Benzylpenicillin versus wide-spectrum beta-lactam antibiotics as empirical treatment of Haemophilus influenzae-associated lower respiratory tract infections in adults; a retrospective propensity score-matched study
verfasst von:
John Thegerström, Viktor Månsson, Kristian Riesbeck, Fredrik Resman
There is consensus that definitive therapy for infections with H. influenzae should include antimicrobial agents with clinical breakpoints against the bacterium. In Scandinavia, benzylpenicillin is the recommended empirical treatment for community-acquired pneumonia (CAP) except in very severe cases. However, the effect of benzylpenicillin on H. influenzae infections has been debated. The aim of this study was to compare the outcomes of patients given benzylpenicillin with patients given wide-spectrum beta-lactams (WSBL) as empirical treatment of lower respiratory tract H. influenzae infections requiring hospital care. We identified 481 adults hospitalized with lower respiratory tract infection by H. influenzae, bacteremic and non-bacteremic. Overall, 30-day mortality was 9% (42/481). Thirty-day mortality, 30-day readmission rates, and early clinical response rates were compared in patients receiving benzylpenicillin (n = 199) and a WSBL (n = 213) as empirical monotherapy. After adjusting for potential confounders, empirical benzylpenicillin treatment was not associated with higher 30-day mortality neither in a multivariate logistic regression (aOR 2.03 for WSBL compared to benzylpenicillin, 95% CI 0.91–4.50, p = 0.082), nor in a propensity score-matched analysis (aOR 2.14, 95% CI 0.93–4.92, p = 0.075). Readmission rates did not significantly differ between the study groups, but early clinical response rates were significantly higher in the WSBL group (aOR 2.28, 95% CI 1.21–4.31, p = 0.011), albeit still high in both groups (84 vs 81%). In conclusion, despite early clinical response rates being slightly lower for benzylpenicillin compared to WSBL, we found no support for increased mortality or readmission rates in patients empirically treated with benzylpenicillin for lower respiratory tract infections by H. influenzae.
Introduction
Haemophilus influenzae is considered the second most common bacterial cause of community-acquired pneumonia (CAP) after Streptococcus pneumoniae [1]. Surveillance data have suggested an increased incidence of invasive infections with H. influenzae in recent years, and since the introduction of capsule type b polysaccharide conjugate vaccines, non-encapsulated strains (NTHi) dominate, followed by capsule type f [2‐4]. This has led to a shift in the clinical epidemiology of severe H. influenzae infections, as most cases now present as pneumonia in older adults or patients with comorbidities, most notably chronic obstructive pulmonary disease (COPD) [2, 3, 5]. With the widespread introduction of conjugated pneumococcal vaccines, there is also concern that the proportion of CAP caused by H. influenzae may increase [6]. Although this has yet to be confirmed, one recent study from Great Britain using molecular diagnostics showed it to be the most common agent in CAP, contributing to 40% of cases [7].
In Scandinavian countries, high-dose benzylpenicillin (PcG) is still recommended as the empirical treatment for patients with CAP requiring hospitalization, with the exception of patients with immunosuppression or very severe presentation (CRB-65 > 2 or concomitant severe sepsis [8]). There is a long tradition of benzylpenicillin treatment in Scandinavia, which remains effective against the majority of pneumococci and has limited collateral ecological effects compared to other empirical alternatives [9].
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The activity of benzylpenicillin against H. influenzae has been debated. Recommendations are based mainly on clinical experience combined with theoretical assumptions from PK/PD simulations and time-killing experiments [10]. The European Committee on Antimicrobial Susceptibility Testing (EUCAST) has not defined clinical breakpoints for benzylpenicillin, referring to insufficient evidence from clinical studies [11]. Moreover, in recent years, the proportion of H. influenzae isolates with reduced susceptibility to aminopenicillins due to alterations in penicillin-binding protein 3 (termed rPBP3) has increased, reaching 10–20% [12, 13]. In addition, a stable proportion (an additional 10–20%) of isolates expresses beta-lactamases [14, 15]. Both of these resistance mechanisms are likely to increase the risk of treatment failure with use of empirical benzylpenicillin. The increase of these resistance mechanisms may make benzylpenicillin a less viable option in the case of H. influenzae CAP. One recent retrospective study from Denmark showed a significantly higher 30-day mortality for patients receiving benzylpenicillin as definitive treatment for H. influenzae bacteremia, compared to those who received cephalosporins or aminopenicillins [16].
Considering the proposed increase in the proportion of H. influenzae as a cause of CAP and the current empirical treatment recommendation of benzylpenicillin, there is a need to assess the outcome of empirical benzylpenicillin treatment in cases of lower respiratory tract infection by H. influenzae. The primary objective of this study was to compare the 30-day mortality between adults who had received benzylpenicillin as empirical treatment for H. influenzae lower respiratory tract infections (with or without bacteremia) requiring hospital care with individuals who had received empirical treatment with wide-spectrum beta-lactams (WSBL). As secondary objectives, 30-day readmission rates and estimations of early clinical response were compared between the two groups.
Materials and methods
Study population and setting
Patients with positive cultures of H. influenzae were identified at the clinical microbiology laboratories in Malmö and Lund, Sweden. The catchment area of these laboratories corresponds to Skåne county in southern Sweden (adult population of 1,045,792 in 2016 [17]), and healthcare was provided by Skåne University Hospital and surrounding regional hospitals. All blood and respiratory tract cultures sampled in the catchment area were analyzed in these two laboratories.
Case definitions and exclusion criteria
Two case definitions were applied: (1) bacteremia with H. influenzae in an individual ≥ 18 years of age 1997–2016 with a lower respiratory tract infection or (2) pure culture of H. influenzae from a respiratory tract sample in an individual hospitalized due to a lower respiratory tract infection 2015–2016.
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Patients aged ≥ 18 years with positive blood cultures of H. influenzae between 1997 and 2016 were identified through the laboratories’ records. All individuals with positive blood cultures were included in the study if they had a concurrent respiratory tract infection, except for those with epiglottitis (in which the recommended treatment in the area is cefotaxim). Recurrent episodes of bacteremia were only recorded once.
Individuals above 18 years of age with positive cultures from sputum or nasopharynx in Skåne county in 2015–2016 were also identified. All individuals with positive cultures were included in the study if (1) they were admitted more than 24 h to a hospital ward due to a lower respiratory tract infection, (2) no other respiratory tract pathogen (see below) was present in any microbiological sample, (3) they had been diagnosed with lower respiratory tract infection (pneumonia or COPD exacerbation) at discharge from hospital, and (4) no alternative foci of infection were identified except the lower respiratory tract.
In cultures from sputum and nasopharyngeal swabs, concurrent growth of Streptococcus pneumoniae, beta-haemolytic streptococci and Moraxella catharrhalis were regularly sought for, and if any of these pathogens were identified in a culture, the patient was excluded. If a respiratory tract sample indicated the presence of influenza virus, respiratory syncytial virus, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Chlamydia psittaci, Legionella pneumophila, or Pneumocystis jirovecii through polymerase chain reaction (PCR), the patient was excluded. Finally, patients were excluded if the presence of Streptococcus pneumoniae or Legionella pneumophila was demonstrated by urine antigen detection tests.
Microbiological methods and antimicrobial susceptibility testing
All blood samples were cultured using the automated BacTAlert system (bioMérieux, Marcy l’Etoile, France) (1997–December 2014) or the BACTEC system (BD diagnostic systems, Sparks, MD) (December 2014–2016). Respiratory tract specimens from sputum and nasopharyngeal swabs were cultured using standard microbiological techniques. Isolates were identified by typical colony morphology on agar plates, through standard biochemical tests and by MALDI Biotyper analysis (Bruker Daltonics, Bremen, Germany). Capsule typing was performed by PCR for H. influenzae isolated from blood. Isolates from respiratory tract samples were not routinely capsule typed and were not saved (and thus not available for capsule typing at the time of the study).
Antimicrobial susceptibility testing was performed according to local laboratory guidelines until 2009, and thereafter according to the EUCAST algorithm [18], which is based upon a disk diffusion screen of 1 U benzylpenicillin on fastidious Mueller Hinton solid medium (MH-F) for identification of beta-lactam resistance. Beta-lactamase production was confirmed by a standard nitrocefin assay in screening-positive cases. Gradient tests (Etest, bioMérieux, Marcy l’Etoile, France) were used to determine the actual MICs of beta-lactam agents if the first disk diffusion screen was positive. Data on antimicrobial susceptibility, including beta-lactam resistance by rPBP3 and beta-lactamase production, were obtained from laboratory records.
Clinical definitions
The following clinical descriptive patient data were recorded from hospital medical records: age, sex, immunosuppression, and comorbidities according to Charlson/Deyo comorbidity index [19]. The study definition of immunosuppression was ongoing primary immune deficiency or immunosuppressive therapy not denoted in the Charlson/Deyo comorbidity index, in order to avoid overfitting in the statistical analysis. Regarding the presenting infection, the following was recorded in addition to the antibiotic treatment strategy: sepsis severity score (SCCM/ESICM/ACCP/ATS/SIS criteria [20]), the maximal concentration of C-reactive protein during hospitalization, the CRB-65 score, and admittance to an intensive care unit. The following was recorded regarding the outcome of the infection: all-cause 30-day mortality, readmission to hospital within 30 days from discharge, and early clinical response. Early clinical response was defined as no signs of fever, tachycardia, hypotension, hypoxemia, or tachypnea on day 4 following admission, according to FDA criteria [21]. Since complete data on all parameters by day 4 were not always available, they were complemented by an evaluation of whether a substantial general improvement of the patient’s condition had occurred by day 4.
Patients were sorted into three groups according to type of empirical antibiotic therapy: (1) patients receiving intravenous (i.v.) benzylpenicillin as empirical therapy, (2) patients receiving any other i.v. beta-lactam agent with clinical breakpoints against H. influenzae, and (3) patients receiving other empirical treatment regimens. Empirical treatment was defined as the initial antibiotic agent the patient received upon admittance, prior to culture results. Clinical outcomes were compared between groups 1 and 2. In the multivariate regressions and propensity score-matched analyses, all patients who received concomitant empirical therapy with another antibiotic active against H. influenzae (fluoroquinolone, tetracycline, aminoglycoside) were excluded.
Statistical analysis
Data were analyzed using Stata 14 (StataCorp, College Station, TX) and SPSS statistics version 24 (IBM, Armonk, NY). The results were expressed as counts and percentages for categorical variables and as medians and interquartile ranges for continuous variables. Comparisons of baseline statistics between the empirical treatment groups were assessed using Chi2-test for categorical variables, the Mann-Whitney U test or the Kruskal-Wallis test for continuous variables. P values ≤ 0.05 were considered statistically significant. Univariate logistic regressions were performed to establish associations between outcomes (30-day all-cause mortality, 30-day readmission, and early clinical response) and collected predictors as well as covariates.
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Multivariate logistic regression models were fitted for the defined outcomes. The main predictor was empirical antibiotic treatment (benzylpenicillin monotherapy versus i.v. WSBL monotherapy). Considering the relatively low number of outcomes, to avoid over-fitting, all multivariate models were fitted using the purposeful selection algorithm [22]. Briefly, the main predictor and all covariates with a p value of < 0.2 in the univariate analysis were included in a crude model. The least significant covariate was step-wise removed from the model, unless the removal changed the adjusted odds ratios by more than 20%, until only significant and strongly influential covariates remained. A separate analysis was performed for 30-day mortality on only bacteremic patients.
A propensity score-matched analysis was performed to assess the effect of the two empirical treatment groups on 30-day mortality, 30-day readmission, and early clinical response. Propensity scores were calculated in a logistic regression using the treatment group as outcome. The following variables were used as covariates in this regression: age (categorized), sex, ICU-care, maximum CRP, CCI, bacteremia, immune suppression, and sepsis severity score. A 1–1 nearest neighbor matching without replacement was performed using the psmatch2 module [23], with a caliper of 0.2. The propensity scores were plotted graphically to verify spread and overlap, and balance in the covariates in the matched cohort was verified (Table 5). Finally, the associations between treatment and outcomes in the matched cohort were assessed in two ways, with full-cohort logistic regression as well as conditional logistic regression on matched pairs. In all analyses, assessments were made only on individuals with complete outcome data for the respective outcome.
The potential effect modification of beta-lactamase production and rPBP3 on the associations between treatment group and outcomes was investigated by stratifying the outcomes per treatment group and resistance mechanism in the propensity-matched cohort and comparing the odds ratios within each strata, including estimation of the beta-coefficient, 95% confidence interval, and p value for the respective interaction term in logistic regressions.
Results
A total of 214 unique episodes of bacteremia with H. influenzae were identified in the catchment area between 1997 and 2016. Of these, 140 individuals had a lower respiratory tract infection (the vast majority had CAP, n = 135, 96%). In addition, a total of 613 unique adult patients had growth of H. influenzae in sputum or nasopharyngeal swabs taken at an emergency department in the catchment area between 2015 and 2016. Of these, 419 were admitted to a hospital ward for more than 24 h. A total of 341 of these patients had been diagnosed with a lower respiratory tract infection (the vast majority were CAP), while at the same time not meeting any of the defined microbiological exclusion criteria. Thus, in total 481 individual cases were included for further analysis (Fig. 1; Appendix Table 6).
Fig. 1
Cases included in the study. Flowchart summarizing the number of included and excluded patients in the study as well as the reason for exclusion. Hi = Haemophilus influenzae. a, bSee appendix Table 6 for diagnosis of the excluded patients. cSee appendix Table 7 for the specific antibiotic agents administered in the different groups
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Descriptive and demographic characteristics of the crude study population
Out of the 481 included patients, 281 (58%) were women. The median age was 75 years (interquartile range (IQR), 66–84). A total of 25 patients (5.2%) met the study criteria of immunosuppression, while the median Charlson comorbidity index (CCI), unadjusted for age, was 2 (IQR 1–3). One out of four patients in the study (n = 120) had COPD. The most commonly confirmed diagnosis was pneumonia (n = 418, 87%) followed by COPD exacerbation (n = 39, 8%). A total of 55 patients (12%) had severe sepsis or septic shock upon admission, whereas 30 (6%) had a CRB-65 score of > 2. The median CRP level was 237 mg/L (IQR 157–318 mg/L), and 21 individuals (4%) were admitted to an ICU. In total, 108 isolates (23%) were screening positive for beta-lactam resistance through rPBP3 in screening, and 65 (14%) were beta-lactamase positive.
Forty-two individuals died within 30 days after cultures were being taken, resulting in an all-cause 30-day mortality of 9%. The 30-day mortality in patients with concurrent bacteremia was 12% (n = 17) and among patients with growth of H. influenzae exclusively in respiratory tract samples 7% (n = 25). The readmission rate 30 days after discharge was 15% (n = 72) for the whole study cohort, whereas 77 patients (16%) failed to meet the criteria of early clinical response on day 4.
Patients were sorted into three groups depending on which empiric antibiotic regimen they had been given. The first group comprised all patients treated with benzylpenicillin (n = 212, 44%), the second group all patients treated with a WSBL antibiotic (total n = 230, 48%; cefotaxim (n = 175), piperacillin-tazobactam (n = 20), cefuroxime (n = 16), imipenem-cilastatin (n = 8), meropenem (n = 8), ampicillin (n = 2), ceftazidime (n = 1)), and the third group those who received alternative treatment options (n = 39, 8%). A comparison of clinical characteristics between the three groups is presented in Appendix Table 8. Concomitant empirical therapy with another agent active against H. influenzae was administered to 13 patients (6%) in the benzylpenicillin group (fluoroquinolone (n = 3), doxycycline (n = 1), aminoglycoside (n = 9)) and to 17 patients (7%) in the wide spectrum beta-lactam group (fluoroquinolone (n = 8), doxycycline (n = 3), aminoglycoside (n = 6)). Thus, 199 patients received benzylpenicillin monotherapy and 213 patients received WSBL monotherapy and were included in the multivariate analysis and formed the basis for propensity score matching (Fig. 1).
Clinical outcome in the two treatment groups according to uni- and multivariate logistic regression analysis
In the group receiving benzylpenicillin as empirical monotherapy, 11 patients (5%) died within 30 days after cultures were taken. In the group receiving WSBL monotherapy, 28 patients (13%) died. There was a significant difference between the two groups in terms of CCI, proportion of patients receiving ICU care, proportion of patients with bacteremia, and sepsis severity. Age, sex, maximal level of CRP, the proportion of immunosuppression, antimicrobial susceptibility to beta-lactam antibiotics, and CRB-65 score did not significantly differ between the two groups (Table 1).
Table 1
Descriptive characteristics of the non-adjusted final cohort on which the logistic regressions are performed, including all individuals receiving empirical monotherapy with benzylpenicillin (PcG) or a wide-spectrum beta-lactam (WSBL). Significant p values are in italics
To compare all-cause 30-day mortality between the group treated with benzylpenicillin and the group treated with WSBL, uni- and multivariate logistic regression was performed (Table 2). In the univariate analyses, a significantly increased 30-day mortality was seen in the group treated with WSBL compared to the benzylpenicillin group. Increasing age, CCI score, sepsis severity, and CRB-65 score were also associated with higher 30-day mortality. In the fitted multivariate model, adjusted for age, sepsis severity, and CCI-score, antibiotic treatment with WSBL was no longer significantly associated with increased mortality (OR 2.03, 95%CI 0.91–4.50, p = 0.082).
Table 2
Univariate and multivariate logistic regressions with 30-day mortality as outcome. Significant p values in the univariate regressions are in italics
Thirty-day mortality (n = 410)
Events = 39
Univariate OR (95% CI)
p
Multivariate adjusted OR (95% CI), n = 399
p
Missing values (n)
WSBL vs PcG (ref) empirical monotherapy
2.59 (1.25–5.35)
0.010
2.03 (0.91–4.50)
0.082
–
Age, continuousa
1.05 (1.02–1.08)
0.003
1.06 (1.03–1.10)
0.001
–
Sex, female vs male (ref)
0.73 (0.38–1.42)
0.35
–
Maximum CRP
1.00 (1.00–1.01)
0.21
4
ICU care
1.48 (0.32–6.81)
0.62
2
CCI category (age not included)
4
0–1
ref. cat
–
ref. cat
–
2–3
1.53 (0.65–3.60)
0.33
0.94 (0.37–2.39)
0.89
4–5
2.17 (0.77–6.12)
0.15
1.06 (0.34–3.36)
0.92
> 5
6.64 (2.29–19.3)
< 0.001
5.44 (1.69–17.5)
0.004
Bacteremia
1.79 (0.91–3.51)
0.093
–
Immune suppression
1.46 (0.41–5.16)
0.56
4
Sepsis severity
8
no
ref. cat
–
ref. cat
–
sepsis
1.53 (0.35–6.73)
0.57
1.40 (0.30–6.42)
0.67
severe sepsis
5.4 (1.08–26.9)
0.04
5.21 (0.96–28.3)
0.056
septic shock
18 (2.1–153)
0.008
28.1 (2.49–316)
0.007
CRB-65b
108
0-1
ref. cat
–
2
3.5 (1.54–7.96)
0.003
3–4
6 (1.99–18.1)
0.001
aUsed as a continuous variable due to no events in the youngest age group
bNot used in the multivariate analysis due to the number of missing values
We also compared mortality in patients with only H. influenzae bacteremia treated with either benzylpenicillin or other intravenous beta-lactams in a multivariate logistic regression model (Appendix Table 9). Thirty-day mortality was higher in the WSBL group, bordering on statistical significance (age- and CCI-adjusted OR 4.86, 95% CI of 0.98–24, p = 0.054), compared to the benzylpenicillin group.
There was no significant association between empirical antibiotic treatment and 30-day readmission rates. Increasing age and CCI were both significantly associated with the risk of readmission in the multivariate regression model (Table 3).
Table 3
Univariate and multivariate logistic regressions with 30-day readmission as outcome. Significant p values in the univariate regressions are in italics
Thirty-day readmission (n = 369)
Events = 63
Univariate OR (95% CI)
p
Multivariate adjusted OR (95%CI), n = 369
p
Missing values (n)
WSBL vs PcG (ref) empirical monotherapy
1.23 (0.72–2.13)
0.45
1.16 (0.66–2.05)
0.61
–
Age, continuousa
1.04 (1.01–1.06)
0.003
1.03 (1.01–1.06)
0.013
–
Sex, female vs male (ref)
0.95 (0.55–1.64)
0.84
–
Maximum CRP
1.00 (0.19–4.05)
0.87
2
ICU care
0.88 (0.32–6.81)
0.62
1
CCI category (age not included)
–
0–1
ref. cat
–
ref. cat
–
2–3
2.27 (1.14–4.55)
0.020
1.80 (0.88–3.68)
0.11
4–5
2.84 (1.20–6.72)
0.018
2.23 (0.92–5.39)
0.075
> 5
4.73 (1.62–13.8)
0.005
3.98 (1.32–12.0)
0.014
Bacteremia
1.44 (0.81–2.56)
0.21
–
Immune suppression
1.15 (0.37–3.55)
0.81
–
Sepsis severity
12
no SIRS
ref. cat
–
sepsis
1.26 (0.47–3.40)
0.65
severe sepsis
2.56 (0.73–8.93)
0.14
septic shock
no events
–
CRB-65b
93
0-1
ref. cat
–
2
1.38 (0.67–2.84)
0.39
3–4
3.18 (1.09–9.28)
0.035
aUsed as a continuous variable due to no events in the youngest age group
bNot used in the multivariate analysis due to the number of missing values
In contrast to 30-day mortality and 30-day readmission rate, the proportion of cases with early clinical response (in which data could be obtained) was higher in the WSBL group (n = 170, 84%) compared with the benzylpenicillin group (n = 153, 81%). This difference was statistically significant in a multivariate regression model after adjustment for age, bacteremia, CCI, and sepsis severity (OR 2.28, 95% CI 1.21–4.31, p = 0.011) (Table 4).
Table 4
Univariate and multivariate logistic regressions with early clinical response as outcome. Significant p values in the univariate regressions are in italics
Early clinical response (n = 392) (events = 323)
Univariate OR (95%CI)
p
Multivariate, adjusted OR (95%CI), n = 385
p
Missing values (n)
WSBL vs PcG (ref) empirical monotherapy
1.28 (0.76–2.16)
0.35
2.28 (1.21–4.31)
0.011
–
Age, continuousa
0.98 (0.96–1.00)
0.031
0.97 (0.95–0.99)
0.012
–
Sex, female vs male (ref)
1.02 (0.60–1.73)
0.93
–
Maximum CRP
0.99 (0.99–1.00)
< 0.001
2
ICU care
0.17 (0.05–0.52)
0.002
–
CCI category (age not included)
–
0–1
ref. cat
–
ref cat
–
2–3
1.33 (0.73–2.45)
0.35
2.72 (1.30–5.70)
0.008
4–5
0.97 (0.44–2.11)
0.93
1.33 (0.54–3.27)
0.532
> 5
0.54 (0.21–1.36)
0.19
0.47 (0.16–1.37)
0.17
Bacteremia
0.28 (0.16–0.49)
< 0.001
0.37 (0.20–0.69)
0.002
–
Immune suppression
2.09 (0.48–9.20)
0.33
–
Sepsis severity
7
no SIRS
ref. cat
–
ref. cat
sepsis
0.31 (0.072–1.34)
0.12
0.27 (0.06–1.21)
0.087
severe sepsis
0.06 (0.013–0.30)
0.001
0.05 (0.010–0.27)
< 0.001
septic shock
0.01 (0.001–0.18)
0.001
0.009 (0.001–0.15)
0.001
CRB-65b
98
0-1
ref. cat
–
2
0.75 (0.37–1.51)
0.41
3–4
0.17 (0.06–0.43)
< 0.001
aUsed as a continuous variable due to no non-events in the youngest age group
bNot used in the multivariate analysis due to the number of missing values
Clinical outcomes in the two treatment groups in the propensity score-matched cohort
To further adjust for potential confounders between the two treatment groups, a propensity score-matched cohort was constructed. The matched cohort consisted of 151 individuals treated with empirical benzylpenicillin monotherapy and 151 individuals receiving empirical WSBL treatment. In this matched cohort, 9 patients (6%) died within 30 days in the benzylpenicillin group and 18 patients (12%) died in the WSBL group (Appendix Table 10). Table 5 shows the balance in covariates between the two groups. The propensity score matching resulted in the omission of the most severely ill patients in the WSBL group, which is reasonable considering that these patients are not recommended empirical benzylpenicillin treatment.
Table 5
Descriptive characteristics for the 8 covariates matched for in the propensity-matched cohort, based on individuals receiving empirical monotherapy with benzylpenicillin (PcG) or a wide-spectrum beta-lactam (WSBL), using a caliper of 0.2 (n = 302)
Covariate
PcG, n = 151
WSBL, n = 151
p
Missing values (n)
Age, n (%)
0.97
–
0–40 years
8 (5.3)
7 (4.6)
40–60 years
11 (7.3)
13 (8.6)
60–80 years
74 (49.0)
74 (49.0)
> 80 years
58 (38.4)
57 (37.8)
Sex, n (%)
Female
95 (62.9)
91 (60.3)
0.64
–
Maximum CRP, median (IQR)
223 (142–306)
226 (167–304)
0.74
–
ICU care, n (%)
3 (2.0)
2 (1.3)
0.65
–
CCI category (age not included), n (%)
0.93
–
0–1
53 (35.1)
58 (38.4)
2–3
71 (47.0)
68 (45.0)
4–5
23 (15.2)
22 (14.6)
> 5
4 (2.7)
3 (2.0)
Bacteremia, n (%)
38 (25.1)
41 (27.2)
0.69
–
Immune suppression, n (%)
8 (5.3)
9 (6.0)
0.80
–
Sepsis severity, n (%)
0.63
–
no SIRS
13 (8.6)
17 (11.3)
sepsis
126 (83.4)
123 (81.5)
severe sepsis
12 (8.0)
10 (6.6)
septic shock
–
1 (0.7)
CRB-65a, n (%)
0.96
79
0–1
82 (70.0)
73 (68.9)
2
28 (23.9)
27 (25.5)
3–4
7 (6.0)
6 (5.7)
aNot used for matching due to the number of missing values
Thirty-day mortality was still higher, but not significantly higher in the WSBL group when comparing the matched groups both in a full cohort logistic regression model (OR 2.14, 95% CI 0.93–4.92, p = 0.075) and in a conditional regression model (OR 1.89, 95% CI 0.84–4.23, p = 0.12). There were still no significant differences in 30-day readmission rates (Appendix Table 10). Early clinical response rates remained significantly higher in the WSBL group both by full cohort logistic regression (OR 2.14, 95% CI 1.07–4.27, p = 0.031) and by conditional logistic regression (OR 2.5, 95% CI 1.20–5.21, p = 0.014).
Effect modification
In order to evaluate any potential effect modification by beta-lactamase production and rPBP3, the odds ratios of the stratified outcomes per treatment group and resistance mechanism in the propensity-matched cohort were compared (Appendix Tables 11and 12). The presence of a beta-lactamase was a significant effect modifier of the association between treatment group and early clinical response (the interaction term for beta-lactamase × treatment group (benzylpenicillin as reference): β = 3.12, 95% CI 0.82–5.43, p = 0.008), explaining a substantial portion of the difference in early clinical response. This was not the case for isolates with rPBP3 (the interaction term for rPBP3 × treatment group (benzylpenicillin as reference): β = 0.74, 95% CI − 1.05–2.54, p = 0.42). Neither the associations between all cause 30-day mortality nor between 30-day readmission rates and treatment group were significantly modified by the presence of either resistance mechanism.
Discussion
In the present study, the all-cause 30-day mortality of severe lower respiratory tract infections caused by H. influenzae was 9%. In an analysis adjusted for potential confounders, empirical monotherapy with benzylpenicillin was not significantly associated with increased risk of mortality or readmission. Early clinical response rates were high in both treatment groups, but significantly higher in the group receiving empirical monotherapy with a WSBL in an adjusted analysis, a difference largely explained by effect modification of benzylpenicillin treatment by beta-lactamase-producing strains.
Previous studies have reported mortality rates between 8 and 22% for Haemophilus bacteremia, results that are in good agreement with our findings of 12% in the bacteremia cohort [4, 5, 16]. Data on fatality rates of in-patients with pneumonia is scarce, with one recent study reporting a 30-day case fatality ratio of 2% [24]. This is lower than what we found in the non-bacteremia group (7%). The lower overall mortality in our study (9%) supports the notion that lower respiratory tract infections with H. influenzae are generally associated with less severe presentation compared with S. pneumoniae [1].
To the best of our knowledge, only one previous report has compared treatment outcome of benzylpenicillin in severe infections by H. influenzae [16]. That study was done in a retrospective cohort of bacteremia cases with various foci of infection, in Copenhagen, Denmark. The authors found a significantly increased 30-day mortality when using benzylpenicillin as a definitive treatment for bacteremia. As for empirical treatment, the results were not significant, but there was a trend towards higher mortality in the benzylpenicillin group (p = 0.06). This study also had a higher overall case fatality rate, reaching 22%. These results contrast our findings, where no such difference in outcome could be shown between treatment groups, neither in the bacteremia cohort nor in the overall study cohort. Since our study population only comprised respiratory tract infections, and empirical, as opposed to definite, treatment with benzylpenicillin, the results are not fully comparable.
In another recent, propensity score-matched study, benzylpenicillin and phenoxymethylpenicillin were compared with WSBL as empirical treatment of pneumonia with CRB-65 score ≤ 2 regardless of etiological agent [25]. No significant difference in mortality was seen between the two groups.
In contrast to 30-day mortality, there was a significantly lower chance of early clinical response among patients treated with benzylpenicillin in our study. However, the early clinical response rate in the benzylpenicillin group was still above 80%, and beta-lactamase production was found to be a significant effect modifier. When comparing patients infected with non-beta-lactamase-producing isolates in the propensity-matched cohort, early clinical response rates were 87% in the benzylpenicillin group compared to 89% in the WSBL group (Appendix Table 11).
The strength of this study includes its substantial size of an unselected, population-based homogenous cohort of cases with H. influenzae respiratory tract infection and a thorough analysis of data. The risk of an indication bias in a retrospective analysis of antibiotic treatment is always substantial. To counter this, the treatment groups were adjusted for known covariates that could confound the outcome association, including age, comorbidities, infection severity, and maximal level of CRP. However, the retrospective design of the study still entails a risk for residual confounding, supported by the counter-intuitive result that the mortality was higher in the wide-spectrum treatment group, and that this difference in outcome was bordering significance in multivariate analysis even after adjusting for confounders. On the other hand, this type of study would be very challenging to perform prospectively, as the causative agent in CAP is rarely known at the start of treatment. Another limitation of this study is its limited power due to the relatively low mortality rate. Given the number of patients in the two treatment groups (n = 199 for the benzylpenicillin group and n = 213 for the WSBL group), a defined α = 0.05 and β = 0.8, and a mortality of 14% in the WSBL group, this study has power to significantly detect an odds ratio of approximately 2, assuming a two-sided test of equality.
We have not performed a statistical comparison between high-dose (3 g t.i.d or higher) and low-dose (1 g t.i.d. or less) benzylpenicillin treatment. Monte Carlo simulations calculated by EUCAST suggest significantly lower target attainment rates for the latter regimen, which might lead to treatment failure [11]. Therefore, current Swedish guidelines advocate the use of high-dose benzylpenicillin in CAP treatment [9]. In our cohort, the fraction of patients receiving high-dose versus low-dose treatment were quite similar (55% (116/212) versus 44% (93/212), appendix Table 8). There was a trend towards fewer case fatalities in the high-dose group (n = 4 versus n = 7), but the number of events was too small to allow further statistical comparison.
Almost all rPBP3 isolates in Europe are still considered susceptible to third generation cephalosporins, whereas the susceptibility to aminopenicillins, and thus also to regular benzylpenicillin remains a matter of controversy [26]. In our study, the presence of rPBP3 isolates does not seem to have any detrimental effect on the clinical outcome in the benzylpenicillin group compared to patients treated with WSBL. Beta-lactamase production, in contrast to rPBP3, was a significant effect modifier, associated with a risk of reduced early clinical response in the benzylpenicillin group. This is intuitive, since third generation cephalosporins are generally stable to beta-lactamases expressed by H. influenzae, whereas benzylpenicillin is not [14]. Thus, beta-lactamase expression may well account for cases of treatment failure in this group. The proportion of beta-lactamase producing strains, however, has been stable over the past decades, whereas the increase in rPBP3 isolates has been worrisome [12, 13].
There has been debate on the optimal empirical treatment of respiratory tract infections and CAP caused by H. influenzae. Although definitive therapy with an agent with clinical breakpoints against H. influenzae always should be used following a positive culture, the present study suggests that empirical benzylpenicillin treatment is not associated with higher mortality in patients with mild to moderate lower respiratory tract infection caused by H. influenzae.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
The study design was reviewed and approved by the Regional Ethical Review Board in Lund, Sweden (Dnr 2016/743, addendum 18-391).
Research involving human participants and/or animals
The study design was reviewed and approved by the Regional Ethical Review Board in Lund, Sweden (Dnr 2016/743, addendum 18-391). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the Helsinki declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors.
Informed consent
Individual informed consent was waived in this retrospective observational study, but information about the study and its purpose was announced in local and regional newspapers. The study design was approved by the regional ethical review board.
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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Patients excluded from the initial cohort due to other foci of infection or other diagnosis
Patients excluded from bacteremia group due to other foci of infection
Epiglottitis
n = 14
Meningitis
n = 11
Abdominal infection
n = 8
Urinary Tract Infection
n = 3
Arthritis
n = 3
Peritoneal infection
n = 2
Gynecological infection
n = 2
Soft tissue infection
n = 2
Aortitis
n = 1
Unknown focus of infection
n = 7
Incomplete medical records
n = 21
Total
n = 74
Patients excluded from the sputum/nasopharyngeal sample group due to other diagnosis
Other respiratory tract pathogens
Influenza virus
n = 11
Streptococcus pneumoniae
n = 6
Respiratory syncytial virus
n = 4
Mycoplasma pneumoniae
n = 3
β-hemolytic Streptococci
n = 3
Legionella pneumonia
n = 1
Pneumocystis jirovecii
n = 1
Chlamydophila pneumoniae
n = 1
Total
n = 30
Other focus of infection than the respiratory tract (w or w/o other pathogens)
Urinary tract infection
n = 7
Escherichia coli bacteremia
n = 4
Staphylococcus aureus bacteremia
n = 3
Streptococcus mitis bacteremia
n = 2
Pseudomonas aeruginosa bacteremia
n = 1
Erysipelas
n = 1
Clostridium difficile enteritis
n = 1
Unknown focus of infection
n = 9
Total
n = 28
No signs of infection
n = 20
Total
n = 78
Table 7
Detailed description of the empirical antibiotic therapy given
Description of the empirical antibiotic treatment given:
Empiric antibiotic treatment (n, %)
Group 1)
Benzylpenicillin
212 (44%)
Total
212 (44%)
Group 2)
Cefotaxime
175 (36%)
Cefuroxime
16 (3%)
Piperacillin-tazobactam
20 (4%)
Imipenem-cilastatin
8 (2%)
Meropenem
8 (2%)
Ampicillin
2 (< 1%)
Ceftazidime
1 (< 1%)
Total
230 (48%)
Group 3)
Doxycycline
12 (2%)
Clindamycine
6 (1%)
Amoxicillin
5 (1%)
Erythromycine
3 (< 1%)
Ciprofloxacine
2 (< 1%)
Phenoximethyl penicillin
2 (< 1%)
Trimetoprim /
sulfamethoxazole
2 (< 1%)
Amoxicillin /
clavulanic acid
1 (< 1%)
Cloxacillin
1 (< 1%)
Levofloxacine
1 (< 1%)
Roxithromycine
1 (< 1%)
No antibiotic treatment
2 (< 1%)
Missing data
1 (< 1%)
Total
39 (8%)
Allergy to penicillin (n, %)
No
461 (96%)
Yes
15 (3%)
Missing data
5 (1%)
Concomitant antibiotic treatment active against
H. influenzae in Benzylpenicillin group
None
199 (94%)
(n, % within group)
Fluoroquinolone
3 (1%)
Doxycycline
1 (< 1%)
Aminoglycoside (1 dose)
9 (4%)
Total
212 (100%)
Concomitant antibiotic treatment active against
H. influenzae in wide-spectrum beta-lactam group
None
213 (93%)
(n, % within group)
Fluoroquinolone
8 (4%)
Doxycycline
3 (1%)
Aminoglycoside (1 dose)
6 (3%)
Total
230 (100%)
Concomitant antibiotic treatment active against
H. influenzae in the miscellaneous group
None
36 (92%)
(n, % within group)
Fluoroquinolone
1 (2%)
Doxycycline
1 (2%)
Aminoglycoside (1 dose)
1 (2%)
Total
39 (100%)
Dosage of benzylpenicillin
1 g t.i.d.
84 (40%)
(n, % within total group)
3 g t.i.d.
104 (49%)
1 g b.i.d.
9 (4%)
2 g t.i.d.
11 (6%)
1 g q.i.d.
1 (< 1%)
Missing data
3 (1%)
Total
212 (100%)
30-day mortality (no of casualties, % within dosage group)
in the benzylpenicillin group sorted by dosage
1 g t.i.d.
5 (6%)
3 g t.i.d.
4 (4%)
1 g b.i.d.
2 (22%)
Other dosages
0
Table 8
Descriptive characteristics of the crude cohort, including all individuals in the study, stratified on treatment group. Significant differences are italics
Univariate and multivariate logistic regressions with outcome 30-day mortality in only bacteremic isolates receiving empirical monotherapy with an i.v. beta-lactam. Significant p values in the univariate regressions are in italics
Thirty-day mortality, (n = 120)
Events = 16
Univariate odds ratio (95%CI)
P
Multivariate adjusted OR (95%CI), n = 116
p
Missing values (n)
WSBL vs PcG (ref) empirical monotherapy
5.55 (1.20–25.7)
0.028
4.86 (0.98–24)
0.054
–
Age, continuousa
1.05 (1.00–1.10)
0.004
1.06 (1.01–1.12)
0.025
–
Sex, female vs male (ref)
0.68 (0.24–1.95)
0.47
–
Maximum CRP
1.00 (1.00–1.01)
0.35
4
ICU care
no events
–
2
CCI category (age not included)
4
0–1
ref. cat
–
ref cat
–
2–3
1.09 (0.27–4.33)
0.91
0.65 (0.15–2.83)
0.57
4–5
3.33 (0.63–17.6)
0.16
1.65 (0.26–10.3)
0.59
> 5
8.0 (1.51–42.4)
0.015
4.59 (0.74–28.6)
0.10
Immune suppression
no events
–
2
Sepsis severity
6
No
ref. cat
–
sepsis
0.72 (0.08–6.86)
0.78
severe sepsis
0.71 (0.06–8.40)
0.79
septic shock
3.33 (0.20–54)
0.40
CRB65b
47
0-1
ref. cat
–
2
1.75 (0.39–7.8)
0.46
3–4
3.75 (0.68–21)
0.13
aUsed as a continuous variable due to no events in the youngest age group
bNot used in the multivariate analysis due to the number of missing values
Table 10
Outcomes stratified by treatment group in the propensity-matched cohort
No
n (%)
logistic regression, OR (95%CI)
conditional logistic regression, OR (95%CI)
Benzyl-penicillin
WSBL
Benzyl-penicillin
WSBL
p value
Benzyl-penicillin
WSBL
p value
30-day all cause mortality, (n = 300)
9/150 (6.0%)
18/150 (12.0%)
1 (ref)
2.14 (0.93–4.92)
0.075
1 (ref)
1.89 (0.84–4.23)
0.12
30-day all cause hospital readmission, (n = 275)
24/143 (16.8%)
21/132 (15.9%)
1 (ref)
0.94 (0.49–1.78)
0.85
1 (ref)
0.89 (0.46–1.72
0.74
Early clinical response at day 4 (n = 292)
119/146 (81.5%)
132/146 (90.4%)
1 (ref)
2.14 (1.07–4.27)
0.031
1 (ref)
2.5 (1.20–5.21)
0.014
Table 11
Potential effect modification of the treatment group by betalactamase production on the respective outcomes in the propensity-matched cohort, balanced by covariates earlier described
Thirty-day all-cause mortality (n = 300)
Benzylpenicillin treatment
Wide-spectrum betalactamase treatment
OR within STRATA of beta-lactamase presence
n with outcome (%)
OR (95% CI), p
OR (95% CI), p
Isolates without betalactamase
8/129 (6.2%)
1 (ref)
16/125 (12.8%)
2.22 (0.91–5.39), p = 0.078
2.22 (0.91–5.39), p = 0.078
Isolates with beta-lactamase
1/21 (4.7%)
0.76 (0.090–6.38), p = 0.80
2/25 (8.0%)
1.32 (0.26–6.60), p = 0.74
1.74 (0.15–20.6), p = 0.66
30-day all-cause readmission (n = 275)
Isolates without betalactamase
21/124 (16.9%)
1 (ref)
19/108 (17.6%)
1.05 (0.53–2.07), p = 0.90
1.05 (0.53–2.07), p = 0.90
Isolates with beta-lactamase
3/19 (15.8%)
0.92 (0.25–3.44), p = 0.90
2/24 (8.3%)
0.45 (0.097–2.04), p = 0.30
0.48 (0.072–3.25), p = 0.46
Early clinical response on day 4 (n = 292)
Isolates without betalactamase
109/125 (87.2%)
1 (ref)
107/120 (89.2%)
1.21 (0.55–2.63), p = 0.63
1.21 (0.55–2.63), p = 0.63
Isolates with beta-lactamase
10/21 (47.6%)
0.13 (0.05–0.36), p < 0.001
25/26 (96.1%)
3.67 (0.46–29.0), p = 0.22
27.5 (3.13–242), p = 0.003
Interaction term for betalactamase × treatment group (Benzyl-pc as ref) for 30-day mortality: β = − 0.24 (− 2.97–2.38), p = 0.86
Interaction term for betalactamase × treatment group (Benzyl-pc as ref) for 30-day readmission: β = − 0.77 (− 2.79–1.25), p = 0.46
Interaction term for betalactamase × treatment group (Benzyl-pc as ref) for early clinical response: β = 3.12 (0.82–5.43), p = 0.008
Table 12
Potential effect modification of the treatment group by rPBP3 on the respective outcomes in the propensity-matched cohort, balanced by covariates earlier described
Thirty-day all-cause mortality (n = 300)
Benzylpenicillin treatment
Wide-spectrum betalactamase treatment
OR within STRATA of rPBP3
n with outcome (%)
OR (95% CI), p
OR (95% CI), p
Isolates without rPBP3
4/110 (3.6%)
1 (ref)
13/121 (10.7%)
3.19 (1.01–10.1), p = 0.048
3.19 (1.01–10.1), p = 0.048
Isolates with rPBP3
5/40 (12.5%)
3.79 (0.96–14.9), p = 0.06
5/29 (17.2%)
5.52 (1.38–22.1), p = 0.016
1.46 (0.38–5.6), p = 0.58
30-day all-cause readmission (n = 275)
Isolates without rPBP3
17/106 (16.0%)
1 (ref)
19/106 (17.9%)
1.14 (0.56–2.34), p = 0.72
1.14 (0.56–2.34), p = 0.72
Isolates with rPBP3
7/37 (18.9%)
1.22 (0.46–3.23), p = 0.69
2/26 (7.7%)
0.44 (0.094–2.02), p = 0.29
0.35 (0.068–1.88), p = 0.22
Early clinical response on day 4 (n = 292)
Isolates without rPBP3
87/105 (82.9%)
1 (ref)
105/117
(89.7%)
1.81 (0.83–3.96), p = 0.14
1.21 (0.55–2.63), p = 0.63
Isolates with rPBP3
32/41 (78.0%)
0.74 (0.30–1.80), p = 0.50
27/29 (93.1%)
2.79 (0.61–12.8), p = 0.19
3.80 (0.75–19.1), p = 0.11
Interaction term for rPBP3 × treatment group (Benzyl-pc as ref) for 30-day mortality: β = − 0.78 (− 2.55–0.99), p = 0.39
Interaction term for rPBP3 × treatment group (Benzyl-pc as ref) for 30-day readmission: β = − 1.16 (− 2.97–0.65), p = 0.21
Interaction term for rPBP3 × treatment group (Benzyl-pc as ref) for early clinical response: β = 0.74 (− 1.05–2.54), p = 0.42
Benzylpenicillin versus wide-spectrum beta-lactam antibiotics as empirical treatment of Haemophilus influenzae-associated lower respiratory tract infections in adults; a retrospective propensity score-matched study
verfasst von
John Thegerström Viktor Månsson Kristian Riesbeck Fredrik Resman
