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ACDIS CCDS Exam Syllabus Topics:

SectionWeightObjectives
Topic 1: Quality, Risk Adjustment & Health Initiatives15%- Severity of Illness (SOI) / Risk of Mortality (ROM)
- Quality reporting, public reporting, and compliance programs
- Risk adjustment models and documentation impact
Topic 2: Clinical Documentation Review & Query Practices20%- Documentation gap identification and resolution
- Concurrent and retrospective chart review methodologies
- Query development, communication, and ethical standards
Topic 3: CDI Program Management & Professional Practice15%- Provider education and training strategies
- Ethics, HIPAA, and professional conduct
- Program metrics, benchmarks, and performance measurement
Topic 4: Coding Guidelines & Official Reporting Standards15%- Coding integrity and compliant documentation practices
- AHIMA/ACDIS Guidelines for Compliant Query Practice
- ICD-10-CM/PCS Official Guidelines for Coding and Reporting
Topic 5: Clinical Knowledge & Disease Processes Application20%- Disease processes across body systems applied to chart review
- Medical terminology, anatomy, physiology, pathophysiology
- Clinical indicators, lab results, medications, diagnostic findings
Topic 6: Healthcare Regulations, Reimbursement & Documentation Requirements – IPPS15%- Inpatient Prospective Payment System (IPPS) fundamentals
- Medicare Severity Diagnostic Related Groups (MS-DRGs)
- Documentation responsibilities of medical and clinical staff

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ACDIS Certified Clinical Documentation Specialist Sample Questions (Q108-Q113):

NEW QUESTION # 108
A physician documents acute kidney injury. The patient's creatinine is 0.8 mg/dL on admission, 0.9 mg/dL the following day, and 0.8 mg/dL at discharge. Urine output remains normal and no renal treatment is provided.
What is the BEST CDI action?

Answer: D

Explanation:
A clinical validation query is appropriate because the documented diagnosis appears inconsistent with the available clinical evidence. The creatinine values remain essentially unchanged, urine output is normal, and there is no apparent treatment or monitoring consistent with acute renal dysfunction.
The CDI specialist cannot simply delete the diagnosis because providers are responsible for establishing diagnoses. Conversely, a diagnosis should not automatically be accepted when substantial clinical evidence raises a legitimate question about its validity.
A compliant query would present the documented AKI together with the pertinent renal findings and request clarification. The provider could confirm AKI and provide supporting clinical reasoning, revise the diagnosis, state that it was ruled out, or document another condition.
Assigning chronic kidney disease would be equally inappropriate because CKD requires evidence of chronic kidney abnormality and cannot be inferred from these laboratory values.
The August 2026 ACDIS/AHIMA query guidance supersedes prior versions and remains the foundational standard for clinical validation and documentation clarification.
Clinical validation protects data integrity because diagnoses influence reimbursement, quality reporting, severity measurement, utilization analysis, and downstream patient information.
CCDS Reference Topics: Clinical validation; AKI; unsupported diagnoses; provider clarification; compliance.
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NEW QUESTION # 109
A CDI program is piloting a new query form to better capture the documentation of pneumonia specificity.
Which of the following would be the BEST indicator to determine the effectiveness of the query form?

Answer: B

Explanation:
The most meaningful indicator is an increased volume of appropriately supported cases grouping to respiratory infection DRGs. The stated purpose of the pilot is not merely to obtain more physician responses; it is specifically to improve documentation of the type or etiology of pneumonia.
When providers document clinically supported pneumonia specificity-for example, an identified bacterial etiology or another qualifying respiratory infection-the coded case may move from a less specific/simple pneumonia grouping into a respiratory infections and inflammations DRG family, depending on the final diagnoses and grouper logic. A trend toward the expected DRG distribution can therefore demonstrate that the form is accomplishing its documentation objective.
Provider response and agreement rates are valuable CDI process metrics, but neither proves that useful specificity was obtained. A physician could respond to every query without adding meaningful diagnostic detail. Likewise, an increase in simple pneumonia DRGs would suggest that the intended specificity is not being captured effectively.
A robust CDI analysis should also verify that any DRG shift reflects clinically valid documentation rather than query pressure or reimbursement-oriented behavior.
CCDS Reference Topics: CDI metrics; query effectiveness; pneumonia specificity; MS-DRG trend analysis.
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NEW QUESTION # 110
A patient presents with fever, productive cough, and infiltrates in the right upper lobe per chest x-ray. The history and physical notes that the patient has pneumonia and hypotension. Cultures are drawn and the patient is admitted for IV antibiotics. On day 2, the patient's condition worsens, and the patient is transferred to the ICU for closer monitoring. The ICU physician documents sepsis. Which of the following statements is MOST accurate?

Answer: A

Explanation:
The key issue is whether the sepsis documented on hospital day 2 was present on admission (POA) or developed after admission. The admission already contains potentially relevant indicators-fever, pneumonia, hypotension, cultures, and IV antibiotic treatment-but a CDI specialist cannot independently determine from those indicators that sepsis was POA. Provider clarification is necessary.
This distinction directly affects principal-diagnosis sequencing. When sepsis and a localized infection such as pneumonia are both responsible for admission, the systemic infection is generally sequenced before the localized infection. Conversely, when the patient is admitted with pneumonia and sepsis develops only after admission, pneumonia is sequenced first.
The POA guidelines also emphasize that a diagnosis may not be recognized until days after admission and that delayed documentation does not automatically mean the condition was hospital-acquired. When timing is unclear, querying the provider is appropriate.
There is no evidence supporting aspiration pneumonia, so option B would introduce an unsupported concept.
Options C and D prematurely determine principal diagnosis without resolving the timing of sepsis.
CCDS Reference Topics: Sepsis sequencing; POA assignment; principal diagnosis; compliant clarification of timing.
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NEW QUESTION # 111
A patient was admitted with weakness, loss of appetite, hemoglobin 7.8, WBC 2,700, and platelet count 58.
The admitting diagnoses on the history and physical were anemia, leukopenia, decreased platelets, and rule out myelodysplastic syndrome. Based on these clinical indicators a CDI specialist should query for which of the following conditions?

Answer: A

Explanation:
The laboratory findings demonstrate reduction in all three major peripheral blood-cell lines: hemoglobin 7.8 indicates anemia, WBC 2,700 indicates leukopenia, and platelets 58 indicate thrombocytopenia. Collectively, this pattern is consistent with pancytopenia, making option C the most appropriate documentation clarification.
The National Cancer Institute defines pancytopenia as a lower-than-normal number of red blood cells, white blood cells, and platelets. Importantly, pancytopenia describes the hematologic state; it does not establish its underlying etiology. Myelodysplastic syndrome was only being ruled out in the scenario, so the CDI specialist should not infer it as the definitive cause.
Thrombocytopenia alone would capture only one component of the abnormal CBC and would fail to represent the simultaneous anemia and leukopenia. Myelophthisis implies marrow displacement or infiltration and cannot be inferred from these counts alone. Likewise, aplastic anemia is a specific bone-marrow failure diagnosis requiring provider determination and supporting diagnostic evaluation.
A compliant query can present pancytopenia as a clinically supported choice while allowing the provider to document another explanation.
CCDS Reference Topics: Hematology; clinical indicators; medical terminology; compliant query opportunity.
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NEW QUESTION # 112
A patient with cirrhosis presents with confusion and asterixis. Ammonia is elevated and the patient improves after lactulose administration. The physician documents "altered mental status due to liver disease." Which clarification would provide the MOST clinically specific documentation?

Answer: B

Explanation:
The findings create a strong clarification opportunity for hepatic encephalopathy. Cirrhosis, altered mental status, asterixis, elevated ammonia, and improvement with lactulose collectively support an encephalopathic process related to hepatic dysfunction.
The CDI specialist should not independently diagnose hepatic encephalopathy from the findings. Instead, the physician should be asked to clarify the condition represented by the documented phrase "altered mental status due to liver disease." Hepatic encephalopathy is clinically more specific than a nonspecific symptom such as altered mental status and has a distinct ICD-10-CM classification. Elevated ammonia alone is not sufficient to establish the diagnosis because ammonia levels do not always correlate directly with the severity of encephalopathy. The entire clinical picture must be considered.
Dementia generally represents a chronic neurocognitive disorder and does not adequately explain the acute presentation. Alcohol withdrawal requires an appropriate history of cessation or reduction plus characteristic withdrawal manifestations. Metabolic acidosis concerns acid-base physiology and is not supported by the described findings.
This is an example of CDI moving documentation from a nonspecific symptom to a clinically meaningful diagnosis without directing the provider to a predetermined answer.
CCDS Reference Topics: Hepatic encephalopathy; cirrhosis; neurologic manifestations; clinical indicators; documentation specificity.
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NEW QUESTION # 113
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