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Title: Donna Bednarski,


1
Give Fluid The BOOT!
  • Donna Bednarski,
  • MSN, RN, ANP-BC, CNN

2
What do we know?
  • Kidneys play a critical role in maintaining the
    effective circulating volume and plasma
    osmolality of the body within narrow limits
  • Under normal circumstances, kidneys can adjust to
    variations in dietary intake by appropriate
    variations in water and electrolyte excretion

3
What do we know?
  • Hypervolemia is the most common cause of
    hypertension (htn), LV hypertrophy, and CVD
    effecting the mortality rate
  • Hypovolemia can cause intradialytic morbidities,
    ischemia, loss of residual kidney function, and
    increased mortality rate

4
What do we know?
  • Body water represents approx 55 60 of total
    body weight in young, lean adults.
  • Water content of fat is less than that of lean
    body mass
  • Body water is divided into two major
    compartments
  • Extracellular accounts for 1/3 total body water
  • Intracellular accounts for 2/3 total body water
  • Interstitial fluid (fluid in between cells)
  • Intravascular fluid
  • Lymph
  • Transcellular fluid (fluid in joints, peritoneal,
    pleural cavities, etc)
  • Fluid shifts occurs often between compartments
    through the semipermeable membranes that separate
    them depending on both fluid and electrolyte
    status

5
Assessment Parameters
  • If a patient is volume overloaded consider
  • Too much sodium intake
  • Too much fluid intake
  • Too little sodium or water removal
  • New or exacerbated co-morbid condition

6
Identification of Patients at Risk for Fluid
Overload
  • Change in body mass
  • Non-adherence to prescribed treatment regimen
  • Barriers to self management
  • Hypertension
  • Ischemic heart disease
  • Acute myocarditis or infective endocarditis
  • Valvular heart disease
  • Acute arrhythmias

7
Identification of Patients at Risk for Fluid
Overload
  • High output failure from shunting via vascular
    access
  • Pulmonary embolism
  • Infections and/or fever
  • Autonomic neuropathy
  • Anemia
  • Carnitine deficiency
  • Amyloidosis
  • Thyrotoxicosis

8
Assessment Subjective
  • Past and current medical history
  • Family history of CV disease
  • Life style habits cigarette smoking, alcohol
    consumption, exercise frequency

9
Assessment Subjective
  • Prescribed medication regimen
  • Adherence?
  • OTC medication utilization
  • Practice patterns?
  • Taking antihypertensives before or after dialysis

10
Assessment Subjective
  • Change in medication that may be nephrotoxic?
  • Assess for medications that may stimulate thirst
    or fluid retention
  • Calcium channel blockers, clinidine, other
    vasodilator meds, e.g. narcotics, analgesics,
    beta blockers

11
Assessment Subjective
  • Recent hospitalizations?
  • Intake and output
  • Decrease in urine volume?
  • Change in intake?
  • Adherence?
  • Other S S Dyspnea, SOB, fatigue, edema, chest
    pain, palpitations

12
Assess Knowledge
  • Diet and fluid management
  • Fluid intake
  • Sodium restrictions
  • Glucose management
  • Intradialytic weight gains
  • S S of hyper and hypovolemia
  • Medication regimen

13
Assessment Objective
  • VS
  • Temperature febrile/afebrile?
  • BP hypertensive, hypotensive, orthostatic
    hypotension?
  • Htn
  • exacerbation of htn can depress ventricular
    function
  • Primary cause of HF in many patients
  • Increases hemodynamic load on the failing
    ventricle in pts with established HF

14
Assessment Objective
  • VS
  • HR Apical and peripheral pulses for quality,
    rate, rhythm
  • RR Rate and quality
  • Pulse Ox, is needed

15
Assessment Objective
  • Wt
  • Trends
  • Intradialytic weight gains?
  • Evidence of body mass change?

16
Assessment Objective
  • Cardiovascular (CV)
  • JVD / neck vein distention
  • Skin Turgor
  • Mucous membranes

17
Assessment Objective
  • Cardiovascular (CV)
  • Presence of edema
  • Palpable swelling produced by expansion of the
    interstitial fluid volume
  • Can be associated with HF, cirrhosis, nephrotic
    syndrome, venous and lymphatic disease

18
Assessment Objective
  • Presence of Edema - Location
  • Peripheral only related to kidney disease, local
    venous disease, or heart failure (HF)
  • Left sided HF present with pulmonary congestion
  • Right sided HF present with peripheral edema
  • Cardiomyopathy usually have equivalent
    involvement of both right and left ventricles
  • Remember bed bound patients!

19
Assessment Objective
  • Cardiovascular (CV)
  • Heart Sounds
  • S1
  • S2
  • Murmurs / change in murmurs

20
Assessment Objective
  • Heart Sounds
  • S3 related to early ventricular filling, low
    pitched, heard best with the bell at apex.
  • Normal in children/young adults
  • gt35 may indicate LV failure or volume overload
  • First clinical sign of CHF
  • S4 related to late ventricular filling, Low
    pitched, head best with bell at apex.
  • Reflects atrial contraction into a noncompliant
    ventricle
  • Can be heard in AS, hypertension, hypertrophic
    cardiomyopathy and CAD

21
Assessment Objective
  • Respiratory
  • Lung Sounds
  • Can reveal subtle physiologic changes
  • Listen for crackles not cleared by coughing
  • Often heard in the right and left lung base and
    correlate well with early left sided HR

22
Assessment Hemodialysis
  • Delivered dose of hemodialysis falls below target
    level evaluate for
  • Laboratory or blood sampling errors
  • Sampling methods
  • Timing of sampling
  • Laboratory error

23
Assessment Hemodialysis
  • 2. Compromised urea clearances
  • Vascular access
  • Blood flow rate inadequate
  • Access recirculation
  • Incorrect needle placement
  • Reversal of blood lines
  • Inappropriate dialyzer size or clearance
  • Inadequate dialyzer reprocessing
  • Excessive dialyzer clotting during dialysis
  • Inadequate dialysate flow rate
  • Dialyzer leaks

24
Assessment Hemodialysis
  • 3. Reduction in treatment times
  • A. Inaccurate assessment of effective treatment
    time
  • B. Uncompensated interruptions in actual
    treatment time
  • Clinical complications (hypotension)
  • Equipment alarms
  • Manipulation of needles
  • Dialysate bypass situations

25
Assessment Hemodialysis
  • 3. Reduction in treatment times (cont.)
  • C. Shortened treatment time
  • Premature d/c of dialysis due to
  • Patient request/demand
  • Dialysis unit issues
  • Clinical complications
  • Delay in initiation of dialysis
  • Missed dialysis treatments

26
Assessment Peritoneal Dialysis
  • Delivered dose of peritoneal dialysis falls below
    target level evaluate for
  • 1. External clamps, kinks or pressure on the
    catheter
  • 2. Gravity driven systems
  • Height of solution bags
  • Distance from lowest point of peritoneal cavity
    to drain bag

27
Assessment Peritoneal Dialysis
  • Delivered dose of peritoneal dialysis falls below
    target level evaluate for
  • 3. Drainage problems related to pt position
  • 4. Peritoneal membrane failure

28
Assessment Lab
  • Laboratory data used to identify
  • Failure of dialysis prescription
  • Loss of residual kidney function
  • Co-Morbid Conditions
  • Hypoalbuminemia potential causes
  • Identify a new CV event or worsening of
    underlying heart disease (HD)
  • Other impacting factors

29
Kick it up a Notch What Is the Evidence?
  • Residual Renal Function
  • How often should it be assessed?
  • What does the assessment include?

30
Assessment Lab
  • Electrolytes
  • BUN / Cr
  • Ca and Mg
  • Glucose
  • Liver function tests
  • Nutrition albumin, transferrin, prealbumin

31
Assessment Lab
  • CBC
  • Anemia is associated with both kidney failure and
    HF
  • The presence of anemia is associated with higher
    mortality risk in patients with HF

32
Assessment Lab
  • Fasting Lipid Profile
  • Primary finding in CKD and dialysis is
    hypertriglyceridemia
  • May contribute to accelerated atherosclerosis
  • Total cholesterol is sometimes normal or low
  • Troponin testing

33
C-Reactive Protein (CRP)
  • Acute phase protein produced by the liver
  • Thought to enhance macrophage phagocytosis and
    complement binding to foreign and damaged cells
  • Only recently studied as a marker of vascular
    inflammation associated with CVD
  • Other factors that may increase CRP
  • Hormone replacement therapy
  • ASA

34
Kick it up a Notch What Is the Evidence?
  • AHA issued a statement about CRP 2007
  • Pts with low CV risk scores immediate testing is
    not warranted
  • Pts risk score is intermediate than CRP may
    assist in predicting CV event or stroke and
    direct evaluation and therapy
  • CRP testing based on this strategy is unclear

35
Homocysteine
  • Amino acid (AA) which cannot be obtained in the
    diet
  • Utilized by changing into other useful AAs
  • A lack of transformation into useful AAs leads to
    hyperhomocysteinema
  • Elevated levels have been linked to increased CVD
    incidences
  • Homocysteine also has prothrombotic properties -
    increased likelihood of clot formation
  • Combines with LDL particles to produce foam cells
    and form the necrotic centers for luminal plaques

36
Kick it up a Notch What Is the Evidence?
  • Treatment of Hyperhomocysteinema
  • Folic acid supplementation
  • 1 mg/day can decrease homocysteine levels up to
    72
  • The evidence to support reducing homocysteine
    levels to decrease heart disease is not yet clear

37
Carnitine
  • An important intermediary in fat metabolism
  • Crucial for energy production in tissues
    dependent upon fatty acid oxidation cardiac and
    skeletal muscle
  • Carnitine is derived from red meat and dairy
    products in the diet
  • Biosyntheses in the liver, kidney, and brain is
    needed to meet normal requirements

38
Carnitine
  • Carnitine deficiency may be a significant problem
    in kidney disease
  • Normal acylcarnitine free carnitine ratio is
    approx 0.16
  • Ratio gt 0.4 is abnormal
  • In hemodialysis pts it is increased to 0.76

39
Brain Natriuretic Peptide (BNP)
  • The natriuretic peptide system impacts salt and
    water handling and pressure regulation and may
    influence myocardial structure and function
  • NP is a natriuretic hormone initially identified
    in the brain but released primarily from the
    heart, particularly the ventricles
  • The release of BNP is increased in heart failure

40
What about BNP?
  • Research shows BNP is markedly higher in patients
    with clinically diagnosed HF compared to those
    without
  • BNPgt100 pg/mL diagnosed HF with a sensitivity,
    specificity, and predictive accuracy of 76 - 90
  • BNP concentrations fall after effective treatment
    of HF so it may be useful in titrating therapy
    but not an established practice

41
Kick it up a Notch What Is the Evidence?What
about BNP and Kidney Failure?
  • BNP is elevated with kidney failure
  • BNP can not be used for the diagnosis or
    management of HF in pts with kidney failure with
    or without dialysis
  • A low BNP would exclude LV dysfunction
  • There is some evidence BNP can be used as a
    marker for mortality - independent from the
    dialysis modality

42
Assessment Echocardiography
  • Evaluates left ventricle size, valvular
    function, wall thickness and pumping function or
    ejection fraction (EF)
  • EF indicates the of blood ejected from the
    ventricle with each heartbeat
  • Normal 50 - 65
  • LV systolic dysfunction EF lt 40

43
Assessment ECG
  • Shows cardiac rhythm /conduction and QRS duration
  • Can detect
  • myocardial ischemia
  • previous MI
  • LV hypertrophy
  • ACS
  • Acute arrhythmias

44
Assessment Radiology
  • CXR
  • Lateral and posterior lateral may assist in
    identifying
  • cardiomegaly
  • pleural effusions
  • pulmonary congestion
  • Abdominal X-Ray
  • Flat plate and lateral views to determine
    position of PD catheter and identification of
    internal kinks

45
Complications of Fluid Overload
  • Hyponatremia (Na lt135mmol/L)
  • S S confusion, lethargy and disorientation,

46
Complications of Fluid Overload
  • Hypertension (htn)
  • Increased fluid volume increases pressure exerted
    by the fluid on the vessel walls
  • Antihypertensive therapy

47
Antihypertensive Agents
  • 3 Categories
  • Sympatholytics
  • Central acting agents (Clonidine, Methyldopa)
  • Beta adrenergic agents (Atenolol, Metoprolol,
    Nadolol)
  • Alpha-1 adrenergic blockers (Prazosin, Terazosin,
    Doxazosin)
  • Mixed adrenergic blockers (Labetalol, Carvedilol)
  • Vasodilators
  • Direct (Diazoxide, Hydralazine, Minoxidil,
    Nitroprusside)
  • Calcium channel blockers (Amlodipine,
    Nicardipine, Nifedipine)
  • Renin-angiotensin-aldosterone system antagonists
  • Angiotensin-converting enzyme (ACE) inhibitors
    (Captopril, Enalapril, Fosinopril, Lisinopril)
  • Angiotensin II receptor blockers (ARBs)
    (Candesartan, Losartan Valsartan)

48
Complications of Fluid Overload
  • Pulmonary Edema
  • Life threatening
  • S S SOB, orthopnea, tachypneic, wet crackles
    and possible heart murmurs and gallop rhythms
  • Confirmed by CXR

49
Complications of Fluid Overload
  • Pulmonary Edema
  • Treatment fluid control
  • Increase ultrafiltration
  • Increase frequency of dialysis
  • Diuretics in those with residual renal function
  • Loop diuretics are most potent and remain
    effective when GFR lt25mL/min

50
Complications of Fluid Overload
  • CHF
  • S S cough, dyspnea, fatigue, tachycardia, may
    or may not have chest discomfort, crackles and
    may have S3 /or S4, elevated JVD, may or may not
    have peripheral edema
  • Can occur in the absence of heart disease fluid
    overload, severe hypertension

51
Complications of Fluid Overload
  • Precipitating factors
  • Cardiac
  • MI
  • Atrial fibrillation and other arrhythmias
  • Underlying cardiac dysfunction
  • Synchrony with right ventricular pacing
  • Non Cardiac
  • Severe hypertension
  • Misc factors anemia, hypo/hyperthyroidism,
    toxins (cocaine/alcohol), fever, infection
    (pneumonia), uncontrolled Db
  • Significant drug interactions negative inotropic
    drugs (verapamil, nifedipine, diltiazem, beta
    blockers) or NSAID
  • Pulmonary emboli

52
Complications of Fluid Overload
  • Confirmed by CXR can range from mild pulmonary
    vascular redistribution to marked cardiomegaly
    and extensive bilateral interstitial markings and
    bilateral perihilar alveolar edema give a typical
    butterfly appearance.
  • Echo identify systolic dysfunction vs diastolic
    dysfunction or valvular disease

53
CHF in Stage 5 Kidney Disease
  • Treatment for general population does not
    necessarily apply
  • Identify/manage associated conditions
  • Htn
  • Ischemic HD
  • Valvular HD
  • High output failure from vascular access
  • Anemia
  • Carnitine deficiency
  • Amyloidosisis
  • Volume Control
  • Pharmacologic

54
Kick it up a Notch What does the evidence say?
ACE Inhibitors
  • Used to treat LV systolic HF or asymptomatic LV
    dysfunction
  • Have been shown in multiple randomized
    prospective trials to improve survival in pts
    with normal or near normal kidney function with
    all degrees of severity of LVSD

55
Kick it up a Notch What does the evidence say?
ACE Inhibitors
  • There are very limited prospective controlled
    studies performed in dialysis patients for use of
    ACE inhibitors
  • Use in the dialysis pts is used based on the
    benefits observed with HF with normal or near
    normal kidney function

56
ACE/ARBs Things to Remember
  • Can decrease protein excretion and may be
    beneficial in slowing the progression of kidney
    disease
  • Useful for pts with LV hypertrophy or ischemic HD
    with LVSD
  • Adverse reactions
  • Angioedema
  • Orthostatic hypotension
  • Hyperkalemia
  • Chronic cough (ARBs produce less cough)
  • Many ACE inhibitors are removed with hemodialysis

57
Kick it up a Notch What does the evidence say?
Beta Blockers
  • A single prospective randomized trial showed beta
    blockers reduced the risk of death in dialysis
    pts with severe dilated cardiomyopathy (LVEF
    lt35)
  • Based on the trial, K/DOQI guidelines suggest
    carvedilol as the preferred beta blocker

58
Beta Blockers Things to Remember
  • They all produce sedation, bradycardia,
    hypotension and HF
  • All require HR and BP monitoring
  • All can mask the S S of hypoglycemia
  • Can precipitate or worsen depression
  • Need dose tapered before D/C to prevent rebound
    htn
  • Most do not require a dosage adjustment in CKD
  • Most are not dialyzable

59
Kick it up a Notch What does the evidence say?
Angiotensin Type II Receptor Blockers (ARBs)
  • In pts with normal or near normal kidney function
    ARBs for the treatment of HF appear to be as or
    possibly slightly less effective than ACE
    inhibitors
  • There are very limited studies addressing the use
    of ARBs in dialysis patient with HF
  • Use of ARBs in ACE intolerant dialysis pts with
    HF based on the utilization in the general HF
    population

60
Kick it up a Notch What does the evidence say?
  • Digoxin
  • Challenging in the dialysis population with the
    narrow therapeutic to toxic ratio
  • Major indication ventricular rate control for
    those in atrial fibrillation
  • Aldosterone Receptor Antagonists
  • Significantly decreases the rate of sudden
    cardiac death in selected HF pts without ESRD
  • Use in dialysis pts is controversial due to risk
    for hyperkalemia
  • Currently not recommended in dialysis pts with HF

61
Treatment of Diastolic HF
  • Pts with preserved LVSF - little data is
    available
  • The following factors need to be addressed
  • Htn
  • HR control
  • Blood volume control
  • Myocardial ischemia

62
Kick it up a Notch What does the evidence say?
  • AHA
  • Recommends early recognition and treatment of
    CAD, hypertension, DM and other CV risk factors
  • Include staging of HF and treatment for each
    stage

63
Barriers to Fluid Removal
  • Hypoalbuminemia
  • Blood Glucose Level
  • Effect upon osmosis and fluid shifts

64
Barriers to Fluid Removal
  • Intradialytic Hypotension
  • Common in patients with myocardial dysfunction
  • Other causes
  • Rapid fluid removal
  • Rapid reduction in plasma osmolality
  • Autonomic neuropathy
  • Diminished cardiac reserve
  • Antihypertensive medications
  • Ingestion of a meal immediately before or during
    dialysis
  • Arrhythmias or pericardial effusion with
    tamponade
  • Other
  • Monitor response to treatment plan

65
Barriers to Fluid Removal
  • Intradialytic Hypotension
  • Treatment
  • Accurate dry weight
  • Steady, constant ultrafiltration
  • Sodium modeling
  • Temperature control
  • Improve CV performance
  • Midodrine
  • Carnitine
  • Avoidance of food
  • Vasopressin infusion

66
Barriers to Fluid Removal
  • Venous insufficiency
  • Incidence increases with age, obesity, history of
    phlebitis or venous thrombosis, leg trauma
  • Differential Dx
  • limited to lower extremities - can be unilateral
  • Often subsides with recumbency
  • Often accompanied by varicosities,
    hyperpigmentation, other signs of venous disease

67
Goals
  • Relieve symptoms
  • Adherence to the prescribed treatment regimen
  • Meet educational deficits
  • Maintain optimal fluid volume status
  • Identify underlying causes and precipitating
    factors
  • Achieve/maintain BP in targeted range
  • Reduction in modifiable risk for CVD

68
Interventions
  • Encourage adherence to therapeutic lifestyle
    changes
  • Diet and weight management
  • Increased physical activity
  • Moderation in alcohol consumption
  • Smoking cessation
  • Encourage adherence to medication therapy
  • Assess patient response to therapy and adjust UF
    and meds as ordered
  • Identify resources to assist in adherence to
    prescribed regimen

69
Fluid Control Adherence
  • Dialysis Staff Encouragement and Fluid Control
    Adherence in Patients on Hemodialysis
  • Yokoyama, et al
  • Nephrology Nursing Journal, May-June 2009
  • Looked at fluid control in 77 patients on
    dialysis and dialysis staff encouragement
  • Measured
  • Dialysis staff support
  • Self-efficacy
  • Health Locus of Control
  • Psychological burden
  • Diet therapy burden
  • Conclusion Dialysis staff encouragement is
    important in improving fluid control adherence

70
Interventions
  • Adjust target dry weight, as needed
  • How do we determine dry weight?
  • No standard measurement
  • Set at the weight below which unacceptable
    symptoms occur
  • The weigh when fluid volume is optimal
    (euvolemic, normotensive)

71
Interventions
  • Individualize dialysis prescription
  • Target hemoglobin levels
  • Modifiable risk factors for CVD
  • Control Hypertension
  • Control of bone metabolism
  • Treatment of anemia
  • Immunize influenza and pneumococcal pneumonia

72
Interventions HD
  • Review dialysis prescription
  • Dialysate sodium concentration
  • Use of isolated ultrafiltration
  • Dialysate temperature
  • Treatment time vs. ultrafiltration requirement
  • Take measures to correct any issues that could
    result in compromised clearances during dialysis
  • Monitor vascular access function

73
Ultrafiltration
  • Determine degree of UF for each dialysis
    treatment and feasibility of reaching UF goal
  • Monitor and adjust UF based on pts response
  • Achieving dry weight through UF should be
    accomplished gradually
  • Blood volume monitoring

74
Blood Volume Monitoring
  • Goal Monitoring blood volume and the changes
    that occur over the course of a treatment
  • As fluid is removed from the intravascular
    compartment at a greater rate than capillary
    refilling, RBCs become more concentrated
    resulting in increased Hct
  • If fluid is shifting at roughly the same rate as
    UF, a steady profile will be displayed
  • BVM may present an opportunity to increase the UF
    rate until an increased Hct or decreased blood
    volume
  • BVM should be used in conjunction with other
    objective assessment tools

75
Sodium Modeling
  • May diminish hypotensive episodes
  • Shifting fluid from intracellular fluid to
    extracellular fluid to improve efficiency of UF
    with increased dialysate sodium
  • Results in a rapid refilling of the vascular space

76
Interventions PD
  • Adjust height of dialysate to enhance drain/fill
    rates
  • Change pts position to enhance dialysate drain
    rates or obtain complete drain
  • Treat constipation
  • PET testing with adjustment of dialysis
    prescription accordingly

77
Education, Education, Education
  • Based on initial assessment and treatment plan
  • Diet and fluid management
  • Fluid intake
  • Sodium restrictions
  • Glucose management
  • Intradialytic weight gains
  • S S of hyper and hypovolemia
  • Medication regimen
  • Understanding of co-morbid conditions

78
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