C-reactive protein point-of-care testing and complementary strategies to improve antibiotic stewardship in children with acute respiratory infections in primary care (2024)

1. Introduction

1.1. Antimicrobial resistance

Bacterial antimicrobial resistance (AMR) is flagged as one of the top 10 threats to global health by the World Health Organization (1). Although it has often been referred to as the “silent pandemic” (2) because its effects are not felt at the place and time they are caused, AMR has been a topic of enduring discussion for many years. The effects of AMR are already drastic today and far from “silent”, causing 1 of 3 hospital deaths due to untreatable secondary bacterial infections (3), and in 2019 a total of 1.27 million deaths globally directly attributable to bacterial AMR, and estimated deaths associated with bacterial AMR at 4.95 million (3). The effects of AMR will be felt even more broadly and severely by our future generations, with 10 million deaths expected globally due to drug-resistant diseases by 2050 (6), with extended impacts on economic stability and increased poverty as early as 2030 (4).

Today's children, if society fails to act and use antibiotics more responsibly, may not have effective treatment for infections that today are cured with a week of antibiotic treatment, essentially catapulting treatment options back 80 years due to the obsolescence of current antibiotics. Already today, AMR is flagged as a threat to neonate survival (5). An effective stewardship of antibiotics could help ensure that the essential life-saving treatment that antibiotics provide remains effective for future generations. That means creating awareness, convictions, and behaviors and supporting mechanisms that ensure antibiotics are used effectively and in a more targeted way. The primary care setting is ideal for children and parents alike to learn about good antibiotic stewardship behaviors, but more importantly a vital setting to influence antibiotic prescribing behaviors, as a considerable portion of antibiotic prescribing is attributable to the primary care of children presenting with an ARTI (6). A recent systematic review and meta-analysis including 86 studies comprising more than 11 million children, concluded a pooled antibiotic prescribing rate of 45.4% for all acutely ill children (7). About one-fifth to one-half of these antibiotic prescriptions are estimated to be inappropriate (7). In most cases of chest infections, particularly when there is no suspected pneumonia, clinicians should not prescribe antibiotics but instead provide safety netting advice. A safety net advice can be defined as an advice about what to do and what to look out for, empowering parents and carers to seek help if the child's condition deteriorates further or if they need more support (8).

1.2. C-reactive protein

CRP is a non-specific inflammatory marker. CRP values correlate well, with the degree of inflammation in the body without identifying the specific cause (9). It raises rapidly (within 4–6 h), but it may take 24–48 h to reach maximum. Indeed, CRP levels can be raised due to auto-immune conditions, cancers, and infections, and therefore cannot with certainty identify if an inflammation is caused by a virus, bacteria, or other. On the other hand, there are documented cases where children's CRP levels remain low despite serious bacterial infections (10, 11). Together with an assessment of other clinical parameters, however, the CRP level is an important predictor of severe ARTI (pneumonia, sepsis) (12). But its main power is, particularly in primary care, to support whether an infection is mild and self-limiting or not. Self-limiting infections are those that tend to resolve themselves without further treatment and represent most respiratory tract infections. If an inflammation is not severe, and appears to be self-limiting, antibiotic treatment will not be beneficial and may even be harmful, causing side effects, alterations to the microbiome (13) and eventually contribute to AMR. If a respiratory tract infection is severe, clinicians should consider starting antibiotic treatment or even urgently refer to a hospital to avoid aggravation or complications, like sepsis. CRP values offer a reliable indicator to complement a general clinical assessment to decide on management. There are opportunities to decrease antibiotic over-consumption by leveraging CRP POCT, when combined with clear guidance and effective communication strategies, for the treatment of children presenting with an ARTI.

2. Evaluation of evidence supporting CRP POCT effectiveness in safely reducing antibiotic prescribing for children presenting with an ARTIs

The use of quantitative CRP POCT to reduce antibiotic prescribing for adults in the primary care settings has been well evaluated, and there is ample evidence indicating a high effectiveness of the tests in safely reducing antibiotic prescribing, especially for adult patients presenting with symptoms of LRTIs (1425). In adults with LRTIs, up to 42% antibiotic prescribing rate reductions were observed (42% relative reduction; 22% absolute reduction, 31% vs. 53%) (19), and more even greater reductions were measured when CRP POCT was combined with targeted communication skills training (19, 20).

While the volume of data regarding the effectiveness of CRP POCT in safely reducing antibiotic prescribing for children is not as complete, an evaluation of current clinical evidence shows a clear opportunity for use in primary care. As in the case of adults presenting to primary care, broader adaptation of CRP POCT to complement the clinical assessment of children presenting in primary care with an ARTI could contribute to safely reducing antibiotic prescribing rates, especially when clear guidance on when to perform CRP POCT and effective communication strategies for clinicians are provided.

The role of CRP in reducing antibiotic prescription in the primary care of children presenting symptoms of respiratory tract infections has been under evaluation for some time, but results have not always been conclusive enough to make clear recommendations (2123). More recent systematic reviews indicate a clear potential to safely reduce antibiotic prescribing for children with ARTIs:

• In 2019, Verbakel et al. and in 2020 Martinez-Gonzales et al. calculated an antibiotic prescribing reduction rate of 44% for children in randomized studies once CRP cut-off guidance was applied, and this without any negative effect on patient outcomes or healthcare processes (RR 0.56, 95% CI 0.33–0.95) (15, 16).

• In 2020, Van Hecke et al. concluded that there is emerging evidence that CRP POCT can be effective at reducing antibiotic prescribing for children with acute RTIs in lower and middle-income countries, but that evidence of the effectiveness in high-income countries is not as abundant (24).

• In the updated systematic review on the impact of the use of CRP on antibiotic prescribing by Smedemark et al. in 2022, a total of four randomized clinical trials including 2,335 children (Althaus 2019; Diederichsen 2000; Do 2016; Schot 2018), collectively found that CRP rapid testing reduces the number of children given an antibiotic prescription by 22%, with this effect being primarily seen in low- and middle-income countries (0.78, 95% CI 0.67–0.91) (25).

The table below summarizes several studies performed in primary care and in emergency department settings related to the effectiveness of CRP POCT in children to safely reduce antibiotic prescribing rates or rule in or out serious infection. The search strategy is detailed in the Appendix.

Overall, it would be useful to generate more context-specific evidence to better understand best practices in utilizing CRP POCT to reduce antibiotic prescribing and consumption in pediatric primary care settings worldwide (15). That said, the authors feel confident that the below guidance, based on the information available today, will allow for a safe and significant contribution to antibiotic stewardship.

3. The use of CRP POCT in the primary care of children presenting with an ARTI

When a physician is deciding to prescribe antibiotics, it may be relevant to perform CRP POCT to support the assumption that those antibiotics will be beneficial and avoid over-prescription. This can help to prevent prescriptions given to worried parents based on “gut feeling” or motivated by a “better safe than sorry” approach and will reassure both the physician and the parent that the right choice has been made.

CRP POCT can help to reduce diagnostic uncertainty and can serve as a way to support communication with parents when antibiotics are not advised. This can be especially useful when parents and children have difficulties in describing the severity of symptoms, or parents are worried and need to be reassured.

A CRP POCT can also support the decision not to prescribe antibiotics, especially when there is any degree of uncertainty. In cases of severe (bacterial) infections, it is important to start antibiotic treatment quickly to avoid exacerbation, complications, and prolonged discomfort. A CRP POCT can be an important component of safety netting procedures to support the decision not to prescribe antibiotics.

Additionally, CRP values can be used to communicate and demonstrate that antibiotic treatment is not recommended to a concerned parent that may have been pushing for or expecting antibiotic treatment. This argumentation value can be especially pertinent for regions where antibiotic use is common-place and access to antibiotics is possible without a prescription.

While using a CRP POCT is useful to complete the clinical assessment of children presenting with ARTIs, the decision whether to perform a test and the ultimate treatment is always at the discretion of the treating physician, considering all clinical and non-clinical factors.

4. Guidance on the interpretation of CRP results for the primary care of children presenting with an ARTI

Simply having a CRP value is not enough to reduce antibiotic prescribing. Clear guidance is key to achieving safe and meaningful reductions. Guidance supports physicians treating children with RTIs in their decision making in order to safely and confidently reduce overall antibiotic prescribing rates, while ensuring that antibiotics are prescribed, or a hospital referral takes place, when needed. However, any guidance must always be interpreted in light of a complete clinical assessment.

Figure 1 offers guidance on the interpretation of CRP values for patients from 6 months to 14 years presenting with an ARTIs, based on the synthesis of several research results and publications—see Table1 and recent systematic reviews and meta-analysis (25). The suggested cut-offs must be interpreted in the context of a complete clinical assessment.

FIGURE 1

C-reactive protein point-of-care testing and complementary strategies to improve antibiotic stewardship in children with acute respiratory infections in primary care (1)

Figure 1. Decision tree/flowchart including the interpretation of CRP values for pediatric population (from 6 months to 14 years) presenting with an acute illness episode due to a respiratory tract infection in primary care.

TABLE 1

C-reactive protein point-of-care testing and complementary strategies to improve antibiotic stewardship in children with acute respiratory infections in primary care (2)

Table 1. Overview of studies examining the role of CRP POCT in safely reducing antibiotic prescribing rates for children with RTIs.

The following treatment considerations are suggested for the CRP ranges listed below, for the primary care of children presenting with an acute illness episode due to a respiratory tract infection:

4.1. If the clinical assessment is non-conclusive, test CRP. If CRP <20 mg/L, avoid prescribing antibiotics

Nearly half of the children tested in the primary care setting for LRTIs will have a CRP below 20 mg/L, showing a considerable potential to rule out the need for antibiotic prescription (10, 22, 34, 35).

In these cases, it is strongly suggested to avoid prescribing antibiotics when the clinical assessment rules out a severe infection. Instead, clinicians should give safety netting advice and ask the child's guardian to monitor the progression of symptoms and in case of exacerbation or persistence to re-contact the physician. Re-consultation should be considered as an option especially in cases where the child presented so early in the progression of the disease (i.e.,: in the first 24 h) that a conclusive clinical evaluation and interpretation of CRP values is difficult or impossible. Consider prescribing symptomatic treatment. In case of worsening of the clinical conditions, clinicians should consider repeating CRP testing, taking into account the possibility of a secondary bacterial infection.

4.2. CRP ≥20 mg/L: the clinical assessment prevails, and CRP values can be used to complement clinical reasoning

For children with CRP values greater than or equal to 20 mg/L, the clinical assessment of the patient prevails, and CRP values can be used to complement clinical reasoning.

• The timing of the CRP measurement with regards to disease progression should be considered.

◦ CRP values are less reliable as predictive indicators during the first 24 h after the onset of a disease (36), and serious (life-threatening) infections such as sepsis can develop within this time.

◦ In the primary care of children, early presentation is common, and in these cases any interpretation of CRP results should be considered carefully and the progression of clinical conditions should be closely monitored. In general, the CRP threshold of 5 mg/L is often exceeded within four to eight hours after an acute inflammatory event, with CRP values peaking at 20–500 mg/L after 48 h (37, 38).

◦ Monitoring CRP over time can help differentiate serious infections from uncomplicated RTIs. If high CRP levels persist during the course of illness, further diagnostic workup should be considered to rule out serious infections.

• The degree of elevation of CRP values should be considered

◦ Higher CRP values indicate a greater urgency to act with regards to starting a course of treatment or referring to a hospital.

◦ Elevated CRP levels do not necessarily mean that antibiotics are a useful course of action, as inflammatory conditions and several viral infections can also increase CRP values in children (39). Be aware that a maximum CRP response with values above 40 mg/L is not infrequently found on days 3–4 in uncomplicated viral RTI (36).

◦ In cases of slightly elevated CRP values that exceed 20 mg/L with few clinical indications of a severe infection, clinicians may consider providing safety netting advice and prescribing symptomatic treatment for a specified period, with potentially a re-consultation if practically possible in case of exacerbation or persistence of symptoms.

◦ In cases of high CRP values (i.e.,: >75 mg/L) it is strongly suggested to start treatment with antibiotics, due to a high risk of a non-self-limiting infection, or to refer to a hospital (10). The child's guardians should monitor for an improvement of symptoms within a specified period of time, and if symptoms persist to arrange a re-consultation or present to a hospital.

◦ CRP levels exceeding 100 mg/L indicate a severe infection for which urgent referral to a hospital should at least be considered alongside thorough clinical assessment and history taking.

• The suspected type of infection plays an important role when making a therapy decision.

◦ Although several studies have found an increase in CRP levels with the severity of otitis media, the use of CRP levels as a guide for antibiotic prescribing in children with suspected ear infections has not specifically been investigated (40, 41). Most children with ARTI in primary care and with CRP ≥ 20 mg/L have viral infections, in which case antibiotics are not recommended. For children under 1 year of age, symptoms of lower RTIs are often associated with viral infections such as the RS-virus, for which antibiotic treatment is not recommended and hospital referral may be necessary (42).

◦ For cases where pneumonia is suspected, consider prescribing antibiotics when CRP values exceed 40 mg/L (43).

While these ranges are broadly applicable, the importance of an individual evaluation of each patient is key and should be leading the final treatment decision.

5. Complementary communication strategies

Both physicians and parents, and one day the children that are being treated, need to play a role as antibiotic stewards. The consultation is a key moment and great opportunity for physicians to offer parents and patients to be partners in the decision-making process. The consultation is typically a moment when symptoms are acute, making the messaging around antibiotic usage relevant and timely. Here below a few communication strategies to have impactful interactions that can educate and sensibilize, but also to put parents at ease with the treatment decision (especially important when access to antibiotics is possible without prescriptions) and potentially to increase satisfaction with regards to the parent/patient-physician interaction.

5.1. Announcement approach

The announcement approach simply states that physicians should give a clear and strong message to the patients, recommending a course of action. While there is no specific evidence regarding the impact of the announcement method on antibiotic use, research has shown that the words of a treating physician carry significant weight in influencing patient and parent acceptance of treatment advice. A study on HPV vaccination rates in the pediatric primary care setting showed that vaccination rates increased by 5% in 3 months by training the vaccine providers on making presumptive announcements (44).

In cases where the clinical evaluation of a physician leads to the decision not to prescribe antibiotic treatment, simple and clear statements like the following could be impactful.

- “Based on my current assessment, your child should not take antibiotics.”

- “We should not start an antibiotic treatment; it could do more harm than good.”

Naturally, there should be a follow-up conversation and further clarification provided where parents or patients express doubts or concerns.

5.2. Decision aids

If a decision aid is available, this could be reviewed together with a parent either in an explanatory fashion, or to engage them in a shared decision-making process. This process would not take much additional consultation time [on average 2.6 min (45)], but could increase the parent's knowledge, understanding and engagement with the antibiotic treatment decision—especially key to increase compliance in areas with easy access to antibiotics. Research has shown that using decision aids does not negatively impact patient satisfaction or health outcomes, and in the case of a decision aid to rule out pneumonia by patients presenting with cough and fever, had the potential to reduce antibiotic prescription by 9,1% (46).

5.3. Communication skills training

While potentially less straightforward to apply than the announcement approach, patient-centric consultation, and shared decision-making (physician-patient) techniques can further increase the effectiveness of a patient/parent-physician interaction. For instance, for adults presenting symptoms of LRTIs the use of CRP POCT reduces antibiotic prescribing by approx. 42% (relative reduction; 22% absolute reduction, 31% vs. 53%) (19), but combining CRP POCT with communication skills training reduces antibiotics prescribing reductions of more than 60% [absolute reduction 44%, 23% vs. 67% (19); RR 0.38; 95% CI 0.36–0.55 (20)]. While there is currently no clinical study available to confirm this, similar increases in efficacy can be expected for the pediatric setting.

During patient-centric consultation the physician takes a more individualized approach to patient care, emphasizing respect for individual preferences and empowering the patient. This involves asking not only for patient conditions and symptoms, but also concerns, perceptions, cultural influences, and taking these into account during treatment consideration.

When applying (physician-patient) shared decision-making techniques, the aim is to involve the patient more actively in the decision-making process, leading to a mutual decision in the best interest of the patient. Best practice combines evidence-based information with the clinical evaluation and experience of the physician, but also the patient's culture, values, and individual preferences.

5.4. Physician-parent interactions that leverage several effective strategies

Trust between physicians and parents is essential. A part of the trust is inherent to a physician's expertise, but a large part of trust is built on an inter-personal relationship based on strong communication. While physicians know how to speak with their patients' parents, and how to explain things to children, it can be useful to have a blueprint for approaches and key messages, especially in a context where the goal is to create a behavioral change that would lead to reduced antibiotic consumption.

Below (Figure 2) are a few key messages and supporting facts that could be transmitted during a consultation. These are not a script, but a number of talking points that could be useful, depending on the parent and patient the physician is facing. It may be pertinent, before introducing too many facts or arguments, to ask an open question such as: “What do you think of antibiotics?” or “To what extent do you think antibiotics would help your child?”. This would allow a physician to gauge the current attitude towards, desire for, and understanding of antibiotics and adjust the messaging accordingly.

FIGURE 2

C-reactive protein point-of-care testing and complementary strategies to improve antibiotic stewardship in children with acute respiratory infections in primary care (3)

Figure 2. Example key messages and supporting facts.

6. Discussion

Based on the available literature, discussions between experts, and the available experience with CRP in adults, the authors recommend using CRP POCT in the primary care of children presenting with ARTIs, to safely reduce antibiotic prescribing rates. While the authors strongly suggest avoiding prescribing antibiotics when CRP values are below 20 mg/L and when the clinical assessment supports ruling out a severe infection, the degree of uncertainty, when it comes to the right cut-off values of CRP for children, is larger than in adults. That is why the most important evidence has been made available to the reader, and why the recommendations are always accompanied by the reminder that the physicians’ clinical examination and reasoning is paramount. For children CRP, irrespective of the CRP value, can be used to complement clinical reasoning.

6.1. The power and precautions surrounding rapid testing at the point-of-care

Having a point-of-care test available in the primary care setting drastically reduces or even eliminates waiting for the test result. This means physicians can immediately complete their clinical analysis with an objective test value and decide a course of action with more security. Patients and their families are not left waiting with doubt and worry, but can be given objective and convincing arguments about a course of action. This will improve the patient outcomes and experiences and improve adherence to the treatment decision. In addition, a CRP POCT can typically be performed by a nurse or medical assistant without requiring training in clinical laboratory sciences (15, 49, 50), allowing diversification of job content, and freeing up time for physicians to spend with patients.

POCT is a process of various elements that need to be considered to reach continuous high quality and to secure patient safety. It is advised to collaborate with POCT or laboratory experts for a proper start of POCT in primary care, and for the ongoing high quality of POCT in routine practice. This includes a workflow according to international standards with a standard operating procedure, proper user instructions at the start, and repeated training on testing performance at the testing site. Furthermore, a set of quality assurance aspects, including technical management of testing devices, tests, and controls, and feedback on technical and user errors, and proper communication of the test results with privacy-proof personal data (preferably within an electronical, closed circle) are recommended. This will increase the chance of ongoing high-quality and patient-safe use of POCT in primary care. To ensure the quality of CRP POCT please note that proper training specific to the CRP test needs to be provided.

6.2. The perils of certainty

As stated before, the treating physician always has the final decision regarding whether or not a CRP test would be a useful addition to their clinical assessment. Sometimes a physician may feel that indications are clear, and a CRP POC test is not needed. A certain degree of confidence is healthy and normal, but there are perils to certainty.

On the one hand, Physicians are generally confident in their antibiotic prescribing decision, with physicians rating 88% of their prescribing decisions at a level of confidence of certain or very certain (51). On the other hand, research has shown that close to half of antibiotics prescribed are not indicated by guidelines or considered over-prescription (47, 52). This underlines the disconnect between confidence levels and appropriateness of prescription. Therefore, it could be recommended to perform a CRP POC test to support and especially re-evaluate the antibiotic prescribing decision regardless of the physician's level of confidence, and to regard unexpected outcomes as learning opportunities that will contribute to better antibiotic prescribing behavior (53) and antibiotic stewardship.

7. Conclusion

To say that antimicrobial resistance is a threat is almost an understatement, with damaging impacts and high costs to both healthcare systems and individual patients already today. Action must be taken on several fronts to reduce the over-use of antibiotics and increase maturity of antibiotic stewardship, to limit antimicrobial resistance and keep the life-saving treatment that antibiotics provide effective for future generations. C-reactive protein point-of-care testing complemented with clear clinical guidance and effective communication techniques leads to better antibiotic stewardship, including a vast reduction of unneeded antibiotic prescriptions. It has the potential to trigger the behavioral change that is needed worldwide, especially with regards to high antibiotic prescribing settings for children presenting in primary care with an acute illness episode due to a respiratory tract infection. CRP POCT in combination with enhanced communication techniques and delayed prescribing should be considered to compliment the clinical assessment of children (6 months to 14 years) presenting with an ARTI in a primary care setting, in order to safely improve the appropriateness of antibiotic prescribing. When CRP values are below 20 mg/L and when the clinical assessment supports ruling out a severe infection, it is strongly suggested to avoid prescribing antibiotics. When CRP values are greater than or equal to 20 mg/L, CRP values can be used to complement clinical reasoning and further treatment considerations.

Further well-designed randomized controlled trials in children are needed to increase the evidence base, particularly on the best cut-off values of CRP in children for management decisions.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Funding

Abbott facilitated and partially funded group discussions leading to the present paper, as an initiative of the Abbott Antibiotic Stewardship Coalition.

Acknowledgments

The authors acknowledge MindGap, the healthcare market research and consultancy, for their facilitation and coordination of the writing process. The authors acknowledge Atilla Altiner for his contributions to content and discussion related to the paper.

Conflict of interest

RH declares to have received honoraria from Abbott, LumiraDx, Future Diagnostics, Photondelta, Cepheid and Roche for advisory board meetings and lecturing. Outside the scope of this article, Ivan Gentile has acted as a consultant for MSD, Gilead, Abbvie, Pfizer, Angelini, Nordic, GSK, and SOBI. Outside the scope of this article, Annamaria Staiano has acted as a consultant for Aboca, Angelini and Novalac; as clinical investigator for Janssen Biologics B.V. and Novalac; speaker for Novartis, Bromatech, Sanofi, Vyvalife; and was clinical investigator for Aboca, Eli Lilly Cork Limited and PAREXEL International Srl. Carl Llor declares to have received honoraria from Abbott for lecturing. Abbott facilitated and partially funded group discussions leading to the present paper, as an initiative of the Abbott Antibiotic Stewardship Coalition, a multi-stakeholder collaboration aiming to reduce antibiotic resistance, by reducing antibiotic over-prescription for RTIs in primary care. Abbott had no input into the content of the publication.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. World Health Organization (WHO), Antimicrobial resistance: Available at: https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance (Accessed July 19, 2022).

2. United Nations Foundation. Antimicrobial resistance is the silent pandemic we can no longer neglect: Available at: https://unfoundation.org/blog/post/antimicrobial-resistance-is-the-silent-pandemic-we-can-no-longer-neglect/ (Accessed July 19, 2022).

3. Antimicrobial Resistance Collaborators. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet. 2022;399(10325):629–55, https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(21)02724-0/fulltext#seccestitle10 doi: 10.1016/S0140-6736(21)02724-0

PubMed Abstract | CrossRef Full Text | Google Scholar

4. United. Global indicator framework for the Sustainable Development Goals and targets of the 2030 Agenda for Sustainable Development. Available at: https://unstats.un.org/sdgs/indicators/Global%20Indicator%20Framework%20after%202020%20review_Eng.pdf (Accessed July 19, 2022).

5. Laxminarayan R, Bhutta ZA. Antimicrobial resistance-a threat to neonate survival. Lancet Glob Health. (2016) 4(10):e676–7. doi: 10.1016/S2214-109X(16)30221-2

CrossRef Full Text | Google Scholar

6. O’Neill J. Tackling Drug-Resistant Infections Globally: Final Report and Recommendations. Review on Antimicrobial Resistance 2016.

7. Burvenich R, Dillen H, Trinh NTH, Freer J, Wynants L, Heytens S, et al. Antibiotic use in ambulatory care for acutely ill children in high-income countries: a systematic review and meta-analysis. Arch Dis Child. (2022) 107:1088–94. doi: 10.1136/archdischild-2022-324227

CrossRef Full Text | Google Scholar

8. Little P, Francis NA, Stuart B, O'Reilly G, Thompson N, Becque T, et al. Antibiotics for lower respiratory tract infection in children presenting in primary care in England (ARTIC PC): a double-blind, randomised, placebo-controlled trial. Lancet. (2021) 398(10309):1417–26. doi: 10.1016/S0140-6736(21)01431-8

CrossRef Full Text | Google Scholar

9. Pfäfflin A, Schleicher E. Inflammation markers in point-of-care testing (POCT). Anal Bioanal Chem. (2009) 393(5):1473–80. doi: 10.1007/s00216-008-2561-3

CrossRef Full Text | Google Scholar

10. Verbakel JY, Lemiengre MB, De Burghgraeve T, De Sutter A, Aertgeerts B, Shinkins B, et al. Should all acutely ill children in primary care be tested with point-of-care CRP: a cluster randomised trial. BMC Med. (2016) 14(1):131. doi: 10.1186/s12916-016-0679-2. Erratum in: BMC Med. (2017) 15(1):93. PMID: 27716201; PMCID: PMC5052874.27317420

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Putto A, Ruuskanen O, Meurman O, Ekblad H, Korvenranta H, Mertsola J, et al. C reactive protein in the evaluation of febrile illness. Arch Dis Child. (1986) 61(1): 24–9. doi: 10.1136/adc.61.1.24

CrossRef Full Text | Google Scholar

12. Rautiainen L, Cirko A, Pavare J, Grope I, Gersone G, Tretjakovs P, et al. Biomarker combinations in predicting sepsis in hospitalized children with fever. BMC Pediatr. (2022) 22:272. doi: 10.1186/s12887-022-03285-3

CrossRef Full Text | Google Scholar

13. Elvers KT, Wilson VJ, Hammond A, Duncan L, Huntley AL, Hay AD, et al. Antibiotic-induced changes in the human gut microbiota for the most commonly prescribed antibiotics in primary care in the UK: a systematic review. BMJ Open. (2020) 10:e035677. doi: 10.1136/bmjopen-2019-035677

CrossRef Full Text | Google Scholar

14. Cooke J, Llor C, Hopstaken R, Dryden M, Butler C. Respiratory tract infections (RTIs) in primary care: narrative review of C reactive protein (CRP) point-of-care testing (POCT) and antibacterial use in patients who present with symptoms of RTI. BMJ Open Respir Res. (2020) 7:e000624. doi: 10.1136/bmjresp-2020-000624

CrossRef Full Text | Google Scholar

15. Verbakel JY, Lee JJ, Goyder C, Tan PS, Ananthakumar T, Turner PJ, Hayward G, Van den Bruel A. Impact of point-of-care C reactive protein in ambulatory care: a systematic review and meta-analysis. BMJ Open. (2019) 9(1):e025036. doi: 10.1136/bmjopen-2018-025036

CrossRef Full Text | Google Scholar

16. Martínez-González NA, Keizer E, Plate A, et al. Point-of-Care C-reactive protein testing to reduce antibiotic prescribing for respiratory tract infections in primary care: systematic review and meta-analysis of randomised controlled trials. Antibiotics. (2020) 9(9):610. doi: 10.3390/antibiotics9090610

CrossRef Full Text | Google Scholar

17. O’Brien K, Gloeckner L, Jordan K, Lucey D, Marshall L, Moran P, et al. EUnetHTA report 2019. Rapid assessment on other health technologies using the HTA Core Model for Rapid Relative Effectiveness Assessment. C-reactive protein point-of-care testing (CRP POCT) to guide antibiotic prescribing in primary care settings for acute respiratory tract infections (RTIs). EUnetHTA Project ID: OTCA012 2019.

18. Tonkin-Crine SK, Tan PS, van Hecke O, Wang K, Roberts NW, McCullough A, et al. Clinician-targeted interventions to influence antibiotic prescribing behaviour for acute respiratory infections in primary care: an overview of systematic reviews. Cochrane Database Syst Rev. (2017) 9(9):CD012252. doi: 10.1002/14651858.CD012252.pub2

CrossRef Full Text | Google Scholar

19. Cals JW, Butler CC, Hopstaken RM, Hood K, Dinant GJ. Effect of point of care testing for C reactive protein and training in communication skills on antibiotic use in lower respiratory tract infections: cluster randomised trial. Br Med J. (2009) 338:b1374. doi: 10.1136/bmj.b1374

CrossRef Full Text | Google Scholar

20. Little P, Stuart B, Francis N, Douglas E, Tonkin-Crine S, Anthierens S, et al. Effects of internet-based training on antibiotic prescribing rates for acute respiratory-tract infections: a multinational, cluster, randomised, factorial, controlled trial. Lancet. (2013) 382(9899):1175–82. doi: 10.1016/S0140-6736(13)60994-0

CrossRef Full Text | Google Scholar

21. Thompson M, Van den Bruel A, Verbakel J, Lakhanpaul M, Haj-Hassan T, Stevens R, Moll H, Buntinx F, Berger M, Aertgeerts B, Oostenbrink R, Mant D. Systematic review and validation of prediction rules for identifying children with serious infections in emergency departments and urgent-access primary care. Health Technol Assess. (2012) 16(15):1–100. doi: 10.3310/hta16150

CrossRef Full Text | Google Scholar

22. Schot MJ, Van den Bruel A, Broekhuizen BD, Cals JW, Noteboom EA, Balemans W, et al. Point-of-care C-reactive protein to assist in primary care management of children with suspected non-serious lower respiratory tract infection: a randomised controlled trial. BJGP Open. (2018) 2(3):bjgpopen18X101600. doi: 10.3399/bjgpopen18X101600

CrossRef Full Text | Google Scholar

23. Dyer EM, Waterfield T, Baynes H. How to use C-reactive protein. Arch Dis Child Educ Pract Ed. (2019) 104(3):150–3. doi: 10.1136/archdischild-2018-315079

CrossRef Full Text | Google Scholar

24. Van Hecke O, Raymond M, Lee JJ, Turner P, Goyder CR, Verbakel JY, et al. In-vitro diagnostic point-of-care tests in paediatric ambulatory care: a systematic review and meta-analysis. PLoS One. (2020) 15(7):e0235605. doi: 10.1371/journal.pone.0235605

CrossRef Full Text | Google Scholar

25. Smedemark SA, Llor C, Aabenhus R, Fournaise A, Jørgensen KJ, Olsen O. Biomarkers as point-of-care tests to guide prescription of antibiotics in people with acute respiratory infections in primary care. Cochrane Database Syst Rev. (2022) 10:CD010130. doi: 10.1002/14651858.CD010130.pub3

CrossRef Full Text | Google Scholar

26. Keitel K, Samaka J, Masimba J, Temba H, Said Z, Kagoro F, et al. Safety and efficacy of C-reactive protein-guided antibiotic use to treat acute respiratory infections in Tanzanian children: a planned subgroup analysis of a randomized controlled noninferiority trial evaluating a novel electronic clinical decision algorithm (ePOCT). Clin Infect Dis. (2019) 69(11):1926–34. doi: 10.1093/cid/ciz080

CrossRef Full Text | Google Scholar

27. Althaus T, Greer RC, Swe MMM, Cohen J, Tun NN, Heaton J, et al. Effect of point-of-care C-reactive protein testing on antibiotic prescription in febrile patients attending primary care in Thailand and Myanmar: an open-label, randomized, controlled trial. Lancet Glob Health. (2019) 7(1):e119–31. doi: 10.1016/S2214-109X(18)30444-3

CrossRef Full Text | Google Scholar

28. Higdon MM, Le T, O’Brien KL, Murdoch DR, Prosperi C, Baggett HC, et al. Association of C-reactive protein with bacterial and respiratory syncytial virus-associated pneumonia among children aged <5 years in the PERCH study. Clin Infect Dis. (2017) 64(suppl_3):S378–86. doi: 10.1093/cid/cix150

CrossRef Full Text | Google Scholar

29. Rebnord IK, Sandvik H, Mjelle AB, Hunskaar S. Factors predicting antibiotic prescription and referral to hospital for children with respiratory symptoms: secondary analysis of a randomised controlled study at out-of-hours services in primary care. BMJ Open. (2017) 7(1):e012992. doi: 10.1136/bmjopen-2016-012992

CrossRef Full Text | Google Scholar

30. Do NT, Ta NT, Tran NT, Than HM, Vu BT, Hoang LB, et al. Point-of-care C-reactive protein testing to reduce inappropriate use of antibiotics for non-severe acute respiratory infections in Vietnamese primary health care: a randomised controlled trial. Lancet Glob Health. (2016) 4:e633–41 doi: 10.1016/S2214-109X(16)30142-5. Erratum in: Lancet Glob Health. 2017 Jan 5(1):e39.

CrossRef Full Text | Google Scholar

31. Díez-Padrisa N, Bassat Q, Morais L, O'Callaghan-Gordo C, Machevo S, Nhampossa T, et al. Procalcitonin and C-reactive protein as predictors of blood culture positivity among hospitalised children with severe pneumonia in Mozambique. Trop Med Int Health. (2012) 17(9):1100–7. doi: 10.1111/j.1365-3156.2012.03035.x

CrossRef Full Text | Google Scholar

32. Diederichsen HZ, Skamling M, Diederichsen A, Grinsted P, Antonsen S, Petersen PH, et al. Randomised controlled trial of CRP rapid test as a guide to treatment of respiratory infections in general practice. Scand J Prim Health Care. (2000) 18(1):39–43. doi: 10.1080/02813430050202541

CrossRef Full Text | Google Scholar

33. Marcus N, Mor M, Amir L, Mimouni M, Waisman Y. Validity of the quick-read C-reactive protein test in the prediction of bacterial pneumonia in the pediatric emergency department. Eur J Emerg Med. (2008) 15(3):158–61. doi: 10.1097/MEJ.0b013e3282f12f52

CrossRef Full Text | Google Scholar

34. Agnello L, Bellia C, Di Gangi M, Lo Sasso B, Calvaruso L, Bivona G, et al. Utility of serum procalcitonin and C-reactive protein in severity assessment of community-acquired pneumonia in children. Clin Biochem. (2016) 49(1-2):47–50. doi: 10.1016/j.clinbiochem.2015.09.008

CrossRef Full Text | Google Scholar

35. Rebnord IK, Sandvik H, Mjelle AB, Hunskaar S. Out-of-hours antibiotic prescription after screening with C reactive protein: a randomised controlled study. BMJ Open. (2016 May) 6(5):e011231. doi: 10.1136/bmjopen-2016-011231 Erratum in: BMJ Open. 2016 Sep 09;6(9):e011231corr1

CrossRef Full Text | Google Scholar

36. Melbye H, Hvidsten D, Holm A, Nordbø SA, Brox J. The course of C-reactive protein response in untreated upper respiratory tract infection. Br J Gen Pract. (2004) 54(506):653–8.

Google Scholar

37. Morley JJ, Kushner I. Serum C-reactive protein levels in disease. Ann NY Acad Sci. (1982) 389:406–18. doi: 10.1111/j.1749-6632.1982.tb22153.x

CrossRef Full Text | Google Scholar

38. Pepys MB, Hirschfield GM. C-reactive protein: a critical update. J Clin Invest. (2003) 111(12):1805–12. doi: 10.1172/JCI200318921

CrossRef Full Text | Google Scholar

39. Appenzeller C, Ammann RA, Duppenthaler A, Gorgievski-Hrisoho M, Aebi C. Serum C-reactive protein in children with adenovirus infection. Swiss Med Wkly. (2002) 132(25-26):345–50.

Google Scholar

40. Garcia C, Salgueiro AB, Luís C, Correia P, Brito MJ. Acute mastoiditis in children: middle ear cultures may help in reducing use of broad spectrum antibiotics. Int J Pediatr Otorhinolaryngol. (2017) 92:32–7 doi: 10.1016/j.ijporl.2016.11.002

CrossRef Full Text | Google Scholar

41. Ovnat Tamir S, Roth Y, Goldfarb A, Grotto I, Marom T. Severity of pneumococcal versus non-pneumococcal acute otitis media in children. Clin Otolaryngol. (2015) 40(4):370–7. doi: 10.1111/coa.12384

CrossRef Full Text | Google Scholar

42. Korppi M, Heiskanen-Kosma T, Jalonen E, Saikku P, Leinonen M, Halonen P, et al. Aetiology of community-acquired pneumonia in children treated in hospital. Eur J Pediatr. (1993) 152(1):24–30. doi: 10.1007/BF02072512

CrossRef Full Text | Google Scholar

43. Alcoba G, Keitel K, Maspoli V, Lacroix L, Manzano S, Gehri M, et al. A three-step diagnosis of pediatric pneumonia at the emergency department using clinical predictors, C-reactive protein, and pneumococcal PCR. Eur J Pediatr. (2017) 176(6):815–24. doi: 10.1007/s00431-017-2913-0

CrossRef Full Text | Google Scholar

44. Brewer NT, Hall ME, Malo TL, et al. Announcements versus conversations to improve HPV vaccination coverage: a randomized trial. Pediatrics. (2017) 139(1):e20161764. doi: 10.1542/peds.2016-1764

CrossRef Full Text | Google Scholar

45. Stacey D, Légaré F, Lewis K, Barry MJ, Bennett CL, Eden KB, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. (2017) 4(4):CD001431. doi: 10.1002/14651858.CD001431.pub5

CrossRef Full Text | Google Scholar

46. Steurer J, Held U, Spaar A, Bausch B, Zoller M, Hunziker R, et al. A decision aid to rule out pneumonia and reduce unnecessary prescriptions of antibiotics in primary care patients with cough and fever. BMC Med. (2011) 9:56. doi: 10.1186/1741-7015-9-56

CrossRef Full Text | Google Scholar

47. Volery M, Scherz V, Jakob W, Bandeira D, Deggim-Messmer V, Lauber-Biason A, et al. Study protocol for the ABERRANT study: antibiotic-induced disruption of the maternal and infant microbiome and adverse health outcomes—a prospective cohort study among children born at term. BMJ Open. (2020) 10(6):e036275. doi: 10.1136/bmjopen-2019-036275

CrossRef Full Text | Google Scholar

48. Bergmann M, Haasenritter J, Beidatsch D, Schwarm S, Hörner K, Bösner S, et al. Coughing children in family practice and primary care: a systematic review of prevalence, aetiology and prognosis. BMC Pediatr. (2021) 21(1):260. doi: 10.1186/s12887-021-02739-4

CrossRef Full Text | Google Scholar

49. Verbakel JY, Aertgeerts B, Lemiengre M, Sutter AD, Bullens DM, Buntinx F. Analytical accuracy and user-friendliness of the afinion point-of-care CRP test. J Clin Pathol. (2014) 67(1):83–6. doi: 10.1136/jclinpath-2013-201654

CrossRef Full Text | Google Scholar

50. Hughes A, Gwyn L, Harris S, Clarke C. Evaluating a point-of-care C-reactive protein test to support antibiotic prescribing decisions in a general practice. Clinical Pharmacist. (2016

Google Scholar

51. Van der Velden AW, van de Pol AC, Bongard E, Cianci D, Aabenhus R, Balan A, et al. Point-of-care testing, antibiotic prescribing, and prescribing confidence for respiratory tract infections in primary care: a prospective audit in 18 European countries. BJGP Open. (2022) 6:BJGPO.2021.0212. doi: 10.3399/BJGPO.2021.0212

CrossRef Full Text | Google Scholar

52. Dekker AR, Verheij TJ, van der Velden AW. Inappropriate antibiotic prescription for respiratory tract indications: most prominent in adult patients. Fam Pract. (2015) 32(4):401–7. doi: 10.1093/fampra/cmv019

CrossRef Full Text | Google Scholar

53. Masic I, Miokovic M, Muhamedagic B. Evidence based medicine—new approaches and challenges. Acta Inform Med. (2008) 16(4):219–25. doi: 10.5455/aim.2008.16.219-225

CrossRef Full Text | Google Scholar

Appendix

We focused on articles included in the last Cochrane reviews. Additionally, we searched the most recent manuscripts using the PubMed database and the following keywords: CRP point of care or CRP AND Acute respiratory tract infections OR Respiratory tract infections AND children.

C-reactive protein point-of-care testing and complementary strategies to improve antibiotic stewardship in children with acute respiratory infections in primary care (2024)

FAQs

What is CRP testing in primary care? ›

C-reactive protein point-of-care testing (CRP POC) is a well-established diagnostic and prognostic tool that, if used in primary care settings, may have a role in the fight against antibiotic over-prescription in patients with LRTI symptoms.

How to reduce CRP level in a child? ›

If your little one's CRP level is high, see a doctor for a correct diagnosis and treatment. While you wait for their visit, make sure they consume a nutritious diet rich in fruits, vegetables, whole grains, and lean proteins. This can enhance their general health and perhaps lessen inflammation.

What is the C reactive protein in antibiotics? ›

CRP aids in the evaluation of disease severity and efficacy of antibiotic therapy. CRP production is proportional to the intensity of infection and inflammation4. Therefore, it is useful in the differentiation of mild and severe infections. If CRP level is < 10 mg/l, bacterial infection is unlikely5.

What is the significance of CRP in pediatrics? ›

Why Are CRP Tests Done? Doctors may order a CRP test if a child has signs of inflammation or infection. They use CRP tests to follow conditions such as inflammatory bowel disease (IBD), arthritis, and lupus. CRP tests also can help doctors see how well treatment for inflammation or infection is working.

How do you perform a CRP test? ›

What happens during a CRP test? A health care professional will take a blood sample from a vein in your arm, using a small needle. After the needle is inserted, a small amount of blood will be collected into a test tube or vial. You may feel a little sting when the needle goes in or out.

What level of C-reactive protein is concerning? ›

You are at low risk of developing cardiovascular disease if your hs-CRP level is lower than 1.0 mg/L. You are at average risk of developing cardiovascular disease if your levels are between 1.0 mg/L and 3.0 mg/L. You are at high risk for cardiovascular disease if your hs-CRP level is higher than 3.0 mg/L.

What happens if C-reactive protein is positive? ›

A high CRP is more than 10mg/L. This shows that there is inflammation somewhere in your body. Other tests might be necessary to find out where or which specific illness or infection is causing the inflammation. If you are being treated for an infection or inflammation, your CRP levels should decrease.

What is an alarming CRP? ›

Generally, a CRP level of less than 10 mg/L is considered normal. CRP levels between 10 and 100 mg/L indicate mild to moderate inflammation, while levels above 100 mg/L indicate severe inflammation.

What level of CRP indicates bacterial infection? ›

Significantly elevated CRP levels tend to occur with severe infections, such as bacterial or fungal infections. Bacterial infection is responsible for about 90% of the cases involving CRP levels higher than 50 mg/l.

What is a normal CRP level for a child? ›

CRP levels ranged from 0.02 to 14.4 mg/l in the children's sera, the median being 0.45 mg/l and the mean 1.65 mg/l. No individual lacking CRP was detected.

What happens if CRP is high in a child with fever? ›

Conclusion: Febrile children with extremely elevated CRP showed greater illness severity (haemodynamic instability, PICU admissions), thus careful clinical attention is desirable in these cases.

How do you treat C-reactive protein? ›

If you're at high risk of cardiovascular disease and your test results show high CRP, your doctor may suggest a statin or other cholesterol-lowering medication. Vitamin C has also been explored as a way to lower CRP levels for people who have an elevated risk of cardiovascular disease.

Why would a doctor order a CRP blood test? ›

What is this test? The C-reactive protein (CRP) test is used to find inflammation in your body. Inflammation could be caused by different types of conditions, such as an infection or autoimmune disorders like rheumatoid arthritis or inflammatory bowel disease. This test measures the amount of CRP in your blood.

What is the CRP test mainly used for? ›

The C-reactive protein (CRP) blood test checks for inflammation in your body. A CRP blood test will show if there is inflammation in your body. A CRP blood test also helps to see how well you are responding to treatment. No special preparation is needed for a CRP blood test.

What does CRP stand for in healthcare? ›

C-reactive protein (CRP) is a protein made by the liver. The level of CRP increases when there's inflammation in the body. A simple blood test can check your C-reactive protein level. A high-sensitivity C-reactive protein (hs-CRP) test is more sensitive than a standard C-reactive protein test.

What diagnosis is CRP covered for? ›

Inflammatory changes lead to progressive disease, which culminates in plaque instability, rupture, thrombosis, and myocardial infarction (MI). CRP testing, CPT code 86140, is eligible for coverage as a diagnostic test for the detection and evaluation of infection, tissue injury, and inflammatory disease.

Top Articles
Latest Posts
Article information

Author: Otha Schamberger

Last Updated:

Views: 6316

Rating: 4.4 / 5 (55 voted)

Reviews: 86% of readers found this page helpful

Author information

Name: Otha Schamberger

Birthday: 1999-08-15

Address: Suite 490 606 Hammes Ferry, Carterhaven, IL 62290

Phone: +8557035444877

Job: Forward IT Agent

Hobby: Fishing, Flying, Jewelry making, Digital arts, Sand art, Parkour, tabletop games

Introduction: My name is Otha Schamberger, I am a vast, good, healthy, cheerful, energetic, gorgeous, magnificent person who loves writing and wants to share my knowledge and understanding with you.