Background
Mycoplasma pneumoniae (
M. pneumoniae) is one of the most common causes of upper and lower respiratory tract infections, particularly in children and young adults. The majority of
M. pneumoniae pneumonia are benign and self-limiting disease. However, some patients may develop severe
M. pneumoniae pneumonia or refractory
M. pneumoniae pneumonia, causing progressive pneumonia or various extrapulmonary complications [
1]. These cases may be related to the occurrence of macrolide-resistant (MR)
M. pneumoniae [
2,
3]. This resistance is associated with point mutations in the V region of the 23S rRNA gene and leads to high-level resistance to macrolides [
4]. Therefore, the efficacy of macrolide treatment was shown to be lower in patients infected with macrolide-resistant isolates than in patients infected with macrolide-sensitive isolates [
5,
6].
In recent years, the global patterns in the proportion of MR
M. pneumoniae infections showed an increasing trend, and the proportion of MR
M. pneumoniae infections was highest in China [
3,
7]. Treatment with the increase in MR
M. pneumoniae has become challenging. Because this resistance may lead to more extrapulmonary complications and severe clinical features [
2], alternative antibiotic treatment can be required, including tetracyclines or fluoroquinolones. To date, no tetracycline resistance has been reported in
M. pneumoniae clinical isolates. In vitro antimicrobial susceptibility testing showed that
M. pneumoniae in all cases was sensitive to tetracyclines, including doxycycline and minocycline [
8].
MR
M. pneumoniae pneumonia is characterized by an excessive immune response against the pathogen as well as direct injury caused by an increasing
M. pneumoniae load [
9]. Study indicates that children with higher
M. pneumoniae abundance in the bronchoalveolar lavage fluid tend to have a longer hospital stay and higher fever peak [
10]. This suggests that the loading of
M. pneumoniae is associated with clinical severity [
11]. Doxycycline, as an alternative drug for treating MR
M. pneumoniae, can inhibit the replication of
M. pneumoniae DNA and reduce the load of pulmonary pathogens [
12]. However, the exact timing of doxycycline treatment has not been established at present. In this study, we aimed to evaluate the efficacy of doxycycline therapy for macrolide-resistant Mycoplasma pneumoniae pneumonia in children at different periods.
Materials and methods
Study subjects
We retrospectively reviewed the medical records of children without prior underlying diseases with Community acquired pneumonia hospitalized at the Ningbo Medical Center Lihuili Hospital between May 2019 and August 2022. All the evaluated patients had signs and symptoms indicative of pneumonia, such as fever, cough, and abnormal chest radiographic findings compatible with pneumonia [
13]. The
M. pneumoniae infection was determined by polymerase chain reaction test of nasopharyngeal aspirates obtained from the patients on admission. Samples positive for
M. pneumoniae were subjected to direct DNA sequencing of the domain V of the 23S rRNA gene to identify A2063G or A2064G mutation site using real-time fluorescent PCR assay kit (Jiangsu Mole Bioscience Co., Ltd, China) in accordance with the manufacturer’s instructions. It took about 2 days to determine whether there is a resistance mutation.
Exclusion criteria were as follow: (1) other pathogens were found before treatment, including bacteria, respiratory syncytial virus, influenza viruses, parainfluenza viruses, coronaviruses, human rhinoviruses, adenoviruses, human metapneumovirus and chlamydia pneumoniae; (2) patients who had been started on treatment for macrolide or doxycycline prior to admission; (3) children who have chronic disease (such as tuberculosis, asthma and immunodeficiency) states predisposing them to recurrent lung infections; (4) discharge within 48 h after enrollment and insufficient data; (5) children younger than 8 years were excluded because they could not be treated with doxycycline.
Methods
In our study, all patients were treated with intravenous azithromycin or oral doxycycline. The dosage of intravenous azithromycin was 10 mg/kg once daily, and oral doxycycline was administered once every 12 h at doses of 2.2 mg/kg, in accordance with the package insert accompanying each drug [
13]. The primary antibiotic selection was made by the attending pediatrician. Oral doxycycline should be used if the patient had a history of exposure to MR
M. pneumoniae. The preferred treatment for
M. pneumoniae pneumonia is macrocyclic antibiotics [
13]. Therefore, before the results of pathogen and
M. pneumoniae mutation site testing are available, intravenous azithromycin was chosen as the primary antibiotic for patients with suspected
M. pneumoniae pneumonia. After obtaining evidence of MR
M. pneumoniae infection, some patients were changed from intravenous azithromycin to oral doxycycline, while others continued treatment with intravenous azithromycin due to inability to tolerate swallowing capsules. According to treatment, these patients were divided into three groups: oral doxycycline treatment alone (DOX group), changed from intravenous azithromycin to oral doxycycline (ATD group) and intravenous azithromycin treatment alone (AZI group). ATD group cases were separated into two sub-groups: intravenous azithromycin treatment<3 days (ATD1 group) and intravenous azithromycin treatment ≥ 3 days (ATD2 group).
Data collection
Clinical information was retrospectively collected from the medical records of the patients. The collected data included demographics, hospitalization period, duration of fever (febrile days before macrolide or doxycycline treatment, febrile days after treatment, time to defervescence), laboratory results upon admission, chest radiographic findings and adverse reactions during treatment. The duration of fever was defined as the number of days for which the patient had a body temperature of ≥ 38℃ with an interval of <24 h between each episode of fever. Defervescence of fever was defined as a decline in body temperature up to < 37.5℃ for > 48 h. All patients underwent chest radiographic examination before admission, and a second chest radiographic examination was performed 7 to 10 days after treatment. The chest radiographic findings were from the records read by two radiologists and classified according to the presence of consolidation lobar, patchy and effusion. If the results of the patient’s X-rays showed that reduction of more than 30% in consolidation and infiltration area compared to before treatment, we consider the patient to be a consolidation and/or infiltration absorption case.
Statistical analysis
SPSS 25.0 statistical software was applied for Propensity score matching (PSM) and analysis. The data were expressed as median (IQR) for continuous variables or as number of cases (percentage) of a specific group for categorical variables. The Kruskal-Wallis test was used for continuous variables. If the variables were statistically significant when compared among more than two groups, they were further analyzed by Mann-Whitney U test for comparing two groups. The Pearson’s Chi-squared or Fisher’s exact test were used for categorical variables. To reduce the effect of possible selective bias, patients in the DOX + ATD1 and ATD2 groups, were matched with those in non-biopsy group for a 1:1 PSM with a caliper value of 0.02. Matching factors included age, gender, fever duration prior to treatment, and chest radiographic before admission. Two-sided p-value < 0.05 was considered to be statistically significant.
Discussion
The incidence of MR
M. pneumoniae has recently increased and has been related to life-threatening or refractory
M. pneumoniae pneumonia in children [
14]. Since the emergence of macrolide resistance has been reported mainly in Asia [
7,
15], prevalence of MR
M. pneumoniae isolated in pediatric patients has increased annually in China [
16]: 88.19% in 2016, 90.93% in 2017, 90.56% in 2018 and 92.90% in 2019. In this study, the total number of
M. pneumoniae pneumonia was 533 cases between May 2019 to August 2022, and 72% (384/533) were MR
M. pneumoniae pneumonia. The prevalence of MR
M. pneumoniae was similar to the data reported, and peaked in 2019 during the study period. There was an uneven distribution among cases in the 2019–2022, which was related to the COVID-19 pandemic. Since January 2020, in response to various public health policies to control the spread of COVID-19 in the pandemic, there was a substantial decrease in respiratory infections in China and many resources were focused on diagnosis and management of COVID-19. During the COVID-19 pandemic, our study also showed an increase in MR
M. pneumoniae infection rates in 2022. The increasing prevalence of MR
M. pneumoniae has become a significant clinical issue in the pediatric patients. Treatment of MR
M. pneumoniae pneumonia in children has become challenging.
M. pneumoniae lacks cell wall and consequently is resistant to beta-lactams and to all antimicrobials targeting the cell wall [
17]. This mycoplasma is intrinsically susceptible to antibiotics that act on the bacterial ribosome and inhibit protein synthesis such as macrolides or tetracyclines or agents that inhibit DNA replication such as fluoroquinolones [
18,
19]. MR
M. pneumoniae is caused by mutations in domain V of the 23s rRNA gene that interfere with the binding of macrolides to rRNA [
15]. A-to-G transition mutation at position 2063 in 23S rRNA genes is the most prevalent in MR
M. pneumoniae isolates, and it is closely followed by the A2064G mutation [
2,
3]. Both mutations can cause high-level resistance to erythromycin and azithromycin in
M. pneumoniae [
20]. This suggests that macrolide may have limited effects on MR
M. pneumoniae infection. Therefore, in cases of MR
M. pneumoniae strains, alternative antibiotic treatment can be required, including tetracyclines such as doxycycline and minocycline [
21,
22]. To date, no tetracycline resistance has been reported in
M. pneumoniae clinical isolates. Doxycycline has good activity against both macrolide-susceptible and macrolide-resistant strains [
22,
23]. As expected, our study found that doxycycline regimens were shown to be more effective than macrolide regimens in patients infected by MR
M. pneumoniae. The duration of fever and hospitalization were significantly longer in patients with macrolide regimens. Compared to intravenous azithromycin treatment, oral doxycycline is more acceptable to children. Therefore, oral doxycycline is likely to be a better treatment of MR
M. pneumoniae infections than macrolide for children above the age of 8 years.
The occurrence of MR
M. pneumoniae infections was likely to lead to treatment failure, which translates into a longer duration of therapy, persistent cough and increased time to resolution of fever compared with treatment-susceptible infection, both in children and in adults [
6,
24]. For the treatment of MR
M. pneumoniae pneumonia presenting clinical and radiological deterioration, adjunctive systemic corticosteroids are sometimes used [
25]. However, too early use large doses corticosteroids could cause suppression of phagocytic function of alveolar macrophages and neutrophils, decrease mobilization of inflammatory cells into areas of infection, and cause changes in antigen presentation and lymphocyte mobilization [
26]. In addition, corticosteroids did not significantly decrease the DNA load of
M. pneumoniae in bronchoalveolar lavage fluid [
27]. Therefore, untimely corticosteroid additional therapy may increase the risk of mixed infection and they may contribute to condition aggravation [
26]. Tetracyclines can inhibit peptide chain lengthening of protein synthesis by acting on the 30 S subunit of
M. pneumoniae ribosomes. Estimated
M. pneumoniae amounts after 3 days clearly decreased from 10
6 copies/mL to 5 × 10
2 copies/mL in those receiving doxycycline [
12]. That indicates doxycycline could decrease the DNA load of
M. pneumoniae. As indicated by our results in, defervescence occurred within 72 h after initiation of doxycycline (66.7%), with poorer results using azithromycin (ATD1 46.7% and ATD2 30%, respectively). However, when doxycycline was administered within 3 days after azithromycin agents, almost 86.7% of patients showed defervescence within 96 h. Because the inflammatory indicators of our study subjects (such as white blood cells, CRP, LDH, etc.) are usually normal or slightly elevated in the early stages, only a very small number of patients have these inflammatory indicators rechecked after treatment. To avoid selection bias, these indicators were not used as evaluation indicators for efficacy. Due to its ability to inhibit virus replication and reduce viral load, patients receiving oral doxycycline treatment in the early stages can quickly improve clinical symptoms and promote the absorption of pulmonary inflammation. This resulted in a significantly lower number of patients using glucocorticoids as adjunctive therapy in the doxycycline group compared to the azithromycin group. Therefore, clinicians should be vigilant for macrolide treatment failure and consider using alternative drugs if symptoms persist or if there are signs of clinical deteriorations.
Tetracyclines are generally well tolerated, with common adverse reactions observed in patients receiving these agents including anorexia, nausea, vomiting, diarrhea, rash, photosensitivity, tooth discoloration [
18,
28]. Most concerning side effect is permanent tooth discoloration. The affinity for mineralizing tissue leads to incorporation into calcifying tissues [
29]. However, due to a low affinity for calcium of doxycycline [
30], there is no or only negligible tooth staining, even in young children aged 2–8 years [
31,
32]. Factors related to tooth discoloration are dosage, duration of treatment, stage of tooth mineralization, and activity of the mineralization process [
33]. In our study, oral doxycycline treatment lengths usually range between 7 and 10 days. No adverse reactions associated with doxycycline was observed during treatment. Further studies were needed to evaluate the adverse effects of doxycycline.
This study has some limitations. The first limitation was its retrospective design, which had the potential to introduce memory bias and led to missing data, most notably for assessment of disease severity. Secondly, due to the limitations of the duration of this study, we collected all the qualified children rather than calculated the sample size in the study period. Therefore, it might lead to selective bias. Finally, all research subjects come from one center with limited sample size. Although the PSM method can deal with the issue of selection bias, the small sample size after matching may lead to less objective and complete display of data features. In the future, it is necessary to carry out prospective randomized studies or to conduct studies involving more subjects through multicenter studies.
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