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. 2024 May 10;56(1):2352606. doi: 10.1080/07853890.2024.2352606

Severe pertussis in infants: a scoping review

Shuai Guo a,b,c, Yu Zhu a,b,c, Qin Guo a,b,c, Chaomin Wan a,b,c,
PMCID: PMC11089926  PMID: 38728617

Abstract

Background

Pertussis (Whooping Cough) is a respiratory infection caused by Bordetella pertussis. Pertussis usually occurs in childhood; severe infections are most common in infants. It can be fatal with severe complications such as pulmonary hypertension, heart failure, and encephalitis.

Objectives

We sought to synthesize the existing literature on severe pertussis in infants and inform further study.

Methods

A scoping review was performed based on the methodological framework developed by Arksey & O’Malley. Search in Pubmed and Embase databases, with no restrictions on the language and date of publication.

Results

Of the 1299 articles retrieved, 64 were finally included. The selected articles were published between 1979 and 2022, with 90.6% (58/64) of the studies in the last two decades. The studies covered epidemiology, pathology, clinical characteristics, risk factors, treatments, and burden of disease.

Conclusion

The literature reviewed suggests that studies on severe pertussis in infants covered a variety of clinical concerns. However, these studies were observational, and experimental studies are needed to provide high-quality evidence.

Keywords: Pertussis, whooping cough, infants

Introduction

Pertussis (Whooping Cough) is a respiratory infection caused by Bordetella pertussis and characterized by paroxysmal coughing ending in a prolonged crowing intake of breath. Pertussis usually occurs in childhood; severe infections are most common in infants. It can be fatal with severe complications such as pulmonary hypertension, heart failure, and encephalitis. Pertussis is a vaccine-preventable disease, and the implementation of pertussis vaccine immunization has led to a decline in the number of pertussis cases and deaths among children since the inception of the WHO Expanded Programme on Immunization in 1974 [1]. However, even in countries with widespread pertussis vaccine coverage, such as the United States, Canada, and Australia [2], the incidence of pertussis has been on the rise again after maintaining a low rate for many years, with outbreaks in some places, which is referred to as ‘re-emergence of pertussis’.

There are multiple challenges to the management of pertussis. The change in the mode of transmission, from the previous child-child epidemic mode to an adult-child epidemic mode after the introduction of the immunization program, makes infants and young children more susceptible to infection [3,4]. Furthermore, given the considerable side effects of whole-cell pertussis vaccine, the acellular pertussis vaccine was introduced at the end of the twentieth century and is already used in many countries and regions. Although acellular pertussis vaccination has fewer adverse events than whole-cell pertussis vaccination, many studies have shown that acellular pertussis vaccination is associated with a higher risk of pertussis morbidity over time [5–7]. The acellular pertussis vaccine only protects against disease, not the infection, which could make it possible for people who were vaccinated with the acellular pertussis vaccine to act as asymptomatic or mildly symptomatic carriers and play an important role in the spread of pertussis in the population [8]. In addition, since the first strain of erythromycin-resistant Bordetella pertussis isolated from a 2-month-old infant with pertussis was reported in Arizona, USA, in 1994, subsequent reports of antibiotic-resistant Bordetella pertussis have been reported in many countries, such as France, China, Iran, Viet Nam [9–13].

Nowadays, pertussis remains a public health problem of great concern, with high rates of morbidity and mortality. WHO estimates that about 24.1 million cases of pertussis and 160,700 children under 5 years of age die of pertussis in a year [14]. According to the United States Centers for Disease Control and Prevention, about one-third of infants with pertussis require hospitalization, and 1% of those cases die [15]. Pertussis is one of the significant causes of illness and death in infants. Therefore, we sought to synthesize the existing literature on severe pertussis in infants and inform further study.

The following research questions were used to guide this evidence review:

  1. How many studies have been published on severe pertussis in infants?

  2. What aspects of the study have been done on severe pertussis in infants?

  3. What study designs have been used in studies on severe pertussis in infants?

Methods

A scoping review was performed based on the methodological framework developed by Arksey & O’Malley [16].

  1. Information sources and Search strategies

    The following terms were used to construct the search strategies in the Pubmed and Embase databases: (Whooping cough or Pertussis) AND (Infant or Newborn or Neonate) AND (Critical illness or Severe or Fatal or Malignant or Fulminant) (Table 1). There were no restrictions on the language and date of publication. The literature was last searched on 30 June 2023.

  2. Literature selection and Inclusion criteria

    Study selection took place in two stages: first, titles and abstracts were reviewed, followed by the full text. Titles and abstracts were reviewed independently by two researchers, the abstracts that did not meet the inclusion criteria or that met the exclusion criteria were discarded. Articles without an available abstract or for which abstracts did not provide sufficient information to determine their exclusion were directly included in the full-text review stage. The full-text review was performed independently by two researchers, and disagreements were resolved by a third researcher. The inclusion of articles met the following criteria: (a) The study subjects were limited to infants under one year of age; (b) The study focuses on severe pertussis infections. Severe infection was defined as infants with pertussis who had hypoxemia, pulmonary hypertension, and heart failure, required respiratory support, were admitted to the intensive care unit, or died. Exclusion of review studies. The final search results were exported to EndNote and duplicate studies were removed.

  3. Results synthesis and Data charts

    We summarize the information extracted from the included studies in the table. Two researchers developed data charts jointly and independently extracted data from articles that fit this study, and then exchanged them for validation. A third researcher solved the disagreement. Variables included author, journal, year of publication, country, language of publication, study design, sample size, sample characteristics, and purpose or topic of the study.

Table 1.

Search strategy.

  Pertussis Infants Severe
MeSH terms Whooping cough Infant Critical illness
Free-text terms Pertussis Newborn* Severe
    Neonat* Fatal
    Infan* Malignant
      Fulminant
Search formula in Pubmed (((Whooping cough[MeSH Terms]) OR (Pertussis[Title/Abstract])) AND ((((Infant[MeSH Terms]) OR (Newborn*[Title/Abstract])) OR (Neonat*[Title/Abstract])) OR (Infan*[Title/Abstract]))) AND (((((Critical illness[MeSH Terms]) OR (Severe[Title/Abstract])) OR (Fatal[Title/Abstract])) OR (Malignant[Title/Abstract])) OR (Fulminant[Title/Abstract]))
Search formula in Embase #1 Pertussis.sh. or Whooping cough.ab.
#2 Infant.sh. or Newborn.ab. or Neonate.ab.
#3 Critical illness.sh. or Severe.ab. or Fatal.ab. or Malignant.ab. or Fulminant.ab.
#4 1 and 2 and 3

Results

The search strategy identified 1299 articles, with 992 articles after deleted duplicates. Screening through titles and abstracts left 107 articles for full-text evaluation. The abstract and full text were not available for four articles, so sufficient information could not be obtained, and a total of 64 studies were finally included (Figure 1).

Figure 1.

Figure 1.

Study selection.

The selected articles were published between 1979 and 2022, with 90.6% (58/64) of the studies in the last two decades. Including studies from 22 countries, the top three numbers were from the United States (25.0%, 16/64), China (9.3%, 6/64), and France (9.3%, 6/64). Out of six publication languages, most studies were published in English (75.0%, 48/64). All study designs were observational studies, with the most case reports (62.5%, 40/64) (Table 2).

Table 2.

Characteristics of the included studies.

Characteristic Categories for each characteristic Number of studies (n = 64)
Date of publication 2022–2018 15
2017–2013 16
2012–2008 13
2007–2003 14
2002–1998 2
1997–1993 1
Before 1992 3
Language of publication Chinese 2
Danish 1
English 48
French 9
Portuguese 1
Spanish 3
Study design Case control study 5
Cohort study 3
Descriptive study (Case analysis) 15
Descriptive study (Case report) 40
Historical control study 1
Place of study Argentina 1
Australia 2
Belgium 2
Canada 3
Chile 3
China 6
Denmark 2
France 6
India 1
Indonesia 1
Italy 1
Netherlands 1
New Zealand 3
Oman 1
Portugal 3
Spain 1
Switzerland 1
Tunisia 2
Türkiye 2
UK 5
USA 16
Viet Nam 2

There are no standardized diagnostic criteria for severe pertussis. In these included studies, severe pertussis was defined as requiring respiratory support, admission to the intensive care unit, or resulting in death. The case reports (Table 3) [17–56] covered clinically severe manifestations and treatments; these severe manifestations are characterized by increased white blood cells, pulmonary hypertension, acute respiratory distress syndrome, encephalopathy, respiratory failure, cardiovascular collapse, and septic shock; of the treatments, most related to a reduction of white blood cells such as leukapheresis (10.0%, 4/40) and exchange transfusion (27.5%, 11/40), in addition to extracorporeal life support (10.0%, 4/40). In infants with severe pertussis and severe leukocytosis, early reduction of white blood cell therapy may be a helpful and rapid life-saving treatment before cardiopulmonary complications develop. Among other studies (except for case reports) (Table 4) [57–80], the major study designs were descriptive studies (62.5%, 15/24), case-control studies (20.8%, 5/24), and cohort studies (12.5%, 3/24); 45.8% (11/24) analyzed the risk factors associated with severe infection or death; Other contents involved epidemiology (12.5%, 3/24), clinical manifestations (8.3%, 2/24), pathological features (12.5%, 3/24), treatment (16.7%, 4/24), and disease burden (4.2%, 1/24). Increased white blood cell (81.8%, 9/11) is one of the risk factors associated with severe infection or death in infants with pertussis shown in most studies, as well as increased lymphocyte, apnea, co-infections, pulmonary hypertension, age, fever, cyanosis, and abnormal liver function.

Table 3.

Study characteristics from case reports.

First author Journal Year Country Language Key element
Long S Cureus 2022 USA English Leukapheresis
Liao Y Open Forum Infect Dis 2022 China English Metagenomics next-generation sequencing
Son PT Vox Sang 2021 Viet Nam English Exchange transfusion
Kolind RS Ugeskr Laeger 2021 Denmark Danish Exchange transfusion
Fueta PO Case Rep Infect Dis 2021 USA English Multidisciplinary management
Rossetti E Blood Purif 2020 Italy English Leukapheresis
Chen X Chinese J Appl Clin Pediatr 2020 China Chinese Leukapheresis
Wei XM Zhongguo Dang Dai Er Ke Za Zhi 2019 China Chinese Exchange transfusion
Alkan G Turk Klinikleri Pediatr 2017 Türkiye English Exchange transfusion
Ganeshalingham A Arch Dis Child 2016 New Zealand English Pulmonary dystrophic calcification
Liko J Public Health Rep 2015 USA English Burden of disease
Chantreuil J Arch Pediatr 2015 France French Exchange transfusion
Assy J Pediatr Infect Dis J 2015 France English Exchange transfusion and Extracorporeal membrane oxygenation
Kurvers RA Eur J Pediatr 2014 Netherlands English C3 deficiency
Al Hanshi S Oman Med J 2014 Oman English Exchange transfusion
Nataprawira HM Case Rep Emerg Med 2013 Indonesia English Severe manifestations
Mata AF Pediatrics 2013 USA English Bronchoscopy with instillation of N-acetylcysteine
Martinez M Pediatr Crit Care Med 2011 Switzerland English Exchange transfusion
Menif K Arch Pediatr 2010 Tunisia French Severe manifestations
Kundrat SL Dimens Crit Care Nurs 2010 USA English Severe manifestations
Freitas J Rev Port Pneumol 2010 Portugal Portuguese Severe manifestations
Berthomieu L Arch Pediatr 2010 France French Severe manifestations
Couchot E Ann Fr Anesth Reanim 2009 France French Extracorporeal membrane oxygenation
Theilen U BMJ 2008 UK English Severe manifestations
Soares S Rev Port Pneumol 2008 Portugal French Severe manifestations
Vaessen S Rev Med Liege 2006 Belgium French Severe manifestations
Grzeszczak MJ Pediatr Crit Care Med 2006 USA English Leukapheresis
Gonzalez-Escudero R Acta Pediatr Esp 2006 Spain Spanish Severe manifestations
Donoso AF Pediatr Infect Dis J 2006 Chile English Exchange transfusion
Donoso A Scand J Infect Dis 2005 Chile English Severe manifestations
De Berry BB Pediatr Surg Int 2005 USA English Extracorporeal membrane oxygenation
Cruces RP Rev Chil Pediatr 2005 Chile Spanish Exchange transfusion
Wauters O Rev Med Liege 2004 Belgium French Severe manifestations
Romano MJ Pediatrics 2004 USA English Exchange transfusion
McEniery JA J Paediatr Child Health 2004 Australia English Nitric oxide and Sildenafil
Pilorget H Arch Pediatr 2003 France French Severe manifestations
Sreenan CD Pediatr Surg Int 2001 Canada English Extracorporeal membrane oxygenation
Corkins M Iowa Med 1991 USA English Severe manifestations
Tam AY Arch Dis Child 1986 China English Salbutamol
Theilade D Anaesthesia 1979 Denmark English Continuous positive airway pressure

Table 4.

Study characteristics from studies other than case reports.

First author Journal Year Country Language Study design Sample size Severe case definition/characterization Study objective
Zhang C BMC Infect Dis 2022 China English Case-control study 336 Infants with pertussis who also had hypoxemia, recurrent apnea, cardiovascular dysfunction, or pertussis encephalopathy were considered to have severe pertussis. To identify risk factors associated with the prognosis of pertussis in infants.
Thuy Nga DT Pediatr Infect Dis J 2022 Viet Nam English Case-control study 108 Severe disease was defined as a need for PICU admission or mechanical ventilation or death during hospitalization. To evaluate associations of Ct values with disease severity and other clinical variables in children with pertussis.
Coquaz-Garoudet M Ann Intensive Care 2021 France English Cohort study 23 Admitted to a PICU To identify factors associated with death in infants affected by malignant pertussis.
Şık G Turk Pediatri Ars 2020 Türkiye English Descriptive study 18 Admitted to a PICU To evaluate the clinical characteristics, risk factors, and prognosis of pertussis in the PICU.
Liu C BMC Infect Dis 2020 China English Case-control study 59 Admitted to a PICU To explore risk factors for death from severe pertussis.
Kavitha TK Indian Pediatr 2020 India English Descriptive study 36 Critical pertussis was defined as pertussis requiring admission to an ICU or resulting in death. To delineate the clinical profile, complications, intensive care needs, and predictors of mortality in children with critical pertussis.
Cherry JD Pediatr Infect Dis J 2018 USA English Descriptive study 100 Admitted to a PICU To gain further insight relating to the characteristics and treatment of pertussis in young infants.
Macdonald-Laurs E Pediatr Infect Dis J 2017 New Zealand English Cohort study 159 Admitted to a PICU To describe changes in pertussis deaths and PICU admissions over the past 2 decades and to determine associations of rates of such severe disease with changes in pertussis identification and in vaccine policy over this period.
Straney L Pediatr Crit Care Med 2016 Australia, New Zealand English Descriptive study 416 Admitted to a ICU To describe admission rates, severity, mortality, and costs of pertussis infections in critically ill infants.
Winter K Clin Infect Dis 2015 USA English Case-control study 236 Death To identify factors for death in young infants hospitalized for B. pertussis infections.
Tiwari TS Pediatrics 2015 USA English Cohort study 45404 Death To investigate the role of ≥1 pertussis vaccinations in preventing pertussis-related deaths and risk markers for death among infants aged <42 days.
Rocha G Pediatr Infect Dis J 2013 Portugal English Descriptive study 18 Admitted to a ICU To better understand the clinical features of pertussis infection in newborns and nonvaccinated infants less than 2 months of age, and to correlate these findings with the outcome.
Nieves D Pediatr Infect Dis J 2013 USA English Descriptive study 10 Admitted to a PICU To analyze data from 10 young infants who received exchange blood transfusions for management of severe pertussis.
Murray EL J Pediatric Infect Dis Soc 2013 USA English Descriptive study 31 Admitted to a PICU To identify factors associated with the poorest outcomes, ie, death and pulmonary hypertension.
Taffarel P Arch Argent Pediatr 2012 Argentina Spanish Descriptive study 41 Admitted to a PICU To describe the evolution of a series of patients with severe pertussis, some of whom received exchange transfusion as an alternative treatment.
Rowlands HE Pediatrics 2010 UK English Historical control study 19 Admitted to a PICU To quantify possible benefits of aggressive leukodepletion.
Bouziri A Med Trop 2010 Tunisia French Descriptive study 10 Admitted to a PICU To determine the prevalence of malignant pertussis in infants admitted to a pediatric intensive care unit for severe acute respiratory failure associated with severe leukocytosis.
Sawal M Pediatr Pulmonol 2009 UK English Descriptive study 10 Death To examine the clinico-pathological features and suggest how they may be related to outcome.
Paddock CD Clin Infect Dis 2008 USA English Descriptive study 15 Death To report the pulmonary histopathologic characteristics of fatal infantile pertussis and use IHC techniques as a tool to provide insights into the complex pathogenesis of this infection.
Vitek CR Pediatr Infect Dis J 2003 USA English Descriptive study 93 Death To characterize the clinical course of the illness and factors potentially associated with a fatal outcome.
Pooboni S Pediatr Pulmonol 2003 UK English Descriptive study 12 Respiratory support To analysis highlight the course and outcome of severe B. pertussis infection treated with extracorporeal membrane oxygenation.
Mikelova LK J Pediatr 2003 Canada English Case-control study 48 Death To describe the clinical course of fatal cases of pertussis and identify predictors of death at the time of presentation for medical care.
Pierce C Intensive Care Med 2000 UK English Descriptive study 13 Admitted to a PICU To identify factors which may be associated with a fulminant course.
Hackman R Pediatr Pathol Lab Med 1996 Canada English Descriptive study 2 Death To describe fatal pertussis histopathology of the lung tissues, including transmission and immunoelectron microscopic studies, together with novel findings in pancreatic tissue.

Discussion

We conducted a scoping review for studies of severe pertussis in infants. These patients’ common critical illness characteristic was a need for intensive care treatment, with specific definitions of severe pertussis given in individual studies. Most of the studies (40/64) were case reports and gave limited information. More than half of the studies described characteristics (or risk factors) of severe course or death from pertussis. There was a significant association between elevated white blood cell counts/pulmonary hypertension and increased severity of the disease/death.

Pulmonary histopathology [74,75,80] demonstrated abundant leukocyte aggregates in small pulmonary arteries, veins, and lymphatics; it was supposed that vascular infiltration and blood hyperviscosity by elevated leukocyte counts may be a factor for pulmonary hypertension and heart failure. Virulence factors, the key pathogenicity determinants of B. pertussis, mediate different stages of disease pathology. The postmortem was pathologically characterized by necrotizing bronchitis, bronchiolitis, pulmonary hemorrhage, edema, and extensive areas of alveolar epithelial necrosis, indicating that toxin-mediated processes or invasive infections damage the bronchi and alveolar epithelium, which could also be responsible for the secondary increased pulmonary vascular resistance, pulmonary hypertension, and subsequent fatal cardiac failure. In the first few months of life, especially in neonates, there is still a prominent muscular component in the arteries, and these vessels are very reactive to constrictive stimuli [81]. Hypoxemia, or coexistent acidosis, can trigger pulmonary vasoconstriction, and result in an acute increase in pulmonary vascular resistance. Thus, critical hypoxemia and heart failure may be due to a combination of factors, and further studies are needed to clarify the pathogenesis of refractory cardiopulmonary failure caused by severe pertussis.

Although the association between leukocyte counts and disease severity is well known, as well as strategies such as leukapheresis and exchange transfusion to reduce high leukocyte counts have been used clinically, there are still no standardized leukocyte cut-off values for initiating the treatment. A total of 18 articles (15 case reports, 3 case series studies) reported the use of leukoreduction therapy in severe pertussis with increased leukocytes, which ranged from 45–204.9 × 109/L. Only one study had proposed a specific quantified leukodepletion strategy, patients were given a suitable treatment respectively based on a leukocyte count greater than 50/70/100 × 109/L with or without cardiopulmonary dysfunction, which made a marked decrease in mortality [72]. Five articles (four case reports and one case series study) reported extracorporeal membrane oxygenation (ECMO). There is no optimal management method for pertussis infants treated with ECMO. Some researchers consider the early use of ECMO as the key to obtaining a good treatment effect and improving survival.

There are some limitations to our review. Due to the strict criteria, that is, the age of infants was younger than 1 year, studies that had a portion of the subjects meet the age criteria may have been missed. We minimized this shortcoming by including studies that had the majority of subjects meet the age criteria. Furthermore, 62.5% of the articles were case reports, which lacked a comprehensive description of the topic they covered. It was difficult to unify the variables in the data charts of the 64 articles, so we characterized case reports by developing the data chart separately.

In summary, the 64 articles included studies on epidemiology, pathology, clinical characteristics, risk factors, treatments, and burden of disease. Although these studies covered a variety of clinical concerns, most of them are descriptive, and targeted studies are still insufficient. Experimental studies are needed to provide high-quality evidence.

Funding Statement

Pediatric Clinical Research Center Foundation of Sichuan Province, China [No. 2017-46-4]. National Project for Clinical Key Specialty Development.

Authors contributions

GS and WCM conceptualized the review. ZY and GQ conducted the title/abstract and full-text screening. GS extracted and synthesized data with inputs from all authors. GS drafted the manuscript. ZY, GQ, and WCM revised for critical content. All authors contributed to the interpretation of findings and approved the version for submission.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Ethical approval

This study was a summary and analysis of the existing literature and ethical approval was not applicable.

Data availability statement

Data sharing is not applicable to this article as no new data were created or analyzed in this study.

References

  • 1.Pertussis vaccines: WHO position paper - September 2015. Wkly Epidemiol Rec. 2015;90:1–10. [PubMed] [Google Scholar]
  • 2.World Health Organization. Pertussis reported cases and incidence . [cited 30 June 2023]. https://immunizationdata.who.int/pages/incidence/PERTUSSIS.html.
  • 3.Kara EO, Campbell H, Ribeiro S, et al. Survey of household contacts of infants with laboratory-confirmed pertussis infection during a national pertussis outbreak in England and Wales. Pediatr Infect Dis J. 2017;36(2):140–145. doi: 10.1097/INF.0000000000001378. [DOI] [PubMed] [Google Scholar]
  • 4.Wiley KE, Zuo Y, Macartney KK, et al. Sources of pertussis infection in young infants: a review of key evidence informing targeting of the cocoon strategy. Vaccine. 2013;31(4):618–625. doi: 10.1016/j.vaccine.2012.11.052. [DOI] [PubMed] [Google Scholar]
  • 5.Klein NP, Bartlett J, Rowhani-Rahbar A, et al. Waning protection after fifth dose of acellular pertussis vaccine in children. N Engl J Med. 2012;367(11):1012–1019. doi: 10.1056/NEJMoa1200850. [DOI] [PubMed] [Google Scholar]
  • 6.Gustafsson L, Hessel L, Storsaeter J, et al. Long-term follow-up of Swedish children vaccinated with acellular pertussis vaccines at 3, 5, and 12 months of age indicates the need for a booster dose at 5 to 7 years of age. Pediatrics. 2006;118(3):978–984. doi: 10.1542/peds.2005-2746. [DOI] [PubMed] [Google Scholar]
  • 7.Schwartz KL, Kwong JC, Deeks SL, et al. Effectiveness of pertussis vaccination and duration of immunity. CMAJ. 2016;188(16):E399–E406. doi: 10.1503/cmaj.160193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Warfel JM, Zimmerman LI, Merkel TJ.. Acellular pertussis vaccines protect against disease but fail to prevent infection and transmission in a nonhuman primate model. Proc Natl Acad Sci U S A. 2014;111(2):787–792. doi: 10.1073/pnas.1314688110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Centers for Disease Control and Prevention (CDC) . Erythromycin-resistant Bordetella pertussis–Yuma County, Arizona, May-October 1994. MMWR Morb Mortal Wkly Rep. 1994;43(44):807–810. [PubMed] [Google Scholar]
  • 10.Guillot S, Descours G, Gillet Y, et al. Macrolide-resistant Bordetella pertussis infection in newborn girl, France. Emerg Infect Dis. 2012;18(6):966–968. doi: 10.3201/eid1806.120091. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Zhang Q, Li M, Wang L, et al. High-resolution melting analysis for the detection of two erythromycin-resistant Bordetella pertussis strains carried by healthy schoolchildren in China. Clin Microbiol Infect. 2013;19(6):E260–262. doi: 10.1111/1469-0691.12161. [DOI] [PubMed] [Google Scholar]
  • 12.Shahcheraghi F, Nakhost Lotfi M, Nikbin VS, et al. The first macrolide-resistant Bordetella pertussis strains isolated from Iranian patients. Jundishapur J Microbiol. 2014;7(6):e10880. doi: 10.5812/jjm.10880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Kamachi K, Duong HT, Dang AD, et al. Macrolide-resistant Bordetella pertussis, Vietnam, 2016-2017. Emerg Infect Dis. 2020;26(10):2511–2513. doi: 10.3201/eid2610.201035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Yeung KHT, Duclos P, Nelson EAS, et al. An update of the global burden of pertussis in children younger than 5 years: a modelling study. Lancet Infect Dis. 2017;17(9):974–980. doi: 10.1016/S1473-3099(17)30390-0. [DOI] [PubMed] [Google Scholar]
  • 15.Centers for Disease Control and Prevention . Pertussis (whooping cough). [cited 30 June 2023]. https://www.cdc.gov/pertussis/about/complications.html
  • 16.Arksey H, O’Malley L.. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8(1):19–32. doi: 10.1080/1364557032000119616. [DOI] [Google Scholar]
  • 17.Long S, Lowe RB.. Severe pertussis infection with hyperleukocytosis in a 10-month-old unvaccinated Amish female: a case report. Cureus. 2022;14(7):e26885. doi: 10.7759/cureus.26885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Liao Y, Li WR, Zhu Y, et al. Invasive Bordetella pertussis infection in infants: a case report. Open Forum Infect Dis. 2022;9(10):ofac478. doi: 10.1093/ofid/ofac478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Son PT, Reda A, Viet DC, et al. Exchange transfusion in the management of critical pertussis in young infants: a case series. Vox Sang. 2021;116(9):976–982. doi: 10.1111/vox.13085. [DOI] [PubMed] [Google Scholar]
  • 20.Kolind RS, Jensen AB, von Linstow ML.. Malignant pertussis in a three-week-old girl. Ugeskr Laeger. 2021;183:V09200691. [PubMed] [Google Scholar]
  • 21.Fueta PO, Eyituoyo HO, Igbinoba O, et al. Cardiopulmonary arrest and pulmonary hypertension in an infant with pertussis case report. Case Rep Infect Dis. 2021;2021:6686185. doi: 10.1155/2021/6686185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Rossetti E, Appierto L, Meschini A, et al. Early leukapheresis depletion in an ex-premature with severe acute respiratory distress syndrome due to Bordetella Pertussis and coronavirus infection. Blood Purif. 2020;49(6):758–760. doi: 10.1159/000507873. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Chen X, Jiang S.. Case report of infant severe pertussis with encephalopathy treated by leukapheresis. Chinese J Appl Clin Pediatr. 2020;35:1908–1910. [Google Scholar]
  • 24.Wei XM, Yang H, Lei M, et al. Blood exchange transfusion for treatment of severe pertussis in an infant. Zhongguo Dang Dai Er Ke Za Zhi. 2019;21:214–217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Alkan G, Keser EM.. Severe pertussis pneumonia in an infant: treated with exchange transfusion: case report. Turkiye Klinikleri J Pediatr. 2017;26(1):32–34. doi: 10.5336/pediatr.2016-52637. [DOI] [Google Scholar]
  • 26.Ganeshalingham A, Anderson BJ, Zuccollo J, et al. Porcelain lung: calcification in severe Bordetella pertussis infection. Arch Dis Child. 2016;101(5):421–421. doi: 10.1136/archdischild-2015-310204. [DOI] [PubMed] [Google Scholar]
  • 27.Liko J, Koenig WJ, Cieslak PR.. Suffer the infants: a severe case of pertussis in Oregon, 2012. Public Health Rep. 2015;130(5):435–439. doi: 10.1177/003335491513000505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Chantreuil J, Fakhri N, Labarthe F, et al. Malignant pertussis and exchange transfusion. Arch Pediatr. 2015;22(1):84–87. doi: 10.1016/j.arcped.2014.10.010. [DOI] [PubMed] [Google Scholar]
  • 29.Assy J, Séguéla PE, Guillet E, et al. Severe neonatal pertussis treated by leukodepletion and early extra corporeal membrane oxygenation. Pediatr Infect Dis J. 2015;34(9):1029–1030. doi: 10.1097/INF.0000000000000781. [DOI] [PubMed] [Google Scholar]
  • 30.Kurvers RA, Westra D, van Heijst AF, et al. Severe infantile Bordetella pertussis pneumonia in monozygotic twins with a congenital C3 deficiency. Eur J Pediatr. 2014;173(12):1591–1594. doi: 10.1007/s00431-013-2107-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Al Hanshi S, Al Ghafri M, Al Ismaili S.. Severe pertussis pneumonia managed with exchange transfusion. Oman Med J. 2014;29(3):e074. doi: 10.5001/omj.2014.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Nataprawira HM, Somasetia DH, Sudarwati S, et al. Critical pertussis in a young infant requiring mechanical ventilation. Case Rep Emerg Med. 2013;2013:125043. doi: 10.1155/2013/125043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Mata AF, Sarnaik AA.. Bronchoscopy with N-acetylcysteine lavage in severe respiratory failure from pertussis infection. Pediatrics. 2013;132(5):e1418–e1423. doi: 10.1542/peds.2013-0912. [DOI] [PubMed] [Google Scholar]
  • 34.Martinez M, Rochat I, Corbelli R, et al. Early blood exchange transfusion in malignant pertussis: a case report. Pediatr Crit Care Med. 2011;12(2):e107–e109. doi: 10.1097/PCC.0b013e3181f3a189. [DOI] [PubMed] [Google Scholar]
  • 35.Menif K, Bouziri A, Khaldi A, et al. Pertussis infection and fatal pulmonary hypertension. Arch Pediatr. 2010;17(11):1550–1552. doi: 10.1016/j.arcped.2010.08.016. [DOI] [PubMed] [Google Scholar]
  • 36.Kundrat SL, Wolek TL, Rowe-Telow M.. Malignant pertussis in the pediatric intensive care unit. Dimens Crit Care Nurs. 2010;29(1):1–5. doi: 10.1097/DCC.0b013e3181be489c. [DOI] [PubMed] [Google Scholar]
  • 37.Freitas J, de Sousa SG, Miguel C, et al. Pertussis keeps on killing. Rev Port Pneumol. 2010;16(2):315–320. doi: 10.1016/s0873-2159(15)30029-5. [DOI] [PubMed] [Google Scholar]
  • 38.Berthomieu L, Boumahni B, Jamal Bey K, et al. Malignant pertussis: 3 case reports. Arch Pediatr. 2010;17(2):144–148. doi: 10.1016/j.arcped.2009.10.020. [DOI] [PubMed] [Google Scholar]
  • 39.Couchot E, Paut O, Ghez O, et al. Extracorporeal membranous oxygenation in severe infant pertussis: a case report. Ann Fr Anesth Reanim. 2009;28(1):74–77. doi: 10.1016/j.annfar.2008.11.007. [DOI] [PubMed] [Google Scholar]
  • 40.Theilen U, Johnston ED, Robinson PA.. Rapidly fatal invasive pertussis in young infants–how can we change the outcome? BMJ. 2008;337(v27 2):a343–a343. doi: 10.1136/bmj.39575.715787.80. [DOI] [PubMed] [Google Scholar]
  • 41.Soares S, Rocha G, Pissarra S, et al. Pertussis with severe pulmonary hypertension in a newborn with good outcome - case report. Rev Port Pneumol. 2008;14(5):687–692. doi: 10.1016/S0873-2159(15)30277-4. [DOI] [PubMed] [Google Scholar]
  • 42.Vaessen S, Anthopoulou A, Bricteux G.. Fatal pertussis infection in a 2 month old infant. Rev Med Liege. 2006;61:145–148. [PubMed] [Google Scholar]
  • 43.Grzeszczak MJ, Churchwell KB, Edwards KM, et al. Leukopheresis therapy for severe infantile pertussis with myocardial and pulmonary failure. Pediatr Crit Care Med. 2006;7(6):580–582. doi: 10.1097/01.PCC.0000235253.19315.56. [DOI] [PubMed] [Google Scholar]
  • 44.Gonzalez-Escudero R, Llorente Otones L, Gonzalez-Tome MI, et al. D. Malignant pertussis in a 25-day-old newborn. Acta Pediatr Esp. 2006;64:297–299. [Google Scholar]
  • 45.Donoso AF, Cruces PI, Camacho JF, et al. Exchange transfusion to reverse severe pertussis-induced cardiogenic shock. Pediatr Infect Dis J. 2006;25(9):846–848. doi: 10.1097/01.inf.0000232630.70138.a2. [DOI] [PubMed] [Google Scholar]
  • 46.Donoso A, León J, Ramírez M, et al. Pertussis and fatal pulmonary hypertension: a discouraged entity. Scand J Infect Dis. 2005;37(2):145–148. doi: 10.1080/00365540510026436. [DOI] [PubMed] [Google Scholar]
  • 47.De Berry BB, Lynch JE, Chung DH, et al. Pertussis with severe pulmonary hypertension and leukocytosis treated with extracorporeal membrane oxygenation. Pediatr Surg Int. 2005;21(8):692–694. doi: 10.1007/s00383-005-1458-x. [DOI] [PubMed] [Google Scholar]
  • 48.Cruces RP, Gonzalez MM, Maldonado VB, et al. Severe pertussis with pulmonary hypertension: cardiorespiratory improvement after exchange transfusion. Rev Chil Pediatr. 2005;76:513–517. [Google Scholar]
  • 49.Wauters O, Brumioul D, Sacré JP, et al. Malignant whooping cough in an infant. Rev Med Liege. 2004;59:555–556. [PubMed] [Google Scholar]
  • 50.Romano MJ, Weber MD, Weisse ME, et al. Pertussis pneumonia, hypoxemia, hyperleukocytosis, and pulmonary hypertension: improvement in oxygenation after a double volume exchange transfusion. Pediatrics. 2004;114(2):e264–e266. doi: 10.1542/peds.114.2.e264. [DOI] [PubMed] [Google Scholar]
  • 51.McEniery JA, Delbridge RG, Reith DM.. Infant pertussis deaths and the management of cardiovascular compromise. J Paediatr Child Health. 2004;40(4):230–232. doi: 10.1111/j.1440-1754.2004.00344.x. [DOI] [PubMed] [Google Scholar]
  • 52.Pilorget H, Montbrun A, Attali T, et al. Malignant pertussis in the young infant. Arch Pediatr. 2003;10(9):787–790. doi: 10.1016/s0929-693x(03)00411-1. [DOI] [PubMed] [Google Scholar]
  • 53.Sreenan CD, Osiovich H.. Neonatal pertussis requiring extracorporeal membrane oxygenation. Pediatr Surg Int. 2001;17(2–3):201–203. doi: 10.1007/s003830000429. [DOI] [PubMed] [Google Scholar]
  • 54.Corkins M, Grose C, Halbur T.. Fatal pertussis in an Iowa infant. Iowa Med. 1991;81:383–384. [PubMed] [Google Scholar]
  • 55.Tam AY, Yeung CY.. Severe neonatal pertussis treated by salbutamol. Arch Dis Child. 1986;61(6):600–602. doi: 10.1136/adc.61.6.600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Theilade D. Nasal continuous positive airway pressure in the treatment of whooping cough. Anaesthesia. 1979;34(10):1028–1031. doi: 10.1111/j.1365-2044.1979.tb06253.x. [DOI] [PubMed] [Google Scholar]
  • 57.Zhang C, Zong Y, Wang Z, et al. Risk factors and prediction model of severe pertussis in infants < 12 months of age in Tianjin, China. BMC Infect Dis. 2022;22(1):24. doi: 10.1186/s12879-021-07001-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Thuy Nga DT, Thi Bich Thuy P, Ainai A, et al. Association between real-time polymerase chain reaction cycle threshold value and clinical severity in neonates and infants infected with Bordetella pertussis. Pediatr Infect Dis J. 2022;41(5):388–393. doi: 10.1097/INF.0000000000003471. [DOI] [PubMed] [Google Scholar]
  • 59.Coquaz-Garoudet M, Ploin D, Pouyau R, et al. Malignant pertussis in infants: factors associated with mortality in a multicenter cohort study. Ann Intensive Care. 2021;11(1):70. doi: 10.1186/s13613-021-00856-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Şık G, Demirbuğa A, Annayev A, et al. The clinical characteristics and prognosis of pertussis among unvaccinated infants in the pediatric intensive care unit. Turk Pediatri Ars. 2020;55(1):54–59. doi: 10.14744/TurkPediatriArs.2020.82435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Liu C, Yang L, Cheng Y, et al. Risk factors associated with death in infants <120 days old with severe pertussis: a case-control study. BMC Infect Dis. 2020;20(1):852. doi: 10.1186/s12879-020-05535-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Kavitha TK, Samprathi M, Jayashree M, et al. Clinical profile of critical pertussis in children at a pediatric intensive care unit in Northern India. Indian Pediatr. 2020;57(3):228–231. doi: 10.1007/s13312-020-1756-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Cherry JD, Wendorf K, Bregman B, et al. An observational study of severe pertussis in 100 infants ≤120 days of age. Pediatr Infect Dis J. 2018;37(3):202–205. doi: 10.1097/INF.0000000000001710. [DOI] [PubMed] [Google Scholar]
  • 64.Macdonald-Laurs E, Ganeshalingham A, Lillie J, et al. Increasing incidence of life-threatening pertussis: a retrospective cohort study in New Zealand. Pediatr Infect Dis J. 2017;36(3):282–289. doi: 10.1097/INF.0000000000001441. [DOI] [PubMed] [Google Scholar]
  • 65.Straney L, Schibler A, Ganeshalingham A, et al. Burden and outcomes of severe pertussis infection in critically ill infants. Pediatr Crit Care Med. 2016;17(8):735–742. doi: 10.1097/PCC.0000000000000851. [DOI] [PubMed] [Google Scholar]
  • 66.Winter K, Zipprich J, Harriman K, et al. Risk factors associated with infant deaths from pertussis: a case-Control study. Clin Infect Dis. 2015;61(7):1099–1106. doi: 10.1093/cid/civ472. [DOI] [PubMed] [Google Scholar]
  • 67.Tiwari TS, Baughman AL, Clark TA.. First pertussis vaccine dose and prevention of infant mortality. Pediatrics. 2015;135(6):990–999. doi: 10.1542/peds.2014-2291. [DOI] [PubMed] [Google Scholar]
  • 68.Rocha G, Flôr-de-Lima F, Soares P, et al. Severe pertussis in newborns and young vulnerable infants. Pediatr Infect Dis J. 2013;32(10):1152–1154. doi: 10.1097/INF.0b013e31829f0b1a. [DOI] [PubMed] [Google Scholar]
  • 69.Nieves D, Bradley JS, Gargas J, et al. Exchange blood transfusion in the management of severe pertussis in young infants. Pediatr Infect Dis J. 2013;32(6):698–699. doi: 10.1097/INF.0b013e31828c3bb3. [DOI] [PubMed] [Google Scholar]
  • 70.Murray EL, Nieves D, Bradley JS, et al. Characteristics of severe Bordetella pertussis infection among infants ≤90 days of age admitted to pediatric intensive care Units - Southern California, September 2009-June 2011. J Pediatric Infect Dis Soc. 2013;2(1):1–6. doi: 10.1093/jpids/pis105. [DOI] [PubMed] [Google Scholar]
  • 71.Taffarel P, Bonetto G, Haimovich A.. Severe pertussis, progression and exchange transfusion as an alternative treatment. Arch Argent Pediatr. 2012;110(4):327–330. doi: 10.5546/aap.2012.327. [DOI] [PubMed] [Google Scholar]
  • 72.Rowlands HE, Goldman AP, Harrington K, et al. Impact of rapid leukodepletion on the outcome of severe clinical pertussis in young infants. Pediatrics. 2010;126(4):e816–e827. doi: 10.1542/peds.2009-2860. [DOI] [PubMed] [Google Scholar]
  • 73.Bouziri A, Hamdi A, Khaldi A, et al. Malignant pertussis: an underdiagnosed illness. Med Trop (Mars). 2010;70:245–248. [PubMed] [Google Scholar]
  • 74.Sawal M, Cohen M, Irazuzta JE, et al. Fulminant pertussis: a multi-center study with new insights into the clinico-pathological mechanisms. Pediatr Pulmonol. 2009;44(10):970–980. doi: 10.1002/ppul.21082. [DOI] [PubMed] [Google Scholar]
  • 75.Paddock CD, Sanden GN, Cherry JD, et al. Pathology and pathogenesis of fatal Bordetella pertussis infection in infants. Clin Infect Dis. 2008;47(3):328–338. doi: 10.1086/589753. [DOI] [PubMed] [Google Scholar]
  • 76.Vitek CR, Pascual FB, Baughman AL, et al. Increase in deaths from pertussis among young infants in the United States in the 1990s. Pediatr Infect Dis J. 2003;22(7):628–634. doi: 10.1097/01.inf.0000073266.30728.0e. [DOI] [PubMed] [Google Scholar]
  • 77.Pooboni S, Roberts N, Westrope C, et al. Extracorporeal life support in pertussis. Pediatr Pulmonol. 2003;36(4):310–315. doi: 10.1002/ppul.10351. [DOI] [PubMed] [Google Scholar]
  • 78.Mikelova LK, Halperin SA, Scheifele D, et al. Predictors of death in infants hospitalized with pertussis: a case-control study of 16 pertussis deaths in Canada. J Pediatr. 2003;143(5):576–581. doi: 10.1067/S0022-3476(03)00365-2. [DOI] [PubMed] [Google Scholar]
  • 79.Pierce C, Klein N, Peters M.. Is leukocytosis a predictor of mortality in severe pertussis infection? Intensive Care Med. 2000;26(10):1512–1514. doi: 10.1007/s001340000587. [DOI] [PubMed] [Google Scholar]
  • 80.Hackman R, Perrin DG, Karmali M, et al. Fatal Bordetella pertussis infection: report of two cases with novel pathologic findings. Pediatr Pathol Lab Med. 1996;16(4):643–653. doi: 10.1080/15513819609168700. [DOI] [PubMed] [Google Scholar]
  • 81.Rudolph AM. High pulmonary vascular resistance after birth: I. Pathophysiologic considerations and etiologic classification. Clin Pediatr (Phila). 1980;19(9):585–590. doi: 10.1177/000992288001900902. [DOI] [PubMed] [Google Scholar]

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