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ISSN 2096-2738 CN 11-9370/R
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Electronic Journal of Emerging Infectious Diseases ›› 2022, Vol. 7 ›› Issue (3): 27-31.doi: 10.19871/j.cnki.xfcrbzz.2022.03.006

• Original Articles • Previous Articles     Next Articles

Analysis of the clinical effect of ambroxol hydrochloride on the treatment of COVID-19

Li Li1, Zhang Xin2, Dai Muwei3, Zheng Huanwei4, Kang Haiyan4, Xu Yi5, Hu Qian4, Yang Li5, Gao Huixia5, Wang Yuling6, Jiang Ping6, Dai Erhei5   

  1. 1. Intensive care unit, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China;
    2. Department of Tuberculosis, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China;
    3. Department of Orthopaedic, The Fourth Hospital of Hebei Medical University and Hebei Cancer Hospital, Shijiazhuang 050019, China;
    4. Department of Infectious Disease, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China;
    5. Department of Laboratory Medicine, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China;
    6. Department of Internal Medicine, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China
  • Received:2022-02-24 Online:2022-07-31 Published:2022-09-08

Abstract: Objective To observe the clinical efficacy and safety of ambroxol hydrochloride on the treatment of Coronavirus disease 2019(COVID-19). Method A total of 68 patients with COVID-19 hospitalized in the Fifth Hospital of Shijiazhuang from January to June 2020 were selected and divided into control group and observation group, with 34 cases in each group. Both observation group and control group were given interferon-α5 million U, atomized, twice a day; arbidol 0.2g, orally, 3 times/d, for 10d. Observation group was treated with ambroxol hydrochloride glucose injection (30 mg, twice a day, iv drip) on the basis of conventional treatment for 2 weeks. The clinical efficacy, changes in serum inflammatory indexes and the incidence of adverse drug reactions were compared between the two groups. Result The total effective rate of observation group (85.3%) was significantly higher than that in the control group (70.6%) (P<0.05). The clinical symptoms improvement time, pulmonary imaging improvement time and hospitalization time in the observation group were shorter than those in the control group, but the differences were not statistically significant (P>0.05). The levels of serum PCT and CRP in the observation group were significantly lower after treatment than before (P<0.05), leukocyte count and lymphocyte count were significantly higher than those before treatment (P<0.05). In the control group the CRP level after treatment was significantly lower than that before treatment (P<0.05), the leukocyte count and lymphocyte count were significantly higher than those before treatment (P<0.05), but there was no significant difference in PCT level before and after treatment (P>0.05). There was no adverse reaction in the observation group and the control group during the treatment period. Conclusion Ambroxol hydrochloride treatment for COVID-19 patients can promote the remission of clinical symptoms and absorption of pulmonary lesions, and reduce inflammatory response, which is worthy of popularization and application.

Key words: Severe acute respiratory syndrome coronavirus 2, Pneumonia, Ambroxol, Clinical effect, C-reactive protein, Procalcitonin