Acupuncture for Persistent Allergic Rhinitis: a Randomised, Sham-Controlled Trial

Objective To investigate the effectiveness and safety of acupuncture in persistent allergic rhinitis (PAR). Design Randomised, single-blind, sham-controlled trial conducted from May 2004 to February 2005. Participants and intervention 80 patients with PAR (age, 16–70 years) were randomly assigned to...

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Veröffentlicht in:Deutsche Zeitschrift für Akupunktur (Heidelberg, Germany : 1977) Germany : 1977), 2008-07, Vol.51 (2), p.45-46
Hauptverfasser: Xue, Charlie C. L., An, Xuedong, Cheung, Thomas P., Da Costa, Cliff, Lenon, George B., Thien, Frank C., Story, David F., Brinkhaus, Benno
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container_end_page 46
container_issue 2
container_start_page 45
container_title Deutsche Zeitschrift für Akupunktur (Heidelberg, Germany : 1977)
container_volume 51
creator Xue, Charlie C. L.
An, Xuedong
Cheung, Thomas P.
Da Costa, Cliff
Lenon, George B.
Thien, Frank C.
Story, David F.
Brinkhaus, Benno
description Objective To investigate the effectiveness and safety of acupuncture in persistent allergic rhinitis (PAR). Design Randomised, single-blind, sham-controlled trial conducted from May 2004 to February 2005. Participants and intervention 80 patients with PAR (age, 16–70 years) were randomly assigned to receive real or sham acupuncture. After a 1-week baseline period, participants were tre ated twice weekly for 8 weeks and followed up for another 12 weeks. Main outcome measures Nasal obstruction, sneezing, rhinorrhoea and nasal itch were each self-assessed daily on a 5-point scale, and scores were aggregated weekly. The sum of the symptom scores (total nasal symptom score, TNSS) was also determined. A secondary outcome was use of PAR relief medication. Results After 8 weeks’ treatment, the weekly mean difference in TNSS from baseline was greater with real (−17.2; 95 % CI, −24.6 to −9.8) than with sham acupuncture (−4.2; 95 % CI, −11.0 to 2.7) (P = 0.01). The decrease in individual symptom score was also greater with real acupuncture for rhinorrhoea (P < 0.01) but not the other symptoms. At the end of follow-up, the greater difference in TNSS from baseline in the real acupuncture group was still apparent: real, −21.0 (95 % CI, −29.1 to −12.9) versus sham, −2.3 (95 % CI, −10.2 to 5.6) (P = 0.001). Moreover, the differences from baseline in all four individual symptom scores were greater for the real than for the sham group (P < 0.05). Real and sham acupuncture were both well tolerated. Conclusion Our findings suggest that acupuncture is effective in the symptomatic treatment of PAR.
doi_str_mv 10.1016/j.dza.2008.04.003
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L. ; An, Xuedong ; Cheung, Thomas P. ; Da Costa, Cliff ; Lenon, George B. ; Thien, Frank C. ; Story, David F. ; Brinkhaus, Benno</creator><creatorcontrib>Xue, Charlie C. L. ; An, Xuedong ; Cheung, Thomas P. ; Da Costa, Cliff ; Lenon, George B. ; Thien, Frank C. ; Story, David F. ; Brinkhaus, Benno</creatorcontrib><description>Objective To investigate the effectiveness and safety of acupuncture in persistent allergic rhinitis (PAR). Design Randomised, single-blind, sham-controlled trial conducted from May 2004 to February 2005. Participants and intervention 80 patients with PAR (age, 16–70 years) were randomly assigned to receive real or sham acupuncture. After a 1-week baseline period, participants were tre ated twice weekly for 8 weeks and followed up for another 12 weeks. Main outcome measures Nasal obstruction, sneezing, rhinorrhoea and nasal itch were each self-assessed daily on a 5-point scale, and scores were aggregated weekly. The sum of the symptom scores (total nasal symptom score, TNSS) was also determined. A secondary outcome was use of PAR relief medication. Results After 8 weeks’ treatment, the weekly mean difference in TNSS from baseline was greater with real (−17.2; 95 % CI, −24.6 to −9.8) than with sham acupuncture (−4.2; 95 % CI, −11.0 to 2.7) (P = 0.01). The decrease in individual symptom score was also greater with real acupuncture for rhinorrhoea (P &lt; 0.01) but not the other symptoms. At the end of follow-up, the greater difference in TNSS from baseline in the real acupuncture group was still apparent: real, −21.0 (95 % CI, −29.1 to −12.9) versus sham, −2.3 (95 % CI, −10.2 to 5.6) (P = 0.001). Moreover, the differences from baseline in all four individual symptom scores were greater for the real than for the sham group (P &lt; 0.05). Real and sham acupuncture were both well tolerated. 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After a 1-week baseline period, participants were tre ated twice weekly for 8 weeks and followed up for another 12 weeks. Main outcome measures Nasal obstruction, sneezing, rhinorrhoea and nasal itch were each self-assessed daily on a 5-point scale, and scores were aggregated weekly. The sum of the symptom scores (total nasal symptom score, TNSS) was also determined. A secondary outcome was use of PAR relief medication. Results After 8 weeks’ treatment, the weekly mean difference in TNSS from baseline was greater with real (−17.2; 95 % CI, −24.6 to −9.8) than with sham acupuncture (−4.2; 95 % CI, −11.0 to 2.7) (P = 0.01). The decrease in individual symptom score was also greater with real acupuncture for rhinorrhoea (P &lt; 0.01) but not the other symptoms. At the end of follow-up, the greater difference in TNSS from baseline in the real acupuncture group was still apparent: real, −21.0 (95 % CI, −29.1 to −12.9) versus sham, −2.3 (95 % CI, −10.2 to 5.6) (P = 0.001). 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L.</creatorcontrib><creatorcontrib>An, Xuedong</creatorcontrib><creatorcontrib>Cheung, Thomas P.</creatorcontrib><creatorcontrib>Da Costa, Cliff</creatorcontrib><creatorcontrib>Lenon, George B.</creatorcontrib><creatorcontrib>Thien, Frank C.</creatorcontrib><creatorcontrib>Story, David F.</creatorcontrib><creatorcontrib>Brinkhaus, Benno</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Deutsche Zeitschrift für Akupunktur (Heidelberg, Germany : 1977)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xue, Charlie C. L.</au><au>An, Xuedong</au><au>Cheung, Thomas P.</au><au>Da Costa, Cliff</au><au>Lenon, George B.</au><au>Thien, Frank C.</au><au>Story, David F.</au><au>Brinkhaus, Benno</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acupuncture for Persistent Allergic Rhinitis: a Randomised, Sham-Controlled Trial</atitle><jtitle>Deutsche Zeitschrift für Akupunktur (Heidelberg, Germany : 1977)</jtitle><stitle>Dtsch Z Akupunkt</stitle><date>2008-07-02</date><risdate>2008</risdate><volume>51</volume><issue>2</issue><spage>45</spage><epage>46</epage><pages>45-46</pages><issn>0415-6412</issn><eissn>1439-4359</eissn><abstract>Objective To investigate the effectiveness and safety of acupuncture in persistent allergic rhinitis (PAR). Design Randomised, single-blind, sham-controlled trial conducted from May 2004 to February 2005. Participants and intervention 80 patients with PAR (age, 16–70 years) were randomly assigned to receive real or sham acupuncture. After a 1-week baseline period, participants were tre ated twice weekly for 8 weeks and followed up for another 12 weeks. Main outcome measures Nasal obstruction, sneezing, rhinorrhoea and nasal itch were each self-assessed daily on a 5-point scale, and scores were aggregated weekly. The sum of the symptom scores (total nasal symptom score, TNSS) was also determined. A secondary outcome was use of PAR relief medication. Results After 8 weeks’ treatment, the weekly mean difference in TNSS from baseline was greater with real (−17.2; 95 % CI, −24.6 to −9.8) than with sham acupuncture (−4.2; 95 % CI, −11.0 to 2.7) (P = 0.01). The decrease in individual symptom score was also greater with real acupuncture for rhinorrhoea (P &lt; 0.01) but not the other symptoms. At the end of follow-up, the greater difference in TNSS from baseline in the real acupuncture group was still apparent: real, −21.0 (95 % CI, −29.1 to −12.9) versus sham, −2.3 (95 % CI, −10.2 to 5.6) (P = 0.001). Moreover, the differences from baseline in all four individual symptom scores were greater for the real than for the sham group (P &lt; 0.05). Real and sham acupuncture were both well tolerated. Conclusion Our findings suggest that acupuncture is effective in the symptomatic treatment of PAR.</abstract><cop>Heidelberg</cop><pub>Springer Medizin</pub><doi>10.1016/j.dza.2008.04.003</doi><tpages>2</tpages></addata></record>
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subjects Acupuncture
Complementary & Alternative Medicine
Hay fever
Journal Club
Medicine
Medicine & Public Health
Pain Medicine
Rhinitis
title Acupuncture for Persistent Allergic Rhinitis: a Randomised, Sham-Controlled Trial
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