Why audiometry before cisplatinCisplatin belongs to the platinum coordination complex group and exerts its antitumor effect by forming DNA cross-links, but the same reactive platinum species also damage cochlear outer hair cells. The resulting injury is
ototoxicity, which typically presents as bilateral, symmetric,
high-frequency sensorineural hearing loss that is dose-dependent and cumulative. Tinnitus often appears first and may be the only early warning sign. Because the damage begins in the basal turn of the cochlea, where high-frequency sounds are processed, routine conversation may remain intact while hearing loss is already progressing on audiometry.
For a patient about to receive the first cycle of cisplatin and etoposide, the nurse must verify that a
baseline audiogram was obtained before treatment. This serves two purposes: it documents pre-existing hearing status, and it provides a reference point for detecting early changes during subsequent cycles.
Key point! Once cisplatin-induced hearing loss occurs, it is generally irreversible, so prevention and early detection are the only realistic strategies.
Evidence from a randomized controlled trial in head and neck cancer patients receiving cisplatin-based chemoradiation confirms that
cisplatin-induced hearing loss is frequent and severe, and that interventions such as trans-tympanic sodium thiosulfate gel are being studied specifically to prevent this ototoxicity
[2]. The trial excluded patients with asymmetric hearing at baseline, which underscores why a pretreatment hearing assessment is essential before cisplatin exposure begins
[2].
Why the other options are incorrect| Test | Primary drug concern | Relevance to cisplatin |
|---|
| Left ventricular ejection fraction | Anthracyclines (doxorubicin, daunorubicin), trastuzumab | Cardiotoxicity is not a defining cisplatin risk; routine baseline EF is not required for cisplatin alone |
| Serum bilirubin and liver enzymes | Docetaxel, other taxanes metabolized hepatically | Cisplatin is primarily nephrotoxic, not hepatotoxic; liver panels are not the priority baseline test |
| Pulmonary function tests | Bleomycin | Bleomycin causes interstitial pneumonitis and pulmonary fibrosis; cisplatin does not carry this specific pulmonary risk |
Watch out! The distractors reflect classic chemotherapy-toxicity pairings. On licensure exams, each option is tied to a specific agent: anthracyclines to cardiac function, bleomycin to pulmonary function, docetaxel to hepatic function, and cisplatin to renal function plus hearing. Recognizing the drug-toxicity match is faster and safer than reasoning from the patient's lung cancer diagnosis alone.
For this patient with
small cell lung cancer and a 40 pack-year smoking history, pre-existing hearing loss from smoking-related vascular damage or age-related presbycusis is possible. That makes baseline audiometry even more important, because it distinguishes treatment-related change from pre-existing deficits. The nurse should also anticipate monitoring
serum creatinine and
BUN before each cisplatin cycle, since nephrotoxicity is the other major dose-limiting toxicity, but the question specifically asks about the baseline test tied to ototoxicity, which is audiometry.
References (research sources)
- [2]
A randomized controlled trial to test the efficacy of trans-tympanic injections of a sodium thiosulfate gel to prevent cisplatin-induced ototoxicity in patients with head and neck cancer.RCT/clinical trialRolland V, Meyer F, Guitton MJ, Bussières R, Philippon D, Bairati I (2019) · DOI: 10.1186/s40463-019-0327-x