Evaluation of Changes in Near Visual Acuity and Required Near Addition Power Following Systemic Chemotherapy

Abstract

Background Near visual acuity (NVA) typically declines with age and after cataract surgery, and it can be influenced by various factors, including diseases and medications. The impacts of systemic chemotherapy on visual functions, particularly accommodation and NVA, have not yet been thoroughly investigated.

Objective The present study is the first to investigate the effects of systemic chemotherapy on NVA and the required near addition power.

Methods A total of 130 eyes from 65 cancer patients [52.3% (n = 34) women, 47.7% (n = 31) men] were evaluated for NVA and required near addition power before and after systemic chemotherapy. Data analysis was performed using SPSS software.

Results The mean age of the participants was 52.63 (13.35) years (age range = 18-80 years). Before chemotherapy, the mean addition power was 1.58 (0.95) D, the mean uncorrected NVA (UCNVA) was 0.50 (0.36) the logarithm of the minimum angle of resolution (logMAR), and the mean corrected NVA (CNVA) was 0.05 (0.24) logMAR. After chemotherapy, changes in addition power were statistically significant (P < 0.05), although changes in NVA were not statistically significant (P > 0.05). UCNVA remained stable in 43.1% of cases, CNVA in 86.9%, and addition power in 46.9%.

Conclusion Based on the findings of this study, systemic chemotherapy does not cause an uncorrectable reduction in NVA. However, it can affect the required near addition power. Further research is recommended to evaluate long-term visual changes in patients undergoing chemotherapy.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The ethics committee of Shahid Beheshti University of Medical Sciences (Tehran, Iran) approved the study protocol

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Footnotes

Email: [tabatabaeefarhotmail.com]

Email: [medicaloptoyahoo.com]

Email: [halehkangarigmail.com]

Email: [mghbr31yahoo.com]

Data Availability

All data produced in the present work are contained in the manuscript

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