Chronic renal failure secondary prevention: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
Sargun Walia (talk | contribs) |
||
Line 6: | Line 6: | ||
*Protective therapy most effective if initiated '''early''', before [[Creatinine]] > 1.5-2.0 mg/dL | *Protective therapy most effective if initiated '''early''', before [[Creatinine]] > 1.5-2.0 mg/dL | ||
**Treat [[Hypertension]] | **Treat [[Hypertension]] | ||
*** Systemic [[hypertension]]--elevated intraglomerular pressure +/or glom hypertrophy | *** Systemic [[hypertension]]--elevated intraglomerular pressure +/or glom hypertrophy. | ||
*** [[Blood Pressure]] (BP) control shown in multiple trials to slow progression of renal disease | *** [[Blood Pressure]] (BP) control shown in multiple trials to slow progression of renal disease. | ||
*** Goal [[Blood pressure]] < 130/80-85; < 125/75 in patients with [[proteinuria]] > 1-2 g/d | *** Goal [[Blood pressure]] < 130/80-85; < 125/75 in patients with [[proteinuria]] > 1-2 g/d. | ||
*** [[ACE inhibitors]] (ACEI) and [[Angiotensin II receptor antagonist|Angiotensin II receptor blockers]] (ARB) preferred 1st line agents due to reno-protective effects | *** [[ACE inhibitors]] (ACEI) and [[Angiotensin II receptor antagonist|Angiotensin II receptor blockers]] (ARB) preferred 1st line agents due to reno-protective effects.<ref name="pmid3651580">{{cite journal |vauthors=Lerche D, Kozlov MM, Markin VS |title=Electrostatic free energy and spontaneous curvature of spherical charged layered membrane |journal=Biorheology |volume=24 |issue=1 |pages=23–34 |date=1987 |pmid=3651580 |doi= |url=}}</ref> | ||
*** Additional agents as needed, including [[diuretics]] if volume overload | *** Additional agents as needed, including [[diuretics]] if volume overload. | ||
** Restrict Dietary Protein | ** Restrict Dietary Protein | ||
*** Controversial – may decrease intraglomerular pressure | *** Controversial – may decrease intraglomerular pressure. | ||
*** Conflicting studies – some show benefit, others do not | *** Conflicting studies – some show benefit, others do not. | ||
*** No significant adverse effects shown in large trial | *** No significant adverse effects shown in large trial. | ||
*** Recommendations | *** Recommendations | ||
**** No restriction (> 0.8 g/kg/d) if [[GFR]] 25-55 mL/min | **** No restriction (> 0.8 g/kg/d) if [[GFR]] 25-55 mL/min. | ||
**** Limit protein to 0.8 g/kg/d if progression or [[Uremia|uremic]] symptoms | **** Limit protein to 0.8 g/kg/d if progression or [[Uremia|uremic]] symptoms. | ||
**** Limit to 0.6 g/kg/d if severe [[renal insufficiency]] ([[GFR]] 13-25 mL/min) | **** Limit to 0.6 g/kg/d if severe [[renal insufficiency]] ([[GFR]] 13-25 mL/min). | ||
*** Close follow-up by dietician given risk of [[malnutrition]] in this population | *** Close follow-up by dietician given risk of [[malnutrition]] in this population. | ||
** Control [[Blood sugar]]: | ** Control [[Blood sugar]]: | ||
*** Tight control ([[HbA1c]] < 7.0, [[Fasting blood sugar 70-120) reduces progression in [[Diabetes Mellitus Type 1|DM I]] | *** Tight control ([[HbA1c]] < 7.0, [[Fasting blood sugar 70-120) reduces progression in [[Diabetes Mellitus Type 1|DM I]]. | ||
*** Unclear if as beneficial in [[Diabetes Mellitus Type 2|DM II]], but potentially helpful | *** Unclear if as beneficial in [[Diabetes Mellitus Type 2|DM II]], but potentially helpful. | ||
===Treat complications=== | ===Treat complications=== | ||
* Volume Overload | * Volume Overload | ||
** Impaired excretion of sodium and water due to decreased [[GFR]] +/- [[Aldosterone|AII/aldo]] activation | ** Impaired excretion of sodium and water due to decreased [[GFR]] +/- [[Aldosterone|AII/aldo]] activation. | ||
** Restrict dietary sodium to 1-2 g/d if [[hypertension]] or [[edema]] | ** Restrict dietary sodium to 1-2 g/d if [[hypertension]] or [[edema]]. | ||
** [[Diuretic]]s | ** [[Diuretic]]s | ||
*** [[Thiazide]]s ineffective if [[GFR]] < 25 mL/min (~[[Creatinine]] > 2-3) | *** [[Thiazide]]s ineffective if [[GFR]] < 25 mL/min (~[[Creatinine]] > 2-3). | ||
*** Switch to [[Loop diuretic]] as [[Creatinine]] rises; may need bid dosing | *** Switch to [[Loop diuretic]] as [[Creatinine]] rises; may need bid dosing. | ||
*** Addition of [[thiazide]] to [[Loop diuretic]] can--additional [[Diuresis]] | *** Addition of [[thiazide]] to [[Loop diuretic]] can--additional [[Diuresis]]. | ||
*** Watch for excessive volume depletion | *** Watch for excessive volume depletion | ||
* [[Hyperkalemia]] | * [[Hyperkalemia]] | ||
** Potassium usually maintained until [[GFR]] < 15-20 mL/min | ** Potassium usually maintained until [[GFR]] < 15-20 mL/min. | ||
**Increased risk of [[hyperkalemia]] with [[Oliguria]], high [[K|potassium]] diet, ([[ACEI|ACE inhibitors]] therapy) | **Increased risk of [[hyperkalemia]] with [[Oliguria]], high [[K|potassium]] diet, ([[ACEI|ACE inhibitors]] therapy). | ||
** Increased risk with many meds: [[ACEI]], [[NSAID]]s, [[Potassium-sparing diuretic]]s, [[digoxin]], [[TMP]] | ** Increased risk with many meds: [[ACEI]], [[NSAID]]s, [[Potassium-sparing diuretic]]s, [[digoxin]], [[TMP]]. | ||
** Increased risk in diabetics with [[Renal tubular acidosis|type IV RTA]] | ** Increased risk in diabetics with [[Renal tubular acidosis|type IV RTA]] | ||
* Management | * Management | ||
** Low potassium diet (< 60 mEq/d) once GFR < 15 mL/min | ** Low potassium diet (< 60 mEq/d) once GFR < 15 mL/min. | ||
** Avoidance of salt substitutes (may contain potassium salts) | ** Avoidance of salt substitutes (may contain potassium salts). | ||
** +/- [[loop diuretic]] | ** +/- [[loop diuretic]] | ||
** Low dose [[Kayexelate]] (5 g with meals) if needed | ** Low dose [[Kayexelate]] (5 g with meals) if needed. | ||
* Calcium/phosphate Abnormalities | * Calcium/phosphate Abnormalities | ||
** Reduced renal synthesis [[Calcitriol]]/[[Vitamin D]]--low serum Calcium-- [[Secondary hyperparathyroidism]] | ** Reduced renal synthesis [[Calcitriol]]/[[Vitamin D]]--low serum Calcium-- [[Secondary hyperparathyroidism]]. | ||
** (Occurs when [[GFR]] < 40 mL/min) | ** (Occurs when [[GFR]] < 40 mL/min) | ||
** Reduced [[GFR]]--phosphate retention | ** Reduced [[GFR]]--phosphate retention | ||
** Elevated [[parathyroid hormone]] ([[PTH]])--mobilization of Calcium from bone; increased excretion phosphate | ** Elevated [[parathyroid hormone]] ([[PTH]])--mobilization of Calcium from bone; increased excretion phosphate. | ||
** Allows maintenance of normal Calcium/phosphate while [[GFR]] > 30 mL/min | ** Allows maintenance of normal Calcium/phosphate while [[GFR]] > 30 mL/min. | ||
** Causes [[renal osteodystrophy]] | ** Causes [[renal osteodystrophy]] | ||
** Once [[GFR]] < 25-30 mL/min, [[hyperphosphatemia]] occurs | ** Once [[GFR]] < 25-30 mL/min, [[hyperphosphatemia]] occurs | ||
** Therapy goals = normalize Calcium/Phosphate and maintain [[parathyroid hormone]] (PTH)< 200 (2-3x uln) | ** Therapy goals = normalize Calcium/Phosphate and maintain [[parathyroid hormone]] (PTH)< 200 (2-3x uln). | ||
*** Calcium/Phosphate management should be initiated when [[Creatinine]] ~ 2 | *** Calcium/Phosphate management should be initiated when [[Creatinine]] ~ 2. | ||
*** Calcium x phosphate product should be < 60 to prevent met calcification | *** Calcium x phosphate product should be < 60 to prevent met calcification. | ||
*** Low phosphate diet: < 800 mg/d (challenging) | *** Low phosphate diet: < 800 mg/d (challenging) | ||
*** Calcium-based oral phosphate binders: Calcium acetate or Calcium carbonate with meals | *** Calcium-based oral phosphate binders: Calcium acetate or Calcium carbonate with meals. | ||
*** Avoid Aluminium-based phosphate binders except for acute therapy of high Calcium x Phosphate products | *** Avoid Aluminium-based phosphate binders except for acute therapy of high Calcium x Phosphate products. | ||
**** (Aluminium toxicity = [[osteomalacia]], [[anemia]], [[encephalopathy]]) | **** (Aluminium toxicity = [[osteomalacia]], [[anemia]], [[encephalopathy]]) | ||
*** Avoid Calcium citrate (increases gastrointestinal absorption of aluminum) | *** Avoid Calcium citrate (increases gastrointestinal absorption of aluminum) | ||
**** RenaGel = new non-Calcium/Aluminium-containing phosphate binder (cationic polymer) | **** RenaGel = new non-Calcium/Aluminium-containing phosphate binder (cationic polymer). | ||
***** (For patients who cannot tolerate Calcium carbonate or need additional agent) | ***** (For patients who cannot tolerate Calcium carbonate or need additional agent) | ||
**** [[Calcitriol]] 0.125-0.25 mg/d improves Calcium & [[Parathyroid hormone]] levels, decreases bone disease | **** [[Calcitriol]] 0.125-0.25 mg/d improves Calcium & [[Parathyroid hormone]] levels, decreases bone disease. | ||
***** (Monitor Calcium--reduce dose if [[Hypercalcemia|hypercalcemic]]) | ***** (Monitor Calcium--reduce dose if [[Hypercalcemia|hypercalcemic]]) | ||
*[[Metabolic Acidosis]] | *[[Metabolic Acidosis]] | ||
**Occurs when [[GFR]] < 25 mL/min due to inability to excrete H+ ions | **Occurs when [[GFR]] < 25 mL/min due to inability to excrete H+ ions. | ||
**Underlying cause = impaired renal ammonia production and bicarbonate reabsorption | **Underlying cause = impaired renal ammonia production and bicarbonate reabsorption. | ||
**Risk = bone buffering of [[acidosis]]--worsened [[Osteodystrophy]] via Calcium/phosphate loss | **Risk = bone buffering of [[acidosis]]--worsened [[Osteodystrophy]] via Calcium/phosphate loss. | ||
**Increased skeletal muscle breakdown--loss of lean body mass | **Increased skeletal muscle breakdown--loss of lean body mass. | ||
**Therapy goal = bicarbonate > 22 mEq/L via alkali therapy (NaHCO3 0.5-1 mEq/kg/d) | **Therapy goal = bicarbonate > 22 mEq/L via alkali therapy (NaHCO3 0.5-1 mEq/kg/d) | ||
*[[Anemia]] | *[[Anemia]] | ||
**[[Normocytic normochromic anemia]] due to reduced [[Erythropoietin]] production | **[[Normocytic normochromic anemia]] due to reduced [[Erythropoietin]] production. | ||
**May be exacerbated by reduced [[RBC]] survival, coexistent iron/folate deficiency, etc. | **May be exacerbated by reduced [[RBC]] survival, coexistent iron/folate deficiency, etc. | ||
**Generally occurs when [[Creatinine]] > 2-3 mg/dL | **Generally occurs when [[Creatinine]] > 2-3 mg/dL. | ||
**If untreated, [[hematocrit]] (Hct) usually stabilizes at ~ 25 | **If untreated, [[hematocrit]] (Hct) usually stabilizes at ~ 25. | ||
**Therapy recommendations = [[Erythropoietin]] if symptomatic [[anemia]] or [[Hemoglobin]] < 10 g/dL (in pre-dialysis patients) | **Therapy recommendations = [[Erythropoietin]] if symptomatic [[anemia]] or [[Hemoglobin]] < 10 g/dL (in pre-dialysis patients). | ||
**Goal [[Hematocrit]] 33-36 | **Goal [[Hematocrit]] 33-36 | ||
**Must replete iron stores first (oral ferrous sulfate) | **Must replete iron stores first (oral ferrous sulfate) | ||
**Initial dose ~ 150 U/kg sc weekly to increase [[Hematocrit]] | **Initial dose ~ 150 U/kg sc weekly to increase [[Hematocrit]]. | ||
**Maintenance dose ~ 75 U/kg weekly once [[Hematocrit]] goal reached | **Maintenance dose ~ 75 U/kg weekly once [[Hematocrit]] goal reached. | ||
**Improves symtoms and may reduce left ventricle (LV) mass (via improvemt of hyperdynamic state) | **Improves symtoms and may reduce left ventricle (LV) mass (via improvemt of hyperdynamic state). | ||
**Side effects = increased [[blood pressure]] (BP); may need to augment [[Antihypertensive]] regimen | **Side effects = increased [[blood pressure]] (BP); may need to augment [[Antihypertensive]] regimen. | ||
===Plan for Renal Replacement Therapy (RRT)=== | ===Plan for Renal Replacement Therapy (RRT)=== | ||
*Indications for [[Dialysis]] | *Indications for [[Dialysis]] | ||
Line 99: | Line 99: | ||
**[[Peritoneal dialysis]] | **[[Peritoneal dialysis]] | ||
**[[Renal transplant]] | **[[Renal transplant]] | ||
*Access for [[hemodialysis]] should be established when [[GFR]] < 25 mL/min (estimated [[Chronic renal failure]] within 1 year) | *Access for [[hemodialysis]] should be established when [[GFR]] < 25 mL/min (estimated [[Chronic renal failure]] within 1 year). | ||
*Diabetics tend to require [[dialysis]] sooner than non-diabetics because more symptomatic at given [[GFR]] | *Diabetics tend to require [[dialysis]] sooner than non-diabetics because more symptomatic at given [[GFR]]. | ||
*Indications for referral to nephrologist | *Indications for referral to nephrologist | ||
**Unclear etiology of new or chronic [[renal insufficiency]] | **Unclear etiology of new or chronic [[renal insufficiency]] |
Revision as of 19:07, 6 August 2018
Chronic renal failure Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Chronic renal failure secondary prevention On the Web |
American Roentgen Ray Society Images of Chronic renal failure secondary prevention |
Risk calculators and risk factors for Chronic renal failure secondary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]
Secondary Prevention
Reduce Progression
- Protective therapy most effective if initiated early, before Creatinine > 1.5-2.0 mg/dL
- Treat Hypertension
- Systemic hypertension--elevated intraglomerular pressure +/or glom hypertrophy.
- Blood Pressure (BP) control shown in multiple trials to slow progression of renal disease.
- Goal Blood pressure < 130/80-85; < 125/75 in patients with proteinuria > 1-2 g/d.
- ACE inhibitors (ACEI) and Angiotensin II receptor blockers (ARB) preferred 1st line agents due to reno-protective effects.[1]
- Additional agents as needed, including diuretics if volume overload.
- Restrict Dietary Protein
- Controversial – may decrease intraglomerular pressure.
- Conflicting studies – some show benefit, others do not.
- No significant adverse effects shown in large trial.
- Recommendations
- No restriction (> 0.8 g/kg/d) if GFR 25-55 mL/min.
- Limit protein to 0.8 g/kg/d if progression or uremic symptoms.
- Limit to 0.6 g/kg/d if severe renal insufficiency (GFR 13-25 mL/min).
- Close follow-up by dietician given risk of malnutrition in this population.
- Control Blood sugar:
- Treat Hypertension
Treat complications
- Volume Overload
- Impaired excretion of sodium and water due to decreased GFR +/- AII/aldo activation.
- Restrict dietary sodium to 1-2 g/d if hypertension or edema.
- Diuretics
- Thiazides ineffective if GFR < 25 mL/min (~Creatinine > 2-3).
- Switch to Loop diuretic as Creatinine rises; may need bid dosing.
- Addition of thiazide to Loop diuretic can--additional Diuresis.
- Watch for excessive volume depletion
- Hyperkalemia
- Potassium usually maintained until GFR < 15-20 mL/min.
- Increased risk of hyperkalemia with Oliguria, high potassium diet, (ACE inhibitors therapy).
- Increased risk with many meds: ACEI, NSAIDs, Potassium-sparing diuretics, digoxin, TMP.
- Increased risk in diabetics with type IV RTA
- Management
- Low potassium diet (< 60 mEq/d) once GFR < 15 mL/min.
- Avoidance of salt substitutes (may contain potassium salts).
- +/- loop diuretic
- Low dose Kayexelate (5 g with meals) if needed.
- Calcium/phosphate Abnormalities
- Reduced renal synthesis Calcitriol/Vitamin D--low serum Calcium-- Secondary hyperparathyroidism.
- (Occurs when GFR < 40 mL/min)
- Reduced GFR--phosphate retention
- Elevated parathyroid hormone (PTH)--mobilization of Calcium from bone; increased excretion phosphate.
- Allows maintenance of normal Calcium/phosphate while GFR > 30 mL/min.
- Causes renal osteodystrophy
- Once GFR < 25-30 mL/min, hyperphosphatemia occurs
- Therapy goals = normalize Calcium/Phosphate and maintain parathyroid hormone (PTH)< 200 (2-3x uln).
- Calcium/Phosphate management should be initiated when Creatinine ~ 2.
- Calcium x phosphate product should be < 60 to prevent met calcification.
- Low phosphate diet: < 800 mg/d (challenging)
- Calcium-based oral phosphate binders: Calcium acetate or Calcium carbonate with meals.
- Avoid Aluminium-based phosphate binders except for acute therapy of high Calcium x Phosphate products.
- (Aluminium toxicity = osteomalacia, anemia, encephalopathy)
- Avoid Calcium citrate (increases gastrointestinal absorption of aluminum)
- RenaGel = new non-Calcium/Aluminium-containing phosphate binder (cationic polymer).
- (For patients who cannot tolerate Calcium carbonate or need additional agent)
- Calcitriol 0.125-0.25 mg/d improves Calcium & Parathyroid hormone levels, decreases bone disease.
- (Monitor Calcium--reduce dose if hypercalcemic)
- RenaGel = new non-Calcium/Aluminium-containing phosphate binder (cationic polymer).
- Metabolic Acidosis
- Occurs when GFR < 25 mL/min due to inability to excrete H+ ions.
- Underlying cause = impaired renal ammonia production and bicarbonate reabsorption.
- Risk = bone buffering of acidosis--worsened Osteodystrophy via Calcium/phosphate loss.
- Increased skeletal muscle breakdown--loss of lean body mass.
- Therapy goal = bicarbonate > 22 mEq/L via alkali therapy (NaHCO3 0.5-1 mEq/kg/d)
- Anemia
- Normocytic normochromic anemia due to reduced Erythropoietin production.
- May be exacerbated by reduced RBC survival, coexistent iron/folate deficiency, etc.
- Generally occurs when Creatinine > 2-3 mg/dL.
- If untreated, hematocrit (Hct) usually stabilizes at ~ 25.
- Therapy recommendations = Erythropoietin if symptomatic anemia or Hemoglobin < 10 g/dL (in pre-dialysis patients).
- Goal Hematocrit 33-36
- Must replete iron stores first (oral ferrous sulfate)
- Initial dose ~ 150 U/kg sc weekly to increase Hematocrit.
- Maintenance dose ~ 75 U/kg weekly once Hematocrit goal reached.
- Improves symtoms and may reduce left ventricle (LV) mass (via improvemt of hyperdynamic state).
- Side effects = increased blood pressure (BP); may need to augment Antihypertensive regimen.
Plan for Renal Replacement Therapy (RRT)
- Indications for Dialysis
- Malnutrition
- Creatinine clearance 10-15 mL/min
- acidosis not responsive to medical therapy
- Volume overload / CHF
- Uremic pericarditis
- Uremic encephalopathy
- Intractable muscle cramps
- Anorexia and nausea not attributable to reversible causes such as peptic ulcer disease
- Protein energy malnutrition
- Hyperkalemia
- Extracellular fluid volume overload
Recent studies have shown no benefits of initiating early dialysis with improved patient survival. [2]However, advanced preparation for dialysis can help avoid complications like poorly functioning fistula for hemodialysis or malfunctioning peritoneal dialysis catheter, sepsis, bleeding and thrombosis.
- RRT modalities
- Access for hemodialysis should be established when GFR < 25 mL/min (estimated Chronic renal failure within 1 year).
- Diabetics tend to require dialysis sooner than non-diabetics because more symptomatic at given GFR.
- Indications for referral to nephrologist
- Unclear etiology of new or chronic renal insufficiency
- For diagnostic evaluation, e.g. biopsy
- GFR < 50 mL/min: i.e. before vascular access/RRT required
References
- ↑ Lerche D, Kozlov MM, Markin VS (1987). "Electrostatic free energy and spontaneous curvature of spherical charged layered membrane". Biorheology. 24 (1): 23–34. PMID 3651580.
- ↑ Cooper BA, Branley P, Bulfone L; et al. (2010). "A randomized, controlled trial of early versus late initiation of dialysis". The New England Journal of Medicine. 363 (7): 609–19. doi:10.1056/NEJMoa1000552. PMID 20581422. Unknown parameter
|month=
ignored (help)