Guide to Clinical Validation, Documentation and Coding ...
Guide to Clinical Validation, Documentation and Coding
Acute Kidney Injury
Acute Kidney Injury
N17.9
Acute Kidney Failure, unspecified
CC
N99.0
Postop (acute) (chronic) kidney failure
Diagnosis: acute kidney injury (nontraumatic); acute kidney failure, unspecified; acute postop kidney failure; acute postop kidney injury
Discussion
Nontraumatic acute kidney injury or impairment (AKI) is the rapid loss of kidney function within 48 hours in either pre-existing normal renal function or with pre-existing renal disease (acute on chronic). It is a syndrome of progressive kidney injury/impairment starting with RISK as an increase in absolute serum creatinine (SCr) of either 0.3 mg/dl (or a percentage increase of 50 percent or 1.5 fold from baseline) or a reduction in urine output and increases in designated stages of injury, failure and with outcomes of LOSS, and end stage kidney disease (ESKD) or end stage renal disease (ESRD). These stages were given the acronym RIFLE by the Acute Dialysis Quality Initiative to develop a uniformly accepted definition of AKI. Acute kidney injury is considered reversible until it progresses to the outcome of complete loss of renal function or ESRD. Treatment depends on both the underlying cause and the severity or stage of AKI.
At the present time, ICD-10-CM makes no distinction between the stages of AKI as identified by the RIFLE Classification system. AKI is classified to N17.9 Acute kidney failure, unspecified. When using the RIFLE Classification system for staging of severity, acute kidney failure represents stage III.
The Acute Kidney Injury Network (AKIN) also developed standardized clinical indicators to help diagnose AKI. The criteria involve the timing and amount of reduction in kidney function. Although these criteria cannot be used for code assignment without physician verification, its presence in the documentation ensures the appropriateness of reporting a code for AKI.
When acute kidney injury (AKI) is documented, if the clinical indicators for acute kidney failure are not met, query the provider if AKI represents "acute kidney insufficiency" (N28.9) as this is the early stage of renal impairment before it evolves into renal failure. Blood urea nitrogen (BUN) and serum creatinine values may be mildly elevated and other clinical symptoms may or may not be present or minimal. RIFLE/AKIN stages I and II represent acute kidney insufficiency, which are milder forms of impairment that do not meet clinical indicators for acute kidney failure.
If AKI is documented and the serum creatinine levels are less than 0.3 mg/L or lasts less than 24 hours, and returns to baseline with no to minor treatment, query for the clinical significance and note the inconsistency with clinical indicators for AKI. If not indicative of acute kidney insufficiency or acute kidney failure, the physician should be queried if the rise in creatinine represents azotemia (R79.89) or if it is integral to another condition, (i.e., hemoconcentration due to dehydration) with minimal rise in BUN/Cr ratio.
Coding Tip When documentation, clinical criteria, and code assignment do not match, query the provider for clarification of the diagnosis.
Linking acute kidney injury to any type of nephropathy does not alter reporting N17.9 for documented AKI. Acute kidney injury/failure can occur in the presence of end stage renal disease when caused by another condition; in such cases, both AKI/AKF and ESRD are reported.
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Acute Kidney Injury
Guide to Clinical Validation, Documentation and Coding
The etiology of AKI should be documented and the link made to the underlying pathology; depending on the underlying condition, the category N17- code may be further defined. For example, if documented as acute kidney injury, meaning acute kidney failure, and is further specified as "with tubular necrosis," code N17.0 would be reported.
The etiologies of acute kidney injury or failure are classified into three categories:
Pre-renal: diminished blood flow to the kidneys or volume loss; oliguria ? severe dehydration ? shock ? embolism ? cardiac failure ? hepatic failure ? sepsis ? excessive diuresis ? hemorrhage ? tense ascites ? peritonitis ? pancreatitis ? burns ? myocardial infarction ? antihypertensive meds, NSAIDS, cyclosporine, tacrolimus, ACE inhibitors ? anesthetics ? renal artery obstruction/renal vein thrombosis
Intrinsic/renal: diseases and disorders of the kidneys ? acute tubular necrosis ? SLE/glomerulonephritis ? Sickle cell disease ? nephrotoxins: IV iodinated radiologic contrast agents ? renal ischemia ? acute pyelonephritis ? acute poststreptococcal glomerulonephritis ? Wegener's granulomatosis ? Goodpasture syndrome ? acute tubulointerstitial nephritis as drug reaction ? acute vascular nephropathy: vasculitis, malignant hypertension, systemic sclerosis ? atheroembolism ? infiltrative diseases: lymphoma, sarcoidosis, leukemia
Post-renal: bilateral obstruction of urinary outflow; anuria ? ureteral calculi ? blood clot ? neoplasm ? BPH ? urethral stricture ? congenital defects ? retroperitoneal fibrosis ? ureteral trauma or surgical ureteral injury
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Guide to Clinical Validation, Documentation and Coding
Acute Kidney Injury
? phimosis
? obstructed indwelling urinary catheter
? anticholinergic meds
Some of the associated conditions of AKI (acute renal failure) (stage III) are:
? cardiac arrhythmia
? hyperkalemia
? acidemia
? hypernatremia
? encephalopathy
When evaluating clinical indicators, it must be noted that when using AKIN criteria, serum creatinine (SCr) levels must represent an elevation (from baseline or seen between two creatinine levels within 48 hours) and not merely a "jump" and that this calculation is based on levels obtained after adequate fluid resuscitation, when possible. RIFLE criteria do not use these parameters. Stage is determined by whichever of the two criteria, serum creatinine (SCr) or Urinary Output (UO), is higher and only after meeting the criteria for AKI.
Coding Tip Code assignment cannot be based on ancillary test results or therapies alone. A diagnosis and its clinical significance must be supported by both physician or other qualified health care professional documentation, and clinical criteria. When it is unclear or there is contradictory information, query the physician or other qualified health care professional for clarification.
Action
In order to assign the ICD-10-CM code for acute kidney injury as a principal diagnosis or comorbidity or as a complication of care, the criteria for official coding guidelines, Uniform Hospital Discharge Data Set (UHDDS) definition, clinical criteria, and physician or other qualified health care professional documentation must be met.
References
AHA Coding Clinic Acute Dialysis Quality Initiative (ADQI): Acute Kidney Injury Network: Medscape Reference: The Merck Manual MLN Matters Number SE1121 National Center for Biotechnology Institute: Regulatory Audits Desk Reference, Optum ICD-10-CM Complete Official Draft Code Set, 2013 DRG Expert, 2013 Edition, Optum ICD-10-CM Clinical Documentation Improvement Desk Reference, 2013, Optum ICD-10-CM Draft Official Guidelines for Coding and Reporting 2014
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Acute Kidney Injury Coding Guideline 1. Physical Evaluation
(routine/expected in italics)
2. Clinical Evaluation (routine/expected in italics)
Guide to Clinical Validation, Documentation and Coding
Clinical Criteria
? Asymptomatic ? Symptoms include those of underlying condition ? Insufficiency: s/s may be absent to minimal ? Anorexia ? Nausea/vomiting ? Decreased urine output ? Asterixis ? hyperreflexia ? Weakness ? Peripheral edema/fluid retention ? orthostasis ? Myoclonic jerks ? Seizures ? Confusion ? Fluid overload ? Uremic pericarditis
? chest pain ? pericardial friction rub ? pericardial tamponade ? Pulmonary edema ? dyspnea ? crackles on auscultation ? Coma
? Serum creatinine with "jump" or < 0.3 mg/L, short-term; indicating hemoconcentration of clinical dehydration
? Serum creatinine (SCr): ? RIFLE and AKIN: - increase of SCr by >/+ 0.3 mg/dl (>/+ 26.4 mol/L or increase to >/+ 150%?200% from baseline [SCr x 1.5-2] [RISK] - increase of SCr to > 200%?300% from baseline [SCr x 2-3] [INJURY] - increase of SCr to > 300% from baseline or SCr >/+ 4.0 mg/dl (>/+ 354 [mol/L] with an acute increase with at least 0.5mg/dl (44 mol/L) [SCr x >3] [FAILURE] or treatment with RRT
? Urine output (UO): ? RIFLE and AKIN: - increase of SCr by >/+ 0.3 mg/dl (>/+ 26.4 mol/L or increase to >/+ 150%?200% from baseline [SCr x 1.5-2] [RISK] - increase of SCr to > 200%?300% from baseline [SCr x 2-3] [INJURY] - increase of SCr to > 300% from baseline or SCr >/+ 4.0 mg/dl (>/+ 354 [mol/L] with an acute increase with at least 0.5mg/dl (44 mol/L) [SCr x >3] [FAILURE] or treatment with RRT
? Urine output (UO): ? RIFLE and AKIN: - I. UO < 0.5 ml/kg/hr for > 6 hours [RISK] - II. UO < 0.5 ml/kg/hr for > 12 hours [INJURY] - III. UO < 0.3 ml/kg/hr for > 24 hours (oliguria) or anuria for 12 hours [FAILURE]
? Serum BUN/Cr ratio > 20/1 ? FENa < 1 (Fractional excretion of sodium) (< 1 prerenal; > 3 ATN) ? GFR ? Urinary sediment, protein, blood, casts ? Urine: specific gravity > 1.018, osmolarity (> 500) ? CBC ? Electrolytes ? Urine Na concentration > 20 ? Postvoid residual bladder volume (postrenal cause suspected) ? Peripheral smear ? Fractional excretion of sodium and urea ? Biomarkers (future)
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Guide to Clinical Validation, Documentation and Coding
Coding Guideline 3. Diagnostic Px
(routine/expected in italics)
4. Therapeutic Tx (routine/expected in italics)
5. Increased Nursing Care and/or Monitoring
6. Extends LOS
Clinical Criteria
? Urine output < 500 mL/day ? Kidney biopsy ? EKG ? Renal scan ? Ultrasound of kidney ? KUB ? IV pyelogram ? Renal arteriography
? Oral hydration ? IV hydration ? Dialysis
? Develops AKI postadmit
? AKI delays discharge ? Discharge delayed due to postprocedure AKI
Acute Kidney Injury
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Acute Kidney Injury
Guide to Clinical Validation, Documentation and Coding
Condition
Evidence Coding Guideline
Physician/Other Qualified Health Care Professional Documentation
ICD-10-CM*
Routine/
1, 2
Expected/
Integral/
Inherent/
Incidental
(italics only)
1, 2
? IP Admit Note: Admitted due to persistent NA
OCG: I.B.5; I.C.18.a; III.B vomiting x two days; requires work-up; mild dehydration with mild AKI; BUN/Cr is
30/1.3 with baseline creatinine 0.9, push
fluid intake. (Query clinical significance of
BUN/creatinine increase and if AKI
represents acute kidney failure, acute
kidney insufficiency, azotemia or
hemoconcentration of dehydration.)
Principal Diagnosis
1, 2, 3, 4, 6
1, 2, 3, 4
OCG: II.C; II.G; I.B.5; I.C.18.a; III.B
AHA CC: 2Q, 2012, pg 5; 3Q, 2011, pg 16, 17; 2Q, 2011, pg 15; 4Q, 2008, pg 192; 2Q, 2003, pg 7; 3Q 2002, pg 28; 1Q, 1993, pg 17
? IP Discharge Summary: AKI due to
? Example: Principal diagnosis is
bladder neck obstruction associated with that condition established
BPH. Treated with dialysis.
after study to be chiefly
responsible for occasioning
the admission of the patient to
the hospital for care.
Comorbidity
1, 2, 3, 4, 5, 6 OCG: I.B.5; I.C.18.a; III.B ? IP Discharge Summary: Final diagnosis:
AHA CC: 2Q, 2012, pg AKI due to SLE nephritis.
5;
? IP Admit Note: Admit due to AKI,
3Q, 2011, pg 16, 17;
decompensated CHF from
2Q, 2011, pg 15;
noncompliance in ESRD by missing
2Q, 2003, pg 7;
dialysis appointment, perform dialysis
4Q, 2008, pg 192;
today.
3Q, 2002, pg 28;
1Q, 1993, pg 17
? Example: Linking acute kidney injury to any type of nephropathy does not alter reporting N17.9 for documented AKI. When two or more diagnoses equally meet the definition of principal diagnosis, any one of the diagnoses may be sequenced first.
Complication of Care
1, 2, 3, 4, 5, 6 OCG: II.G; I.B.5; I.C.18.a; ? IP Discharge Summary: Discharge was
III.B
delayed due to post on-pump CABG
AHA CC: 2Q, 2012, pg induced AKI with ATN.
5;
? IP Admit Note: Admit due to AKI from
3Q, 2011, pg 16, 17;
renal artery thrombosis, s/p kidney
2Q, 2011, pg 15;
transplant (affecting the function of the
4Q, 2008, pg 192;
transplanted organ).
3Q, 2002, pg 28;
1Q, 1993, pg 17
? Example: Report by sequencing postprocedure (acute) (chronic) kidney failure N99.0 before an additional code for type of kidney disease.
? Example: Report complication resulting from surgery or other medical care. Sequence complication code first followed by additional code to specify nature of complication if not included in complication code. For complications in T80?T88 range, follow with a code for the specific complication.
Poisoning or 1, 2, 3, 4, 5, 6 OCG: I.B.5; I.C.18.a; III.B ? IP Admit Note: Admit due to AKI from ? Example: Report poisoning:
Adverse Effect of Medication/ Chemical
AHA CC: 2Q, 2012, pg 5;
3Q, 2011, pg 16, 17; 2Q, 2011, pg 15; 4Q, 2008, pg 192; 3Q, 2002, pg 28; 1Q, 1993, pg 17
"Spice" abuse, chronic abuser
Identify drug/chemical by
(poisoning).
T36?T50 with fifth or sixth
? IP Progress Note: AKI due to contrast dye character of intent + N17.9
following IV pyelogram (adverse effect) Nature of adverse drug effect
? IP Admit Note: Admit due to Prograf
(manifestation).
toxicity induced AKI, s/p lung transplant ? Example: Report adverse
(adverse effect) (not affecting the
effect: Nature of adverse drug
function of the transplanted organ).
effect: N17.9 (adverse
condition) + T36?T50 with
fifth or sixth character 5.
*ICD-10-CM codes referenced pertain only to those indicated at the beginning of this diagnosis.
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