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استفاده از پروکلسی‌تونین برای آغاز یا قطع تجویز آنتی‌بیوتیک‌ها در عفونت‌های حاد دستگاه تنفسی

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پیشینه

عفونت‌های حاد تنفسی (acute respiratory infections; ARI) شامل گروه بزرگ و ناهمگونی از عفونت‌ها از جمله باکتری، ویروس، و سایر اتیولوژی‌ها می‌شود. در سال‌های اخیر، پروکلسی‌تونین (procalcitonin; PCT)، یک نشانگر خونی برای عفونت‌های باکتریال، به‌نظر می‌رسد ابزار امیدوار کننده‌ای برای بهبود تصمیم‌گیری در مورد درمان با آنتی‌بیوتیک باشد (درمان آنتی‌بیوتیکی هدایت شده با PCT). چندین کارآزمایی تصادفی‌سازی و کنترل شده (randomised controlled trials; RCTs) امکان استفاده از پروکلسی‌تونین را برای شروع و توقف آنتی‌بیوتیک‌ها در جمعیت بیماران مختلف مبتلا به ARI و شرایط مختلف از جمله مجموعه مراقبت‌های اولیه در بخش‌های اورژانس، بخش‌های بیمارستانی، و بخش مراقبت‌های ویژه نشان دادند. با این حال، تاثیر استفاده از پروکلسی‌تونین بر پیامدهای بالینی مشخص نیست. این یک نسخه به‎روز از مرور کاکرین و متاآنالیز (meta‐analysis) داده‌های فردی شرکت‌کنندگان است که ابتدا در سال 2012 منتشر شد و به دنبال بررسی ایمنی نظارت بر تجویز آنتی‌بیوتیکی بر مبنای هدایت PCT بود.

اهداف

هدف این مرور سیستماتیک ارزیابی ایمنی و اثربخشی استفاده از پروکلسی‌تونین برای شروع یا توقف آنتی‌بیوتیک‌ها در طیف وسیعی از بیماران مبتلا به ARI با شدت متفاوت و در شرایط بالینی متفاوت، بر اساس داده‌های فردی شرکت‌کنندگان بود.

روش‌های جست‌وجو

ما پایگاه ثبت مرکزی کارآزمایی‌های کنترل‌ شده کاکرین (CENTRAL)، را که شامل پایگاه ثبت تخصصی گروه عفونت‌های حاد تنفسی در کاکرین، MEDLINE، و Embase بود، در فوریه 2017 برای شناسایی کارآزمایی‌های مناسب جست‌وجو کردیم. هم‌چنین ClinicalTrials.gov را برای شناسایی کارآزمایی‌های در حال انجام در اپریل 2017 جست‌وجو کردیم.

معیارهای انتخاب

RCTهای مربوط به شرکت‌کنندگان بزرگسال مبتلا به ARI را که درمان آنتی‌بیوتیکی را بر اساس الگوریتم پروکلسی‌تونین (الگوریتم نظارت بر تجویز آنتی‌بیوتیک با هدایت PCT) یا مراقبت معمول دریافت کردند، وارد مرور کردیم. کارآزمایی‌هایی را که به‌طور انحصاری بر کودکان متمرکز بودند یا از پروکلسی‌تونین با هدفی غیر از هدایت آغاز و طول مدت درمان آنتی‌بیوتیک استفاده کردند؛ از مطالعه خارج کردیم.

گردآوری و تجزیه‌وتحلیل داده‌ها

دو تیم از نویسندگان مرور به‌طور مستقل متدولوژی را بررسی کرده و داده‌ها را از مطالعات اولیه استخراج کردند. نقاط پایانی اولیه شامل مورتالیتی به هر علتی و شکست درمان در 30 روز بود، که تعاریف آنها بین کارآزمایی‌ها هماهنگ بودند. نقاط پایانی ثانویه استفاده از آنتی‌بیوتیک، عوارض جانبی مرتبط با آنتی‌بیوتیک، و طول مدت بستری در بیمارستان بود. نسبت شانس (OR) و 95% فاصله اطمینان (CI) را با استفاده از رگرسیون لوجستیک سلسله مراتبی چند متغیری تعدیل شده برای سن، جنس، و تشخیص‌های بالینی با استفاده از مدل اثر‐ثابت محاسبه کردیم. کارآزمایی‌های مختلف به عنوان اثرات تصادفی به مدل اضافه شدند. ما تجزیه‌و‌تحلیل حساسیت طبقه‌بندی شده را بر اساس شرایط بالینی و نوع ARI انجام دادیم. متاآنالیز داده‌های جمع‌آوری شده را نیز انجام دادیم.

نتایج اصلی

از 32 RCT واجد شرایط، 18 کارآزمایی جدید برای به‎روز کردن در سال 2017 وارد شدند، ما داده‌های فردی شرکت‌کننده را از 26 کارآزمایی شامل 6708 شرکت‌کننده به دست آوردیم، که آنها را در متاآنالیز اصلی داده‌های فردی شرکت‌کننده وارد کردیم. داده‌های فردی شرکت‌کنندگان را در چهار کارآزمایی به دست نیاوردیم و دو کارآزمایی افراد مبتلا به ARIهای تایید شده را وارد نکردند. با توجه به رویکر درجه‌‏بندی توصیه‏، ارزیابی، توسعه و ارزشیابی (GRADE)، کیفیت شواهد مربوط به پیامدهای مرگ‌ومیر و مواجهه با آنتی‌بیوتیک بالا بود، و برای پیامدهای شکست درمان و عوارض جانبی مرتبط با آنتی‌بیوتیک متوسط بود.

نقاط پایانی اصلی: 286 مورد مرگ‌ومیر در 3336 شرکت‌کننده هدایت شده با پروکلسی‌تونین (8.6%) در مقایسه با 336 مورد مرگ‌ومیر در 3372 شرکت‌کننده در گروه کنترل (10.0%)، در نتیجه مرگ‌ومیر مرتبط با درمان هدایت شده با پروکلسی‌تونین بسیار کمتر بود (OR تعدیل شده: 0.83؛ 95% CI؛ 0.70 تا 0.99؛ 0.037 = P). ما نمی‌توانیم مرگ‌و‌میر را در کارآزمایی‌های مربوط به مراقبت‌های اولیه تخمین بزنیم؛ زیرا فقط یک مورد مرگ‌ومیر در شرکت‌کننده گروه کنترل گزارش شده بود. شکست درمان در شرکت‌کنندگان هدایت شده با پروکلسی‌تونین به‌طور معنی داری پائین نبود (23.0% در برابر 24.9% در گروه کنترل؛ OR تعدیل شده: 0.90؛ 95% CI؛ 0.80 تا 1.01؛ 0.068 = P). نتایج میان زیر‐گروه‌ها بر اساس شرایط بالینی و نوع عفونت تنفسی مشابه بود، و هیچ شواهدی در مورد اصلاح تاثیر وجود نداشت (P برای اثر متقابل > 0.05). نقاط پایانی ثانویه: هدایت درمان با پروکلسی‌تونین در مواجهه با آنتی‌بیوتیک، با کاهش 2.4 روزه (5.7% در برابر 8.1% روز؛ 95% CI؛ 2.71‐ تا 2.15‐؛ 0.001 > P)، و با خطر عوارض جانبی مرتبط با آنتی‌بیوتیک کمتری همراه بود (16.3% در برابر 22.1%؛ OR تعدیل شده: 0.68؛ 95% CI؛ 0.57 تا 0.82؛ 0.001 > P). طول مدت بستری در بیمارستان و بخش مراقبت‌های ویژه در هر دو گروه مشابه بود. تجزیه‌وتحلیل حساسیت داده‌های گردآوری شده بر اساس هر 32 کارآزمایی واجد شرایط، نتایج مشابهی را نشان داد.

نتیجه‌گیری‌های نویسندگان

این متاآنالیز به‌روز شده از داده‌های فردی شرکت‌کنندگان از 12 کشور نشان می‌دهد که استفاده از پروکلسی‌تونین برای هدایت آغاز و طول مدت درمان آنتی‌بیوتیک منجر به کاهش خطر مرگ‌ومیر، مصرف آنتی‌بیوتیک پائین‌تر، و کاهش خطر عوارض جانبی مرتبط با آنتی‌بیوتیک می‌شود. نتایج مربوط به شرایط بالینی مختلف و انواع ARI مشابه بود، بنابراین از استفاده از پروکلسی‌تونین در زمینه نظارت بر تجویز آنتی‌بیوتیک در افراد مبتلا به ARI حمایت می‌کند. پژوهش‌های با کیفیت بالا در آینده برای تایید نتایج در بیماران با سیستم ایمنی سرکوب شده و بیماران مبتلا به عفونت‌های غیر‐تنفسی ضروری است.

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

خلاصه به زبان ساده

تست سطح پروکلسی‌تونین (procalcitonin) خون برای تعیین زمان شروع و توقف تجویز آنتی‌بیوتیک‌ها در بزرگسالان مبتلا به عفونت‌های حاد دستگاه تنفسی

سوال مطالعه مروری

تاثیرات استفاده از پروکلسی‌تونین در شروع یا قطع تجویز آنتی‌بیوتیک‌ها در افراد مبتلا به عفونت‌های حاد تنفسی در مقایسه با مراقبت معمول بر مرگ‌ومیر و شکست درمان چیست؟

پیشینه

در افراد مبتلا به عفونت‌های حاد تنفسی، استفاده غیر‐ضروری از آنتی‌بیوتیک‌ها به‌طور قابل توجهی باعث افزایش مقاومت باکتری، هزینه‌های پزشکی، و خطر حوادث جانبی مرتبط با دارو می‌شود. نشانگر خونی پروکلسی‌تونین در عفونت‌های باکتریال افزایش می‌یابد و زمانی که عفونت بیماران بهبود می‌یابد، کاهش پیدا می‌کند. پروکلسی‌تونین را می‌توان در خون بیماران توسط آزمایش‌های مختلف تجاری موجود با زمان چرخش حدود یک تا دو ساعت اندازه‌گیری و از تصمیم‌گیری بالینی در مورد شروع و قطع درمان آنتی‌بیوتیک حمایت کرد.

تاریخ جستجو

در 10 فوریه 2017، جست‌وجوهای الکترونیکی انجام دادیم. در 12 اپریل 2017، کارآزمایی‌های در حال انجام را جست‌وجو کردیم.

ویژگی‌های مطالعه

تمام کارآزمایی‌های وارد شده، شرکت‌کنندگان مبتلا به عفونت‌های حاد تنفسی را برای دریافت آنتی‌بیوتیک‌ها بر اساس سطوح پروکلسی‌تونین (گروه هدایت شده با پروکلسی‌تونین) یا یک گروه کنترل تصادفی‌سازی کردند. این کارآزمایی‌ها در بخش مراقبت‌های اولیه، اورژانس و بخش‌های درمانی، و بخش مراقبت‌های ویژه انجام شدند. شرکت‌کنندگان وارد شده مبتلا به عفونت‌های حاد تنفسی فوقانی یا تحتانی بودند از جمله پنومونی، برونشیت (bronchitis)، تشدید بیماری مزمن انسدادی ریه و سایر عفونت‌ها.

منابع تامین مالی مطالعه

تمام مطالعات، کارآزمایی‌های آغاز شده توسط محققان بودند. نیمی از کارآزمایی‌ها توسط آژانس‌های ملی حمایت مالی شدند یا منبع مالی را گزارش نکردند، و نیمی از کارآزمایی‌ها بودجه را از صنعت بیومارکر دریافت کردند (برای مثال Thermo Fisher Scientific).

نتایج کلیدی

6708 شرکت‌کننده را در 26 کارآزمایی و 12 کشور مورد مطالعه قرار دادیم. مرگ‌ومیر در 30 روز به‌طور قابل توجهی در شرکت‌کنندگان هدایت شده با پروکلسی‌تونین در مقایسه با شرکت‌کنندگان کنترل کمتر بود (286 مورد مرگ‌ومیر در 3336 شرکت‌کننده هدایت شده با پروکلسی‌تونین (8.6%) در برابر 336 مورد مرگ‌ومیر در 3372 شرکت‌کننده گروه کنترل (10.0%)). تفاوت معنی‌داری در رابطه با شکست درمان وجود نداشت. نتایج مربوط به شرایط مختلف بالینی (مراقبت‌های اولیه، بخش اورژانس، بخش مراقبت‌های ویژه) و انواع عفونت تنفسی مشابه بود. با توجه به مواجهه قبلی با آنتی‌بیوتیک، شرکت‌کنندگان در گروه هدایت شده توسط پروکلسی‌تونین کاهش 2.4 روزه در مواجهه با آنتی‌بیوتیک و کاهش عوارض جانبی مرتبط با آنتی‌بیوتیک داشتند (16.3% در برابر 22.1%).

کیفیت شواهد

کیفیت شواهد برای مرگ‌ومیر و مواجهه با آنتی‌بیوتیک بالا بود. اکثر کارآزمایی‌ها از کورسازی استفاده نکردند، اما ما انتظار نداشتیم که مرگ‌ومیر تحت تاثیر این محدودیت، دارای سوگیری (bias) شود. کیفیت شواهد برای شکست درمان و عوارض جانبی مرتبط با آنتی‌بیوتیک متوسط بود زیرا تعریف این نقاط پایانی میان کارآزمایی‌ها یکسان نبود.

Authors' conclusions

Implications for practice

Emerging bacterial resistance to multiple antibiotic agents calls for more stringent efforts to reduce the empiric use of antimicrobial agents in self limited and non‐bacterial diseases and to shorten the duration of antibiotic treatment in bacterial infection with clinical resolution. The results of our study suggest that procalcitonin (PCT) is a safe and effective tool to guide clinical decisions for antibiotic initiation and duration of treatment. In all trials, PCT was used to inform physicians about the need for initiation or discontinuation of antibiotic therapy, or both. However, there were differences in PCT protocols among trials depending on the clinical setting (see Table 1 for details about PCT recommendations used in the individual trials) (Schuetz 2011a; Schuetz 2015). In brief, PCT was mainly used to inform about initiation of antibiotic treatment in primary care trials, and re‐measurement of PCT was recommended in participants not being treated with antibiotics and not showing a resolution of illness at follow‐up. In the emergency room and hospital ward setting, PCT was used to inform about initiation of antibiotic treatment (mainly in low‐risk patients with bronchitis or chronic obstructive pulmonary disease exacerbation), and also about discontinuation of treatment in community‐acquired pneumonia patients. In intensive care unit patients, PCT was mainly used to monitor treatment and discontinue antibiotics in participants with clinical improvement and a drop in PCT levels. Thus for clinical practice, PCT should also be adapted to clinical settings and the risk of patients ‐ similar to patients with suspicion of pulmonary embolism where D‐dimer levels are used differently depending on the pre‐test probability (Konstantinides 2008).

The use of PCT to guide initiation and duration of antibiotic treatment in people with acute respiratory infections (ARIs) was associated with lower mortality rates and significantly reduced antibiotic consumption and associated side effects across different clinical settings and ARI diagnoses. Of note, mortality was very low in primary care patients, and we were thus not able to assess the effect of PCT on mortality. The use of PCT embedded in clinical algorithms has the potential to improve the antibiotic management of ARI patients and has substantial clinical and public health implications to reduce antibiotic exposure and the associated risk of antibiotic resistance. Several assays for the measurement of PCT are currently available (Schuetz 2017), and the US Food and Drug Administration recently cleared the Vidas assay, among others, for antibiotic stewardship and prognostication of patients using a PCT kinetics algorithm (Schuetz 2016). Importantly, all trials have used highly sensitive assays to measure PCT in order to have optimal sensitivity and thus test performance. Factors such as accessibility and time taken to get reports of the tests are equally important in whether PCT will be used in the clinical decision‐making process for antibiotic therapy in ARIs. In this regard, a point‐of‐care test would be important, especially for the primary care setting (Kutz 2016).

Importantly, all trials included PCT into clinical algorithms, and physicians could deviate from the PCT algorithm if needed. Poststudy surveys have been published in order to better understand the effects and challenges of PCT testing in clinical practice (Albrich 2012; Balk 2017). 

Implications for research

Future studies should establish cost‐effectiveness by considering country‐specific costs of PCT measurement (around USD 20 to USD 30 per sample) and potential savings in consumption of antibiotics and other healthcare resources (Stojanovic 2017). 

In addition, it would be interesting to conduct a head‐to‐head trial comparing a PCT strategy to a strategy based on another biomarker, such as C‐reactive protein (CRP) or interleukin‐6 (Meili 2015; Meili 2016). A similar randomised controlled trial was recently conducted in primary care in the Netherlands with a treatment algorithm based on either CRP levels, communication training, or both, compared to a control group (Cals 2009). The trial authors reported a 42% relative reduction in antibiotic use with CRP guidance, which was similar to the effect of communication training in this setting. However, the usefulness of CRP for antibiotic guidance outside the primary care setting is not yet supported by controlled intervention trials.

While there is strong evidence for the use of PCT in respiratory infections, its role in other infections remains unclear. Several studies have investigated PCT as a diagnostic and antibiotic stewardship marker in different types of infections (Albrich 2012; Drozdov 2015; Sager 2017). However, larger trials powered for safety are needed to understand the effect of PCT outside respiratory infections.

Summary of findings

Open in table viewer
Summary of findings for the main comparison. Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections

Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections

Patient or population: people with acute respiratory tract infections
Settings: primary care, emergency department, intensive care unit
Intervention: PCT‐guided care
Comparison: standard care

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No. of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Standard care

PCTalgorithm

Mortality
Follow‐up: 30 days

Study population

OR 0.83
(0.70 to 0.99)

6708
(26 studies)

⊕⊕⊕⊕
High1

100 per 1000

86 per 1000

(76 to 95)

Treatment failure
Clinical assessment3
Follow‐up: 30 days

Study population

OR 0.90
(0.80 to 1.01)

6708
(26 studies)

⊕⊕⊕⊝
Moderate2 3

249 per 1000

230 per 1000

(216 to 245)

Antibiotic‐related side effects

Follow‐up: 30 days

Study population

221 per 1000

163 per 1000

(145 to 182)

OR 0.68
(0.57 to 0.82)

3034
(6 studies)

⊕⊕⊕⊝
Moderate4

Antibiotic exposure
Total days of antibiotic therapy in all randomised participants

The mean antibiotic exposure in the control groups was
8.1 days.

The mean antibiotic exposure in the intervention groups was
2.43 dayslower
(2.15 to 2.71)

6708
(26 studies)

⊕⊕⊕⊕
High1

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; OR: odds ratio: PCT: procalcitonin

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1No downgrading for serious concerns. Still, there is some concern about unconcealed allocation in several trials in the emergency department and intensive care settings. There is also some concern about low adherence with the PCT algorithm in the intervention group. We consider unblinded outcome assessment as not relevant for the outcome of death.
2Downgraded one level for serious inconsistency: trials used differing definition of treatment failure and some rare events were not systematically assessed among trials.
3For the primary care setting, treatment failure was defined as death, hospitalisation, acute respiratory infection (ARI)‐specific complications (e.g. empyema for lower ARI, meningitis for upper ARI), recurrent or worsening infection, and participants reporting any symptoms of an ongoing respiratory infection (e.g. fever, cough, dyspnoea) at follow‐up. For the emergency department setting, treatment failure was defined as death, intensive care unit (ICU) admission, rehospitalisation after index hospital discharge, ARI‐associated complications (e.g. empyema or acute respiratory distress syndrome for lower ARI), and recurrent or worsening infection within 30 days of follow‐up. For the ICU setting, treatment failure was defined as death within 30 days of follow‐up.
4Downgraded one level for incomplete reporting: only 6 trials reported side effects from antibiotics, and none of these trials were conducted in the ICU setting.

Background

Acute respiratory infections (ARIs) account for over 10% of global disease burden and are the most common reason for antibiotic therapy in primary care and hospital settings (Evans 2002; Gonzales 1997; Zaas 2014).

Description of the condition

Acute respiratory infections comprise a heterogeneous group of infections including bacterial, viral, and other aetiologies. As many as 75% of all antibiotic doses are prescribed for ARIs, despite their mainly viral cause (Doan 2014; Evans 2002). Early initiation of adequate antibiotic therapy is the cornerstone in the treatment of bacterial ARIs and is associated with improved clinical outcomes (Hoare 2006; Kumar 2006; Kumar 2009; Liberati 2009b; Spurling 2010). However, overuse of antibiotics by overprescription in outpatients with bronchitis (Arnold 2005), for instance, and prolonged duration of antibiotic therapy in people with bacterial ARIs in the hospital and intensive care unit (ICU) settings is associated with increased resistance to common bacteria, high costs, and adverse drug reactions (Gonzales 1997; Goossens 2005; Lawrence 2009; Zaas 2014).

Description of the intervention

The presence of a diagnostic 'gold standard' or reference standard represents the best available method for establishing the presence or absence of a disease. Optimally, a morphological verification such as histopathology or, in the case of ARIs, growth of typical pathogens in blood cultures or sputum cultures can be obtained to establish the 'correct' diagnosis. Regrettably, the use of blood cultures as the assumed gold standard in ARIs lacks sensitivity, specificity, or both, with only around 10% of people with pneumonia having positive cultures and some of them being false positives (Muller 2010). In this diagnostic uncertainty, surrogate biomarker to estimate the likelihood for the presence of a bacterial infection and to grade disease severity are of great interest (Schuetz 2015). In such a circumstance, two fundamentally different concepts are employed. One concept tends to ignore potential dilemmas in the accuracy of the alleged gold standard but assumes a well‐defined illness, which is represented by the assumption drawn following a diagnostic test or a clinical diagnosis. The second concept discards alleged gold standards and focuses on patient outcomes. In the case of ARIs, the clinical benefit of a diagnostic biomarker, such as procalcitonin (PCT), can be measured by clinical outcomes of randomised intervention studies, assuming that if the person recovered without antibiotics then there was no relevant bacterial illness.

In recent years, PCT has emerged as a promising marker for the diagnosis of bacterial infections because higher levels are found in severe bacterial infections but remain fairly low in viral infections and non‐specific inflammatory diseases (Muller 2000; Muller 2001; Muller 2010). Procalcitonin is released in multiple tissues in response to bacterial infections via a direct stimulation of cytokines, such as interleukin (IL)‐1β, tumour necrosis factor (TNF)‐ɑ, and IL‐6. Conversely, PCT production is blocked by interferon gamma, a cytokine released in response to viral infections (Muller 2000). Hence, PCT may be used to support clinical decision making for the initiation and discontinuation of antibiotic therapy in different types of infections and indications (Sager 2017; Schuetz 2016). Randomised controlled trials (RCTs) have demonstrated the feasibility of such a strategy in different ARI patient populations and different settings ranging from primary care to emergency departments and hospital wards to medical and surgical ICUs (Bloos 2016; Branche 2015; Corti 2016; De Jong 2016; Deliberato 2013; Layios 2012; Long 2014; Maravić‐Stojković 2011; Oliveira 2013; Shehabi 2014; Verduri 2015; Wang 2016).

How the intervention might work

Procalcitonin levels correlate with the risk of relevant bacterial infections and decrease upon recovery. Procalcitonin testing may therefore help physicians decide in which patients antibiotics are needed and when it is safe to stop treatment (Kutz 2015). The use of PCT in clinical protocols may thus decrease antibiotic consumption in two ways: by preventing unnecessary antibiotic prescriptions and by limiting durations of antibiotic treatment (Sager 2017; Schuetz 2011a).

Why it is important to do this review

While several RCTs have evaluated PCT‐guided antibiotic treatment, most individual trials included participants with different types of respiratory and non‐respiratory infections and lacked the statistical power to assess the risk for mortality and severe infectious disease complications associated with PCT‐guided decision making. Previous meta‐analyses of RCTs investigating the effect of PCT algorithms on antibiotic use focused on the critical care setting, people with suspicion of bacterial infections, and people with sepsis and respiratory infections (Heyland 2011; Hoeboer 2015; Tang 2009; Wacker 2013). However, these meta‐analyses used aggregated data and were not able to investigate the effects of PCT on different ARI diagnoses and on outcomes other than mortality. A previous meta‐analysis based on individual participant data published in the Cochrane Library did not find a significant difference in clinical outcomes, but confidence intervals remained relatively wide (Schuetz 2012). Safety of using PCT for antibiotic decision making remained thus unproven.

Objectives

The aim of this systematic review based on individual participant data was to assess the safety and efficacy of using procalcitonin for starting or stopping antibiotics over a large range of patients with varying severity of ARIs and from different clinical settings.

Methods

Criteria for considering studies for this review

Types of studies

Prospective RCTs comparing a strategy to initiate or discontinue antibiotic therapy based on PCT levels with a control arm without PCT measurements were eligible for inclusion. Participants were randomised to receive antibiotics either based on PCT levels ('PCT‐guided' group) or a control group without knowledge of PCT levels, including antibiotic management based on usual care or guidelines. We did not include non‐randomised studies.

Types of participants

We included adult participants with clinical diagnoses of ARIs: either a lower ARI including community‐acquired pneumonia (CAP), hospital‐acquired pneumonia (HAP), ventilator‐associated pneumonia (VAP), acute bronchitis, exacerbation of asthma, or exacerbation of chronic obstructive pulmonary disease (COPD); or an upper ARI including common cold, rhino‐sinusitis, pharyngitis, tonsillitis, or otitis media. We also included people with sepsis and suspected ARIs in the analyses. We excluded trials if they focused exclusively on children or used PCT to escalate antibiotic therapy. We made no exclusions based on language of reports or clinical setting. We included trials from primary care, emergency departments, and medical and surgical ICUs.

Types of interventions

Strategies to initiate or discontinue antibiotic therapy based on PCT levels compared with usual care were eligible.

Types of outcome measures

We defined primary and secondary outcomes to a follow‐up time of 30 days. For trials with shorter follow‐up periods, we used the available information (i.e. until hospital discharge). We excluded all trials with different follow‐up times for mortality in a sensitivity analysis.

Primary outcomes

  1. All‐cause mortality following randomisation up to a follow‐up time of 30 days.

  2. Setting‐specific treatment failure within 30 days of inclusion.

For the primary care setting, we defined treatment failure as death, hospitalisation, ARI‐specific complications (e.g. empyema for lower ARIs, meningitis for upper ARIs), recurrent or worsening infection, and still having ARI‐associated discomfort at 30 days. For the emergency department setting, we defined treatment failure as death, ICU admission, rehospitalisation after index hospital discharge, ARI‐associated complications (e.g. empyema or acute respiratory distress syndrome for lower ARIs), and recurrent or worsening infection within 30 days of follow‐up. For the medical and surgical ICU setting, we defined treatment failure as death within 30 days of follow‐up and recurrent or worsening infection.

Secondary outcomes

  1. Antibiotic use (initiation of antibiotics, duration of antibiotics, and total exposure to antibiotics (total amount of antibiotic days divided by total number of participants)).

  2. Length of hospital stay for hospitalised participants.

  3. Length of ICU stay for critically ill participants.

  4. Number of days with restricted activities within 14 days after randomisation for primary care participants.

  5. Antibiotic‐related side effects.

Search methods for identification of studies

We updated the search strategy for this review in February 2017 in collaboration with the Cochrane Acute Respiratory Infections Group's Information Specialist. We performed data collection based on the protocol of a previous meta‐analysis of individual participant data published in the Cochrane Library (Schuetz 2008).

Electronic searches

We updated the searches for this review in February 2017, running the search across all databases from the date of inception to 10 February 2017. We screened all new references identified by the search. We searched the following databases for published studies:

  • The Cochrane Central Register of Controlled Trials (CENTRAL; 2017, Issue 1), part of the Cochrane Library, which includes the Cochrane Acute Respiratory Infections Group's Specialised Register, www.cochranelibrary.com/ (accessed 10 February 2017) (Appendix 1);

  • MEDLINE Ovid (1966 to 10 February 2017) (Appendix 2);

  • Embase.com (1980 to 10 February 2017) (Appendix 3).

We used the search strategy in Appendix 4 to conduct searches for the 2012 version of this review (Schuetz 2012).

We also searched for ongoing and completed trials in the following trial register:

  • US National Institutes of Health Ongoing Trials Register ClinicalTrials.gov (www.clinicaltrials.gov/; searched 12 April 2017).

We did not apply any language or publication restrictions.

Searching other resources

We contacted experts for further eligible trials.

Data collection and analysis

We requested individual participant data from the investigators of all included trials. We checked all provided data against published reports, and if needed, corrected any discrepancies.

We prepared this review update according to PRISMA guidelines and the PRISMA‐IPD guideline (Liberati 2009a; Stewart 2015).

Selection of studies

At least two review authors (RS, YW, PS) independently assessed trial eligibility based on titles, abstracts, full‐text reports, and further information from investigators as needed.

Data extraction and management

We checked data from each trial against reported results and resolved any queries with the principal investigator, trial data manager, or statistician. The mortality and adverse outcome rates from trials included in this review may differ slightly from previous reports because we treated data in a consistent manner across all trials.

Assessment of risk of bias in included studies

Two review authors (RS, YW) assessed the methodological quality of each included study using the Cochrane 'Risk of bias' tool and resolved any disagreements by discussion (Higgins 2011). Methodological criteria included: adequate sequence generation and concealment of treatment allocation; blinding of participants, physicians and clinical outcome assessment; whether the study was free of selective reporting; and the proportion of participants lost to follow‐up. We documented the proportion of participants in the PCT group that adhered to the PCT algorithm used in each study, defining adherence to the PCT algorithm of lower than 70% as high risk of bias, and, if not reported, as unclear risk. Due to the study design of the included studies, physicians were aware of the participants' study group because in the intervention group physicians used the PCT result for decision making about antibiotic treatment, while in the control group no PCT result was communicated to the physicians. Blinding of physicians was therefore not feasible, resulting in an unclear risk for performance bias in all studies.

We assessed the quality of evidence at the outcome level using the GRADE approach (GRADEpro GDT 2014).

Measures of treatment effect

We calculated odds ratios (ORs) and 95% confidence intervals (CIs) using multivariable hierarchical logistic regression for the co‐primary endpoints of mortality from any cause and treatment failure (Thompson 2001; Turner 2000). We fitted corresponding linear and logistic regression models for continuous and binary secondary endpoints, respectively. We calculated Kaplan‐Meier curves for time to death for graphical display.

We used Stata version 12.1 (College Station, TX) for statistical analyses (Stata 12.1).

Unit of analysis issues

The unit of our primary analysis was the individual study participant. We analysed all participants in the study group to which they were randomised. We calculated summary estimates using aggregated data from individual trials as a sensitivity analysis.

Dealing with missing data

We received the full data sets from all trials included in the individual participant data analysis (n = 26) with all available follow‐up information (if recorded in the trials).

We assumed in our main analysis that participants lost to follow‐up did not experience an event. We explored if a complete‐case analysis (excluding participants lost to follow‐up) or an analysis assuming that participants lost to follow‐up experienced an event would change the results for the primary outcomes of mortality and treatment failure in sensitivity analyses. We checked all individual participant data against the published results but did not find significant differences that warranted further exploration.

Assessment of heterogeneity

We performed prespecified analyses stratified by clinical setting (i.e. primary care, emergency department, ICU) and ARI diagnosis (CAP, COPD, bronchitis, VAP) to investigate the consistency of results across our heterogeneous patient populations in terms of disease severity. We formally tested for potential subgroup effects by adding the clinical setting and ARI diagnosis in turn to the regression model together with the corresponding interaction term with the PCT group as a fixed‐effect model. We assessed heterogeneity by estimating the I2 statistic (the percentage of total variance across trials that is due to heterogeneity rather than chance) in meta‐analyses using aggregated data and by testing for heterogeneity using the Cochran Q test (Higgins 2003).

Assessment of reporting biases

We assessed reporting bias by attempting to identify if the study was included in a trial registry, a protocol was available, and if the methods section provided a list of outcomes. We compared listed outcomes from those sources to outcomes reported in the published papers.

Data synthesis

We used multivariable hierarchical logistic regression to combine participant data from the trials (Thompson 2001; Turner 2000). Apart from the group variable indicating the use of a PCT algorithm, we included important prognostic factors such as participant age and ARI diagnosis as an additional fixed effect; to account for within‐ and between‐trial variability, we added a categorical trial variable to the model as a random effect. In meta‐analyses with aggregated trial data we calculated summary ORs using a random‐effects model and the Mantel‐Haenszel facility of Review Manager 5 (RevMan 2014).

GRADE and 'Summary of findings' table

We created a 'Summary of findings' table using the following outcomes: all‐cause mortality at 30 days, setting‐specific treatment failure at 30 days, total exposure to antibiotics, and antibiotic‐related side effects (summary of findings Table for the main comparison). The results reported in this table correspond to the main IPD analysis and are slightly different from the aggregate data analysis. We used the five GRADE considerations (study limitations, consistency of effect, imprecision, indirectness, and publication bias) to assess the quality of a body of evidence as it relates to the studies that contribute data to the meta‐analyses for the prespecified outcomes (Atkins 2004). We used the methods and recommendations in Section 8.5 and Chapter 12 of the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011), employing GRADEpro GDT software (GRADEpro GDT 2014). We justified all decisions to down‐ or upgrade the quality of studies using footnotes, and we made comments to aid the reader's understanding of the review where necessary.

Subgroup analysis and investigation of heterogeneity

We performed prespecified analyses stratified by clinical setting and ARI diagnosis and formally tested for potential subgroup effects by adding an interaction term into the statistical model.

Sensitivity analysis

We performed prespecified sensitivity analyses based on the main quality indicators: allocation concealment, blinded outcome assessment, adherence to the PCT algorithm (we defined low adherence to PCT algorithms as < 70%), and follow‐up time for mortality other than one month. We also performed an aggregate data meta‐analysis using all trials with potentially eligible participants.

Results

Description of studies

See: Characteristics of included studies, Characteristics of excluded studies, and Characteristics of ongoing studies tables.

Results of the search

After removal of duplicates, we identified 998 records that we further assessed based on title and abstracts, excluding 919 records. We obtained 79 full‐text study reports, and following assessment excluded 39 that did not meet our inclusion criteria. Eight studies were ongoing trials. From 32 eligible RCTs (9909 participants) including 18 new trials for this 2017 update, we obtained individual participant data from 26 trials including 6708 participants, which were included in the main individual participant data meta‐analysis (see Figure 1). We did not obtain individual participant data for four trials, and two trials did not include participants with confirmed ARIs. The sensitivity aggregate analysis includes all 32 trials.


Study flow diagram.Abbreviations: ARI: acute respiratory infection; IPD: individual participant data; RCT: randomised controlled trial

Study flow diagram.

Abbreviations: ARI: acute respiratory infection; IPD: individual participant data; RCT: randomised controlled trial

Included studies

We included a total of 26 studies involving 6708 participants in the main individual participant data meta‐analysis. Study characteristics are presented in Table 1.

Open in table viewer
Table 1. Characteristics of included trials

Study ID

Country

Setting, type of trial

Clinical diagnosis

Type of PCTalgorithm and PCTcut‐offs used (µg/L)

N: ARI participants (study total)

Primary endpoint

Follow‐up time

Reasons for exclusion of patients

Annane 2013

France

ICU, multicentre

Severe sepsis without overt source of infection and negative blood culture

Initiation and duration; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 5.0)

0 (62)

Participants on AB on day 5 post randomisation

Hospital stay

62 non‐ARI patients (4 of them with post randomisation consent withdrawal)

Bloos 2016

Germany

ICU, multicentre

Severe sepsis or septic shock

Discontinuation at day 4, 7, and 10; R against AB: < 1.0 or > 50% drop to previous value

219 (1180)

28‐day mortality

3 months

91 post randomisation exclusions (informed consent not obtainable), 870 not ARI patients

Bouadma 2010

France

ICU, multicentre

Suspected bacterial infections during ICU stay without prior AB (> 24 h)

Initiation and duration; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 1.0)

394 (630)

All‐cause mortality

2 months

9 post randomisation exclusions (8 withdrew consent, 1 randomised twice); 227 non‐ARI patients

Branche 2015

USA

ED, medical ward, single centre

Lower ARI

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

265 (300)

Antibiotic exposure and safety

3 months

35 non‐ARI patients

Briel 2008

Switzerland

Primary care, multicentre

Upper and lower ARI

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

458 (458)

Days with restricted activities

1 month

No exclusions

Burkhardt 2010

Germany

Primary care, multicentre

Upper and lower ARI

Initiation; R against AB: < 0.25; R for AB: > 0.25

550 (571)

Days with restricted activities

1 month

21 post randomisation exclusions (2 withdrew consent, 1 due to loss of sample, 15 with autoimmune, inflammatory, or systemic disease, 2 with advanced liver disease, 1 with prior use of antibiotics)

Christ‐Crain 2004

Switzerland

ED, single centre

Lower ARI with X‐ray confirmation

Initiation; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

219 (243)

AB use

2 weeks

24 non‐ARI patients

Christ‐Crain 2006

Switzerland

ED, medical ward, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

286 (302)

AB use

6 weeks

16 non‐ARI patients

Corti 2016

Denmark

ED, single centre

AECOPD

Initiation and duration; R against AB < 0.25 (0.15)/80% decrease; R for AB > 0.25

120 (120)

AB use

28 days

No exclusions

De Jong 2016

Netherlands

ICU, multicentre

Critically ill patients with presumed infection

Duration; R against AB: < 0.5 or > 80% drop

994 (1575)

AB use

1 year

29 post randomisation exclusions (25 protocol violations, 4 withdrew informed consent), 552 non‐ARI patients

Deliberato 2013

Brazil

ICU, single centre

Septic patients with proven bacterial infection

Duration; R against AB: < 0.5 or > 90% drop

66 (81)

AB use

ICU discharge or 14 days' post randomisation

15 non‐ARI patients

Ding 2013

China

ICU, single centre

Acute exacerbation of pulmonary fibrosis

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

0 (78)

AB use

1 month

10 post randomisation exclusions (7 lost to follow‐up, 3 withdrew informed consent), 68 data not shared

Hochreiter 2009

Germany

Surgical ICU, single centre

Suspected bacterial infections and > 1 SIRS criteria

Duration; R against AB: < 1 or > 65% drop over 3 d

43 (110)

AB use

Hospital stay

67 non‐ARI patients

Kristoffersen 2009

Denmark

ED, medical ward, multicentre

Lower ARI without X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25 (> 0.5)

210 (223)

AB use

Hospital stay

13 post randomisation exclusions (3 no PCT testing, 6 not meeting inclusion criteria, 4 withdrew informed consent)

Layios 2012

Belgium

ICU, single centre

Suspected infection

Initiation; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 1.0)

160 (509)

AB use

1 month

120 no PCT measurements, 10 missing data, 219 non‐ARI patients

Lima 2016

Brazil

ED, medical ward, single centre

Febrile neutropenia

Duration; R against AB: < 0.5 for 2 days or > 90% drop than highest measured concentration

0 (62)

AB use

28 days

1 post randomisation exclusion (withdrew informed consent), 62 non‐ARI patients

Long 2009

China

ED, outpatients, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

127 (149)

AB use

1 month

22 post randomisation exclusions due to withdrawal of consent

Long 2011

China

ED, outpatients, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

156 (172)

AB use

1 month

16 post randomisation exclusions (6 lost to follow‐up, 7 withdrew consent, 3 with final diagnosis other than CAP)

Long 2014

China

ED, single centre

Severe acute exacerbation of asthma

Initiation; R against AB: < 0.25 (< 0.1); R for AB: > 0.25

180 (180)

AB use

1 year

No exclusions

Maravić‐Stojković 2011

Serbia

ICU surgical, single centre

Infection after open heart surgery

Initiation; R for AB: > 0.5

5 (205)

AB use, AB cost

Hospital stay

200 non‐ARI patients

Najafi 2015

Iran

ICU, single centre

SIRS without apparent source of infection

Initiation; R for AB: > 2

0 (60)

AB use

Hospital stay

60 patient data not shared

Nobre 2008

Switzerland

ICU, single centre

Suspected severe sepsis or septic shock

Duration; R against AB: < 0.5 (< 0.25) or > 80% drop; R for AB: > 0.5 (> 1.0)

52 (79)

AB use

1 month

27 non‐ARI patients

Ogasawara 2014

Japan

Medical ward, single centre

Aspiration pneumonia

Predefined duration; AB for 3 d: < 0.5; AB for 5 d: 0.5 to 1.0; AB for 7 d: > 1

0 (105)

Relapse and 30‐day mortality

1 month

9 post randomisation exclusions (2 withdrew consent, 7 others), 96 data not shared

Oliveira 2013

Brazil

ICU, multicentre

Severe sepsis or septic shock

Discontinuation; initial < 1.0: R against AB: 0.1 at day 4; initial > 1.0: R against: > 90% drop

58 (97)

AB use

28 days or hospital discharge

3 post randomisation exclusions (2 withdrew consent, 1 technical problems), 36 patients with a final diagnosis other than ARI

Schroeder 2009

Germany

Surgical ICU, single centre

Severe sepsis following abdominal surgery

Duration; R against AB: < 1 or > 65% drop over 3 d

8 (27)

AB use

Hospital stay

19 non‐ARI patients

Schuetz 2009

Switzerland

ED, medical ward, multicentre

Lower ARI with X‐ray confirmation

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

1304 (1381)

AB use

1 month

22 post randomisation exclusions due to withdrawal of consent, 55 non‐ARI patients

Shehabi 2014

Australia

ICU, multicentre

Suspected sepsis, undifferentiated infections

Duration; R against AB: < 0.25 (< 0.1) or > 90% drop

156 (400)

AB use

3 months

6 post randomisation exclusions (6 withdrew consent), 238 non‐ARI patients

Stolz 2007

Switzerland

ED, medical ward, single centre

Exacerbated COPD

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

208 (226)

AB use

2 to 3 weeks

18 post randomisation exclusions (absence of COPD)

Stolz 2009

Switzerland, USA

ICU, multicentre

VAP when intubated > 48 h

Duration; R against AB: < 0.5 (< 0.25) or > 80% drop; R for AB: > 0.5 (> 1.0)

101 (101)

AB‐free days alive

1 month

No exclusions

Tang 2013

China

ED, single centre

Exacerbation of asthma

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25

0 (265)

AB use

6 weeks

10 post randomisation exclusions (5 lost to follow‐up, 3 died, 2 withdrew consent), 255 data not shared

Verduri 2015

Italy

ED, medical ward, multicentre

AECOPD

Initiation; R against AB:< 0.1; R for AB: > 0.25

178 (183)

Number of exacerbations

6 months

5 post randomisation exclusions (5 lost to follow‐up because they did not meet the inclusion criteria)

Wang 2016

China

ICU, single centre

AECOPD

All participants had initial PCT < 0.1; AB group treated with AB for at least 3 days, control group no AB in the first 10 days

191 (194)

Treatment success within 10 days

30 days

3 post randomisation exclusions (3 with pneumonia according to CT scan)

AB: antibiotic
AECOPD: acute exacerbation of chronic obstructive pulmonary disease
ARI: acute respiratory infection
CAP: community‐acquired pneumonia
COPD: chronic obstructive pulmonary disease
CT: computed tomography
d: days
ED: emergency department
h: hours
ICU: intensive care unit
PCT: procalcitonin
R: recommendation for or against antibiotics
SIRS: systemic inflammatory response syndrome
VAP: ventilator‐associated pneumonia

Participants

Baseline characteristics of included participants were similar in the PCT and control groups with respect to important prognostic features (Table 2). Most participants were recruited either in the emergency department or ICU setting, and CAP was the most frequent ARI diagnosis, reported in more than 40% of participants.

Open in table viewer
Table 2. Baseline characteristics of included participants

Parameter

Control (n = 3372)

PCT group (n = 3336)

Demographics

Age (year), mean (SD)

61.2 ± 18.4

60.7 ± 18.8

Male gender, n (%)

1910 (56.6%)

1898 (56.9%)

Clinical setting, no (%)

Primary care

501 (14.9%)

507 (15.2%)

Emergency department

1638 (48.6%)

1615 (48.4%)

Intensive care unit

1233 (36.6%)

1214 (36.4%)

Primary diagnosis

Total upper ARI, n (%)

280 (8.3%)

292 (8.8%)

Common cold

156 (4.6%)

149 (4.5%)

Rhino‐sinusitis, otitis

67 (2.0%)

73 (2.2%)

Pharyngitis, tonsillitis

46 (1.4%)

61 (1.8%)

Total lower ARI, n (%)

3092 (91.7%)

3044 (91.2%)

Community‐acquired pneumonia

1468 (43.5%)

1442 (43.2%)

Hospital‐acquired pneumonia

262 (7.8%)

243 (7.3%)

Ventilator‐associated pneumonia

186 (5.5%)

194 (5.8%)

Acute bronchitis

287 (8.5%)

257 (7.7%)

Exacerbation of COPD

631 (18.7%)

621 (18.6%)

Exacerbation of asthma

127 (3.8%)

143 (4.3%)

Other lower ARI

131 (3.9%)

144 (4.3%)

Procalcitonin upon enrolment

PCT< 0.1 ug/L

921 (35.6%)

981 (30.9%)

PCT 0.1 to 0.25 ug/L

521 (20.1%)

608 (19.2%)

PCT > 0.25 to 0.5 ug/L

308 (11.9%)

383 (12.1%)

PCT > 0.5 to 2.0 ug/L

358 (13.8%)

520 (16.4%)

PCT > 2.0 ug/L

482 (18.6%)

679 (21.4%)

ARI: acute respiratory infection
COPD: chronic obstructive pulmonary disease
PCT: procalcitonin
SD: standard deviation

Settings

Trials were conducted in 12 countries: Switzerland, Germany, France, Italy, USA, China, Denmark, Netherlands, Brazil, Belgium, Australia, and Serbia. Trials were conducted in different clinical settings including primary care, emergency departments and medical wards, and ICU. There were two primary care trials with upper and lower respiratory infection patients; 11 emergency department and medical ward trials with lower ARI patients; and 13 ICU trials with mostly septic patients due to infections of the lower respiratory tract.

Interventions

Procalcitonin algorithms used in the different trials were similar in concept and recommended initiation and/or continuation of antibiotic therapy based on similar PCT cut‐off levels (reviewed in Schuetz 2011a). However, there were differences: some trials in primary care and the emergency department used only a single PCT measurement on admission to guide initiation of antibiotics, while the other trials (predominantly in hospitalised patients with severe infections) used repeated measurements for guiding the duration of treatment. One trial used a point‐of‐care device (Corti 2016). Adherence to algorithms varied, ranging from 44% to 100% (Table 3).

Open in table viewer
Table 3. Quality assessment of trials

Study ID

Allocation concealment

Blinded
outcome assessment

Follow‐up for mortality

Adherence to PCT algorithm in PCT group

Follow‐up for mortality

Annane 2013

Yes (central randomisation)

No

58/58 (100%)

63% adherence

LOS

Bloos 2016

Yes (central randomisation)

No

1045/1089 (96%)

49.6% adherence

28 days and 90 days

Bouadma 2010

Yes (central randomisation)

Yes

393/394 (100%)

47% adherence

28 days and 60 days

Branche 2015

Yes (central randomisation using blocks of 4)

No

250/300 (83.3%)

64% adherence

1 month and 3 months

Briel 2008

Yes (central randomisation)

Yes

454/458 (99%)

85% adherence

28 days

Burkhardt 2010

Yes (central randomisation)

Yes

546/550 (99%)

87% adherence

28 days

Christ‐Crain 2004

No (alternating weeks)

No

230/243 (95%)

83% adherence

10 to 14 days

Christ‐Crain 2006

Yes (sequentially numbered, opaque, sealed envelopes)

No

300/302 (99%)

87% adherence

56 days

Corti 2016

Yes (randomisation algorithm was concealed to treating clinicians and participants)

No

120/120 (100%)

61.1% adherence

28 days

De Jong 2016

Yes (central randomisation)

No

1546/1546 (100%)

44% adherence

28 days and 1 year

Deliberato 2013

Yes (opaque, sealed envelopes)

No

81/81 (100%)

52% adherence

LOS

Ding 2013

Yes (central randomisation)

No

68/78 (87.2%)

Not reported

30 days

Hochreiter 2009

No (unconcealed drawing of lots)

No

43/43 (100% until discharge)

Not reported

LOS

Kristoffersen 2009

Yes (central randomisation)

No

210/210 (100% until discharge)

59% adherence

LOS

Layios 2012

Not reported

No

509/509 (100%)

Not reported

Intensive care unit LOS

Lima 2016

Yes (sequentially numbered, opaque, sealed envelopes)

No

61/62 (98.4%)

73.3% adherence

28 days and 90 days

Long 2009

No (odd and even patient ID numbers)

No

127/127 (100%)

Not reported

Not reported

Long 2011

No (odd and even patient ID numbers)

No

156/156 (100%)

Not reported

28 days

Long 2014

Yes (central randomisation)

No

169/180 (93.9%)

96.6% adherence

LOS and 1 year

Maravić‐Stojković 2011

Yes (central randomisation)

No

205/205 (100%)

Not reported

30 days and LOS

Najafi 2015

Yes (central randomisation)

No

30/30 (100%)

Not reported

LOS

Nobre 2008

Yes (sequentially numbered, opaque, sealed envelopes)

No

52/52 (100%)

81% adherence

28 days and LOS

Ogasawara 2014

Not reported

No

96/96 (100%)

Not reported

30 days

Oliveira 2013

Yes (central randomisation)

No

94/94 (100%)

86.2% adherence

28 days

Schroeder 2009

No (unconcealed drawing of lots)

No

8/8 (100% until discharge)

Not reported

LOS

Schuetz 2009

Yes (central randomisation)

Yes

1358/1359 (100%)

91% adherence

28 days

Shehabi 2014

Yes (central randomisation)

Yes

394/394 (100%)

Not reported

LOS and 90 days

Stolz 2007

Yes (sequentially numbered, opaque, sealed envelopes)

Yes

208/208 (100%)

Not reported

6 months

Stolz 2009

Yes (sequentially numbered, opaque, sealed envelopes)

No

101/101 (100%)

Not reported

28 days

Tang 2013

Yes (sequentially numbered, opaque, sealed envelopes)

Yes

258/265 (97.4%)

Not reported

6 weeks

Verduri 2015

Yes (central randomisation)

No

178/178 (100%)

Not reported

6 months

Wang 2016

Yes (those responsible for allocation concealment were not involved in the measurement of results)

No

191/191 (100%)

82.3% adherence (17 participants in the control group received AB)

30 days

LOS: length of stay
PCT: procalcitonin

Comparators

In control group participants, PCT was not used to guide treatment decisions, but this decision was up to the treating physician team. In some trials, physicians were asked to follow antibiotic guidelines for control group participants (Briel 2008; Schuetz 2009). In one trial, the control group was guided with C‐reactive protein levels (Oliveira 2013).

Funding sources

All studies were investigator‐initiated trials. Half of the trials were funded by national agencies or did not report funding; the other half of the trials received funding from the biomarker industry (e.g. Thermo Fisher Scientific).

Excluded studies

We excluded a total of 39 studies due to wrong intervention (n = 1), wrong population (n = 2), and wrong design (not RCT) (n = 36). A total of nine studies reported as ongoing in the 2012 review were now available for assessment; we included four of these studies in this current update (Annane 2013; Bloos 2016; De Jong 2016; Lima 2016), and did not include five studies due to wrong population (paediatrics).

Ongoing studies

Our searches of the trial register identified seven ongoing studies that we will assess for inclusion for the next review update (Ongoing studies). These studies focus on the utility of PCT in people with pneumonitis (NCT02862314), pulmonary embolism (NCT02261610), lower respiratory infection (NCT02130986), heart failure (NCT02787603), and intraoperative positive‐end expiratory pressure optimisation (NCT02931409). Two trials are antibiotic efficacy trials (NCT02332577; NCT02440828).

Risk of bias in included studies

The overall risk of bias is presented graphically in Figure 2 and Figure 3. The risk of bias was mostly low for random sequence generation, allocation concealment, incomplete outcome data, and selective reporting; unclear for blinding of personnel in all studies; and mostly high for blinding of outcome assessment.


'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.


'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.

'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.

Allocation

All studies randomised participants to intervention (PCT testing) or control groups. A total of 25 trials with mainly computer‐generated lists and centralised randomisation were at low risk of selection bias. Seven trials were at high or unclear risk of selection bias. Risk for selection bias with regard to random sequence generation was due to weekly allocation (Christ‐Crain 2004), unnumbered envelopes (Christ‐Crain 2006; Stolz 2007), use of odd and even patient identification numbers (Long 2009; Long 2011), and unconcealed drawing of lots (Hochreiter 2009; Schroeder 2009).

Blinding

None of the included trials blinded physicians to group allocation because PCT was used for decision making in the intervention group, thus all trials had unclear risk for blinding of participants and personnel.

All trials used blinded outcome assessment (Briel 2008; Bouadma 2010; Branche 2015; Layios 2012; Schuetz 2009; Shehabi 2014; Stolz 2007; Tang 2013), employing blinded telephone interviews to assess vital status and other outcomes.

Incomplete outcome data

The included trials had a high follow‐up for mortality with few participants lost to follow‐up (Table 3). In seven trials, outcome assessment was done after hospital or ICU discharge (Deliberato 2013; Hochreiter 2009; Kristoffersen 2009; Layios 2012; Long 2009; Schroeder 2009; Shehabi 2014). One trial had a high number of post randomisation exclusions (six in the intervention arm versus four in the control group) and thus had an unclear risk of bias (Ding 2013).

Selective reporting

No reporting bias was found when study protocols and final results were compared. However, we did not find registration numbers for four trials (Ding 2013; Layios 2012; Maravić‐Stojković 2011; Najafi 2015), which we considered to be at unclear risk of bias. We found no evidence of reporting bias by visual inspection of funnel plots (Figure 4).


Funnel plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Funnel plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Other potential sources of bias

Another potential source of bias relates to low adherence to the PCT algorithms, particularly for safety endpoints. Overall, adherence varied, ranging from 44% to 100% (Table 3).

With regard to funding, 16 trials reported no industry funding (six did not report any funding, 10 reported public funding), and in 16 trials Thermo Fisher, the producer of the PCT assay, funded or co funded the studies by providing free‐of‐charge PCT kits or additional research funds, or both.

Effects of interventions

See: Summary of findings for the main comparison Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections

Primary outcomes

1. All‐cause mortality following randomisation up to a follow‐up time of 30 days

There were 286 deaths in 3336 PCT‐guided participants (8.6%) compared to 336 in 3372 controls (10.0%) resulting in a significantly lower mortality associated with PCT‐guided therapy (adjusted odds ratio (OR) 0.83, 95% confidence interval (CI) 0.70 to 0.99, P = 0.037) (Table 4). This effect was consistent across clinical settings (P for interaction > 0.05), although mortality could not be estimated in primary care trials because only one death was reported in a control group participant. The effect on mortality was also consistent among different ARI diagnoses (CAP, COPD, bronchitis, VAP) (P for interaction > 0.05). As a further sensitivity analysis and to investigate heterogeneity among trials, we also calculated an aggregate data meta‐analysis based on the aggregate results of all 32 potentially eligible trials (thus not limited to ARI participants only). In this analysis, the results proved robust, although the mortality estimate did not reach statistical significance (OR 0.89, 95% CI 0.78 to 1.01; Analysis 1.1; Figure 5). There was no evidence of heterogeneity (I2 = 0%).


Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Open in table viewer
Table 4. Clinical endpoints overall and stratified by setting and ARI diagnosis

Control group

PCT group

Measures of effect: adjusted OR or difference (95% CI), P value

P for interaction

Overall

3372

3336

30 days mortality, n (%)

336 (10.0%)

286 (8.6%)

0.83 (0.70 to 0.99), P = 0.037

NA

Treatment failure, n (%)

841 (24.9%)

768 (23.0%)

0.90 (0.80 to 1.01), P = 0.068

NA

Length of ICU stay, mean (±SD)

13.3 ± 16.0

13.7 ± 17.2

0.39 (‐0.81 to 1.58), P = 0.524

NA

Length of hospital stay, mean (±SD)

13.7 ± 20.6

13.4 ± 18.4

‐0.19 (‐0.96 to 0.58), P = 0.626

NA

Antibiotic‐related side effects, n (%)

336 (22.1%)

247 (16.3%)

0.68 (0.57 to 0.82), P < 0.001

NA

According to setting

Primary care

501

507

30 days mortality, n (%)

1 (0.2%)

0 (0.0%)

NA

NA

Treatment failure, n (%)

164 (32.7%)

159 (31.4%)

0.96 (0.73 to 1.25), P = 0.751

0.715

Days with restricted activities, mean (±SD)

8.9 ± 4.2

8.9 ± 4.1

0.07 (‐0.44 to 0.59), P = 0.777

NA

Antibiotic‐related side effects, n (%)

128 (25.7%)

102 (20.2%)

0.65 (0.46 to 0.91), P = 0.012

0.596

Emergency department

1638

1615

30 days mortality, n (%)

62 (3.8%)

57 (3.5%)

0.91 (0.63 to 1.33), P = 0.635

0.546

Treatment failure, n (%)

292 (17.8%)

259 (16.0%)

0.87 (0.72 to 1.05), P = 0.141

0.807

Length of hospital stay, mean (±SD)

8.2 ± 10.5

8.1 ± 7.5

‐0.14 (‐0.73 to 0.44), P = 0.631

0.684

Antibiotic‐related side effects, n (%)

208 (20.3%)

145 (14.4%)

0.66 (0.52 to 0.83), P = 0.001

0.596

Intensive care unit

1233

1214

30 days mortality, n (%)

273 (22.3%)

229 (19.0%)

0.84 (0.69 to 1.02), P = 0.081

0.619

Length of ICU stay, mean (±SD)

14.8 ± 16.2

15.3 ± 17.5

0.56 (‐0.82 to 1.93), P = 0.427

0.849

Length of hospital stay, mean (±SD)

26.3 ± 26.9

25.8 ± 23.9

‐0.33 (‐2.28 to 1.62), P = 0.739

0.641

According to diagnosis

Community‐acquired pneumonia

1468

1442

30 days mortality, n (%)

206 (14.1%)

175 (12.2%)

0.82 (0.66 to 1.03), P = 0.083

0.958

Treatment failure, n (%)

385 (26.2%)

317 (22.0%)

0.78 (0.66 to 0.93), P = 0.005

0.052

Length of ICU stay, mean (±SD)

10.5 ± 10.3

11.9 ± 13.3

1.45 (0.15 to 2.75), P = 0.029

0.119

Length of hospital stay, mean (±SD)

13.3 ± 15.7

13.9 ± 16.1

0.74 (‐0.25 to 1.73), P = 0.143

0.094

Antibiotic‐related side effects, n (%)

186 (27.7%)

127 (19.1%)

0.62 (0.48 to 0.80), P < 0.001

0.227

Exacerbation of COPD

631

621

30 days mortality, n (%)

24 (3.8%)

19 (3.1%)

0.8 (0.43 to 1.48), P = 0.472

0.847

Treatment failure, n (%)

110 (17.4%)

104 (16.7%)

0.94 (0.70 to 1.27), P = 0.704

0.676

Length of hospital stay, mean (±SD)

9.3 ± 13.9

8.4 ± 7.2

‐0.60 (‐1.84 to 0.64), P = 0.342

0.658

Antibiotic‐related side effects, n (%)

30 (10.9%)

29 (10.5%)

0.93 (0.53 to 1.63), P = 0.805

0.198

Acute bronchitis

287

257

30 days mortality, n (%)

0 (0.0%)

2 (0.8%)

NA

NA

Treatment failure, n (%)

55 (19.2%)

52 (20.2%)

1.11 (0.72 to 1.70), P = 0.643

0.4

Length of hospital stay, mean (±SD)

2.6 ± 5.7

2.2 ± 4.7

‐0.21 (‐0.90 to 0.48), P = 0.556

0.97

Antibiotic‐related side effects, n (%)

54 (21.6%)

39 (17.3%)

0.77 (0.49 to 1.22), P = 0.263

0.657

Ventilator‐associated pneumonia

186

194

30 days mortality, n (%)

29 (15.6%)

23 (12.0%)

0.75 (0.41 to 1.39), P = 0.366

0.644

Treatment failure, n (%)

51 (27.4%)

44 (22.7%)

0.78 (0.48 to 1.28), P = 0.332

0.522

Length of ICU stay, mean (±SD)

23.5 ± 20.5

21.8 ± 19.1

‐1.74 (‐5.64 to 2.17), P = 0.383

0.441

Length of hospital stay, mean (±SD)

33.8 ± 27.6

32.0 ± 23.1

‐2.14 (‐7.04 to 2.75), P = 0.391

0.448

Measures of effect: dichotomous outcomes are reported as adjusted OR (95% CI) and continuous outcomes are adjusted mean differences and confidence intervals

ARI: acute respiratory infection
CI: confidence interval
COPD: chronic obstructive pulmonary disease
ICU: intensive care unit
NA: not applicable
OR: odds ratio
PCT: procalcitonin
SD: standard deviation

2. Setting‐specific treatment failure within 30 days of inclusion

Treatment failure was not significantly lower in PCT‐guided participants (23.0% versus 24.9%, adjusted OR 0.90, 95% CI 0.80 to 1.01, P = 0.068). These results were similar among subgroups by clinical setting and type of respiratory infection (P for interaction > 0.05). With an OR of 0.90 (95% CI 0.81 to 0.99), treatment failure was significantly lower in PCT group participants in an aggregate data meta‐analysis based on all 32 potentially eligible trials (thus relying on the original definition of treatment failure as used in the trials). There was no evidence of heterogeneity (I2 = 0%) (Figure 6). We also performed several predefined sensitivity analyses, which showed no evidence for interactions (see summary in Table 5).


Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.2 Treatment failure at 30 days.

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.2 Treatment failure at 30 days.

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Table 5. Sensitivity analysis

Mortality

Main analysis

Control group

PCT group

Adjusted OR (95% CI), P value

P for interaction

All participants

336 (10.0%)

286 (8.6%)

0.83 (0.70 to 0.99), P = 0.037

NA

Adherence

High adherence

82 (4.5%)

75 (4.1%)

0.88 (0.63 to 1.22), P = 0.434

0.617

Low adherence (< 70% or not reporting)

254 (16.4%)

211 (14.0%)

0.83 (0.67 to 1.02), P = 0.073

Allocation

Low risk for allocation concealment bias

305 (10.6%)

250 (8.8%)

0.80 (0.67 to 0.97), P = 0.021

0.229

High risk for allocation concealment bias (or not reporting)

31 (6.5%)

36 (7.3%)

1.12 (0.66 to 1.91), P = 0.672

Blinding

Blinded outcome assessment

113 (6.5%)

102 (5.9%)

0.85 (0.64 to 1.13), P = 0.259

0.537

No blinded outcome assessment

223 (13.8%)

184 (11.5%)

0.81 (0.65 to 1.01), P = 0.062

Follow‐up

Follow up for mortality at 1 month

275 (10.7%)

224 (8.9%)

0.81 (0.67 to 0.99), P = 0.039

0.325

Follow up for mortality < 1 month

61 (7.6%)

62 (7.6%)

0.94 (0.64 to 1.38), P = 0.756

Treatment failure

Control group

PCT group

Adjusted OR (95% CI), P value

P for interaction

All participants

841 (24.9%)

768 (23.0%)

0.90 (0.80 to 1.01), P = 0.068

NA

Adherence

High adherence

419 (23.1%)

381 (21.0%)

0.89 (0.76 to 1.04), P = 0.148

0.752

Low adherence (< 70% or not reporting)

422 (27.1%)

387 (25.5%)

0.92 (0.77 to 1.08), P = 0.301

Allocation

Low risk for allocation concealment bias

776 (26.8%)

699 (24.6%)

0.89 (0.79 to 1.01), P = 0.069

0.486

High risk for allocation concealment bias (or not reporting)

65 (13.6%)

69 (13.8%)

0.99 (0.68 to 1.44), P = 0.939

Blinding

Blinded outcome assessment

412 (23.5%)

367 (21.1%)

0.88 (0.75 to 1.03), P = 0.117

0.574

No blinded outcome assessment

429 (26.5%)

401 (25.1%)

0.94 (0.79 to 1.11), P = 0.438

CI: confidence interval
NA: not applicable
OR: odds ratio
PCT: procalcitonin

Secondary outcomes

1. Antibiotic use (initiation of antibiotics, duration of antibiotics, and total exposure to antibiotics (total amount of antibiotic days divided by total number of participants))

Procalcitonin guidance was associated with a reduction in total antibiotic exposure (mean 8.1 days compared to 5.7 days, regression coefficient ‐2.43 days (95% CI ‐2.71 to ‐2.15), P < 0.001). Also, duration of antibiotic treatment in treated participants was shorter (mean 9.4 days compared to 8.0 days, adjusted coefficient ‐1.83 days (95% CI ‐2.15 to ‐1.5), P < 0.001) (Table 6).

Open in table viewer
Table 6. Antibiotic treatment overall and stratified by setting and ARI diagnosis

Parameter

Control group

PCT group

Measures of effect: adjusted OR or difference (95% CI), P value

P for interaction

Overall

3372

3336

Initiation of antibiotics, n (%)

2894 (86.3%)

2351 (71.5%)

0.27 (0.24 to 0.32), P < 0.001

Duration of antibiotics (days), mean (±SD)

9.4 ± 6.2

8.0 ± 6.5

‐1.83 (‐2.15 to ‐1.50), P < 0.001

Total exposure of antibiotics (days), mean (±SD)

8.1 ± 6.6

5.7 ± 6.6

‐2.43 (‐2.71 to ‐2.15), P < 0.001

Setting‐specific outcomes

Primary care

501

507

Initiation of antibiotics, n (%)

316 (63.1%)

116 (22.9%)

0.13 (0.09 to 0.18), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

7.3 ± 2.5

7.0 ± 2.8

‐0.52 (‐1.07 to 0.04), P = 0.068

0.064

Total exposure of antibiotics (days), mean (±SD)

4.6 ± 4.1

1.6 ± 3.2

‐3.02 (‐3.45 to ‐2.58), P < 0.001

0.101

Emergency department

1638

1615

Initiation of antibiotics, n (%)

1354 (83.2%)

1119 (71.3%)

0.49 (0.41 to 0.58), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

9.8 ± 5.4

7.3 ± 5.1

‐2.45 (‐2.86 to ‐2.05), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

8.2 ± 6.2

5.2 ± 5.4

‐3.02 (‐3.41 to ‐2.62), P < 0.001

< 0.001

Intensive care unit

1233

1214

Initiation of antibiotics, n (%)

1224 (99.8%)

1116 (91.9%)

0.02 (0.01 to 0.05), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

9.5 ± 7.4

8.8 ± 7.8

‐1.23 (‐1.82 to ‐0.65), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

9.5 ± 7.4

8.1 ± 7.9

‐1.44 (‐1.99 to ‐0.88), P < 0.001

< 0.001

Disease‐specific outcomes

Community‐acquired pneumonia

1468

1442

Initiation of antibiotics, n (%)

1455 (99.4%)

1340 (92.9%)

0.08 (0.04 to 0.15), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

10.5 ± 6.2

8.0 ± 5.7

‐2.45 (‐2.87 to ‐2.02), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

10.4 ± 6.2

7.5 ± 5.9

‐2.94 (‐3.38 to ‐2.50), P < 0.001

0.004

Exacerbation of COPD

631

621

Initiation of antibiotics, n (%)

453 (71.8%)

266 (42.8%)

0.29 (0.23 to 0.36), P < 0.001

0.017

Duration of antibiotics (days), mean (±SD)

7.4 ± 5.3

7.2 ± 6.7

‐1.15 (‐2.00 to ‐0.31), P = 0.007

0.003

Total exposure of antibiotics (days), mean (±SD)

5.3 ± 5.6

3.1 ± 5.6

‐2.22 (‐2.83 to ‐1.60), P < 0.001

0.506

Acute bronchitis

287

257

Initiation of antibiotics, n (%)

189 (65.9%)

68 (26.5%)

0.18 (0.12 to 0.26), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

7.1 ± 3.0

6.4 ± 3.5

‐0.35 (‐1.15 to 0.45), P = 0.393

0.359

Total exposure of antibiotics (days), mean (±SD)

4.7 ± 4.2

1.7 ± 3.3

‐2.95 (‐3.59 to ‐2.31), P < 0.001

0.33

Ventilator‐associated pneumonia

186

194

Initiation of antibiotics, n (%)

186 (100.0%)

193 (99.5%)

NA

NA

Duration of antibiotics (days), mean (±SD)

13.1 ± 7.9

10.8 ± 8.7

‐2.22 (‐3.80 to ‐0.65), P = 0.006

0.253

Total exposure of antibiotics (days), mean (±SD)

13.1 ± 7.9

10.8 ± 8.7

‐2.45 (‐4.09 to ‐0.82), P = 0.003

0.786

Note: Duration refers to the total days of antibiotic therapy in participants in whom antibiotics were initiated. Total exposure refers to the total days of antibiotic therapy in all randomised participants.

Measures of effect: dichotomous outcomes are reported as adjusted OR (95% CI) and continuous outcomes are adjusted mean differences and confidence intervals

ARI: acute respiratory infection
CI: confidence interval
COPD: chronic obstructive pulmonary disease
NA: not applicable
OR: odds ratio
PCT: procalcitonin
SD: standard deviation

2. Length of hospital stay for hospitalised participants

However, the effect on antibiotic consumption differed according to clinical setting. In the primary care setting, lower antibiotic exposure was mainly due to lower initial prescription rates (P < 0.001 for interaction between primary care setting and PCT group on antibiotic prescriptions). Similarly, lower antibiotic exposure due to lower prescription rates was found in selected infections such as acute bronchitis (adjusted OR 0.18, 95% CI 0.12 to 0.26; P for interaction < 0.001). Lower antibiotic prescription rates (adjusted OR 0.49, 95% CI 0.41 to 0.58) and shorter duration of antibiotic therapy in participants with initiation of antibiotic (adjusted coefficient ‐2.45 days, 95% CI ‐2.86 to ‐2.05) contributed to the lower overall exposure in the emergency department setting.

Length of hospital stay and ICU stay were similar in both groups with no evidence for different effects in subgroups (P for interaction > 0.05).

3. Length of ICU stay for critically ill participants

For the ICU setting, the lower exposure was mainly explained by shorter treatment durations (adjusted difference in days ‐1.23, 95% CI ‐1.82 to ‐0.65). Similarly, for CAP, the lower exposure was mainly explained by shorter durations (adjusted difference in days ‐2.45, 95% CI ‐2.87 to ‐2.02).

4. Number of days with restricted activities within 14 days after randomisation for primary care participants

For studies conducted in the primary care setting, there was no difference in days with restricted activities of daily living between PCT and control group participants (days, 8.9 ± 4.2 versus 8.9 ± 4.1, regression coefficient 0.07 (95% CI ‐0.44 to 0.59), P = 0.777).

5. Antibiotic‐related side effects

There was also a significant reduction in antibiotic‐related side effects (16.3% versus 22.1%, adjusted OR 0.68, 95% CI 0.57 to 0.82, P < 0.001). This outcome was only assessed in some of the primary care and emergency department trials (n = 6), and not in ICU trials. There was no evidence for subgroup effects (P for interaction > 0.05).

Discussion

Summary of main results

This updated systematic review and meta‐analysis included 32 trials, of which 26 trials were used for the main individual participant data analysis. Trials were conducted in 12 countries and included different clinical settings and types of respiratory infections. There was mostly low risk for random sequence generation, allocation concealment, incomplete outcome data, and selective reporting. There was unclear risk in all studies for blinding of personnel, and mostly high risk for blinding of outcome assessment. The results indicate a significant reduction in mortality (high‐quality evidence according to GRADE, summary of findings Table for the main comparison) and non‐significant result for treatment failure (moderate‐quality evidence according to GRADE, summary of findings Table for the main comparison) when PCT was used to guide initiation and duration of antibiotic treatment in ARI participants compared to control participants. Additionally, antibiotic consumption and side effects from antibiotics were significantly reduced across different clinical settings and types of ARIs. There was no effect on length of hospital stay and ICU length of stay. Results were similar in subgroup and sensitivity analyses including an aggregate data analysis with all 32 potentially eligible trials. Limitations include incomplete individual participant data, with four research groups not agreeing to the sharing of individual participant data; incomplete follow‐up information in some of the trials where no outcome assessment was done after 30 days of enrolment; differences in definitions of treatment failure among trials; and exclusion of some patient populations such as immunosuppressed people. Still, results from this updated individual participant data meta‐analysis support the use of PCT in the context of antibiotic stewardship in people with ARIs.

Overall completeness and applicability of evidence

The strengths of our review include an explicit study protocol, a comprehensive search to retrieve all relevant trials, access to individual participant‐level data from all but four of the included trials, and standardised outcome definitions across trials, thereby overcoming limitations of meta‐analyses using aggregated data. To minimise the risk of data‐driven associations, we prespecified a limited number of prognostic factors and subgroup variables for our statistical model. We allowed for potential clustering effects by using random‐effects models for included trials. Our results proved robust in sensitivity analyses focusing on high‐quality trials and on participants with complete follow‐up data.

The accuracy of PCT for diagnosing bacterial infections has been called into question by previous meta‐analyses of observational studies, which demonstrated mixed results (Jones 2007; Simmonds 2005; Tang 2007; Uzzan 2006). However, a more recent meta‐analysis using positive culture as the reference method found moderate to high discrimination of systematic inflammatory response syndrome and sepsis (Wacker 2013). Since there are no available gold standards for the diagnosis of the clinical conditions included in our analysis, most studies used clinical consensus criteria, which may differ among studies. Rather than relying on these imperfect diagnostic criteria, we were able to assess the value of PCT algorithms by means of RCTs measuring clinically relevant, participant‐level outcomes.

Despite these merits, this review has several limitations. We limited our analysis to adults with ARIs who were mostly immunocompetent, and excluded some pathogens (i.e. Legionella or Pseudomonas infections). The results of these trials may therefore not be generalised to people who are immunocompromised, with specific pathogens or infections other than ARIs, or children. Previous RCTs have shown that PCT guidance also reduces antibiotic exposure in a neonatal sepsis population but not in children with fever without a source (Manzano 2010). We found several ongoing RCTs in children evaluating PCT algorithms that should shed further light on the benefits and harms of PCT use for children. The included trials compared the PCT strategy to a control group where antibiotic therapy was guided based on 'usual practice' or based on current guideline recommendations. The magnitude of antibiotic reduction obviously correlates strongly with antibiotic prescription patterns, and in regions of low antibiotic prescription the PCT strategy may have smaller effects.

Quality of the evidence

Characteristics of the individual trials are presented in Table 1. Most trials had a follow‐up of one month, with two trials assessing outcome after 14 to 21 days and several trials following participants until hospital discharge (or ICU discharge) only. Procalcitonin algorithms used in the different trials were similar in concept and recommended initiation and/or continuation of antibiotic therapy based on similar PCT cut‐off levels (Table 1). However, there were differences: some trials in primary care and the emergency department used only a single PCT measurement on admission to guide initiation of antibiotics (Burkhardt 2010; Christ‐Crain 2004), while the other trials (predominantly in hospitalised participants with severe infections) used repeated measurements for guiding the duration of treatment. Adherence to algorithms was variable. In terms of methodological quality, trials had concealed allocation, but in several trials blinded outcome assessment was not done. All trials achieved complete or near‐complete follow‐up for mortality. None of the trials blinded participants or physicians to group allocation. The overall quality of the evidence according to GRADE was moderate to high (summary of findings Table for the main comparison).

Potential biases in the review process

Due to the differences in patient populations included in this analysis, which ranged from primary care to the ICU, we adapted the definition of treatment failure to clinical settings by including setting‐specific components in this composite outcome. This may challenge the clinical interpretation in the overall analysis.

Agreements and disagreements with other studies or reviews

While mortality did not differ significantly in our initial meta‐analysis (adjusted OR 0.94, 95% CI 0.71 to 1.23) (Schuetz 2012), we found a significantly lower mortality rate in PCT‐guided participants in this update. This result was robust in subgroup analyses and in our sensitivity analysis. Also, when considering all trials in the aggregate data analysis, mortality tended to be reduced, although not significantly (OR 0.89, 95% CI 0.78 to 1.01). Importantly, the largest‐yet ICU trial from the Netherlands has reported a significantly lower mortality in PCT‐guided participants (De Jong 2016).

Two of the included individual trials reported reduced length of stay, particularly within the ICU. Yet, despite a marked reduction in the duration of antibiotic therapy across trials and settings, there was no difference in length of ICU and hospital stay between the two groups in our comprehensive analysis. One might expect that clinically stable patients with discontinued intravenous antibiotics could be safely discharged unless there are extenuating circumstances. Perceived needs by physicians to further monitor these patients in the unit or inability to transfer patients to other inpatient or aftercare locations may partly explain this finding.

There is ongoing controversy about the diagnostic performance of PCT and other blood markers to correctly identify patients with a bacterial infection. In fact, several observational studies have questioned the added value of PCT in addition to clinical signs, such as a primary care study authored by van Vugt and colleagues reporting no additional benefit of PCT to a clinical assessment (van Vugt 2013). Importantly, in the context of respiratory infections, diagnostic studies are limited by the lack of a reference standard, with blood cultures only detecting a minority of cases (e.g. only 10% to 20% of patients with clinically and radiologically confirmed CAP have positive blood cultures) (Muller 2010; Wacker 2013). Interventional research, such as the trials included in the current analysis, do not rely on a reference standard but compare resource use (e.g. antibiotics) and clinical outcomes in people with and without use of the diagnostic marker. For the primary care setting, PCT had a very strong effect on antibiotic consumption (reduction of antibiotic exposure by 70%, from 4.6 to 1.6 days) without compromising disease resolution and patient safety. Of note, we were not able to assess the effect of PCT on mortality due to the very low risk situation with only one non‐survivor (control group) among the 1008 included participants.

The available evidence from RCTs, as summarised in this report, supports the use of PCT for de‐escalation of antibiotic therapy for people with ARIs. The same may not be true for escalation of antibiotic therapy when PCT levels increase as demonstrated in a recent large sepsis trial (Jensen 2011), where PCT‐guided escalation of diagnostic procedures and antimicrobial therapy in the ICU did not improve survival and led to organ‐related harm and prolonged ICU stays.

Study flow diagram.Abbreviations: ARI: acute respiratory infection; IPD: individual participant data; RCT: randomised controlled trial
Figuras y tablas -
Figure 1

Study flow diagram.

Abbreviations: ARI: acute respiratory infection; IPD: individual participant data; RCT: randomised controlled trial

'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 2

'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.

Funnel plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.
Figuras y tablas -
Figure 4

Funnel plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.
Figuras y tablas -
Figure 5

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.1 Mortality at 30 days.

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.2 Treatment failure at 30 days.
Figuras y tablas -
Figure 6

Forest plot of comparison: 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, outcome: 1.2 Treatment failure at 30 days.

Comparison 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, Outcome 1 Mortality at 30 days.
Figuras y tablas -
Analysis 1.1

Comparison 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, Outcome 1 Mortality at 30 days.

Comparison 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, Outcome 2 Treatment failure at 30 days.
Figuras y tablas -
Analysis 1.2

Comparison 1 Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting, Outcome 2 Treatment failure at 30 days.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 1 Mortality at 30 days stratified by adherence.
Figuras y tablas -
Analysis 2.1

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 1 Mortality at 30 days stratified by adherence.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 2 Treatment failure at 30 days stratified by adherence.
Figuras y tablas -
Analysis 2.2

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 2 Treatment failure at 30 days stratified by adherence.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 3 Mortality at 30 days stratified by allocation concealment.
Figuras y tablas -
Analysis 2.3

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 3 Mortality at 30 days stratified by allocation concealment.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 4 Treatment failure at 30 days stratified by allocation concealment.
Figuras y tablas -
Analysis 2.4

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 4 Treatment failure at 30 days stratified by allocation concealment.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 5 Mortality at 30 days stratified by blinded outcome assessment.
Figuras y tablas -
Analysis 2.5

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 5 Mortality at 30 days stratified by blinded outcome assessment.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 6 Treatment failure at 30 days stratified by blinded outcome assessment.
Figuras y tablas -
Analysis 2.6

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 6 Treatment failure at 30 days stratified by blinded outcome assessment.

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 7 Mortality at 30 days stratified by follow up.
Figuras y tablas -
Analysis 2.7

Comparison 2 Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses, Outcome 7 Mortality at 30 days stratified by follow up.

Summary of findings for the main comparison. Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections

Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections

Patient or population: people with acute respiratory tract infections
Settings: primary care, emergency department, intensive care unit
Intervention: PCT‐guided care
Comparison: standard care

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No. of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Standard care

PCTalgorithm

Mortality
Follow‐up: 30 days

Study population

OR 0.83
(0.70 to 0.99)

6708
(26 studies)

⊕⊕⊕⊕
High1

100 per 1000

86 per 1000

(76 to 95)

Treatment failure
Clinical assessment3
Follow‐up: 30 days

Study population

OR 0.90
(0.80 to 1.01)

6708
(26 studies)

⊕⊕⊕⊝
Moderate2 3

249 per 1000

230 per 1000

(216 to 245)

Antibiotic‐related side effects

Follow‐up: 30 days

Study population

221 per 1000

163 per 1000

(145 to 182)

OR 0.68
(0.57 to 0.82)

3034
(6 studies)

⊕⊕⊕⊝
Moderate4

Antibiotic exposure
Total days of antibiotic therapy in all randomised participants

The mean antibiotic exposure in the control groups was
8.1 days.

The mean antibiotic exposure in the intervention groups was
2.43 dayslower
(2.15 to 2.71)

6708
(26 studies)

⊕⊕⊕⊕
High1

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; OR: odds ratio: PCT: procalcitonin

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1No downgrading for serious concerns. Still, there is some concern about unconcealed allocation in several trials in the emergency department and intensive care settings. There is also some concern about low adherence with the PCT algorithm in the intervention group. We consider unblinded outcome assessment as not relevant for the outcome of death.
2Downgraded one level for serious inconsistency: trials used differing definition of treatment failure and some rare events were not systematically assessed among trials.
3For the primary care setting, treatment failure was defined as death, hospitalisation, acute respiratory infection (ARI)‐specific complications (e.g. empyema for lower ARI, meningitis for upper ARI), recurrent or worsening infection, and participants reporting any symptoms of an ongoing respiratory infection (e.g. fever, cough, dyspnoea) at follow‐up. For the emergency department setting, treatment failure was defined as death, intensive care unit (ICU) admission, rehospitalisation after index hospital discharge, ARI‐associated complications (e.g. empyema or acute respiratory distress syndrome for lower ARI), and recurrent or worsening infection within 30 days of follow‐up. For the ICU setting, treatment failure was defined as death within 30 days of follow‐up.
4Downgraded one level for incomplete reporting: only 6 trials reported side effects from antibiotics, and none of these trials were conducted in the ICU setting.

Figuras y tablas -
Summary of findings for the main comparison. Procalcitonin algorithm compared to standard care for guiding antibiotic therapy in acute respiratory tract infections
Table 1. Characteristics of included trials

Study ID

Country

Setting, type of trial

Clinical diagnosis

Type of PCTalgorithm and PCTcut‐offs used (µg/L)

N: ARI participants (study total)

Primary endpoint

Follow‐up time

Reasons for exclusion of patients

Annane 2013

France

ICU, multicentre

Severe sepsis without overt source of infection and negative blood culture

Initiation and duration; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 5.0)

0 (62)

Participants on AB on day 5 post randomisation

Hospital stay

62 non‐ARI patients (4 of them with post randomisation consent withdrawal)

Bloos 2016

Germany

ICU, multicentre

Severe sepsis or septic shock

Discontinuation at day 4, 7, and 10; R against AB: < 1.0 or > 50% drop to previous value

219 (1180)

28‐day mortality

3 months

91 post randomisation exclusions (informed consent not obtainable), 870 not ARI patients

Bouadma 2010

France

ICU, multicentre

Suspected bacterial infections during ICU stay without prior AB (> 24 h)

Initiation and duration; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 1.0)

394 (630)

All‐cause mortality

2 months

9 post randomisation exclusions (8 withdrew consent, 1 randomised twice); 227 non‐ARI patients

Branche 2015

USA

ED, medical ward, single centre

Lower ARI

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

265 (300)

Antibiotic exposure and safety

3 months

35 non‐ARI patients

Briel 2008

Switzerland

Primary care, multicentre

Upper and lower ARI

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

458 (458)

Days with restricted activities

1 month

No exclusions

Burkhardt 2010

Germany

Primary care, multicentre

Upper and lower ARI

Initiation; R against AB: < 0.25; R for AB: > 0.25

550 (571)

Days with restricted activities

1 month

21 post randomisation exclusions (2 withdrew consent, 1 due to loss of sample, 15 with autoimmune, inflammatory, or systemic disease, 2 with advanced liver disease, 1 with prior use of antibiotics)

Christ‐Crain 2004

Switzerland

ED, single centre

Lower ARI with X‐ray confirmation

Initiation; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

219 (243)

AB use

2 weeks

24 non‐ARI patients

Christ‐Crain 2006

Switzerland

ED, medical ward, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

286 (302)

AB use

6 weeks

16 non‐ARI patients

Corti 2016

Denmark

ED, single centre

AECOPD

Initiation and duration; R against AB < 0.25 (0.15)/80% decrease; R for AB > 0.25

120 (120)

AB use

28 days

No exclusions

De Jong 2016

Netherlands

ICU, multicentre

Critically ill patients with presumed infection

Duration; R against AB: < 0.5 or > 80% drop

994 (1575)

AB use

1 year

29 post randomisation exclusions (25 protocol violations, 4 withdrew informed consent), 552 non‐ARI patients

Deliberato 2013

Brazil

ICU, single centre

Septic patients with proven bacterial infection

Duration; R against AB: < 0.5 or > 90% drop

66 (81)

AB use

ICU discharge or 14 days' post randomisation

15 non‐ARI patients

Ding 2013

China

ICU, single centre

Acute exacerbation of pulmonary fibrosis

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

0 (78)

AB use

1 month

10 post randomisation exclusions (7 lost to follow‐up, 3 withdrew informed consent), 68 data not shared

Hochreiter 2009

Germany

Surgical ICU, single centre

Suspected bacterial infections and > 1 SIRS criteria

Duration; R against AB: < 1 or > 65% drop over 3 d

43 (110)

AB use

Hospital stay

67 non‐ARI patients

Kristoffersen 2009

Denmark

ED, medical ward, multicentre

Lower ARI without X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25 (> 0.5)

210 (223)

AB use

Hospital stay

13 post randomisation exclusions (3 no PCT testing, 6 not meeting inclusion criteria, 4 withdrew informed consent)

Layios 2012

Belgium

ICU, single centre

Suspected infection

Initiation; R against AB: < 0.5 (< 0.25); R for AB: > 0.5 (> 1.0)

160 (509)

AB use

1 month

120 no PCT measurements, 10 missing data, 219 non‐ARI patients

Lima 2016

Brazil

ED, medical ward, single centre

Febrile neutropenia

Duration; R against AB: < 0.5 for 2 days or > 90% drop than highest measured concentration

0 (62)

AB use

28 days

1 post randomisation exclusion (withdrew informed consent), 62 non‐ARI patients

Long 2009

China

ED, outpatients, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

127 (149)

AB use

1 month

22 post randomisation exclusions due to withdrawal of consent

Long 2011

China

ED, outpatients, single centre

CAP with X‐ray confirmation

Initiation and duration; R against AB: < 0.25; R for AB: > 0.25

156 (172)

AB use

1 month

16 post randomisation exclusions (6 lost to follow‐up, 7 withdrew consent, 3 with final diagnosis other than CAP)

Long 2014

China

ED, single centre

Severe acute exacerbation of asthma

Initiation; R against AB: < 0.25 (< 0.1); R for AB: > 0.25

180 (180)

AB use

1 year

No exclusions

Maravić‐Stojković 2011

Serbia

ICU surgical, single centre

Infection after open heart surgery

Initiation; R for AB: > 0.5

5 (205)

AB use, AB cost

Hospital stay

200 non‐ARI patients

Najafi 2015

Iran

ICU, single centre

SIRS without apparent source of infection

Initiation; R for AB: > 2

0 (60)

AB use

Hospital stay

60 patient data not shared

Nobre 2008

Switzerland

ICU, single centre

Suspected severe sepsis or septic shock

Duration; R against AB: < 0.5 (< 0.25) or > 80% drop; R for AB: > 0.5 (> 1.0)

52 (79)

AB use

1 month

27 non‐ARI patients

Ogasawara 2014

Japan

Medical ward, single centre

Aspiration pneumonia

Predefined duration; AB for 3 d: < 0.5; AB for 5 d: 0.5 to 1.0; AB for 7 d: > 1

0 (105)

Relapse and 30‐day mortality

1 month

9 post randomisation exclusions (2 withdrew consent, 7 others), 96 data not shared

Oliveira 2013

Brazil

ICU, multicentre

Severe sepsis or septic shock

Discontinuation; initial < 1.0: R against AB: 0.1 at day 4; initial > 1.0: R against: > 90% drop

58 (97)

AB use

28 days or hospital discharge

3 post randomisation exclusions (2 withdrew consent, 1 technical problems), 36 patients with a final diagnosis other than ARI

Schroeder 2009

Germany

Surgical ICU, single centre

Severe sepsis following abdominal surgery

Duration; R against AB: < 1 or > 65% drop over 3 d

8 (27)

AB use

Hospital stay

19 non‐ARI patients

Schuetz 2009

Switzerland

ED, medical ward, multicentre

Lower ARI with X‐ray confirmation

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

1304 (1381)

AB use

1 month

22 post randomisation exclusions due to withdrawal of consent, 55 non‐ARI patients

Shehabi 2014

Australia

ICU, multicentre

Suspected sepsis, undifferentiated infections

Duration; R against AB: < 0.25 (< 0.1) or > 90% drop

156 (400)

AB use

3 months

6 post randomisation exclusions (6 withdrew consent), 238 non‐ARI patients

Stolz 2007

Switzerland

ED, medical ward, single centre

Exacerbated COPD

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25 (> 0.5)

208 (226)

AB use

2 to 3 weeks

18 post randomisation exclusions (absence of COPD)

Stolz 2009

Switzerland, USA

ICU, multicentre

VAP when intubated > 48 h

Duration; R against AB: < 0.5 (< 0.25) or > 80% drop; R for AB: > 0.5 (> 1.0)

101 (101)

AB‐free days alive

1 month

No exclusions

Tang 2013

China

ED, single centre

Exacerbation of asthma

Initiation and duration; R against AB: < 0.25 (< 0.1); R for AB: > 0.25

0 (265)

AB use

6 weeks

10 post randomisation exclusions (5 lost to follow‐up, 3 died, 2 withdrew consent), 255 data not shared

Verduri 2015

Italy

ED, medical ward, multicentre

AECOPD

Initiation; R against AB:< 0.1; R for AB: > 0.25

178 (183)

Number of exacerbations

6 months

5 post randomisation exclusions (5 lost to follow‐up because they did not meet the inclusion criteria)

Wang 2016

China

ICU, single centre

AECOPD

All participants had initial PCT < 0.1; AB group treated with AB for at least 3 days, control group no AB in the first 10 days

191 (194)

Treatment success within 10 days

30 days

3 post randomisation exclusions (3 with pneumonia according to CT scan)

AB: antibiotic
AECOPD: acute exacerbation of chronic obstructive pulmonary disease
ARI: acute respiratory infection
CAP: community‐acquired pneumonia
COPD: chronic obstructive pulmonary disease
CT: computed tomography
d: days
ED: emergency department
h: hours
ICU: intensive care unit
PCT: procalcitonin
R: recommendation for or against antibiotics
SIRS: systemic inflammatory response syndrome
VAP: ventilator‐associated pneumonia

Figuras y tablas -
Table 1. Characteristics of included trials
Table 2. Baseline characteristics of included participants

Parameter

Control (n = 3372)

PCT group (n = 3336)

Demographics

Age (year), mean (SD)

61.2 ± 18.4

60.7 ± 18.8

Male gender, n (%)

1910 (56.6%)

1898 (56.9%)

Clinical setting, no (%)

Primary care

501 (14.9%)

507 (15.2%)

Emergency department

1638 (48.6%)

1615 (48.4%)

Intensive care unit

1233 (36.6%)

1214 (36.4%)

Primary diagnosis

Total upper ARI, n (%)

280 (8.3%)

292 (8.8%)

Common cold

156 (4.6%)

149 (4.5%)

Rhino‐sinusitis, otitis

67 (2.0%)

73 (2.2%)

Pharyngitis, tonsillitis

46 (1.4%)

61 (1.8%)

Total lower ARI, n (%)

3092 (91.7%)

3044 (91.2%)

Community‐acquired pneumonia

1468 (43.5%)

1442 (43.2%)

Hospital‐acquired pneumonia

262 (7.8%)

243 (7.3%)

Ventilator‐associated pneumonia

186 (5.5%)

194 (5.8%)

Acute bronchitis

287 (8.5%)

257 (7.7%)

Exacerbation of COPD

631 (18.7%)

621 (18.6%)

Exacerbation of asthma

127 (3.8%)

143 (4.3%)

Other lower ARI

131 (3.9%)

144 (4.3%)

Procalcitonin upon enrolment

PCT< 0.1 ug/L

921 (35.6%)

981 (30.9%)

PCT 0.1 to 0.25 ug/L

521 (20.1%)

608 (19.2%)

PCT > 0.25 to 0.5 ug/L

308 (11.9%)

383 (12.1%)

PCT > 0.5 to 2.0 ug/L

358 (13.8%)

520 (16.4%)

PCT > 2.0 ug/L

482 (18.6%)

679 (21.4%)

ARI: acute respiratory infection
COPD: chronic obstructive pulmonary disease
PCT: procalcitonin
SD: standard deviation

Figuras y tablas -
Table 2. Baseline characteristics of included participants
Table 3. Quality assessment of trials

Study ID

Allocation concealment

Blinded
outcome assessment

Follow‐up for mortality

Adherence to PCT algorithm in PCT group

Follow‐up for mortality

Annane 2013

Yes (central randomisation)

No

58/58 (100%)

63% adherence

LOS

Bloos 2016

Yes (central randomisation)

No

1045/1089 (96%)

49.6% adherence

28 days and 90 days

Bouadma 2010

Yes (central randomisation)

Yes

393/394 (100%)

47% adherence

28 days and 60 days

Branche 2015

Yes (central randomisation using blocks of 4)

No

250/300 (83.3%)

64% adherence

1 month and 3 months

Briel 2008

Yes (central randomisation)

Yes

454/458 (99%)

85% adherence

28 days

Burkhardt 2010

Yes (central randomisation)

Yes

546/550 (99%)

87% adherence

28 days

Christ‐Crain 2004

No (alternating weeks)

No

230/243 (95%)

83% adherence

10 to 14 days

Christ‐Crain 2006

Yes (sequentially numbered, opaque, sealed envelopes)

No

300/302 (99%)

87% adherence

56 days

Corti 2016

Yes (randomisation algorithm was concealed to treating clinicians and participants)

No

120/120 (100%)

61.1% adherence

28 days

De Jong 2016

Yes (central randomisation)

No

1546/1546 (100%)

44% adherence

28 days and 1 year

Deliberato 2013

Yes (opaque, sealed envelopes)

No

81/81 (100%)

52% adherence

LOS

Ding 2013

Yes (central randomisation)

No

68/78 (87.2%)

Not reported

30 days

Hochreiter 2009

No (unconcealed drawing of lots)

No

43/43 (100% until discharge)

Not reported

LOS

Kristoffersen 2009

Yes (central randomisation)

No

210/210 (100% until discharge)

59% adherence

LOS

Layios 2012

Not reported

No

509/509 (100%)

Not reported

Intensive care unit LOS

Lima 2016

Yes (sequentially numbered, opaque, sealed envelopes)

No

61/62 (98.4%)

73.3% adherence

28 days and 90 days

Long 2009

No (odd and even patient ID numbers)

No

127/127 (100%)

Not reported

Not reported

Long 2011

No (odd and even patient ID numbers)

No

156/156 (100%)

Not reported

28 days

Long 2014

Yes (central randomisation)

No

169/180 (93.9%)

96.6% adherence

LOS and 1 year

Maravić‐Stojković 2011

Yes (central randomisation)

No

205/205 (100%)

Not reported

30 days and LOS

Najafi 2015

Yes (central randomisation)

No

30/30 (100%)

Not reported

LOS

Nobre 2008

Yes (sequentially numbered, opaque, sealed envelopes)

No

52/52 (100%)

81% adherence

28 days and LOS

Ogasawara 2014

Not reported

No

96/96 (100%)

Not reported

30 days

Oliveira 2013

Yes (central randomisation)

No

94/94 (100%)

86.2% adherence

28 days

Schroeder 2009

No (unconcealed drawing of lots)

No

8/8 (100% until discharge)

Not reported

LOS

Schuetz 2009

Yes (central randomisation)

Yes

1358/1359 (100%)

91% adherence

28 days

Shehabi 2014

Yes (central randomisation)

Yes

394/394 (100%)

Not reported

LOS and 90 days

Stolz 2007

Yes (sequentially numbered, opaque, sealed envelopes)

Yes

208/208 (100%)

Not reported

6 months

Stolz 2009

Yes (sequentially numbered, opaque, sealed envelopes)

No

101/101 (100%)

Not reported

28 days

Tang 2013

Yes (sequentially numbered, opaque, sealed envelopes)

Yes

258/265 (97.4%)

Not reported

6 weeks

Verduri 2015

Yes (central randomisation)

No

178/178 (100%)

Not reported

6 months

Wang 2016

Yes (those responsible for allocation concealment were not involved in the measurement of results)

No

191/191 (100%)

82.3% adherence (17 participants in the control group received AB)

30 days

LOS: length of stay
PCT: procalcitonin

Figuras y tablas -
Table 3. Quality assessment of trials
Table 4. Clinical endpoints overall and stratified by setting and ARI diagnosis

Control group

PCT group

Measures of effect: adjusted OR or difference (95% CI), P value

P for interaction

Overall

3372

3336

30 days mortality, n (%)

336 (10.0%)

286 (8.6%)

0.83 (0.70 to 0.99), P = 0.037

NA

Treatment failure, n (%)

841 (24.9%)

768 (23.0%)

0.90 (0.80 to 1.01), P = 0.068

NA

Length of ICU stay, mean (±SD)

13.3 ± 16.0

13.7 ± 17.2

0.39 (‐0.81 to 1.58), P = 0.524

NA

Length of hospital stay, mean (±SD)

13.7 ± 20.6

13.4 ± 18.4

‐0.19 (‐0.96 to 0.58), P = 0.626

NA

Antibiotic‐related side effects, n (%)

336 (22.1%)

247 (16.3%)

0.68 (0.57 to 0.82), P < 0.001

NA

According to setting

Primary care

501

507

30 days mortality, n (%)

1 (0.2%)

0 (0.0%)

NA

NA

Treatment failure, n (%)

164 (32.7%)

159 (31.4%)

0.96 (0.73 to 1.25), P = 0.751

0.715

Days with restricted activities, mean (±SD)

8.9 ± 4.2

8.9 ± 4.1

0.07 (‐0.44 to 0.59), P = 0.777

NA

Antibiotic‐related side effects, n (%)

128 (25.7%)

102 (20.2%)

0.65 (0.46 to 0.91), P = 0.012

0.596

Emergency department

1638

1615

30 days mortality, n (%)

62 (3.8%)

57 (3.5%)

0.91 (0.63 to 1.33), P = 0.635

0.546

Treatment failure, n (%)

292 (17.8%)

259 (16.0%)

0.87 (0.72 to 1.05), P = 0.141

0.807

Length of hospital stay, mean (±SD)

8.2 ± 10.5

8.1 ± 7.5

‐0.14 (‐0.73 to 0.44), P = 0.631

0.684

Antibiotic‐related side effects, n (%)

208 (20.3%)

145 (14.4%)

0.66 (0.52 to 0.83), P = 0.001

0.596

Intensive care unit

1233

1214

30 days mortality, n (%)

273 (22.3%)

229 (19.0%)

0.84 (0.69 to 1.02), P = 0.081

0.619

Length of ICU stay, mean (±SD)

14.8 ± 16.2

15.3 ± 17.5

0.56 (‐0.82 to 1.93), P = 0.427

0.849

Length of hospital stay, mean (±SD)

26.3 ± 26.9

25.8 ± 23.9

‐0.33 (‐2.28 to 1.62), P = 0.739

0.641

According to diagnosis

Community‐acquired pneumonia

1468

1442

30 days mortality, n (%)

206 (14.1%)

175 (12.2%)

0.82 (0.66 to 1.03), P = 0.083

0.958

Treatment failure, n (%)

385 (26.2%)

317 (22.0%)

0.78 (0.66 to 0.93), P = 0.005

0.052

Length of ICU stay, mean (±SD)

10.5 ± 10.3

11.9 ± 13.3

1.45 (0.15 to 2.75), P = 0.029

0.119

Length of hospital stay, mean (±SD)

13.3 ± 15.7

13.9 ± 16.1

0.74 (‐0.25 to 1.73), P = 0.143

0.094

Antibiotic‐related side effects, n (%)

186 (27.7%)

127 (19.1%)

0.62 (0.48 to 0.80), P < 0.001

0.227

Exacerbation of COPD

631

621

30 days mortality, n (%)

24 (3.8%)

19 (3.1%)

0.8 (0.43 to 1.48), P = 0.472

0.847

Treatment failure, n (%)

110 (17.4%)

104 (16.7%)

0.94 (0.70 to 1.27), P = 0.704

0.676

Length of hospital stay, mean (±SD)

9.3 ± 13.9

8.4 ± 7.2

‐0.60 (‐1.84 to 0.64), P = 0.342

0.658

Antibiotic‐related side effects, n (%)

30 (10.9%)

29 (10.5%)

0.93 (0.53 to 1.63), P = 0.805

0.198

Acute bronchitis

287

257

30 days mortality, n (%)

0 (0.0%)

2 (0.8%)

NA

NA

Treatment failure, n (%)

55 (19.2%)

52 (20.2%)

1.11 (0.72 to 1.70), P = 0.643

0.4

Length of hospital stay, mean (±SD)

2.6 ± 5.7

2.2 ± 4.7

‐0.21 (‐0.90 to 0.48), P = 0.556

0.97

Antibiotic‐related side effects, n (%)

54 (21.6%)

39 (17.3%)

0.77 (0.49 to 1.22), P = 0.263

0.657

Ventilator‐associated pneumonia

186

194

30 days mortality, n (%)

29 (15.6%)

23 (12.0%)

0.75 (0.41 to 1.39), P = 0.366

0.644

Treatment failure, n (%)

51 (27.4%)

44 (22.7%)

0.78 (0.48 to 1.28), P = 0.332

0.522

Length of ICU stay, mean (±SD)

23.5 ± 20.5

21.8 ± 19.1

‐1.74 (‐5.64 to 2.17), P = 0.383

0.441

Length of hospital stay, mean (±SD)

33.8 ± 27.6

32.0 ± 23.1

‐2.14 (‐7.04 to 2.75), P = 0.391

0.448

Measures of effect: dichotomous outcomes are reported as adjusted OR (95% CI) and continuous outcomes are adjusted mean differences and confidence intervals

ARI: acute respiratory infection
CI: confidence interval
COPD: chronic obstructive pulmonary disease
ICU: intensive care unit
NA: not applicable
OR: odds ratio
PCT: procalcitonin
SD: standard deviation

Figuras y tablas -
Table 4. Clinical endpoints overall and stratified by setting and ARI diagnosis
Table 5. Sensitivity analysis

Mortality

Main analysis

Control group

PCT group

Adjusted OR (95% CI), P value

P for interaction

All participants

336 (10.0%)

286 (8.6%)

0.83 (0.70 to 0.99), P = 0.037

NA

Adherence

High adherence

82 (4.5%)

75 (4.1%)

0.88 (0.63 to 1.22), P = 0.434

0.617

Low adherence (< 70% or not reporting)

254 (16.4%)

211 (14.0%)

0.83 (0.67 to 1.02), P = 0.073

Allocation

Low risk for allocation concealment bias

305 (10.6%)

250 (8.8%)

0.80 (0.67 to 0.97), P = 0.021

0.229

High risk for allocation concealment bias (or not reporting)

31 (6.5%)

36 (7.3%)

1.12 (0.66 to 1.91), P = 0.672

Blinding

Blinded outcome assessment

113 (6.5%)

102 (5.9%)

0.85 (0.64 to 1.13), P = 0.259

0.537

No blinded outcome assessment

223 (13.8%)

184 (11.5%)

0.81 (0.65 to 1.01), P = 0.062

Follow‐up

Follow up for mortality at 1 month

275 (10.7%)

224 (8.9%)

0.81 (0.67 to 0.99), P = 0.039

0.325

Follow up for mortality < 1 month

61 (7.6%)

62 (7.6%)

0.94 (0.64 to 1.38), P = 0.756

Treatment failure

Control group

PCT group

Adjusted OR (95% CI), P value

P for interaction

All participants

841 (24.9%)

768 (23.0%)

0.90 (0.80 to 1.01), P = 0.068

NA

Adherence

High adherence

419 (23.1%)

381 (21.0%)

0.89 (0.76 to 1.04), P = 0.148

0.752

Low adherence (< 70% or not reporting)

422 (27.1%)

387 (25.5%)

0.92 (0.77 to 1.08), P = 0.301

Allocation

Low risk for allocation concealment bias

776 (26.8%)

699 (24.6%)

0.89 (0.79 to 1.01), P = 0.069

0.486

High risk for allocation concealment bias (or not reporting)

65 (13.6%)

69 (13.8%)

0.99 (0.68 to 1.44), P = 0.939

Blinding

Blinded outcome assessment

412 (23.5%)

367 (21.1%)

0.88 (0.75 to 1.03), P = 0.117

0.574

No blinded outcome assessment

429 (26.5%)

401 (25.1%)

0.94 (0.79 to 1.11), P = 0.438

CI: confidence interval
NA: not applicable
OR: odds ratio
PCT: procalcitonin

Figuras y tablas -
Table 5. Sensitivity analysis
Table 6. Antibiotic treatment overall and stratified by setting and ARI diagnosis

Parameter

Control group

PCT group

Measures of effect: adjusted OR or difference (95% CI), P value

P for interaction

Overall

3372

3336

Initiation of antibiotics, n (%)

2894 (86.3%)

2351 (71.5%)

0.27 (0.24 to 0.32), P < 0.001

Duration of antibiotics (days), mean (±SD)

9.4 ± 6.2

8.0 ± 6.5

‐1.83 (‐2.15 to ‐1.50), P < 0.001

Total exposure of antibiotics (days), mean (±SD)

8.1 ± 6.6

5.7 ± 6.6

‐2.43 (‐2.71 to ‐2.15), P < 0.001

Setting‐specific outcomes

Primary care

501

507

Initiation of antibiotics, n (%)

316 (63.1%)

116 (22.9%)

0.13 (0.09 to 0.18), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

7.3 ± 2.5

7.0 ± 2.8

‐0.52 (‐1.07 to 0.04), P = 0.068

0.064

Total exposure of antibiotics (days), mean (±SD)

4.6 ± 4.1

1.6 ± 3.2

‐3.02 (‐3.45 to ‐2.58), P < 0.001

0.101

Emergency department

1638

1615

Initiation of antibiotics, n (%)

1354 (83.2%)

1119 (71.3%)

0.49 (0.41 to 0.58), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

9.8 ± 5.4

7.3 ± 5.1

‐2.45 (‐2.86 to ‐2.05), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

8.2 ± 6.2

5.2 ± 5.4

‐3.02 (‐3.41 to ‐2.62), P < 0.001

< 0.001

Intensive care unit

1233

1214

Initiation of antibiotics, n (%)

1224 (99.8%)

1116 (91.9%)

0.02 (0.01 to 0.05), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

9.5 ± 7.4

8.8 ± 7.8

‐1.23 (‐1.82 to ‐0.65), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

9.5 ± 7.4

8.1 ± 7.9

‐1.44 (‐1.99 to ‐0.88), P < 0.001

< 0.001

Disease‐specific outcomes

Community‐acquired pneumonia

1468

1442

Initiation of antibiotics, n (%)

1455 (99.4%)

1340 (92.9%)

0.08 (0.04 to 0.15), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

10.5 ± 6.2

8.0 ± 5.7

‐2.45 (‐2.87 to ‐2.02), P < 0.001

< 0.001

Total exposure of antibiotics (days), mean (±SD)

10.4 ± 6.2

7.5 ± 5.9

‐2.94 (‐3.38 to ‐2.50), P < 0.001

0.004

Exacerbation of COPD

631

621

Initiation of antibiotics, n (%)

453 (71.8%)

266 (42.8%)

0.29 (0.23 to 0.36), P < 0.001

0.017

Duration of antibiotics (days), mean (±SD)

7.4 ± 5.3

7.2 ± 6.7

‐1.15 (‐2.00 to ‐0.31), P = 0.007

0.003

Total exposure of antibiotics (days), mean (±SD)

5.3 ± 5.6

3.1 ± 5.6

‐2.22 (‐2.83 to ‐1.60), P < 0.001

0.506

Acute bronchitis

287

257

Initiation of antibiotics, n (%)

189 (65.9%)

68 (26.5%)

0.18 (0.12 to 0.26), P < 0.001

< 0.001

Duration of antibiotics (days), mean (±SD)

7.1 ± 3.0

6.4 ± 3.5

‐0.35 (‐1.15 to 0.45), P = 0.393

0.359

Total exposure of antibiotics (days), mean (±SD)

4.7 ± 4.2

1.7 ± 3.3

‐2.95 (‐3.59 to ‐2.31), P < 0.001

0.33

Ventilator‐associated pneumonia

186

194

Initiation of antibiotics, n (%)

186 (100.0%)

193 (99.5%)

NA

NA

Duration of antibiotics (days), mean (±SD)

13.1 ± 7.9

10.8 ± 8.7

‐2.22 (‐3.80 to ‐0.65), P = 0.006

0.253

Total exposure of antibiotics (days), mean (±SD)

13.1 ± 7.9

10.8 ± 8.7

‐2.45 (‐4.09 to ‐0.82), P = 0.003

0.786

Note: Duration refers to the total days of antibiotic therapy in participants in whom antibiotics were initiated. Total exposure refers to the total days of antibiotic therapy in all randomised participants.

Measures of effect: dichotomous outcomes are reported as adjusted OR (95% CI) and continuous outcomes are adjusted mean differences and confidence intervals

ARI: acute respiratory infection
CI: confidence interval
COPD: chronic obstructive pulmonary disease
NA: not applicable
OR: odds ratio
PCT: procalcitonin
SD: standard deviation

Figuras y tablas -
Table 6. Antibiotic treatment overall and stratified by setting and ARI diagnosis
Comparison 1. Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mortality at 30 days Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.89 [0.78, 1.01]

1.1 Primary care trials

2

1008

Odds Ratio (M‐H, Random, 95% CI)

0.32 [0.01, 7.98]

1.2 Emergency department trials

14

3805

Odds Ratio (M‐H, Random, 95% CI)

0.97 [0.70, 1.36]

1.3 Intensive care unit trials

16

5233

Odds Ratio (M‐H, Random, 95% CI)

0.88 [0.77, 1.00]

2 Treatment failure at 30 days Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.90 [0.81, 0.99]

2.1 Primary care trials

2

1008

Odds Ratio (M‐H, Random, 95% CI)

0.94 [0.72, 1.22]

2.2 Emergency department trials

14

3805

Odds Ratio (M‐H, Random, 95% CI)

0.85 [0.69, 1.05]

2.3 Intensive care unit trials

16

5233

Odds Ratio (M‐H, Random, 95% CI)

0.92 [0.81, 1.05]

Figuras y tablas -
Comparison 1. Procalcitonin algorithm versus no procalcitonin algorithm stratified by clinical setting
Comparison 2. Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mortality at 30 days stratified by adherence Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.89 [0.78, 1.01]

1.1 Adherence to procalcitonin algorithm > 70%

14

4422

Odds Ratio (M‐H, Random, 95% CI)

1.05 [0.81, 1.37]

1.2 Adherence to procalcitonin algorithm < 70% or not available

18

5624

Odds Ratio (M‐H, Random, 95% CI)

0.85 [0.73, 0.97]

2 Treatment failure at 30 days stratified by adherence Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.90 [0.81, 0.99]

2.1 Adherence to procalcitonin algorithm > 70%

14

4422

Odds Ratio (M‐H, Random, 95% CI)

0.87 [0.75, 1.02]

2.2 Adherence to procalcitonin algorithm < 70% or not available

18

5624

Odds Ratio (M‐H, Random, 95% CI)

0.92 [0.81, 1.04]

3 Mortality at 30 days stratified by allocation concealment Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.89 [0.78, 1.01]

3.1 Trials with concealed allocation

22

7968

Odds Ratio (M‐H, Random, 95% CI)

0.88 [0.76, 1.01]

3.2 Trials without concealed allocation

10

2078

Odds Ratio (M‐H, Random, 95% CI)

0.95 [0.70, 1.28]

4 Treatment failure at 30 days stratified by allocation concealment Show forest plot

32

10046

Odds Ratio (M‐H, Random, 95% CI)

0.90 [0.81, 0.99]

4.1 Trials with concealed allocation

22

7968

Odds Ratio (M‐H, Random, 95% CI)

0.91 [0.82, 1.02]

4.2 Trials without concealed allocation

10

2078

Odds Ratio (M‐H, Random, 95% CI)

0.82 [0.64, 1.04]

5 Mortality at 30 days stratified by blinded outcome assessment Show forest plot

32

10046

Odds Ratio (M‐H, Fixed, 95% CI)

0.89 [0.78, 1.00]

5.1 Trials with blinded outcome assessment

9

4664

Odds Ratio (M‐H, Fixed, 95% CI)

1.05 [0.84, 1.32]

5.2 Trials without blinded outcome assessment

23

5382

Odds Ratio (M‐H, Fixed, 95% CI)

0.82 [0.70, 0.95]

6 Treatment failure at 30 days stratified by blinded outcome assessment Show forest plot

32

10046

Odds Ratio (M‐H, Fixed, 95% CI)

0.90 [0.81, 0.99]

6.1 Trials with blinded outcome assessment

9

4664

Odds Ratio (M‐H, Fixed, 95% CI)

0.92 [0.79, 1.06]

6.2 Trials without blinded outcome assessment

23

5382

Odds Ratio (M‐H, Fixed, 95% CI)

0.88 [0.77, 1.01]

7 Mortality at 30 days stratified by follow up Show forest plot

32

10046

Odds Ratio (M‐H, Fixed, 95% CI)

0.89 [0.78, 1.00]

7.1 Trials with 1 month follow up for mortality

18

7337

Odds Ratio (M‐H, Fixed, 95% CI)

0.85 [0.74, 0.98]

7.2 Trials with different follow up for mortality

14

2709

Odds Ratio (M‐H, Fixed, 95% CI)

1.01 [0.78, 1.30]

Figuras y tablas -
Comparison 2. Procalcitonin algorithm versus no procalcitonin algorithm, sensitivity analyses