Effect of ketorolac tromethamine on pain management in patients with condyloma acuminata treated with 5-aminolevulinic acid photodynamic therapy

•The application of ketorolac tromethamine significantly relieves pain within 24 h after ALA-PDT.•Ketorolac tromethamine combined with two-step irradiation is a safe and effective method to relieve pain produced by ALA-PDT.•The application of ketorolac tromethamine combined with two-step irradiation...

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Published inPhotodiagnosis and photodynamic therapy Vol. 54; p. 104646
Main Authors Chen, Xiaomeng, Liu, Chang, Cao, Shuanglin, Wang, Xin
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.08.2025
Elsevier
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Abstract •The application of ketorolac tromethamine significantly relieves pain within 24 h after ALA-PDT.•Ketorolac tromethamine combined with two-step irradiation is a safe and effective method to relieve pain produced by ALA-PDT.•The application of ketorolac tromethamine combined with two-step irradiation improves patient satisfaction. Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions. To investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA). A total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 min, followed by 80 mW/cm² for 16 min; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 min (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 min (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 h, and any adverse reactions after therapy. During ALA-PDT, the median pain scores at 1 min and 5 min in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 min: 2.0, 4.0, and 4.5, respectively; at 5 min: 5.0, 6.0, and 7.0, respectively). At 10 min and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 min: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 min. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1–3), with most reporting pain relief within 24 h. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4–7), with pain lasting >24 h in most cases, showing a statistically significant difference (χ2 = 70.925, P < 0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1 %), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3 %) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ2 = 10.351, P = 0.025). The application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.
AbstractList Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions.BACKGROUNDPhotodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions.To investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA).OBJECTIVETo investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA).A total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 minutes, followed by 80 mW/cm² for 16 minutes; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 minutes (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 minutes (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 hours, and any adverse reactions after therapy.METHODSA total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 minutes, followed by 80 mW/cm² for 16 minutes; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 minutes (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 minutes (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 hours, and any adverse reactions after therapy.During ALA-PDT, the median pain scores at 1 minute and 5 minutes in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 minute: 2.0, 4.0, and 4.5, respectively; at 5 minutes: 5.0, 6.0, and 7.0, respectively). At 10 minutes and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 minutes: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 minutes. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1-3), with most reporting pain relief within 24 hours. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4-7), with pain lasting more than 24 hours in most cases, showing a statistically significant difference (χ2=70.925, P<0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1%), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3%) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ2=10.351, P=0.025).RESULTSDuring ALA-PDT, the median pain scores at 1 minute and 5 minutes in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 minute: 2.0, 4.0, and 4.5, respectively; at 5 minutes: 5.0, 6.0, and 7.0, respectively). At 10 minutes and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 minutes: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 minutes. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1-3), with most reporting pain relief within 24 hours. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4-7), with pain lasting more than 24 hours in most cases, showing a statistically significant difference (χ2=70.925, P<0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1%), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3%) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ2=10.351, P=0.025).The application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.CONCLUSIONSThe application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.
Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions. To investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA). A total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 min, followed by 80 mW/cm² for 16 min; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 min (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 min (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 h, and any adverse reactions after therapy. During ALA-PDT, the median pain scores at 1 min and 5 min in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 min: 2.0, 4.0, and 4.5, respectively; at 5 min: 5.0, 6.0, and 7.0, respectively). At 10 min and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 min: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 min. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1-3), with most reporting pain relief within 24 h. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4-7), with pain lasting >24 h in most cases, showing a statistically significant difference (χ = 70.925, P < 0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1 %), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3 %) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ = 10.351, P = 0.025). The application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.
•The application of ketorolac tromethamine significantly relieves pain within 24 h after ALA-PDT.•Ketorolac tromethamine combined with two-step irradiation is a safe and effective method to relieve pain produced by ALA-PDT.•The application of ketorolac tromethamine combined with two-step irradiation improves patient satisfaction. Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions. To investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA). A total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 min, followed by 80 mW/cm² for 16 min; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 min (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 min (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 h, and any adverse reactions after therapy. During ALA-PDT, the median pain scores at 1 min and 5 min in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 min: 2.0, 4.0, and 4.5, respectively; at 5 min: 5.0, 6.0, and 7.0, respectively). At 10 min and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 min: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 min. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1–3), with most reporting pain relief within 24 h. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4–7), with pain lasting >24 h in most cases, showing a statistically significant difference (χ2 = 70.925, P < 0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1 %), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3 %) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ2 = 10.351, P = 0.025). The application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.
Background: Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or non-invasive. However, patients often experience significant pain during the treatment. How to alleviate the pain experienced by patients during photodynamic therapy has become a key focus of current discussions. Objective: To investigate the pain control and its safety and feasibility of ketorolac tromethamine combined with two-step irradiation in 5-aminolevulinic acid photodynamic therapy (ALA-PDT) for the treatment of condyloma acuminatum (CA). Methods: A total of 92 patients were randomly assigned into the following three groups in this study. The first group, the combination group, received ketorolac tromethamine combined with the two-step irradiation (irradiation at 65 mW/cm² for 5 min, followed by 80 mW/cm² for 16 min; total energy: 96 J/cm²). The second group, the ketorolac group, received ketorolac tromethamine with irradiation at 80 mW/cm² for 20 min (96 J/cm²). The third group, the control group, used cold air analgesia with irradiation at 80 mW/cm² for 20 min (96 J/cm²). Pain scores during irradiation were recorded for all patients, using Visual Analogue Scale (VAS). Additionally, a questionnaire was taken to assess treatment satisfaction, pain improvement within 24 h, and any adverse reactions after therapy. Results: During ALA-PDT, the median pain scores at 1 min and 5 min in the combination group were lower than those in the ketorolac group and the control group (median pain scores at 1 min: 2.0, 4.0, and 4.5, respectively; at 5 min: 5.0, 6.0, and 7.0, respectively). At 10 min and at the end of the treatment, the median pain scores in the combination group and the ketorolac group were lower than those in the control group (median pain scores at 10 min: 6.0, 6.0, and 7.0, respectively; at the end of treatment: 3.0, 4.0, and 5.0, respectively). All three groups reached peak pain levels between 5 and 10 min. After irradiation, the majority of patients in the combination group and the ketorolac group experienced mild pain (VAS scores of 1–3), with most reporting pain relief within 24 h. In contrast, the majority of patients in the control group experienced significant pain (VAS scores of 4–7), with pain lasting >24 h in most cases, showing a statistically significant difference (χ2 = 70.925, P < 0.001). In terms of adverse reactions, all three groups experienced pain, with some patients also exhibiting redness and swelling, erosion, itching, scabbing, and other symptoms. And there were no statistically significant differences in adverse reactions among the three groups (P>0.05). Regarding treatment satisfaction, the vast majority of patients in the combination group reported being very satisfied (87.1 %), with no patients expressing dissatisfaction. However, in the control group, 5 patients expressed dissatisfaction, and only 16 patients (53.3 %) reported being very satisfied. The ketorolac group had a satisfaction level that fell between the other two groups. The differences among the three groups were statistically significant (χ2 = 10.351, P = 0.025). Conclusions: The application of ketorolac tromethamine can effectively relieve the pain of CA patients during ALA-PDT, especially in the later stages of treatment. Combining ketorolac tromethamine with the two-step irradiation method can further reduce pain generated in the initial stage of ALA-PDT and improve patient satisfaction with the treatment.
ArticleNumber 104646
Author Chen, Xiaomeng
Wang, Xin
Cao, Shuanglin
Liu, Chang
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  givenname: Xiaomeng
  surname: Chen
  fullname: Chen, Xiaomeng
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  givenname: Chang
  surname: Liu
  fullname: Liu, Chang
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  givenname: Shuanglin
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  surname: Wang
  fullname: Wang, Xin
  email: xinwang@ntu.edu.cn
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Keywords Ketorolac tromethamine
Condyloma acuminatum
Photodynamic therapy
Pain
5-aminolevulinic acid
Language English
License This is an open access article under the CC BY-NC-ND license.
Copyright © 2025. Published by Elsevier B.V.
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OpenAccessLink https://doaj.org/article/6a893b3c3080495384da3a4dc1b66359
PMID 40409692
PQID 3207202600
PQPubID 23479
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crossref_primary_10_1016_j_pdpdt_2025_104646
elsevier_sciencedirect_doi_10_1016_j_pdpdt_2025_104646
elsevier_clinicalkey_doi_10_1016_j_pdpdt_2025_104646
PublicationCentury 2000
PublicationDate 2025-08-01
PublicationDateYYYYMMDD 2025-08-01
PublicationDate_xml – month: 08
  year: 2025
  text: 2025-08-01
  day: 01
PublicationDecade 2020
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Photodiagnosis and photodynamic therapy
PublicationTitleAlternate Photodiagnosis Photodyn Ther
PublicationYear 2025
Publisher Elsevier B.V
Elsevier
Publisher_xml – name: Elsevier B.V
– name: Elsevier
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Snippet •The application of ketorolac tromethamine significantly relieves pain within 24 h after ALA-PDT.•Ketorolac tromethamine combined with two-step irradiation is...
Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local minimally or...
Background: Photodynamic therapy is widely used to treat condyloma acuminatum, which has the advantages of proven efficacy, low recurrence rates, and local...
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SubjectTerms 5-aminolevulinic acid
Adult
Aminolevulinic Acid - administration & dosage
Aminolevulinic Acid - therapeutic use
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Condyloma acuminatum
Condylomata Acuminata - drug therapy
Female
Humans
Ketorolac tromethamine
Ketorolac Tromethamine - administration & dosage
Ketorolac Tromethamine - therapeutic use
Male
Middle Aged
Pain
Pain Management - methods
Pain Measurement
Photochemotherapy - adverse effects
Photochemotherapy - methods
Photodynamic therapy
Photosensitizing Agents - administration & dosage
Photosensitizing Agents - adverse effects
Photosensitizing Agents - therapeutic use
Young Adult
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Title Effect of ketorolac tromethamine on pain management in patients with condyloma acuminata treated with 5-aminolevulinic acid photodynamic therapy
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