key: cord-0040635-ahknexy0 authors: Pappas, Diane E. title: The Common Cold date: 2017-07-18 journal: Principles and Practice of Pediatric Infectious Diseases DOI: 10.1016/b978-0-323-40181-4.00026-8 sha: f2d38da952953f1321f5effb9bd87fb0dab679d9 doc_id: 40635 cord_uid: ahknexy0 nan In temperate climates in the northern hemisphere, the predictable yearly epidemic of colds begins in September and continues unabated until spring. This sustained epidemic curve is a result of successive waves of different respiratory viruses moving through the community ( Fig. 26.1 ). The epidemic begins with a sharp rise in the frequency of rhinovirus infections in September (after children return to school), which is followed by PIVs in October and November. RSV and HCoVs circulate during the winter months, and infection due to influenza virus peaks in the late winter. The epidemic ends with a small resurgence of rhinovirus infections in the spring. Adenovirus infection occurs at a constant rate throughout the cold season. The frequency of colds varies with age. A 10-year study in the 1970s of families with children who did not attend a childcare facility showed that the peak incidence of colds occurs in preschool children 1 to 5 years old, with a frequency of 7.4 to 8.3 colds per year. 5 In a 52-week longitudinal study of 108 individuals in 26 households in Utah, which included diaries of illness and testing of weekly self-collected or family-collected anterior nares specimens by FilmArray, an automated polymerase chain reaction (PCR) system for virus detection, respiratory symptoms were identified for 38% of person-weeks for children younger than 5 years and 20% for older children and adults. Sixty percent of respiratory illnesses were associated with virus detection, but only approximately 50% of virus detections were associated with symptoms (especially rhinovirus and bocavirus). 6 Viral transmission occurs primarily in the home setting, although the exact mechanism of spread has not been established. Colds can be spread by a small-particle (<5 µm in diameter) aerosol, which infects when 21 A yellow or white nasal discharge may result from the higher number of PMNs, whereas the enzymatic activity of PMNs (due to myeloperoxidase and other enzymes) may cause a green nasal discharge. A potent chemoattractant for PMNs is produced by cells in culture infected with rhinovirus. 22 The chemoattractant has been identified as interleukin-8 (IL-8). 23 Elevated levels of IL-8 and other cytokines (e.g., IL-1β, IL-6) also have been demonstrated in the nasal secretions of infected individuals. 24, 25 Elevated levels of albumin and kinins (predominantly bradykinin) in nasal secretions coincide with the onset of symptoms in experimental rhinovirus infection. 20 The elevated concentration of albumin and kinins likely results from exudation of plasma proteins due to greater vascular permeability in the nasal submucosa. The method by which viral infection initiates this vascular leak has not been determined. The release of kinins resulting from plasma exudation may augment the symptoms of the cold. Bradykinin alone can cause rhinitis and sore throat when sprayed into the noses of uninfected individuals. 26 The paranasal sinuses usually are involved during an uncomplicated cold. In one study, CT scans obtained during the acute phase of illness revealed abnormalities of one or more sinuses in 27 (87%) of 31 young adults. 27 Without antibiotic therapy, there was complete resolution or marked improvement of the sinus abnormalities in 11 (79%) of the 14 subjects for whom second CT scans were obtained 2 weeks later. In another study, MRI revealed that 60% of children with URIs had major abnormalities in their paranasal sinuses, which tended to resolve without antibiotic therapy. 28 It is not known whether sinus abnormalities result from viral infection of the sinus mucosa or from impaired sinus drainage due to viral rhinitis. Nose blowing can generate enough pressure to force fluid from the nasopharynx into the paranasal sinuses, suggesting that nose blowing may force mucus containing viruses, bacteria, and inflammatory mediators into the paranasal sinuses during a cold. 29 The middle ear can be involved during uncomplicated colds. Studies have shown that two thirds of school-aged children develop abnormal middle ear pressures within 2 weeks after the onset of a cold. 30 Otitis media was not diagnosed during the study because ears were not examined, and none of the children sought medical care. It is not known whether the abnormal middle ear pressures result from viral infection of the mucosa of the middle ear and eustachian tube or from viral nasopharyngitis with secondary eustachian tube dysfunction. Symptoms of the common cold do not vary by specific causative virus. In older children and adults, rhinorrhea, nasal obstruction, and sore or scratchy throat are typical. The rhinorrhea is initially clear but may become colored as the illness proceeds, and patients can cough or sneeze. Fever (>38°C) is uncommon in adults. Other symptoms are malaise, sinus fullness, and hoarseness. Objective findings are minimal except for mild erythema of the nasal mucosa or pharynx. Symptoms resolve in 5 to 7 days. Compared with adults, infants and preschool children with colds are more likely to have fever (>38°C) and moderate enlargement of the anterior cervical lymph nodes (Table 26. 2). 1 Rhinorrhea may not be noticed until the nasal discharge becomes colored. Nasal congestion can disrupt sleep and lead to fatigue and irritability. The illness often persists in infants and preschool children for 10 to 14 days. 31 inhaled; by large-particle (>10 µm in diameter) droplets, which infect by landing on nasal or conjunctival mucosa; or by direct transfer through hand-to-hand contact. 7 A small-particle aerosol is an effective method of transfer for influenza virus 8 and coronavirus 9 but not for RSV. 10 Rhinoviruses are most likely spread by large-particle droplets or direct transfer. Rhinoviruses can survive as long as 2 hours on human hands and up to several days on other surfaces. Studies have shown that infected young adults commonly have rhinovirus on their hands, which can be efficiently transferred to the hands of uninfected individuals during brief contact. Infection results when the uninfected person transfers the virus from the hands on to his or her nasal or conjunctival mucosa. Sneezing and coughing are ineffective modes of rhinovirus transmission, 11 although there is some evidence that the virus also can be transmitted by aerosols generated by coughing, talking, and breathing. 12 Inoculation of the oral mucosa with rhinovirus 13 or RSV 14 does not result in infection. Symptoms of the common cold do not appear to result from destruction of nasal mucosa because nasal biopsy specimens from young adults with natural and experimentally induced colds show intact nasal epithelium during symptomatic illness. 15, 16 Study by in situ hybridization of nasal biopsy specimens obtained during rhinovirus infection indicates that replication occurs in only a small number of epithelial cells. 17, 18 In vitro studies have shown that rhinovirus and coronavirus produce no detectable cytopathic effect when replicating in a cultured monolayer of nasal epithelial cells, whereas influenza virus A and adenovirus produce obvious damage. 19 The symptoms of the common cold appear to result from release of cytokines and other mediators from infected nasal epithelial cells and from an influx of polymorphonuclear cells (PMNs). Nasal washings of volunteers experimentally infected with rhinovirus showed a 100-fold increase in PMN concentration 1 to 2 days after inoculation. 20 The influx of PMNs coincides with the onset of symptoms and correlates with a Antibiotics have no role in the treatment of uncomplicated URIs in children. Antibiotic therapy does not hasten resolution of the viral infection or reduce the likelihood of occurrence of secondary bacterial infection. 42 Antibiotics are indicated only in cases of secondary bacterial infection, such as sinusitis and acute otitis media. Supportive measures remain the mainstay of treatment for the common cold in children. Bulb suction with saline drops (i.e., ≈1 teaspoon of salt in 2 cups of water) may help relieve nasal congestion and remove secretions. One study suggests that honey given at bedtime may help reduce cough in children with URIs, although honey is not recommended for children younger than 12 months because of the risk of exposure to Clostridium botulinum spores. 43 Vapor rub applied to the chest and neck of children between the ages of 2 and 11 years may help reduce nighttime cough. 44 The common cold usually resolves in about 10 to 14 days in infants and children. New-onset fever and earache during this period may herald the development of bacterial otitis media, which occurs in about 5% of colds in preschool children. Persistence of nasal symptoms for longer than 10 days was thought to signify the development of a secondary bacterial sinusitis, but a study found that 20 children hospitalized for preseptal or orbital cellulitis, indicative of bacterial sinusitis, had symptoms of acute respiratory tract infection for 7 or fewer days before hospitalization, suggesting that the complications of rhinosinusitis can occur during the first few days of a cold. 45 Bacterial pneumonia is an uncommon secondary infection. For children with underlying reactive airways disease, wheezing is common during the course of a viral URI; at least 50% of asthma exacerbations in children are associated with viral infection. Children who experience more than one lower respiratory tract infection (e.g., croup, bronchiolitis) during their first year of life have an increased risk of asthma thereafter. 46 Other complications are epistaxis, eustachian tube dysfunction, conjunctivitis, and pharyngitis. Symptoms of the common cold appear to result from the effects of inflammatory mediators released in response to the viral infection of the respiratory tract. As the determinants of this process are further elucidated, treatments may be developed that can interrupt or ameliorate release of inflammatory mediators and prevent or reduce the symptoms of the common cold. Vaccines are unlikely to be useful for prevention because of the large number of serotypes of some cold viruses and the lack of lasting immunity to others. The use of alcohol-based hand gels has been suggested as a means of reducing secondary transmission of respiratory illnesses in the home, 47 but this approach was not shown to be effective in one field trial. 48 Virucidal tissues have been effective in preventing viral passage and transmission and may reduce secondary transmission by about 30%. 49, 50 Until new methods are developed, prevention of the common cold is limited to avoiding selfinoculation (i.e., transfer of virus from contaminated fingers to nasal or conjunctival mucosa) by removing virus through handwashing or by killing virus with application of a virucide to the hands. The differential diagnoses of a cold include allergic rhinitis, vasomotor rhinitis, intranasal foreign body, and sinusitis. A diagnosis of allergic rhinitis is suggested by a seasonal pattern of clear rhinorrhea, absence of associated fever, and family history of allergy. Possible associated conditions are asthma and eczema. Physical findings consistent with allergic rhinitis include allergic shiners (i.e., dark circles under the eyes) and nasal salute (i.e., wiping or rubbing the nose with a transverse or upward movement of the hand). Detection of numerous eosinophils on microscopic examination of the nasal mucus using Hansel stain confirms the diagnosis of allergic rhinitis. A diagnosis of vasomotor rhinitis is suggested by a chronic course without fever or sore throat. The diagnosis of bacterial sinusitis is suggested by persistent rhinorrhea or cough, or both, for more than 10 days. 32 The diagnosis of a cold is based on history and physical examination; typically, laboratory tests are not useful. The rapid test for detecting RSV, influenza, parainfluenza, and adenovirus antigens in nasal secretions can be used to confirm the diagnosis. RSV, rhinovirus, influenza viruses, parainfluenza viruses, and adenoviruses also can be isolated in cell culture. Because HCoVs cannot be detected reliably in cell culture, a serologic titer elevation can be used for diagnosis if necessary. PCR assays for detection of all the respiratory viruses are available increasingly in clinical laboratories, but there is a lack of standardization and validation for many of the tests offered. Meaningful interpretation of PCR results remains challenging because PCR detection of virus can occur in several clinical scenarios, including coinfection with multiple viruses, viral detection during the incubation period, subclinical infection, infection with the identified virus, variable duration of viral shedding, and sequential infection with different serotypes of the same species. 33 Other methods of detection can be used but are rarely needed. No antiviral agents are available that are effective for treatment of the common cold. Although an array of medications may be used to relieve symptoms, there is little scientific evidence to support the use of symptomatic treatments in children. Because the common cold is a self-limited illness with symptomatology that is largely subjective, a substantial placebo effect can suggest that various treatments have some efficacy. Inadequate blinding of placebo recipients in a study can make an ineffective treatment appear effective. In adults with colds, first-generation antihistamines (e.g., chlorpheniramine) have been shown to provide modest symptomatic relief, with decreases in nasal discharge, sneezing, nose blowing, and duration of symptoms, 34 presumably because of the anticholinergic effects of these medications. A randomized, double-blind, placebo-controlled study of preschool children with URIs showed that treatment with an antihistamine-decongestant combination (i.e., brompheniramine maleate and phenylpropanolamine hydrochloride) produced no improvement in cough, rhinorrhea, or nasal congestion, although a larger proportion of the treated children (47% vs. 26%) were asleep 2 hours after treatment. 35 Numerous decongestants, antitussives, and expectorants are available over the counter, but there is no evidence to support their use in children. A study of phenylephrine, a topical decongestant, for the treatment children 6 to 18 months old showed no decrease in nasal obstruction with its use during a URI. 36 In a study comparing placebo, dextromethorphan, and codeine for cough suppression in children 18 months to 12 years old, cough decreased in all patients within 3 days, but there was no difference in cough reduction among the three treatment groups. 37 Guaifenesin, an expectorant, has not been shown to change the volume or quality of sputum or the frequency of cough in young adults with colds. 38 Echinacea preparations, often thought to be effective in the treatment of the common cold, have no effect on the prevention or treatment of rhinovirus infection. 39 Similarly, intranasal zinc gluconate has had no effect for the treatment of colds 40 or prevention of experimental rhinovirus colds. 41 In January, 2008, the US Food and Drug Administration issued an advisory strongly recommending that over-the-counter cold and cough medications not be given to infants because of the risk of life-threatening side effects. Epidemiology, pathogenesis, and treatment of the common cold Community surveillance of respiratory virus among families in the Utah Better Identification of Germs-Longitudinal Viral Epidemiology (BIG-LoVE) study Mechanisms of transmission of rhinovirus infections Transmission of rhinovirus colds by selfinoculation Histopathologic examination and enumeration of polymorphonuclear leukocytes in the nasal mucosa during experimental rhinovirus colds Paranasal sinus findings in children during respiratory infections evaluated with magnetic resonance imaging Viral and bacterial interactions in the upper respiratory tract Epidemiology, pathogenesis, and treatment of the common cold Human bocavirus infections in hospitalized children and adults Viral etiology of common cold in children Newly identified respiratory viruses in children with asthma exacerbation not requiring admission to hospital Illness in the Home Community surveillance of respiratory virus among families in the Utah Better Identification of Germs-Longitudinal Viral Epidemiology (BIG-LoVE) study Mechanisms of transmission of rhinovirus infections An outbreak of influenza aboard a commercial airliner Mechanism of transmission of coronavirus 229E in human volunteers Modes of transmission of respiratory syncytial virus Hand-to-hand transmission of rhinovirus colds Exhalation of respiratory viruses by breathing, coughing, talking Transmission of rhinovirus colds by self-inoculation Infectivity of respiratory syncytial virus by various routes of inoculation Light and scanning electron microscopy of nasal biopsy material from patients with naturally acquired common colds Histopathologic examination and enumeration of polymorphonuclear leukocytes in the nasal mucosa during experimental rhinovirus colds Detection of rhinovirus infection of the nasal mucosa by oligonucleotide in situ hybridization Localization of human rhinovirus replication in the upper respiratory tract by in situ hybridization Respiratory virus infection of monolayer cultures of human nasal epithelial cells Kinins are generated during experimental rhinovirus colds Study of bacteria in the nasal cavity and nasopharynx during naturally acquired common colds Rhinovirus infection of human embryonic lung fibroblasts induces the production of a chemoattractant for polymorphonuclear leukocytes Elaboration of interleukin 8 (IL-8) from fibroblast (MRC-5) cells and human nasal epithelium in response to rhinovirus (RV) challenge [abstract B43 Respiratory syncytial virus-induced cytokine production by a human bronchial epithelial cell line Nasal cytokine production in viral acute upper respiratory infection of childhood Nasal provocation with bradykinin induces symptoms of rhinitis and a sore throat Computed tomographic study of the common cold Paranasal sinus findings in children during respiratory infections evaluated with magnetic resonance imaging Nose blowing propels nasal fluid into the paranasal sinuses Viral respiratory infection in schoolchildren: effects on middle ear pressure Clinical course of acute infection of the upper respiratory tract in children: a cohort study Sinusitis in children Viral and bacterial interactions in the upper respiratory tract Effectiveness of antihistamines in the symptomatic management of the common cold Is an antihistamine-decongestant combination effective in temporarily relieving symptoms of the common cold in preschool children? Effect of topical adrenergic decongestants on middle ear pressure in infants with common colds Efficacy of cough suppressants in children Antitussive effect of guaifenesin in young adults with natural colds: objective and subjective assessment An evaluation of Echinacea angustifolia in experimental rhinovirus infections Treatment of naturally acquired common colds with zinc: a structured review Ineffectiveness of intranasal zinc gluconate for prevention of experimental rhinovirus colds Upper respiratory tract infection Effect of honey, dextromethorphan, and no treatment on nocturnal cough and sleep quality for coughing children and their parents Vapor rub, petrolatum, and no treatment for children with nocturnal cough and cold symptoms Timing of rhinosinusitis complications in children Early respiratory infections, asthma, and allergy: 10-year follow-up of the Oslo birth cohort Illness transmission in the home: a possible role for alcohol-based hand gels A randomized, controlled trial of a multifaceted intervention including alcohol-based hand sanitizer and hand-hygiene education to reduce illness transmission in the home Two randomized, controlled trials of virucidal nasal tissues in the prevention of natural upper respiratory infections Efficacy of virucidal nasal tissues in interrupting familial transmission of respiratory agents The author wishes to highlight the dominant contribution of J. Owen Hendley to our understanding of respiratory viruses and to this chapter. The pediatric infectious diseases community recognizes our great loss with his death.All references are available online at www.expertconsult.com.