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Medical Journal, Armed Forces India logoLink to Medical Journal, Armed Forces India
. 2011 Jul 21;67(2):194. doi: 10.1016/S0377-1237(11)60036-1

Supplemental oxygen therapy in bleomycin-induced pulmonary toxicity

Rohit Verma 1
PMCID: PMC4920794  PMID: 27365803

Dear Editor,

I read with interest the case report “Reversible Bleomycin Toxicity”.1 The authors have mentioned high-dose oxygen exposure as one of the risk factors for pulmonary toxicity. This is an important aspect of Bleomycin-induced pulmonary toxicity, as supplemental oxygen therapy is considered to be a synergistic toxin with Bleomycin, particularly in the setting of general anaesthesia and hyperbaric oxygen therapy (HBOT). The dosage of oxygen which can result in toxicity has not been quantified. Even a modest increase in fraction of inspired oxygen (FiO2) to 0.32 or 0.45, intra-operatively, has reportedly resulted in lung toxicity and death.2 Further, the duration of this relationship is not well characterised. An exposure to Bleomycin in the past six months is considered by some to be a significant risk factor;2 however for delivery of HBOT, even a remote history of Bleomycin therapy is an absolute contraindication.3

In patients with history of exposure to Bleomycin, requiring oxygen administration, inspired oxygen concentration is recommended to be kept at the lowest level, typically at FiO2 of 0.22–0.25, that provides adequate tissue oxygenation. A single breath, carbon monoxide diffusion capacity (DLco) is considered to be the most predictive of potential pulmonary toxicity where HBOT is being considered.4

The authors in their case report have not described if the patient received any supplemental oxygen therapy after the administration of Bleomycin. Also, they report that the initial pulmonary function test revealed moderate restrictive defect with impaired gas exchange, and the repeat pulmonary function test was normal. It has not been mentioned if DLco was performed and how significantly it improved after resolution of lung lesions. The finding of improved DLco may have a positive bearing if the patient subsequently requires supplemental oxygen therapy for any reason.

REFERENCES

  • 1.Debnath J, Singh HP, George RA. Reversible Bleomycin toxicity. MJAFI. 2010;66:290–291. doi: 10.1016/S0377-1237(10)80071-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Goldiner P, Carlon GC, Cvitkovic E. Factors influencing postoperative morbidity and mortality in patients treated with bleomycin. BMJ. 1978;1:1664–1669. doi: 10.1136/bmj.1.6128.1664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Kindwall EP. Contraindications and side effects to hyperbaric oxygen therapy. In: Kindwall EP, Whelan HT, editors. Hyperbaric Medicine Practice. 2nd ed. Best Publishing Company; Flagstaff AZ: 1999. pp. 83–98. [Google Scholar]
  • 4.Comis RL. Detecting bleomycin pulmonary toxicity: a continued conundrum. J Clin Oncol. 1990;8:765–767. doi: 10.1200/JCO.1990.8.5.765. [DOI] [PubMed] [Google Scholar]

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