1. Introduction
Patient Profile
Patient C. T.
Age 15 years old
Gender 15
Anthropometrics

●               Height

●               Weight

●               BMI

●               Usual Body Weight (UBW) ●            Ideal Body Weight (IBW)

In addition, please address any

weight changes within the past six months

Upon Admit:

178 cm

54 kg

17.0 kg/m2    (9%ile, Z-score = -1.3)

57kg

66.019 kg

Expected wt gain for age: 11-14g/day

Some wt loss upon admit from recent illness and fatigue over past couple weeks. No other wt concerns upon admit.

Chief Complaint (CC) on Current Admission Persistent cough, fatigue, body aches, epistaxis, weight loss
Primary Diagnosis(es) AKI, ANCA Vasculitis
Secondary Diagnosis(es) Hypoxia
Reason patient was chosen for study Complex medical stay, recent weight loss, nutrition support required
Date the study began and ended 7/18-7/29
Focus of this study NFPE, Nutrition support
  1. Patient History
Past Medical History
Previous Diagnosis(es) Seizure in 2018, but otherwise previously healthy
Past Hospital Admissions None
Relevant Family Medical History
Maternal History of scleroderma
Paternal None significant
Social History
Occupation Student
Marital and family status Lives w/ parents
Educational level Currently a sophomore in high school
Health insurance Select Health
Number of children and ages none
Family responsibilities child
Home environment Positive- no current concerns
Standards of living Positive environment
Religion None mentioned
Lifestyle History
Alcohol none
Tobacco none
Exercise Plays some sports including baseball and soccer
Sleep Mom reports he sleeps around 8-10hrs
Current medications, vitamins, supplements, or illicit drug use none
  1. Pathophysiology
Organ(s)/systems involved Respiratory/Lungs Renal system/Kidneys
Function of organ(s)/systems involved Allow for a gas exchange from the outside environment to the bloodstream. 1 Act as filters for getting rid of waste within the body while also return essential substances such as vitamins, amino acids, hormones, glucose, and additional particles back into the bloodstream to be used by the body.5
Diagnosis (discussion) Hypoxia, risk for pulmonary

hemorrhage, pulmonary vasculitis

Renal dysfunction,

hyperkalemia, granulomatosis

Etiology Not enough blood flow to the lungs. Presumably via vessel restriction related to the ANCA vasculitis2 Glomerulus filtration has been impaired and results in reduction of kidney functions as particles cannot be filtered and buildups occur within the kidney.9
Symptoms Cough, fatigue, SOB Decreased urinary output, fatigue, nausea, shortness of breath5
Physiological consequences Low )2 levels, poor perfusion, increased WOB Volume overload, decreased immunity, uremic retention5
Diagnostic criteria Abnormal gas exchange (Fio2 ratio), low blood oxygen levels.2 Urea and creatinine levels via a blood test. Low urine volume10
Relevant labs required Na, blood gas, FiO2, O2 levels3 Urea, Creatinine, BUN, Na, K,

Cl10

MNT/nutrition treatment options Lower kcal needs  to ensure that lower amounts of gas are produced in the bloodstream via carbohydrate digestion and energy production.

Overfeeding the patient could exacerbate the hypoxia and add to respiratory distress.4

All nutrition interventions are expected to be low in K. For TPNs, K is typically often removed all together and low Cl is included at smaller amounts. For enteral nutrition, formulas low in K and Na are recommended.9

C.T. was a previously healthy 15 year old male living in Reno, Nevada who developed a cough two months ago. He originally thought the cough was related to allergies. He also had fatigue, body aches, epistaxis (bloody noses), weight loss, and was staying in his room a lot. He was evaluated a couple of times by his primary care physician where a chest xray was completed and shown to be normal. Three weeks ago his eyes were noted to be red but again thought it was related to allergies. Mother reported that his skin color was different and he was evaluated again by his primary care physician and labs were drawn. When his labs came back a few days later, he was sent to Reno Children’s hospital where he was admitted for further evaluation and care.

In the ED, he had abnormal labs of sodium at 129, potassium 5.4, BUN of 110, creatinine of 11.1 and a bicarbonate of 17. Nephrology was consulted for renal failure. ANCA antibodies were sent to be tested and came back positive. A hemodialysis catheter was placed for renal failure and dialysis was performed for two consecutive days. He was then intubated for a renal biopsy. While suctioning, he had a significant bit of mucus plugs and old blood but he was able to be extubated after the procedure and was on 1 Liter of oxygen through his nasal cannula, but acutely had hypoxia and required an increase of oxygen from 1 L to 4 L without increased WOB. He then was escalated to 20 L high flow nasal cannula with an FIo2% 80%. Due to his diagnosis of ANCA Vasculitis, the decision was made to transfer him to Primary Children’s hospital for a rheumatology consultation. He was then admitted to the Pediatric ICU due to hypoxia requiring HFNC and high risk for pulmonary hemorrhage. He was intubated upon admission.

4.   Present Medical Status and Treatment

Lab Tests
Lab Test Value Abnormal Value Normal Reference Value/Range
Sodium 136 (low) 135-145
Potassium 5.6 high 3.6-5.2
Cl 95 low 96-106
BUN 125 HIGH 6-24
Protein total 6.3 6-8.3
Creatinine 10.42 high 0.7-1.3
Calcium 7.7 low 2.1-2.6
Hemoglobin 10.7 low 13.8-17.2
Hematrocrit 31.3% 41%-50%
Medications
Medication Treatment for: Drug/Food Interactions and/or side effects Duration of treatment
Heparin Flush saline none ongoing
protonix Heartburn, cough none PRN
labetalol Treat high blood pressure Possible nausea (uncommon) PRN
Methylprednisolone Inflammation, kidney issues Possible lactose interactions Ongoing
Vit D Low vit D labs Supplement in lack of nutrition Ongoing
Treatment/Medical Procedures and Nutrition Implications
Procedure/Surgery Results from diagnostic tests/procedures, and/or surgical procedure findings Nutritional Implications
ECMO Cardiopulmonary support NPO status, TPN when stable
Trach Placement Need for ventilatory needs Lower kcal needs
Kidney Biopsy Testing Kidney tissue none
Dialysis Filtering electrolytes in blood Limit Na, K, phosphorus in nutrition
  1. ’s hospital course was complicated by shock requiring vasoactive medications,acute hypoxemic respiratory failure requiring mechanical ventilation, pulmonary hemorrhage requiring VV ECMO, acute renal failure requiring CRRT, bilateral pneumothoraces and pneumomediastinum, seizure, and pericardial effusion s/p pericardiocentesis and pericardial drain placement. Infectious concerns during admission include influenza A with persistent lactobacillus bacteremia and pleural effusion, invasive pulmonary aspergillosis and pericardial fluid positive for Rhizopus.

The patient was currently working through trach adjustments and ventilatory management, and significant weight loss was observed and recorded during the current admission. Began trophic feeding to preserve gut function until he tolerated feedings.

Aim to transition to full feeds with an NG tube in place.

C.T. was diagnosed with ANCA Vasculitis is a very rare auto-immune disease that  is characterized by a condition that causes vessel inflammation sometimes causing necrosis and can quickly lead to mortality and morbidity.11

5.   Medical Nutrition Therapy

Nutrition History:

-C.T. was a previously healthy 15 year old male who had no issues eating. He was on a regular diet prior to admission and was not taking any oral supplements or medications. Mom reported that the patient has appeared to have lost weight recently and stated that his usual body weight is around 57 kg.

-Upon admission to Primary Children’s hospital, C.T. likely received 75% goal nutrition over the past week via his previous hospital stay. TPN was initiated within 3-5 days of admission.

-C. T. is currently determined to be at a “high” nutrition risk level

Current Prescribed Diet: NPO

  • NPO diet prescribed upon admission due to hospital and ASPEN critical care protocol. Will start TPN after 3-5 days of NPO status.
  • Current Needs:

○ Intubated: 30 kcal/kg 1.5 g/kg protein,  40 ml/kg fluids

○ Extubated: 38-44 kcal/kg, 0.9 g/kg protein, 40 ml/kg fluids

  • Feeding Goal TPN: D12%, AA 1.5 g/kg, SMOF 0.88 g/kg (GIR 2.9 mg/kg/min) =

29.2 kcal/kg & 40 mL/kg; carnitine added at 15 mg/kg/d

  • Feeding Goal NG:

○ Intubated: Nepro at 38ml/hr x 24hrs = 30 kcal/kg, 1.4 g/kg protein, 17 ml/kg fluid

○ Extubated: Nepro at 55 ml/hr x 24 hrs = 44 kcal/kg, 2g/kg protein, 24ml/kg

Other

Nutrition Goals: Meet nutrition needs to aid age-appropriate weight gain

Nutrition Interventions: NPO, Nutrition support when medically appropriate

Nutrition Diagnosis

PES Statement
Problem (the nutrition diagnosis) Inadequate Oral Intake
Etiology (factors contributing to the nutrition diagnosis) Decreased ability to consume sufficient energy, nutrients
Signs/symptoms (findings from the nutrition assessment that determine the nutrition diagnosis) NPO status
Statement:

Inadequate Oral intake related to decreased ability to consume sufficient energy, nutrients as evidenced by NPO status.

Summary of Conclusions:

C.T. is currently NPO status which is appropriate as he is newly admitted into the ICU, and per ICU nutrition recommendations, remains NPO prior to possible surgeries and during the acute stabilization phase in the ICU.6,8 Expecting that nutrition will be started within five days, there is priority to begin enteral nutrition if medically appropriate to maintain the gastrointestinal system.7 If enteral nutrition is not appropriate, TPN needs have already been calculated in that case and will be started no later than day 5. 8

6.   Prognosis

C.T. is currently in a medical state needing complete 24 hour support including kidney, cardiovascular, and pulmonary support around the clock. The current stabilization process is prioritized to maintain renal function and transition off of NPO status to begin enteral feedings. Pt will remain in ICU until no longer needing ventilatory support and medications that require ICU care. Transition aims to transition to medical and rehab floor as the patient continues to stabilize and eventually return back home. Patient and family are receiving support via social workers from the hospital and hoping to be able to transition home soon.

7.   References

  1. Haddad M, Sharma S. Physiology, Lung. In: StatPearls. Treasure Island (FL): StatPearls Publishing; July 18, 2022.
  2. Bhutta BS, Alghoula F, Berim I. Hypoxia. In: StatPearls. Treasure Island (FL): StatPearls Publishing; May 8, 2022.
  3. Michiels C. Physiological and pathological responses to hypoxia. Am J Pathol. 2004;164(6):1875-1882. doi:10.1016/S0002-9440(10)63747-9
  4. Dixit SB, Tiwari NR, Zirpe KG, et al. How Have Nutrition Practices in the ICU Changed in the Last Decade (2011-2020): A Scoping Review. Cureus.

2021;13(6):e15422. Published 2021 Jun 3. doi:10.7759/cureus.15422

  1. Ogobuiro I, Tuma F. Physiology, Renal. In: StatPearls. Treasure Island (FL): StatPearls Publishing; July 26, 2021.
  2. Friedrich S, Meybohm P, Kranke P. Nulla Per Os (NPO) guidelines: time to revisit?.

Curr Opin Anaesthesiol. 2020;33(6):740-745.

doi:10.1097/ACO.0000000000000920

  1. Mehta Y, Sunavala JD, Zirpe K, Tyagi N, Garg S, Sinha S, Shankar B,

Chakravarti S, Sivakumar MN, Sahu S, Rangappa P, Banerjee T, Joshi A, Kadhe G. Practice Guidelines for Nutrition in Critically Ill Patients: A Relook for Indian Scenario. Indian J Crit Care Med. 2018 Apr;22(4):263-273. doi:

10.4103/ijccm.IJCCM_3_18. PMID: 29743765; PMCID: PMC5930530.

  1. Singer P, Blaser AR, Berger MM, et al. ESPEN guideline on clinical nutrition in the intensive care unit. Clin Nutr. 2019;38(1):48-79. doi:10.1016/j.clnu.2018.08.037
  2. Binda V, Moroni G, Messa P. ANCA-associated vasculitis with renal involvement. J Nephrol. 2018;31(2):197-208. doi:10.1007/s40620-017-0412-z

10.Bindroo S, Quintanilla Rodriguez BS, Challa HJ. Renal Failure. In: StatPearls. Treasure Island (FL): StatPearls Publishing; February 24, 2022.

11.Yates M, Watts R. ANCA-associated vasculitis. Clin Med (Lond). 2017 Feb;17(1):60-64. doi: 10.7861/clinmedicine.17-1-60. PMID: 28148583; PMCID: PMC6297586.

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