ACDIS Updated CCDS Exam Questions and Answers by sahib

When severe sepsis is documented, coding requires the underlying systemic infection first, followed by the appropriate severe-sepsis code and additional code(s) for the acute organ dysfunction. Therefore, the sepsis code is sequenced first, followed by the severe-sepsis code and acute kidney injury.

The FY 2026 ICD-10-CM Official Guidelines state that severe sepsis requires at least two codes: one for the underlying systemic infection and another from subcategory R65.2-. Additional codes identify associated acute organ dysfunction. A code from R65.2- cannot serve as the principal diagnosis.

The UTI identifies the localized source but does not replace the systemic infection as principal diagnosis when sepsis is the condition chiefly responsible for admission. Likewise, the AKI is a manifestation of the severe systemic process and is not sequenced before the sepsis in this scenario.

For CDI specialists, the essential documentation element is the relationship between sepsis and the acute organ dysfunction. Organ dysfunction alone does not automatically permit severe-sepsis coding; provider documentation must establish the association when it is not inherent.

CCDS Reference Topics: Sepsis; severe sepsis; organ dysfunction; sequencing; principal diagnosis.

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The relevant Hospital Value-Based Purchasing domain is the Safety domain, corresponding most closely to option D. CMS's FY 2026 Hospital VBP program maintains a Safety domain that includes healthcare-associated infection performance measures, including C. difficile infection. CMS's current VBP Safety dataset specifically identifies C. difficile among its healthcare-associated infection measures.

It is important to distinguish the domain from an individual measure. “Hospital-acquired infection” describes the type of quality measure, but the formal broader scoring domain is Safety. PSI 90 is also associated with patient safety measurement, but it is not the name of the overall VBP domain.

From a CDI standpoint, documentation accuracy matters because coded and quality-reporting data can influence organizational performance assessment. However, documentation of C. difficile alone does not automatically establish that an infection qualifies as a hospital-onset event for every quality program. Timing and the applicable measure specifications determine whether an individual episode enters a particular healthcare-associated infection metric.

Therefore, CDI professionals should accurately capture the infection and its clinical circumstances without attempting to classify an event as hospital acquired solely to influence quality scores.

CCDS Reference Topics: Hospital VBP; Safety domain; healthcare-associated infections; C. difficile; quality reporting.

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This is an appropriate clinical validation query because the provider has documented a diagnosis while the available clinical information appears inconsistent with that diagnosis.

The CDI specialist should not automatically accept every documented diagnosis when substantial contradictory clinical evidence exists. Conversely, CDI cannot independently delete the physician's diagnosis or replace the physician's clinical judgment.

The query should objectively identify the documented severe malnutrition and relevant contradictory findings—for example, stable weight, adequate nutritional intake, and absence of documented muscle or fat loss—and ask the provider to clarify whether severe malnutrition remains clinically appropriate, whether another nutritional condition better describes the patient, whether the diagnosis has been ruled out, or whether additional clinical reasoning supports it.

The query must remain neutral and should not mention the MCC status or potential reimbursement effect of severe malnutrition.

The August 2026 ACDIS/AHIMA compliant-query guidance supersedes previous editions and is the current foundational standard for compliant documentation clarification.

CCDS Reference Topics: Clinical validation; malnutrition; conflicting clinical indicators; compliant queries; documentation integrity.

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Pulmonary vascular congestion accompanied by pleural effusions is classically associated with congestive heart failure, particularly left-sided or biventricular decompensation. Increased left-sided cardiac filling pressure raises pulmonary venous and capillary hydrostatic pressure, promoting interstitial and alveolar fluid accumulation. Fluid may also migrate into the pleural space, producing unilateral or bilateral pleural effusions.

Additional radiographic indicators of heart failure may include cardiomegaly, cephalization of pulmonary vessels, interstitial edema, Kerley B lines, perihilar alveolar opacities, and bilateral effusions. These findings should always be interpreted alongside symptoms and other clinical evidence such as dyspnea, orthopnea, edema, BNP/NT-proBNP, echocardiography, and response to diuretics.

COPD more commonly demonstrates hyperinflation, flattened diaphragms, and increased lucency rather than pulmonary vascular congestion. Cor pulmonale refers to right-sided cardiac dysfunction resulting from pulmonary disease and does not typically produce the classic pulmonary venous congestion pattern. Pulmonary embolism may have a normal chest radiograph or nonspecific abnormalities, but pulmonary vascular congestion with effusions is not its characteristic pattern.

For CDI purposes, imaging provides a clinical indicator but does not independently establish the diagnosis or acuity of heart failure.

CCDS Reference Topics: Heart failure pathophysiology; chest radiography; clinical indicators; cardiopulmonary terminology.

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