Module 4: Casefinding
This module consists of four units which will deal with some basic procedures for casefinding in a healthcare facility.
After completing this module, cancer abstractors will be able to:
Module 4 Units:
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Unit 4.1: Casefinding
Casefinding is a system for identifying every patient - inpatient or outpatient, who is diagnosed and/or treated with a reportable diagnosis of cancer.
Casefinding is one of the most important duties a cancer registrar performs. Cancer data collection begins by identifying those patients with a clinical or pathological diagnosis of cancer. All healthcare facilities should create a casefinding system to ensure all reportable cases are identified. It is important that all personnel involved in the casefinding be thoroughly familiar with reportable diagnoses. (See Module 2 and Module 3)
A clinical diagnosis results when a recognized medical practitioner says the patient has a cancer or carcinoma; the case is reportable. Some malignancies are never histologically or cytologically confirmed. A diagnosis of cancer can be made during a diagnostic workup e.g. imaging exams, radiographic scans, tumor markers, blood work, visualization of tumor at exploratory laparotomy, etc. These cases are reportable based on the clinical diagnosis. A clinical diagnosis may be recorded in the final diagnosis on the face sheet or other parts of the medical record.
Note: A pathology report normally takes precedence over a clinical diagnosis. If the patient has a negative biopsy, the case would not be reported.
Exception 1: If the physician treats a patient for cancer in spite of the negative biopsy, report the case.
Exception 2: If enough time has passed that it is reasonable to assume that the physician has seen the negative pathology, but the clinician continues to call this a reportable disease, report the case. A reasonable amount of time would be equal to or greater than 6 months.
A pathologic diagnosis is based upon tissue specimens taken during surgical procedures or autopsies; positive hematological findings relative to leukemia are included, as well as bone marrow exams. This type diagnosis can also be based upon examination of cells e.g. sputum cytology, fine needle aspirate (FNA), peritoneal washings, or examination of cells in pleural fluid. (See Module 3)
Casefinding is an important part of the cancer registry. All healthcare facilities must perform casefinding in order to assure that all reportable cases are submitted to the Tennessee Cancer Registry and to adhere to the reporting requirements.
Cancer registrars do not wait for cancer information to filter in to a registry. Registrars should become actively involved in casefinding so that the cancer information they receive is as complete as possible. Cancer registrars often accomplish this by visiting other areas of the healthcare facility to ensure that no cancer data or cases are missed.
Unit 4.2: Types of Casefinding Methods
There are two types of casefinding methods used by registries: active and passive.
Active Casefinding
Passive Casefinding
Active and passive case finding ensures more complete cancer case reporting. The most effective casefinding system includes reviewing specimen reports e.g. pathology, cytology, bone marrow, and autopsy reports, as well as, non-specimen reports e.g. disease indices, radiology reports, or oncology logs.
Unit 4.3: Casefinding Sources
There are several source documents available for casefinding. The documents may vary from one facility to another based on what specialty departments exist. In general the source documents in a hospital can include, but are not limited to, the following:
Specimen Sources
Pathology and Cytology Reports: Generally, 90 percent of all cancers are histologically confirmed. The reviewing of all pathology and cytology reports is essential to complete cancer reporting. The cancer registrar or designated personnel should review ALL these reports.
Non-Specimen Sources
Important: Review of only one type of source document cannot identify all cancer cases diagnosed and/or treated in a facility. USE AS MANY SOURCES AS POSSIBLE TO ASSURE COMPLETE CASE ASCERTAINMENT.
Casefinding and abstracting are not done at the same time.
Unit 4.4: Cancer-Screening List of ICD-9-CM Codes for Casefinding
| 042 | AIDS (review cases for AIDS-related malignancies) |
| 140.0-208.9 | Malignant neoplasms |
| 203.1 | Plasma cell leukemia (9733/3) |
| 205.1 | Chronic neutrophilic leukemia (9963/3) |
| 210.0-229.9 | Benign neoplasms |
| 230.0-234.9 | Carcinoma in-situ |
| 235.0-238.9 | Neoplasms of uncertain behavior |
| 238.4 | Polycythemia vera (9950/3) |
| 238.6 | Solitary plasmacytoma (9731/3); Extramedullary plasmacytoma (9731/3) |
| 238.7 | Chronic myeloproliferative disease (9960/3); Myelosclerosis with myeloid metaplasia (9961/3); Essential thrombocythemia (9962/3); Refractory cytopenia with multilineage dysplasia (9985/3); Myelodysplastic syndrome with 5q-syndrome (9986/3); Therapy-related myelodysplastic syndrome (9987/3) |
| 239.0-239.9 | Neoplasms of unspecified behavior |
| 273.2 | Gamma heavy chain disease; Franklin’s disease |
| 273.3 | Waldenstrom’s macroglobulinemia |
| 273.9 | Unspecified disorder of plasma protein metabolism (screen for potential 273.3 miscodes) |
| 284.9 | Refractory anemia (9980/3) |
| 285.0 | Refractory anemia with ringed sideroblasts (9982/3); Refractory anemia with excess blasts (9983/3); Refractory anemia with excess blasts in transformation (9984/3) |
| 288.3 | Hypereosinophilic syndrome (9964/3) |
| 289.8 | Acute myelofibrosis (9932/3) |
| V07.3 | Other prophylactic chemotherapy (screen for miscoded malignancies) |
| V07.8 | Other specified prophylactic measures |
| V10.0-V10.9 | Personal history of malignancy |
| V58.0 | Admission for radiotherapy |
| V58.1 | Admission for chemotherapy |
| V66.1 | Convalescence following radiotherapy |
| V66.2 | Convalescence following chemotherapy |
| V67.1 | Radiation follow-up |
| V67.2 | Chemotherapy follow-up |
| V71.1 | Observation for suspected malignant neoplasm |
| V76.0-V76.9 | Special screening for malignant neoplasm. |
Casefinding Codes for Benign Brain and CNS Tumors
| 225 | Benign neoplasm of brain and other parts of central nervous system |
| 225.0 | Benign neoplasm of the brain |
| 225.1 | Benign neoplasm of the cranial nerves |
| 225.2 | Benign neoplasm of the cerebral meninges; cerebral meningioma |
| 225.3 | Benign neoplasm of spinal cord, cauda equina |
| 225.4 | Benign neoplasm of spinal meninges; spinal meningioma |
| 225.8 | Benign neoplasm of other specified sites of nervous system |
| 225.9 | Benign neoplasm of nervous system, part unspecified |
| 227.3 | Benign neoplasm of pituitary, craniopharyngeal duct, carniobuccal pouch, hypophysis, Ratke’s pouch, sella trucica |
| 227.4 | Benign neoplasm of pineal gland, pineal body |
| 237 | Neoplasm of uncertain behavior of endocrine glands and nervous system |
| 237.0 | Neoplasm of uncertain behavior of pituitary gland and craniopharyngeal duct |
| 237.1 | Neoplasm of uncertain behavior of pineal gland |
| 237.5 | Neoplasm of uncertain behavior of brain and spinal cord |
| 237.6 | Neoplasm of uncertain behavior of meninges: NOS, cerebral, spinal |
| 237.7 | Neurofibromatosis |
| 237.70 | Neurofibromatosis, Unspecified von Recklinghausen’s Disease |
| 237.71* | Neurofibromatosis, Type One von Recklinghausen’s Disease |
| 237.72 | Neurofibromatosis, Type Two von Recklinghausen’s Disease |
| 237.9 | Neoplasm of uncertain behavior of other and unspecified parts of nervous system; cranial Nerves |
The suspense file should be reviewed periodically to ensure that cases are completed promptly; within six months after date of diagnosis.
Module 4 Review and Quiz
Casefinding is a system for locating every patient, either inpatient or outpatient, who is diagnosed and/or treated with a reportable diagnosis.
All healthcare facilities must perform case finding. Although these facilities may use different source documents, the procedures involved in their casefinding cycles are similar.
In the casefinding process, a suspense file is kept so that the status of casefinding can be ascertained at any time.
There are two types of casefinding methods used by healthcare facilities: active and passive.
In active casefinding procedures, cancer registrars retrieve and screen the source documents (such as disease indices, pathology reports, and so on).
A benefit of active casefinding procedures is that this method is more thorough and accurate, because the registry personnel have extensive training in terminology that identifies reportable cases.
In case of passive casefinding the cancer registrar relies on other health care professionals to notify the registrar of potentially reportable cases.
A concern with passive casefinding is that non-cancer registry staff are not as familiar with reporting terminology and rules, so incomplete casefinding may occur.
A combination of active and passive casefinding is a commonly used system in registries.
There are many casefinding sources; Reliance on multiple sources is necessary to obtain a complete description of the patient's cancer experience.
Review of all inpatient and outpatient admissions and discharges facilitates quick casefinding process since these documents present clinical or pathological diagnosis of cancer.
One method of casefinding is the reviewing of all pathology and cytology reports which is essential to complete cancer reporting. The cancer registrar or designated personnel should review ALL these reports.
Other casefinding sources include cytology and autopsy reports, nuclear medicine documents, radiation oncology and medical oncology logs.
After identifying a potential case from a casefinding source, the registrar processes the case into a suspense file.
The suspense file contains information on cases that are potentially reportable.
The suspense file can be maintained in at least two ways:
The suspense file should be reviewed periodically to ensure that cases are completed promptly.
Quiz for Module 4
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