Draft 2
Running head: ACADEMIC CLINICAL SOAP NOTE 1
Academic Clinical Soap Note
Grand Canyon University
ANP 650
September 25, 2019
ACADEMIC CLINICAL SOAP NOTE
SUBJECTIVE
Chief Complaint:
Patient is in clinic today for second peptide receptor radionuclide treatment (PRRT)
with Lutathera treatment.
Background:
This is a pleasant 47-year-old female with a history of metastatic pancreatic
neuroendocrine tumor. She was initially diagnosed in October 2016 presenting with
pneumonia with an incidental lung nodule noted. Biopsy demonstrated low-grade
neuroendocrine of 1%. She then was noted to have metastatic disease in the right breast
biopsy proven in February 2017. Somatostatin analog therapy was initiated then. When the
patient progressed in September 2017 she was transitioned to Afinitor. A right thyroid nodule
was noted and biopsied in December 2018 with benign findings. That due to Tait scan in
January 2019 showed progression of disease. She was transitioned to Capoten for one cycle
with recurrence of pancreatitis as well as development of splenic vein thrombus in February
2019. She had persistent pancreatitis in March 2019 on CT imaging. After, GI tumor board
review at Stony Brook University Hospital she was found to be metastatic low-grade
neuroendocrine tumor more likely pancreatic origin. Because of persistent abdominal pain
she underwent celiac plexus block in May 2019. She was subsequently referred for peptide
receptor radionuclide therapy/ Lutathera and received first dose on 7/17/2019. She has
recently moved to Florida 3 weeks ago and presents to reestablish for continuation of
Lutathera treatment at Moffitt Cancer Center.
Family History:
Father died of prostate cancer in 1998. Mother had diabetes, heart disease, and
hypertension, she passed in 2010. Patient state she had several uncles that died from cancer,
but she does not recall which cancer they had.
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ACADEMIC CLINICAL SOAP NOTE
Medication:
Insulin (Lantus) glargine 20 unit(s), SubQ, DAILY.
fluticasone nasal (Flonase 50 mcg/inh nasal spray) 2 spray(s), NASAL, DAILY.
pancrelipase 6000 units oral delayed release capsule, PO, QID.
Simvastatin 10 mg, 1 tab(s), PO, Bedtime
Metoprolol 50 mg, 1 tab(s), PO, Daily
NIFEdipine 30 mg, 1 tab(s), PO, Daily
Losartan (losartan 100 mg oral tablet) 100 mg, 1 tab(s), PO, AS NEEDED.
Multivitamin (Multi Vitamin+) PO, DAILY
Vitamin C lozenge 500 mg, 1 tab(s), PO, Daily
Multivitamin with iron (Iron 100 Plus) PO, DAILY.
Multivitamin (Vitamin B Complex oral capsule) 1 cap(s), PO, Daily
Biotin (biotin 5000 mcg oral tablet, disintegrating) PO, DAILY
Review of Systems:
Constitutional: She has a long-term history of fatigue. Weight loss of 30lb since beginning
of 2019. No fever, no chills, no weakness, no decrease activity.
Eye: No recent visual problem, No double vision.
Ear/Nose/Mouth/Throat: No dry mouth, No nasal congestion, No mouth sores, No
mucositis.
Respiratory: No shortness of breath, No cough, No sputum production.
Cardiovascular: No palpitations, No bradycardia, No tachycardia.
Breast: No nipple discharge.
Gastrointestinal: Occasionally nausea with no vomiting. She has constipation alternating
with diarrhea. Stomach pain 4 on scale 0-10. Last bowel movement today.
Genitourinary: No dysuria, No hematuria.
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ACADEMIC CLINICAL SOAP NOTE
Gynecologic: Negative.
Hematological/Lymphatics : No bruising tendency, No bleeding tendency.
Endocrine : No cold intolerance, No heat intolerance.
Immunologic : No recurrent fevers, No recurrent infections.
Musculoskeletal : No claudication.
Integumentary : No rash.
Neurologic: Alert and oriented X4.
Psychiatric: Not delusional, No hallucinations.
OBJECTIVE
Vital Signs:
Temperature: 98.65 Heart Rate: 74, Blood Pressure: 112/74, Respiratory Rate: 14,
SpO2: 100%, Weight: 57.3kg, Height: 5 ft 6 in and BMI: 21.1
Physical Examination:
General: Compared weight chart and noted a 30lb weight loss. Alert and oriented, No acute
distress.
HEENT: Oropharynx clear, Normocephalic, Oral mucosa is moist.
Cardiovascular: Normal rate, Good pulses equal in all extremities.
Respiratory: Lungs are clear to auscultation, Symmetrical chest wall expansion.
Gastrointestinal: Pain elected on lite palpation soft. Non-tender, Non-distended.
Hematological/Lymphatics: Lymphatic exam: Right, Submandibular, 10 mm ( By 10 mm ).
Extremities: Normal range of motion, No deformity, Normal gait.
Integumentary: Warm, Intact.
Neurologic: Normal sensory, No focal defects.
Cognition and Speech: Speech clear and coherent, Functional cognition intact.
Psychiatric: Cooperative, Appropriate mood & affect
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ACADEMIC CLINICAL SOAP NOTE
Labs/Imaging/ Diagnostic Test Result:
Abnormal Labs: Glucose- 219 H: Mean Cell Volume: 94.2 H: RDW: 52.7 H:
Diagnostic Data: Detailed review of the PET/CT: demonstrates numerous metastatic
avid lesions within the soft tissues and osseous structures involving bilateral breasts, liver,
pancreas, metastatic lesion in the left peritoneum and irregular mass in the left pelvis and
persistent multiple osseous metastasis.
ASSESSMENT/CLINICAL IMPRESSIONS
Health Problems:
1. Neuroendocrine Tumor D3A.8
2. Pancreatitis K85
3. Diabetes E23.2
4. Hyperlipidemia E78.49
Differential Diagnosis:
ICD-10 K29: Zollinger-Ellison Syndrome- is characterized by gastric acid
hypersecretion resulting in severe acid-related peptic disease and diarrhea. The tumors are
thought to emerge from the delta cells that are found in the pancreas and it was founded to
account for about 25% to 40% of gastrinomas. The rest of the endocrine tumors to include the
50- 70% of abnormal cells were found in the small digestive tract, while about 5% emerge
from other intra-stomach area. “Gastric not only directly stimulates parietal cell secretion but
also causes expansion of the mass of parietal cells. The increase in parietal cells results in an
increase in basal acid output and maximal acid output. This substantial secretion of acid
results in gastroesophageal reflux disease (GERD) symptoms and damage to the mucosal
lining of the GI tract, causing peptic ulcers. In addition, the acid inactivates pancreatic
enzymes, which contributes to the diarrhea, steatorrhea, and malabsorption of lipid-soluble
nutrients (www.epocrate.com.2019).”
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ACADEMIC CLINICAL SOAP NOTE
ICD-10 E34.0: Carcinoid Syndrome- progress in some people with carcinoid tumors
and is identified by cutaneous flushing, abdominal cramps, and diarrhea. There are a number
of symptoms relevant to CS that healthcare work looks for such as the abnormal labs are the
first to investigate then there are the physical manifestations. Carcinoid syndrome is seen in
individuals who have an underlying carcinoid tumor that has spread to the liver. Carcinoid
syndrome is a rare condition that effect about 10% of the population. “Carcinoid syndrome
may be more prevalent than suspected because diagnosis is difficult and sometimes
overlooked; some patients may not exhibit all three of the hallmark symptoms of flushing,
wheezing, and diarrhea (www.raredisease.org. 2019).”
ICD-10 D35.00: Pheochromocytoma- Is the type of “tumor arising from
catecholamine-producing chromaffin cells of the adrenal medulla that classically presents
with headaches, diaphoresis, and palpitations in the setting of paroxysmal hypertension
(www.epocrate.com 2019).” This disease secrete adrenaline in an uncontrolled manner and
can cause severe medical issues including heart disease, stroke, and ultimate this can lead to
death.
PLAN COMPONENT MANAGEMENT:
Research has shown that there are few neuroendocrine tumors that may not have a
clear primary tumor site and these tumors will be treated based on the histology. Many
neuroendocrine tumors tend to poorly differentiated and may grow and spread rapidly. In
order to get a better understanding of the tumor dynamic imaging studies a long with scopes
to see the internal area of the tumor body will be utilized by the provider. EUS and biopsy
may be done to confirm the cell type. The initially diagnostic test can start with the CT of the
chest, abdomen, and/ or pelvis, MRI, FDG_PET/ CT scan, and biochemical testing. The
patient that has a poorly differential neuroendocrine tumor the treatment option ideally
utilizes a combination of options. The doctor will decide which treatment will work best, for
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ACADEMIC CLINICAL SOAP NOTE
the patient at that time; “one treatment option is the surgical option this will include resection
+ adjuvant chemotherapy +/- radiation therapy. There is locoregional surgical option that
involves radiation therapy and chemotherapy given at the same time or one treatment after
the other or just chemotherapy only. If the neuroendocrine tumor is metastatic than the
treatment option is chemotherapy and every three months the patient will come into the clinic
and have his/ her lab drawn and CT or MRI completed to check the progression of the
treatment and at the time the provider and patient will decide based on the diagnostic report
how to proceed (www.nccn.org. 2019).”
Providers at the Moffitt cancer center have used peptide receptor radionuclide therapy
(PRRT) with great success. “The FDA approval of Lutathera, a peptide receptor radionuclide
therapy (PRRT), on January 26, 2018, for a new era in treatment options for the
neuroendocrine tumor (www.newRx.org. 2016).” When PRRT is use it was found to
manifest long term effectiveness to the treatment of neuroendocrine tumor while also
allowing the patient to maintain a high-quality lifestyle. The patient can use PRRT repeatedly
with very little side effects and rarely these patients were dialysis dependent.
“All PRRT candidates must first be seen by an Oncologist in order to be evaluated for
treatment. The requests for PRRT treatment should be for a GI oncology consult (De Visser,
M., 2008).” Cost associated with the PRRT can be costly but patient who do not have
insurance, Medicare/ Medicaid there are programs that can help with getting qualified for
therapy. The PRRT drug can be offered free to the patient that do not have insurance but there
will be costs for medications to help with the side effect of PRRT such as nausea and
vomiting, and there will be costs to the institution and medical personnel providing the
service.
Disposition/ Discharge Plan:
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ACADEMIC CLINICAL SOAP NOTE
“Peptide Receptor Radionuclide Therapy uses radiation to kill cancer cells, this mean
that this medication works differently than other cancer drugs. PRRT is given in a hospital
setting and have two components to the therapy (Thang. S. P., et.al 2018).” There is the tumor
targeted part that finds the cancer cell with a receptor called somatostatin. Then there is the
radioactive component that actually kills the cancer cell. This cancer infusion is given up to
four times and eight weeks apart from each infusion. Once the infusion has completed the
patient will be given an injection of long acting octreotide to decrease the cancer from
growing or spreading. The patient will be given anti-nausea medication, amino acid hydration
solution medication, and then 45 minutes later the patient will receive the PRRT treatment.
The nurse will explain during the discharge planning that it is imperative that the
patient must drink a lot of fluids/ water and urinate frequently before, during and after
treatment because this will help the radiation to leave the body. Patient should also limit close
contact with pregnant women, children, and immune compromised patient for the first two
weeks after therapy to prevent exposure and the patient must practice good hand hygiene with
soap and water often. Expected outcome of PRRT is to “reduce the risk of cancer spreading,
growing, or getting worse by 79% compared to a larger than normal dose of long-acting
octreotide (www.carcinoid.org. 2019).”
Health Education/ Promotion and Disease Prevention:
Patient education/ health promotion include “minimize radiation exposure during and
after treatment with PRRT-consistent with institutional good radiation safety practices and
patient management procedures, monitor blood cell counts because of myelosuppression;
treatment may be placed on hold, dose educed, or permanently discontinue PRRT treatment
based on negative reaction to treatment, hepatotoxicity can cause a decrease in blood levers
therefore monitor transaminases, bilirubin and albumin. Due to neuroendocrine hormonal
crisis patient must be monitored for flushing, diarrhea, hypotension, bronchoconstriction or
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ACADEMIC CLINICAL SOAP NOTE
other signs and symptoms, embryo-fetal toxicity can occur with PRRT in which the fetal
harm can come about. Advise females and males of reproductive potential of the potential
risk to a fetus and to use effective contraception and PRRT can cause infertility
(www.carcinoid.org. 2019).” Patient are also instructed to make sure they continue to update
their medication list to prevent adverse reaction. Disease prevention focus is on consuming
half the patient body weight in water daily, eating a healthy diet that consist of fresh fruit and
vegetable, avoid white pasta and rice, organic meats, fruits, and vegetables is considered a
better choice (think rainbow colors when it comes to healthy eating). Maintaining a healthy
weight and BMI. Patient are instructed to work out 150 minutes per week about 3 to 4 times
in that week, stress reduction is another prevention option, and finally getting enough rest so
that the body can fight off the cancer cell that is circulating in the body.
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ACADEMIC CLINICAL SOAP NOTE
References
Carcinoid Syndrome. (2019). Retrieved from https://rarediseases.org/rare-diseases/carcinoid-
syndrome/
de Visser, M., Verwijnen, S. M., & de Jong, M. (2008). Update: Improvement strategies for
peptide receptor scintigraphy and radionuclide therapy. Cancer Biotherapy &
Radiopharmaceuticals, 23(2), 137-57.
doi:http://dx.doi.org.lopes.idm.oclc.org/10.1089/cbr.2007.0435
Neuroendocrine cancer; long-term experience supports efficacy and safety of PRRT for
treating neuroendocrine tumors. (2016, Nov 06). NewsRx Health Retrieved from
https://lopes.idm.oclc.org/login?url=https://search-proquest-
com.lopes.idm.oclc.org/docview/1832797816?accountid=7374
Pheochromocytoma. (2019). Retrieved from
https://online.epocrates.com/diseases/16332/Pheochromocytoma/Risk-Factors
Thang, S. P., Mei, S. L., Kong, G., Hofman, M. S., Callahan, J., Michael, M., & Hicks, R. J.
(2018). Peptide receptor radionuclide therapy (PRRT) in european neuroendocrine
tumour society (ENETS) grade 3 (G3) neuroendocrine neoplasia (NEN) - a single-
institution retrospective analysis. European Journal of Nuclear Medicine and
Molecular Imaging, 45(2), 262-277.
doi:http://dx.doi.org.lopes.idm.oclc.org/10.1007/s00259-017-3821-2
Treatment Guideline: Neuroendocrine Tumors. (2019). Retrieved from
https://www.nccn.org/patients/guidelines/neuroendocrine/88/
What is LUTATHERA®? (2019). Retrieved from https://www.carcinoid.org/wp-
content/uploads/2018/07/AAA_Lu177_US_0058_LUTATHERA_lutetitum_Lu177_d
otatate_Patient_Fact-Sheet_Final-July-2018.pdf
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ACADEMIC CLINICAL SOAP NOTE
Zollinger-Ellison syndrome. (2019). Retrieved from
https://online.epocrates.com/diseases/40824/Zollinger-Ellison-syndrome/Etiology27,
2018, from https://www.atsjournals.org/doi/citedby/10.1513/pats.200604-099SS
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- References