notes utilize the following format –
Disease name –
What are signs and symptoms? –
Special considerations for this disease? –
How do you manage disease? –
When do you refer to specialist(s)?
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, Mid-term Exam – modules 1-4 –
Module 1 -
Vaccinations >>
should not be delayed due to minor illnesses, even if they illicit low-grade fever. However, for
moderate to severe infections, vaccinations could be postponed. Premature infants should follow
a schedule for immunizations based on their chronological age, not their gestational age. Vaccine
doses should not be adjusted (reduced) for premature or low-birthweight patients. Chronic
diseases are not outright contra-indications; however, vaccination with DTaP should be deferred
until the neurologic condition has been clarified and/or is stable.
Rotavirus vaccines –
• Rotarix –doses s/b given 28 days apart – for infants, given at age 2 mo and 4 mo. –
completed by 24 weeks.
• Rotateq – 3 doses completed by 32 weeks of age.
Immunodeficient children should not be given live-virus vaccines. These include –
• Oral polio vaccine [OPV, not available in the United States]
• Rotavirus
• MMR
• VAR
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, • MMRV
• yellow fever
• LAIV (live attenuated)
• Live-bacteria vaccines (BCG or live typhoid fever vaccine).
If malignancy is in remission or chemo hasn’t been administered within 90 days they can receive
live virus vaccine.
Known allergies and vaccines –
MMR, IPV, and VAR contain microgram quantities of neomycin, and IPV also contains trace
amounts of streptomycin and polymyxin B; children with known anaphylactic responses to
these antibiotics should not be given these vaccines.
Trace quantities of egg antigens may be present in both inactivated and live influenza and yellow
fever vaccines. Guidelines for influenza vaccination in children with egg allergies have recently
changed. The trace amounts of egg protein are generally considered below the threshold needed
to induce an allergic reaction and there has been no increased risk of anaphylaxis documented in
children with severe egg allergies. Therefore, children with severe egg allergy can be vaccinated
with influenza vaccine with no special precautions beyond those for any other vaccine.
RV vaccine –
Rare incidence (1 in 20k-100k) of intussusception. Med should be avoided in pt’s w/ hx of
chronic GI issues (Hirschsprung’s dz, hx of intussusception, or immune conditions. RV1 should
not be given to infants with a severe latex allergy; container for RV1 med has latex. Both
vaccines (RV1 + RV5) are contraindicated in infants with severe combined immunodeficiency
(SCID). RV vaccines should be avoided in infants whose mother received a biologic response
modifier (eg, etanercept) during pregnancy. Vaccination should be deferred in infants with acute
moderate or severe gastroenteritis. Hospitalized children should wait until post discharge to
receive their first dose.
Developmental >>
Typical things children should be able to do, by age –
• They can lift their heads with good control at 3 months.
• Sit independently at 6 months – question involved a 4mo.
• What can they do at 4mo??
• Roll over from front to back by 6 months?
• Hand to hand transfer 5-6 months.
• Pincer grasp 8-10 months.
• crawl at 9 months.
• Pinch grasp at 12 months.
• walk at 1 year.
o The child learning to walk has a wide based gait at first. Next, he or she walks
with legs closer together, the arms move medially, a heel toe gait develops, and
the arms swing symmetrically by 18–24 months.
• Feed self by 15 months.
• Scoop with a spoon, throw ball at 18 months.
• run by 18 months.
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, • 18 Bmonths B– Bwould Bbe Bconcerning Bif Bthey Bare Bnot Bmaking Beye Bcontact Bor
Bfeeding Bthemselves.
• Speech B/ Blanguage B–
o Babbling Breaches Ba Bpeak Bat Bage B12 Bmonths.
o The Bchild Bthen Bmoves Binto Ba Bstage Bof Bhaving Bneeds Bmet Bby Busing Bindividual
Bwords Bto Brepresent Bobjects Bor Bactions. BIt Bis Bcommon Bat Bthis Bage Bfor Bchildren
Bto Bexpress Bwants Band Bneeds Bby Bpointing Bto Bobjects Bor Busing Bother Bgestures.
o Children Busually Bhave B5–10 Bcomprehensible Bwords Bby B12–18 Bmonths; Bby
Bage B2 Byears Bthey Bare Bputting B2–3 Bwords Binto Bflexible Bphrases, B50% Bof
Bwhich Bstrangers Bcan Bunderstand Band Bfluidly Buse Babout B50 Bwords Bfor
Bvarious Bneeds.
o The Bacquisition Bof Bexpressive Bvocabulary Bexpands Bsignificantly Bbetween B12 Band
B24 Bmonths Bof Bage. BAs Bthey Bage, Bchildren Bbecome Bmore Bunderstanding.
o By Bkindergarten Bage B– Bthey Bcan Bunderstand B100% Bof Bthe Blanguage.
o approximately B75% Bof Bspeech Bunderstandable Bat B3 Byears Bold,
o about B100% Bof Bspeech Bis Bunderstandable Bby B4 Byears Bold.
Tanner BStages B>>
System Bfor Bdescribing Bpredictable Bsteps Bduring Bsexual
Bmaturation. BCenters Bon Btwo, Bindependent Bcriteria B–
• Appearance B– Bpubic Bhair Bin Bmales Band Bfemales
• Genital Bdevelopment B–
o Males B– Bincreased Btesticular Bvolume, Bpenile Bgrowth.
o Females B– Bbreast Bdevelopment
Tanner BStages B– Bbe Bable Bto Bstage Bby Bage.
• Stage B1 B– Bpre-pubertal
o No Bpubic Bhair, Beither Bsex
• Stage B2 B–
o Soft Bpubic Bhair, Bboth Bsexes
o M B– Bmeasurable Btestes Benlargement
o F B– Bbreast Bbuds Bappear
• Stage B3 B–
o Pubic Bhair Bbecomes Bcoarser.
o M B– Bpenis Bbegins Bto Benlarge Bin Bsize, Blength
o F B– Bbreast Bmounds Bform
• Stage B4 B–
o Pubic Bhair Bbegins Bto Bcover Bthe Bpubic Barea.
o M B– Bpenis Bbegins Bto Bwiden
o F B– Bbreast Benlargement Bforms B“mound Bon Bmound” Bbreast Bcontour
• Stage B5 B– Badult
o Pubic Bhair Bextends Bto Bthe Binner Bthigh.
o M B– Bpenis, Btests Benlarge Bto Badult Bsize
o F B– Bbreast Btakes Bon Badult Bcontour
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