Professional Documents
Culture Documents
Signs/Symptoms:
Clinical signs and symptoms of T2DM may include polyuria (excessive urination),
polydipsia (excessive thirst), unexplained weight loss, fatigue, and blurred vision. Patients might
also experience slow wound healing and increased susceptibility to infections. Diabetic patients
may experience hyperglycemia, or high blood sugar, as well as hypoglycemia, or low blood
sugar. Signs and symptoms of hyperglycemia include increased thirst and dry mouth, frequent
urination, tiredness, blurred vision, and recurrent infections. Signs and symptoms of
hypoglycemia include fast heartbeat, shaking, sweating, anxiety, irritability or confusion,
dizziness, and hunger. Any signs and symptoms of hyperglycemia or hypoglycemia should be
addressed immediately and if the situation is emergent, the patient should call 911 and seek
medical attention.
Pathology:
The pathology of T2DM involves a complex interplay of insulin resistance in peripheral
tissues (muscle and adipose) and impaired insulin secretion from pancreatic beta cells. This
results in an inability of cells to efficiently take up glucose, leading to hyperglycemia. Chronic
hyperglycemia contributes to microvascular and macrovascular complications, affecting organs
such as the eyes, kidneys, nerves, and cardiovascular system.
A healthy pancreas efficiently regulates glucose levels through well-maintained islet
architecture, appropriate beta-cell response to elevated glucose, and balanced intra-islet
signaling. In type 2 diabetes (T2DM), pancreatic function is characterized by insulin resistance,
leading to compensatory hyperinsulinemia. Over time, beta-cell dysfunction develops, resulting
in reduced glucose-stimulated insulin secretion (GSIS). The altered architecture of pancreatic
islets, with decreased beta-cells and increased alpha-cells, disrupts intra-islet signaling and
impairs metabolic homeostasis.¹
If left unmanaged, T2DM can impact the entire body. Insulin resistance in peripheral
tissues, including skeletal muscles, leads to impaired glucose uptake, contributing to
hyperglycemia. In the bones, T2DM is associated with an increased risk of bone fractures and
reduced bone mineral density, potentially affecting bone health. Digestion and nutrient
absorption may be affected by gastrointestinal complications such as gastroparesis and altered
gut microbiota, which promotes proinflammatory cytokine release. Chronic hyperglycemia may
lead to skin complications, including increased susceptibility to infections and delayed wound
healing. Increased insulin resistance and hyperglycemia have been linked to non-alcoholic fatty
liver disease (NAFLD), which can progress to more severe liver conditions.¹ T2DM is a leading
cause of diabetic nephropathy, characterized by impaired kidney function and proteinuria.¹ The
effects of T2DM on the cardiovascular system significantly increase the risk of cardiovascular
diseases, including heart attacks and strokes, often exacerbated by hypertension and
dyslipidemia. T2DM may also impair immune function, leading to an increased susceptibility to
infections. The nervous system effects of T2DM are associated with peripheral neuropathy,
impacting sensory and motor functions, and may have implications for cognitive function.¹
Finally, adipose tissue dysfunction contributes to insulin resistance and metabolic disturbances in
T2DM.
Epidemiology:
T2DM has reached epidemic proportions globally, with a rising prevalence linked to
lifestyle changes, aging populations, and urbanization. The condition is more prevalent in adults
but is increasingly diagnosed in children and adolescents. According to the World Health
Organization (WHO), in 2022, approximately 422 million people worldwide were living with
diabetes, and this number is expected to rise.² Diabetes is the seventh leading cause of death
among Americans.² Diabetes is a major cause of blindness, kidney failure, heart attacks, stroke,
and lower limb amputation. Seventy-five percent of people with diabetes live in low- and
middle-income countries. Alaska Native adults (13.6) and non-Hispanic Blacks (12.1%) have the
highest rates of diabetes in the US.² Currently, 8.7 million Americans are living with
undiagnosed diabetes, meaning that 22.8% of adults with diabetes are undiagnosed.²
Comorbidities:
Individuals with T2DM often present with a spectrum of comorbidities that exacerbate
the disease's impact on overall health. Common comorbidities include hypertension,
hyperlipidemia, retinopathy, nephropathy, and neuropathy. Elevated blood pressure, or
hypertension, is prevalent in individuals with T2DM, contributing to an increased risk of
cardiovascular complications. Hyperlipidemia, characterized by elevated levels of cholesterol
and triglycerides, is frequently observed in T2DM patients, further enhancing cardiovascular
risk. Diabetes can lead to retinal damage, affecting vision and potentially leading to blindness if
left untreated. Diabetes is a leading cause of kidney disease, marked by impaired kidney function
and proteinuria.³ Type 2 diabetes is the leading cause of dialysis in the United States and one in
three adults with diabetes suffers from kidney disease.³ Diabetes and Hypertension are the major
causes of kidney failure in the United States.³
Peripheral neuropathy can result in sensory and motor deficits, impacting daily
functioning. Chronic high blood sugar, as well as increased triglycerides in the blood from
diabetes, can cause nerve damage.³ Peripheral neuropathy affects the feet, legs, and sometimes
hands and arms. Nearly one-third to one-half of people with diabetes have peripheral
neuropathy.³ Autonomic neuropathy damages the nerves of internal organs, which can affect
heart rate, blood pressure, and the digestive system, as well as masking hypoglycemia symptoms.
Focal neuropathies typically damage a single nerve, such as in the hand, torso, or leg. The most
common focal neuropathy type experienced by adults with diabetes includes entrapment
syndromes such as carpal tunnel syndrome.³ Proximal neuropathy is rare but disabling, affecting
the hip, buttock, or thigh on one side of the body. This type of neuropathy typically does not
spread to both sides of the body and symptoms gradually improve over months or years.
Case Presentation:
Patient, age 68, presents with Type 2 Diabetes Mellitus. She was diagnosed 12 years ago
in her home country of Zimbabwe and arrived in the United States in 2018 with her husband and
5 adult children. Recently, her diabetes has become more uncontrolled. During the session, she
reported that her husband died of stomach cancer last year and that she lacks proper social
support. She also reports stress from being unable to bring her husband back to their home
country.
The major stressors described by the patient included family conflict over how she
handled her husband’s passing. She stated that she was unable to return to Zimbabwe for her
husband to pass peacefully due to financial constraints, as well as not being able to receive her
medications while there. This caused conflict not only with her 5 children but with her extended
family. She chose to cremate her husband’s body due to financial reasons, which caused her to
lose the relationship with two of her children. As evidenced by the patient’s recounting, she has
been struggling to self-monitor her glucose and follow a carbohydrate-consistent diet due to
stress and low mood as a result of her lack of psychosocial support during what she reported to
be the most stressful time of her life. A detailed timeline of patient encounters from 6/22/23 to
1/4/24, covering the patient's husband's illness, the patient’s medication changes,
hospitalizations, and his eventual passing can be seen below as follows:
6/22/23: The case worker reports the patient’s husband is sick. The patient cannot work
due to health issues. The patient requested assistance with securing food. She was
referred to Groceries to Go and enrolled in NYC Cares. She was referred to a social
worker. Currently, she is experiencing financial, food, and social barriers to care.
7/5/23: She was prescribed Ozempic but has not not taken it. She is waiting to confirm
her cancer history, specifically pancreatic cancer. She denies any history of pancreatitis.
Her husband is in the hospital. The patient reports not adhering to a carbohydrate-
consistent diet due to visiting him often. The doctor states there is not much more they
can do for him. At this time the patient is experiencing medical and social barriers to
care.
8/15/23: The patient arrived 1hr 20m late to apt, as she was coming from the hospital
visiting her husband. At this time the patient is experiencing social barriers to care.
8/17/23: There is a note for acute kidney injury (AKI). The patient reported stopping
Ozempic due to hypoglycemic intolerance. She is positive for nephropathy (eGFR 40),
proteinuria, and retinopathy. The husband was discharged from the hospital, went home
for 3 days, went into cardiac arrest, and was re-admitted.
8/22/23: The patient missed her scheduled nutrition appointment.
9/24: The patient reports that her husband passed away and she stated that she would like
to see a social worker.
9/28: Repeat referral to SW. The original referral was placed 06/2023.
10/3/23: The patient missed her scheduled nutrition appointment.
10/29/2023: The patient had a hypoglycemic event after her husband’s memorial service.
At three am, her blood glucose was 53 mg/dL and her daughter called 911. Paramedics
arrived and assisted in regulating the patient’s glucose levels but the patient was not taken
to the ER.
1/4/24: As of today the patient has still not seen a social worker.
NCP Assessment:
Client History:
Medical History:
Hypertension
Hyperlipidemia
Retinopathy
Anemia
Microalbuminuria
Susrgical History:
Cataract Removal surgery (2003, Zimbabwe)
Hysterectomy (2003, Zimbabwe)
Family History:
Mother (Deceased) Hypertension
Father (Deceased) No Known Problems
Sister Diabetes
Brother Diabetes
Paternal Grandfather Diabetes
Social History:
The patient reports a lack of social support post-husband’s death. She reports that her daughter
lives in Brooklyn and is supportive.
cultural: The patient is unable to return to her home country to bury her husband or practice any
cultural rites of passing.
financial: The patient requested financial assistance and assistance securing food.
1. atorvastatin HMG-CoA Take 1 tablet (40 mg) by avoid grapefruit, avoid alcohol⁴
(LIPITOR) 40 MG reductase mouth daily.
tablet inhibitor⁴
3. Ferrous sulfate Oral iron Take 1 tablet (325 take 1-2 hours before eating⁴
(FERATAB) 325(65 supplement⁴ mg total) by mouth
FE) MG tablet daily.
6. Losartan (COZAAR) Angiotensin II Take 1 tablet (25 mg total) avoid potassium-containing salt
25 MG tablet receptor blockers by mouth substitutes⁴
(ARBs) nightly.
7. Metoprolol tartrate Beta blocker, take 0.5 tablets (12.5 mg) Take 2 hours apart from
(LOPRESSOR) 25 mg antiadrenergic, twice daily. multivitamin/multimineral, take
tablet antiarrhythmic⁴ with or immediately after food.
Beta-adrenergic receptor blocking
agents (aka beta-blockers) may alter
serum lipid profiles. Increases in
serum VLDL and LDL cholesterol
and triglycerides, as well as
decreases in HDL cholesterol, have
been reported with some beta-
blockers. Patients with preexisting
hyperlipidemia may require closer
monitoring during beta-blocker
therapy, and adjustments⁴
8. NIFEdipine Calcium channel 1 tablet orally daily take 2 hours apart from
(ADALAT CC) 60 MG blocker⁴ multivitamin/multimineral, avoid
ER 24 hr tablet grapefruit juice, avoid alcohol⁴
9. Polyvinyl alcohol 1.4 Eye lubricant - Administer 1 drop (15 ml) n/a
% (LIQUIFILM ophthalmic to both eyes 4 (four) times
TEARS) 1.4 % a day.
ophthalmic solution
10. Sodium zirconium Calcium channel Take 1 packet (5 g total) take 2 hours apart from
cyclosilicate blocking agents⁴ and mix with 3 multivitamin/multimineral, avoid
(LOKELMA) 5 g packet tablespoons of water grapefruit juice, avoid alcohol⁴
and take by mouth
daily.
Supplements: none
Food and Supply Availability: The patient prepares her food. The patient requested assistance
with securing food. She was referred to Groceries to Go and enrolled in NYC Cares.
Anthropometrics:⁶
● Ht: 1.52 m (4’ 11.84”)
● Wt (current):71.2 kg (157 lb)
● BMI: 30.82 kg/m² (overweight)
● DBW: 45.5 kg
● % UBW: 101
● % wt Δ: -1.28
● % DBW: 156%
Labs:
Component Lab Value Etiology (if Normal Range⁴ Date
applicable)⁴
HGB 9.4 (L) May be 2/2 anemia⁴ Female: 12–16 g/dL⁴ 11/29/2023
Interpretation:
The patient’s elevated creatinine level (1.27 mg/dL) aligns with T2DM's impact on
kidney function. Chronic hyperglycemia in diabetes can lead to diabetic nephropathy,
contributing to impaired renal function and elevated creatinine levels. Reduced eGFR (46
mL/min/1.73m²) is consistent with diabetic nephropathy, indicating decreased kidney filtration
capacity. Persistent hyperglycemia damages the renal microvasculature, leading to impaired
glomerular filtration. Elevated BUN (22.0 mg/dL) is in line with impaired kidney function
associated with diabetic nephropathy. BUN levels rise as the kidneys struggle to excrete urea, a
waste product. The patient’s high glucose levels (159 mg/dL) are indicative of uncontrolled
diabetes. The patient's reported challenges in self-monitoring and dietary adherence,
compounded by emotional stress, likely contribute to poor glycemic control. Low hemoglobin
(9.4 g/dL) and hematocrit (31.4%) levels suggest the presence of anemia. Anemia is a common
complication of chronic diseases, including diabetes, and can result from a combination of
factors such as nutritional deficiencies and chronic inflammation. While the iron level is within
the normal range, it is important to monitor for changes as anemia management may require
attention to iron status. Anemia in diabetes can be multifactorial. The patient’s lipid profile
within the very-high-risk range indicates the need for cardiovascular risk management.
Individuals with diabetes often experience dyslipidemia, contributing to increased cardiovascular
risk. Despite being in the very-high-risk-range, her lab values are normal at the moment. For this
reason, her nutrition intervention and follow-up appointment will only address diabetes unless
her lab values change. Her elevated HBA1C levels (ranging from 7.4% to 14.0%) indicate
persistent hyperglycemia and uncontrolled diabetes. Emotional stress, as reported by the patient,
can further exacerbate glycemic fluctuations. These lab values underscore the effects of diabetes-
related complications on multiple organ systems, which further emphasizes the need for a
continuum of care that addresses not only glycemic control but also the patient's psychosocial
well-being and associated comorbidities.
Nutrition Needs:⁶
Estimated nutrition needs are based on the Hospital’s Standards of Care.⁶ Please see Appendix 2
for the full Standards of Care.
NCP: Diagnosis:
1. Altered nutrition-related laboratory values NC-2.2 related to endocrine dysfunction as
evidenced by elevated HgbA1C 10%.⁷
2. Inability to manage self-care NB-2.3 related to spousal death as evidenced by
uncontrolled glucose levels and hypoglycemic event on 10/29/23.⁷
NCP: Intervention:
Medical:
Medical interventions for diabetes management include pharmacotherapy and creating a blood
glucose monitoring plan. The pharmacotherapy includes the patient continuing her regimen of
insulin glargine (LANTUS SOLOSTAR) and empagliflozin (JARDIANCE). Psychosocial
support can be applied in medication management to ensure that the patient understands how to
use her lancet device to properly monitor her blood sugar at home, as well as understanding
normal and abnormal blood glucose values. The Hospital protocol is that Outpatient Dietitians
counsel on the reason for referral. This patient was referred for diabetes education, therefore
hypertension management will be managed by the pharmacy.
Nutritional:
Food and/or nutrient delivery ND Meal and Snacks (1); Modify distribution, type, or
amount of food and nutrient ND-1.2⁸
The current diet order for this patient is a carbohydrate-consistent diet. Based on the patient’s
diet recall, she is consuming large quantities of carbohydrates at a time, as well as consuming
carbohydrates on their own, which both elevate blood sugar. The patient was educated on a
carbohydrate-consistent diet and how to measure carbohydrate portions using measuring cups.
She was instructed to read nutrition labels on food packages to understand how many
carbohydrates foods contain.
Education:
Nutrition Education–Content (1); Recommended modifications E-1.5⁸
During the session, the patient was educated on food groups and encouraged to include
foods from all food groups in her diet based on the MyPlate method. The patient was also
educated on how to prepare balanced meals including non-starchy vegetables, whole grains, lean
protein, and healthy fats. The education portion of the session addressed foods containing
carbohydrates and appropriate portion sizes. The patient was encouraged to increase her intake of
non-starchy vegetables and increase moderate-intensity physical activity as she is able. She was
also encouraged to consume adequate amounts of fiber and water. The patient verbalized
understanding and asked relevant questions. Education handouts were provided. The patient
stated that she wants to lower the blood sugar to the target range, and the patient wants to
improve her understanding and compliance with a carbohydrate-consistent diet, Patient
education completed.
Counseling:
Theoretical Basis/Approach (1); Health Belief Model C-1.2⁸
The Health Belief Model, as applied to diabetes, considers several key factors influencing
health-related behaviors. The patient's assessment of the severity of their diabetes can motivate
them to engage in preventive measures. Cues to action are triggers that prompt the patient to take
action, such as a doctor's visit or adopting healthier habits. Perceived benefits and barriers are
what the patient believes are the benefits and obstacles to managing their diabetes. Finally, self-
efficacy allows the provider to assess the patient's confidence in their ability to achieve their
goals.
Rationale:
Several studies show that among older adults, spousal illness or death is associated with
poor health outcomes.¹² Some stress hormones, such as norepinephrine, epinephrine, cortisol, β-
endorphin, and growth hormone, can affect glucose homeostasis by interfering with various
metabolic functions, such as insulin release, glucose utilization, and hepatic glucose
production.¹² Divorce, separation, and widowed status are viewed as among the most stressful of
life events but have not been fully explored with diabetes mortality.¹² Several studies have shown
that divorced men often lose the social support of their spouses, who are also typically their
primary caregivers. Husbands’ illness or death might increase financial hardship, which often
leads to increased depressive symptoms for widows.¹² This is because Marriage promotes
healthful behaviors & reduces the risk of chronic disease.¹³ Some widowed men are more likely
to cope with the loss of a spouse by engaging in more dangerous activity leading to early
morbidity and mortality related to alcohol and drug use, accidents, homicide, and suicide.¹² For
women, a deterioration of the husband’s health of one step in a range from "very good" to "very
poor" is associated with a significant increase of 0.15 percentage points in HbA1c levels, and
losing a husband in very good health is associated with a significant increase in glycemic levels
of 0.76 percentage points. ¹²
Psychosocial care is particularly important for diabetic patients, as diabetic patients are
three times more likely to have depression than non-diabetic patients.¹³ In addition to stressors
related to type 2 diabetes, Black patients statistically become sicker and die from T2DM at
significantly higher rates than non-Black patients.¹³ Black patients are at a higher risk for stress
and depression due to poor adjustment to their diagnosis and lifestyle changes.¹³ This
maladjustment can be exacerbated by a lack of family, community, or professional support, such
as a lack of cultural relevance, social isolation due to diet changes, increased social barriers to
care, and medical racism.¹³ As a result of the increased difficulty in self-managing blood glucose
levels, Black patients are four times more likely to experience blindness, amputations, and renal
disease due to unmanaged diabetes and experience a 20% higher risk of fatality.¹³ Black patients
must be screened for non-diet factors that may affect their ability to self-manage their diabetes
such as income, financial barriers, social support, and cultural relevance of nutrition education
being provided.
Practitioners can incorporate social support strategies into patient care in many ways.
Empowering patients assists with self-management by improving self-efficacy. Cultural
competency, such as using the patient's native language and including cultural foods, can
promote self-care across populations. Using faith-based and community-based organizations that
are of value to specific cultural groups not only aids in diabetes management but can help
prevent diabetes in vulnerable populations by providing culturally appropriate education backed
by trusted community leaders.¹³
Continuum of Care:
Psychosocial care is defined as social support, psychological support, emotional support,
material resources, and education that help to manage glucose levels.¹³ Upon a new T2DM
diagnosis, patients experience major changes to their lives including but not limited to diet
changes, new medications, major lifestyle changes, social isolation, fatalism, and guilt or shame.
Psychosocial care is often overlooked when considering diabetes management and has been
proven effective in reducing stigma, promoting social functioning, and improving overall quality
of life.¹³ Providing a continuum of care such as referrals to social workers, specialist providers
such as nephrologists, and communicating with all providers about relevant findings ensures that
all of the patient’s needs, including emotional and psychological, are considered when treating
any patient. By providing a continuum of care, the patient will have the support needed to make
major life changes that otherwise may be too cumbersome to manage on their own.
Future Exams:
02/24/2023 RETINOPATHY SCREEN
0/11/29/2023 PNEUMOCOCCAL 65+ YEARS VACCINE (3 - PPSV23 or PCV20)
04/04/2024 A 1 C (MANAGEMENT)
01/04/2024 NUTRITION FOLLOW UP
08/17/2024 NEPHROPATHY (eGFR, MICROALBUMIN)~
09/14/2024 MAMMOGRAM
10/04/2024 LIPID PANEL
08/07/2029 TDAP/TD VACCINE
Urine Output
:
Goal: 0.3-0.5
ml/kg/hr
Critically ill Penn State 2003b (vented; 1.2-2.0 g/kg 1 ml/kcal *Typically used after NCM1
adults non-obese) Up to 2 g/kg the first week of JPEN3
Penn State 2010 (vented; IBW if BMI critical illness EAL2
obese)* 30-40 **Typically used ASPEN3
11-14 kcal/kg Up to 2.5 within the first week of AND2
ABW (vented; BMI 30- g/kg IBW if critical illness (7-10
50)** BMI >40 days)
22-25 kcal/kg IBW (vented;
BMI > 50)**
Monitor MAP
Monitor propofol rate
12-25 kcal/kg** (per
ASPEN 2022 update, can
be used for all critical care
patients per clinical
judgement)
HIV 30 -35 kcals/kg 1.0-1.5 g/kg 30 - 35 ml/kg NCM1
asymptomatic Asymptoma Asymptomati AND3
35-40 kcals/kg tic; c EAL2
symptomatic; weight loss 1.5 - 2.0 35 - 40 ml/kg
OR g/kg Symptomatic
MSJ Symptomati Fluid control
c; 2.0 -2.5 for those
g/kg CD 4 experiencing
<200, ESRD
presence of
AIDS
defining
condition
&/or
opportunisti
c infection
CHF 22-25 1.1 – 1.4 20-25 ml/kg Malnutrition is present NCM1
Kcal/kg(maintenance) g/kg actual (or as in 36-53% of CHF III-IV AND3
30-35 Kcal/kg BW indicated by EAL2
(repletion) (normally MD for fluid
20-22 Kcal/kg (weight nourished or restrictions) Maintain:
reduction) malnourishe Na+ ~140 mEq/dL
OR d) K+ 4-5 mEq/dL
MSJ/ Monitor:
HBE + 15-25% (minimal Zn, Mg, Ca, replete as
PA) needed
25-45%
(hypermetabolism)
Multiple
Gestation:
96 g/day
(RDI + 50
g/d) starting
in the 2nd
trimester
Lactation:
1.3 g/kg
Oncology 25-30 Kcal/kg (Non- 1 – 1.5 25-35 ml/kg NCM1
ambulatory or g/kg
Sedentary Adults) (non-
30-35 Kcal/kg (Slightly stressed
Hypermetabolic )
patients) 1.5-2.5 g/kg
35 Kcal/kg (hypermeta
(Hypermetabolic or bolic/stem
severely stressed cell
patients) transplant/p
rotein-losing
enteropathy
)
Pancreatitis Moderate to severe Moderate to 1 ml/kcal For patients with mild NCM1
pancreatitis: severe acute pancreatitis,
25-35 kcal/kg pancreatitis initiate nutrition
Chronic Pancreatitis: 35 1.2-1.5 g/kg support if unable to
kcal/kg Chronic advance to a PO diet
Pancreatitis: within 7 days
1-1.5 g/kg
Standard enteral
formulations are
appropriate
If EN is not feasible,
consider PN after 7
days from onset of
symptoms
Chronic Pancreatitis:
Consider addition of
PERT Enzyme
Kidney 25-35 kcal/kg (include kcal 0.8-1.2g/kg 500 ml + UOP Sodium: 2.0-3.0 g/day NCM1
Disease: from continuous renal (non- AKI w/ CRRT Potassium: 2.0-3.0 EAL2
replacement therapy - catabolic, – no g/day
CRRT) without restriction Phosphorus: 8-15
Acute Renal dialysis) mg/kg
Failure
1.2-1.5g/kg
(catabolic
and/or
initiation of
dialysis/CRR
T)
Kidney CK 25-35 kcal/kg IBW 0.55-0.66 1 ml/kcal *Vegetable protein NCM1
Disease D g/kg/d diets may have EAL2
: (st (metabolical beneficial effects on
ag ly stable) (In CKD health by a variety of
e Stages 1-4, mechanisms but
1- fluids are insufficient evidence
5); 0.6-0.8 usually to definitively
no g/kg/d unlimited) recommend a
n- (diabetic) particular protein type.
dia
lysi
s OR Advise patients to
gradually reduce Pro
intake and/or
0.28-0.43 encourage occasional
g/kg/d with meatless meals
additional
keto acid
analogs
(sufficient
energy
intake e.g.
>30kcal/kg
per day, pro
intake level
can be
safely
decreased
to 0.55 to
0.6g/kg/d)
CK 25-35 kcal/kg IBW 1.0-1.2 1000 ml + Potassium and NCM1
D g/kg/d UOP Phosphorus should be K/DOQI4
5D (patients at (the fluid adjusted to maintain
on risk of recommenda serum levels within
Dia hyperglycem tion is to normal range (It is
lysi ia and/or ensure that reasonable to consider
s hypoglycemi overhydratio bioavailable of
a, higher n and phosphorus sources;
levels of underhydrati additives > animal >
dietary pro on are vegetable). Limit
intake may avoided: sodium intake to less
need to be target of UFR than 2.3 g/day.
considered) less than 13
ml/hour/kg)
Pressure 30-35kcal/kg (Stages I-IV, 1.25-1.5g/kg 30ml/kg Juven (Arginine and NPUAP7
ulcer DTI, Unstageable) (Stages I-IV, (Stages I-II) Glutamine) 1 packet NCM1
Unstageable 30-35ml/kg BID (Stages II-IV,
, DTI) (Stages III-IV, Unstageable, DTI).
DTI, Juven contains
Unstageable) Arginine, Glutamine,
HMB, C, E, and Zinc.
Consider d/c
additional zinc. TUL for
elemental zinc is 40
mg.
Pediatrics 0-6 Months: 1-10kg: PNCM6
0-6 Months: 108kcal/kg 2.2g/kg 100ml/kg Texas
6-12 Months: 98kcal/kg 6-12 11-20kg: Children’
1-3 Years: 102kcal/kg Months: 100ml/kg + s8
4-6 Years: 90kcal/kg 1.6g/kg 50ml/kg
7-10 Years: 70kcal/kg 1-3 Years: above 10kg
1.2g/kg >20kg:
Males 4-6 Years: 1500ml +
11-14 Years: 55kcal/kg 1.2g/kg 20ml/kg
15-18 Years: 45kcal/kg 7-10 Years: above 20kg
1.0g/kg
Females
11-14 Years: 47kcal/kg Males
15-18 Years: 40kcal/kg 11-14
Years:
1.0g/kg
15-18
Years:
0.9g/kg
Females
11-14
Years:
1.0g/kg
15-18
Years:
0.8g/kg
**These are standard guidelines. Clinical judgement always prevails**
2. World Health Organization. Diabetes Fact Sheet. World Health Organization; 2022. Accessed
January 13, 2024. https://cdn.who.int/media/docs/default-source/searo/nde/sde-diabetes-fs.pdf?
sfvrsn=7e6d411c_2
3. Diabetic kidney disease - niddk. National Institute of Diabetes and Digestive and Kidney
Diseases. Accessed January 25, 2024.
https://www.niddk.nih.gov/health-information/diabetes/overview/preventing-problems/diabetic-
kidney-disease#:~:text=Diabetes%20is%20the%20leading%20cause,with%20diabetes%20has
%20kidney%20disease.&text=The%20main%20job%20of%20the,body%20needs%20to
%20stay%20healthy.
4. Width M, Reinhard T. The Essential Pocket Guide for Clinical Nutrition. 3rd ed. Jones &
Bartlett Learning; 2021.
5. Nutrition assessment and monitoring and evaluation ... Accessed January 25, 2024.
https://www.andeal.org/vault/2440/editor/docs/idnt_assess_me_v3.pdf.
6. Academy of Nutrition and Dietetics Nutrition Care Manual, 2022, accessible online at
www.nutritioncaremanual.org.
7. Academy of Nutrition and Dietetics. International Dietetics & Nutrition Terminology (IDNT)
- Nutrition Diagnosis Guide. [Accessed January 13, 2024]. Available from:
https://www.andeal.org/vault/2440/editor/Docs/IDNT_Diagn_v3.pdf
8. Academy of Nutrition and Dietetics. International Dietetics & Nutrition Terminology (IDNT)
- Nutrition Intervention Guide. [Accessed January 13, 2024]. Available from:
https://www.andeal.org/vault/2440/editor/Docs/IDNT_Interv_v3.pdf
9. Kellogg M. TIP # 114 the four processes in motivational interviewing. Molly Kellogg.
December 12, 2014. Accessed January 13, 2024. https://mollykellogg.com/tip-114-the-four-
processes-in-motivational-interviewing/.
10. The spirit of motivational interviewing | HMA. Accessed January 25, 2024.
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