Participants with a secondary hordeolum during or after the treatment period and seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Adverse effects · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Resolution of hordeolum at short term · people with acute hordeolum
Acupuncture plus conventional treatments may leads to higher resolution of hordeolum at short term compared with conventional treatments alone (low certainty).
1 finding from 1 review
Resolution of hordeolum between 8 and 30 days after diagnosis, or that closest to 14 days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants who required surgical incision and drainage after the treatment period or seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants experiencing the occurrence of a chalazion after the treatment period or seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants experiencing the recurrence of a hordeolum within six months and one year · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants with a secondary hordeolum during or after the treatment period and seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Adverse effects · people with acute hordeolum
Acupuncture plus conventional treatments led to lower adverse effects compared with conventional treatments alone; GRADE not reported.
1 finding from 1 review
Participants who required surgical incision and drainage after the treatment period or seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants experiencing the occurrence of a chalazion after the treatment period or seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants experiencing the recurrence of a hordeolum within six months and one year · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Participants with a secondary hordeolum during or after the treatment period and seven days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Adverse effects · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Resolution of hordeolum at short term · people with acute hordeolum
Acupuncture showed no clear difference in resolution of hordeolum at short term compared with topical antibiotics plus warm compresses (low certainty).
1 finding from 1 review
Resolution of hordeolum between 8 and 30 days after diagnosis, or that closest to 14 days after diagnosis · people with acute hordeolum
The review found no eligible studies for this question.
1 finding from 1 review
Intervention not reported
Uncorrected visual acuity (UCVA) of 20/20 or better · participants aged 18‐60 years with myopia ranging in severity up to 12 diopters (D)
It is very uncertain whether the intervention changes uncorrected visual acuity (UCVA) of 20/20 or better (very low certainty).
1 finding from 1 review
RR 0.96 [0.82, 1.13]
Studies not reported
Very low
Intervention not reported
Uncorrected visual acuity (UCVA) of 20/40 or better · participants aged 18‐60 years with myopia ranging in severity up to 12 diopters (D)
It is very uncertain whether the intervention changes uncorrected visual acuity (UCVA) of 20/40 or better (very low certainty).
1 finding from 1 review
RR 0.9 [0.67, 1.21]
Studies not reported
Very low
Intervention not reported
Proportion of participants who lost two or more lines of best‐corrected visual acuity (BCVA) · participants aged 18‐60 years with myopia ranging in severity up to 12 diopters (D)
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Eyes within ± 0.5 D of target refraction · participants aged 18‐60 years with myopia ranging in severity up to 12 diopters (D)
It is very uncertain whether the intervention changes eyes within ± 0.5 D of target refraction (very low certainty).
1 finding from 1 review
RR 0.69 [0.48, 0.99]
Studies not reported
Very low