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<IndexPatientGuideline ID="x22866" Name="Guideline Statement 28" IsComponent="true" Changed="20260429T19:36:00" Created="20260427T18:18:39" Published="20260506T19:42:11" SiteBaseUrl="https://www.auanet.org" Locale="" XPowerPath="/Home/Guidelines &amp; Quality/Guidelines/Clinical Guidelines/BPH Guideline/Combination Therapy/Guideline Statement 28">
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  <Header type="string" UID="faf9fd2842b549d09e761cd943c2be20" label="Header" readonly="false" hidden="false" required="false" indexable="false" CIID="">Guideline Statement 28</Header>
  <BodyCopy type="xhtml" UID="41a2d8598c364193bbfe9ad86d7bcd3c" label="Body Copy" readonly="false" hidden="false" required="false" indexable="false" Height="" CIID="">&lt;p&gt;&lt;strong&gt;In patients with moderate to severe predominant storage LUTS, clinicians may offer beta-3 agonists alone or in combination with an AB as a treatment option. (&lt;em&gt;Conditional Recommendation; Evidence Level: Grade C&lt;/em&gt;) &lt;/strong&gt;&lt;/p&gt;</BodyCopy>
  <DiscussionLinkName type="string" UID="b364402056154f78b38cd8d663eaf3ba" label="Discussion Link Name" readonly="false" hidden="false" required="false" indexable="false" CIID="">Discussion</DiscussionLinkName>
  <DiscussionTitle type="string" UID="ceedafe4ad314b5d8d3225bc0083b81c" label="Discussion Title" readonly="false" hidden="false" required="false" indexable="false" CIID="">Discussion</DiscussionTitle>
  <DiscussionBody type="xhtml" UID="9bbbac02721d4eefba59c63ee7ff9007" label="Discussion Body" readonly="false" hidden="false" required="false" indexable="false" Height="" CIID="">&lt;p&gt;The use of beta-3 agonists in combination with ABs has emerging evidence of safety and symptomatic improvement. Vibegron, randomized to placebo, in men with LUTS/BPH with predominant storage LUTS on ABs or 5-ARIs, showed a significant improvement in urgency, frequency, and nocturia.&lt;sup&gt;205&lt;/sup&gt; Mirabegron used alone in patients with BOO did not adversely affect Q&lt;sub&gt;max&lt;/sub&gt; and detrusor pressure at Q&lt;sub&gt;max &lt;/sub&gt;compared with placebo after 12 weeks of treatment.&lt;sup&gt;206&lt;/sup&gt;&lt;/p&gt;
&lt;p&gt;One RCT (n=706) in two publications compared a beta-3 agonist combined with an AB to AB monotherapy.&lt;sup&gt;207, 208&lt;/sup&gt;&amp;nbsp;The PLUS trial enrolled men who had been taking tamsulosin for at least two months for LUTS/BPH;&amp;nbsp;almost all&amp;nbsp;had moderate or severe symptoms at baseline. Patients were randomized to add-on mirabegron or continued tamsulosin monotherapy.&amp;nbsp;At 12-weeks&amp;nbsp;follow-up, symptoms and quality of life were similar between combination therapy and monotherapy groups. Adverse event rates were similar between groups. The AUA/SUFU OAB Guideline supports the use of monotherapy with beta-3 agonists in patients with predominant storage LUTS and BPH.&lt;sup&gt;52&lt;/sup&gt;&amp;nbsp;&amp;nbsp;&lt;/p&gt;</DiscussionBody>
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