- Open Access
Cough quality in children: a comparison of subjective vs. bronchoscopic findings
Respiratory Research volume 6, Article number: 3 (2005)
Cough is the most common symptom presenting to doctors. The quality of cough (productive or wet vs dry) is used clinically as well as in epidemiology and clinical research. There is however no data on the validity of cough quality descriptors. The study aims were to compare (1) cough quality (wet/dry and brassy/non-brassy) to bronchoscopic findings of secretions and tracheomalacia respectively and, (2) parent's vs clinician's evaluation of the cough quality (wet/dry).
Cough quality of children (without a known underlying respiratory disease) undergoing elective bronchoscopy was independently evaluated by clinicians and parents. A 'blinded' clinician scored the secretions seen at bronchoscopy on pre-determined criteria and graded (1 to 6). Kappa (K) statistics was used for agreement, and inter-rater and intra-rater agreement examined on digitally recorded cough. A receiver operating characteristic (ROC) curve was used to determine if cough quality related to amount of airway secretions present at bronchoscopy.
Median age of the 106 children (62 boys, 44 girls) enrolled was 2.6 years (IQR 5.7). Parent's assessment of cough quality (wet/dry) agreed with clinicians' (K = 0.75, 95%CI 0.58–0.93). When compared to bronchoscopy (bronchoscopic secretion grade 4), clinicians' cough assessment had the highest sensitivity (0.75) and specificity (0.79) and were marginally better than parent(s). The area under the ROC curve was 0.85 (95%CI 0.77–0.92). Intra-observer (K = 1.0) and inter-clinician agreement for wet/dry cough (K = 0.88, 95%CI 0.82–0.94) was very good. Weighted K for inter-rater agreement for bronchoscopic secretion grades was 0.95 (95%CI 0.87–1). Sensitivity and specificity for brassy cough (for tracheomalacia) were 0.57 and 0.81 respectively. K for both intra and inter-observer clinician agreement for brassy cough was 0.79 (95%CI 0.73–0.86).
Dry and wet cough in children, as determined by clinicians and parents has good clinical validity. Clinicians should however be cognisant that children with dry cough may have minimal to mild airway secretions. Brassy cough determined by respiratory physicians is highly specific for tracheomalacia.
Cough is the most common symptom presenting to medical practitioners in Australia, the UK and USA [1–3]. Cough quality, specifically dry versus we t or productive cough, is often used in epidemiological [5–7] and clinical research [8, 9]. Clinically, physicians also often differentiate between dry and wet cough [10–12] but there are no studies that have evaluated if these are reproducible descriptors. In adults, productive cough is usually obvious but children however often swallow their sputum and hence a 'wet cough' is used inter-changeably with 'productive cough' to describe cough quality in young children who are unable to expectorate [10, 13]. It is known that nocturnal cough is unreliably reported in both children  and adults  but there is no data on cough quality. Wet and dry cough are determined subjectively as there are no 'gold standards'. To date there are no human studies that have identified the objective relationship of the cough descriptors to mucus secretory states.
The sound of a cough is due to vibration of larger airways and laryngeal structures during turbulent flow in expiration [16, 17]. It is not known which generation of the airways is involved when the human ear identifies a wet cough and currently there are no validated human models that allow measurement of increased airway mucus. Mucus hypersecretory states in human diseases can occur from a variety of mechanisms which include; hypersecretion of stored mucin, hypertrophy or hyperplasia of goblet cells and/or increased synthesis from over-expression of mucin genes . In disease states, it is not known which mechanism or site of production is the most important but in smokers with chronic bronchitis, a common cause of productive cough in adults, the larger bronchi (bronchi of diameter >4 mm ie segmental bronchi and above)  are the site of greatest inflammation . Flexible bronchoscopy allows an in-vivo visual assessment of larger airways usually to the 3rd (lobar bronchi) or 4th generation (segmental bronchi) in young children.
The study aims were to compare (1) cough quality (wet vs dry and brassy vs non-brassy) with bronchoscopic findings of secretions and tracheomalacia respectively and, (2) parent(s) vs clinician's evaluation of the cough quality (wet and dry). We hypothesised that clinical assessment of cough is good compared to bronchoscopic findings and that a wet cough is related to presence of airway secretions.
Children electively admitted for bronchoscopy without a known underlying respiratory diagnosis were seen by a member of the research team 0.5–3 hours prior to bronchoscopy. The clinician's assessment of cough quality (wet or dry) was recorded on a standardised sheet (based on the cough present on the day of the bronchoscopy), before the parent(s) independently evaluated the current (the morning of, or last 12 hours) cough quality (wet or dry) of their child. For clinician's assessment of wet/dry cough, when no spontaneous cough was heard or if child was too young to elicit a cough, cough quality (wet or dry) was deemed 'non-assessable'. Clinicians also rated cough as 'brassy' or 'non-brassy' based on coughs heard anytime before bronchoscopy. For assessment of reliability of cough quality (wet/dry and brassy/non-brassy), 21 cooperative children had their coughs digitally recorded (Acer Pocket PC n11, Taiwan) using music compact disc quality format (44.1 kHz, 16 bit) on the morning of their bronchoscopy. These stored cough sounds were later replayed (using headphones 30–10,000 Hz, Lanier, Japan) from a computer and re-scored in a blinded manner (blinded to the child's name and cough quality assigned earlier) for wet/dry and brassy/non-brassy qualities. Written consent was obtained from a parent and the study approved by the hospital's ethics committee on human research.
Bronchoscopy and quantification of secretions seen during bronchoscopy
Flexible bronchoscopy was performed under general anaesthesia as previously described [20–22]. Briefly, anaesthesia was induced with sevoflurane in 100% oxygen administered through a Jackson Rees T piece circuit, the vocal cords and upper trachea then sprayed (4 mg/kg lignocaine via a Cass needle). Atropine was given intravenously to most children aged <12 months. In all children a video flexible bronchoscope (BF 3C160, Olympus, Tokyo, Japan) entered the circuit via the port of a swivel right angle connector attached to a facemask. Images were projected onto a monitor (Sony Trinitron, Tokyo, Japan).
A respiratory consultant (ABC or IBM) blinded to the child's history and cough quality scored the bronchoscopy sheet quantifying the amount of secretions at the time of the bronchoscopy in real time. When no scorer was available, the session was videotaped and played back. A secretion quantification card (figure 1) was visible to the scorer at all times. Secretions were quantified according to amount of mucus in the airways in relation to lumen size (fig 1) and scored from the trachea to the level of lobar bronchi (total of 9; trachea, right main stem, right upper lobe, right middle lobe, right lower lobe, left main stem, left upper lobe, left lingula, left lower lobe). When segmental bronchi were seen, the worst segment (ie segment with most secretions) was scored. These scores were used to obtain a final grade of bronchoscopic secretions (BS) from grades 1 to 6;
BS Grade 1 = Nil secretions
BS Grade 2 = Near dry = Bubbles only in < half total number of bronchi involved
BS Grade 3 = Minimal = Bubbles found in > half total number of bronchi involved or Secretion type-I in < half total number of bronchi involved
BS Grade 4 = Mild = Secretion type-I, > half total number of bronchi involved or Secretion type-II, < half total number of bronchi involved
BS Grade 5 = Mod = Secretion type-II, > half total number of bronchi involved or Secretion type-III, < half total number of bronchi involved
BS Grade 6 = Large = Secretion type-III, > half total number of bronchi involved Inter-rater reliability of BS grading was assessed by replaying the videotapes of the recorded bronchoscopy of 20 children, with the 2nd assessor blinded to the child's condition.
BAL was obtained from the macroscopically most abnormal lobe; when changes were generalised, BAL was obtained from the right middle lobe. Cell count was performed on the cell suspension, cytocentrifuge slides were prepared and stained (modified Wright's stain) for cell differential profile. All cellular examinations were performed by cytologists blinded to the children's medical history.
Data were not normally distributed and thus non parametric analyses were used; medians and inter-quartile range (IQR) were used for all descriptive data and Kruskal Wallis for comparisons between groups. Cohen's kappa (K) with 95%CI was utilised for inter and intra-observer reliability and graded from 'poor' (K<0.2) to 'very good' (K = 0.81–1.0). For calculation of sensitivity and specificity, negative and positive predictive values (NPV, PPV); cough quality was assigned to dry when a history of cough was absent and bronchoscopy findings at two cut offs (grades 3 and 4) of BS grades were taken as the 'gold standard' eg for cut-off at BS grade 3, BS grades 1–2 were defined as no secretions and BS grades = 3 defined as secretions present. To determine if cough quality (wet/dry) was predictive of amount of secretions found during bronchoscopy, a receiver operating characteristic (ROC) curve was generated  where cough quality wet/dry was considered the true positive/negative and the bronchoscopic secretion scoring (1 to 6) as the ordinal rating scale. Two tailed p value of < 0.05 was considered significant. SPSS ver 11.1 was utilised for most statistical calculation.
Median age of the 106 children (62 boys, 44 girls) enrolled was 2.6 years (IQR 5.7). Indications for bronchoscopy were chronic cough (n = 44, 41.5%), wheeze (n = 21, 19.8%), stridor (n = 16, 15.4%), investigation of persistent radiological changes (n = 14, 13.5%), recurrent pneumonia (n = 6, 5.8%), suspicion of aspiration lung disease (n = 3, 2.9%), BAL and suspected foreign body (n = 1 each, 2%). In four children, BS grades were not obtained (session was inadvertently not recorded and 'blinded' clinician not present at bronchoscopy). Scores of BS were done in real time in all but 9 children.
In 30 children, cough was non-assessable. Agreement between clinicians and parents assessment of cough quality (wet/dry) was good (K = 0.75, 95%CI 0.58, 0.93). For cough quality of 'wet/dry', cough assessed by clinicians had the highest specificity, sensitivity, NPV, PPV and positive likelihood ratio for both BS cut-offs (tables 1 and 2). Parent(s) assessment were less precise but only marginally so. The area under the fitted ROC curve (figure 2) was 0.85 95%CI 0.77, 0.92. The specificity, NPV and likelihood ratio for brassy cough assessed against gold standard bronchoscopic finding of tracheomalacia was good (table 1) but less than that for cough quality of wet/dry.
There was little difference in sensitivity and specificity between children grouped by indication for bronchoscopy (cough or other indications). Values were marginally better in older children (tables 4 and 5 in supplementary data additional file 2). Area under the fitted ROC curve was similar for both age groups (aged ≤ 2 years = 0.811, 95%CI 0.79, 0.84; age >2 = 0.84, 95%CI 0.74, 0.95). Agreement for clinicians vs parents cough quality (dry/wet) was better in children aged ≤ 2 years (K = 0.85, 95%CI 0.57, 1.0; n = 42 but 18 non-assessable) than that for those age >2 years (K = 0.70, 95%CI 0.49, 0.92; n = 64, but 12 non-assessable) (see additional file 1).
Using recorded coughs, kappa scores were 'very good' for both intra-observer and inter-clinician agreement for wet and dry cough (K = 1.0 and 0.88 [95%CI 0.82–0.94] respectively). There was only one disagreement in wet and dry cough between clinicians and in this child the cough was mildly wet (BS grade of 3). Kappa scores for intra-observer and inter-observer clinician agreement for brassy cough was good, K in both was 0.79, 95%CI 0.73, 0.86. Inter-rater agreement for BS grades was 'very good' (weighted K = 0.95, 95%CI 0.87–1).
Cellularity for total cell count, percentages of neutrophils and macrophages were significantly different between children grouped by BS grade cut-offs of 3 and 4 as well as wet/dry cough (table 3).
We have shown that clinical assessment of cough quality of wet/dry cough generally relates to bronchoscopic secretions determined using a standardised scoring system (BS grades). When cough is wet, secretions were always present; when cough was dry secretions if present, were usually minimal or mild. Clinicians were marginally better than parents at assessing wet/dry cough and agreement between the 2 groups was good. When clinicians detected presence of a brassy cough, tracheomalacia was usually present. Inter-rater clinician agreement for cough qualities of dry/wet and brassy/non brassy was good.
Accuracy and reliability of symptoms are important in clinical and research settings. Cane and colleagues [25, 26]. found that parental reports of wheeze and stridor are often not accurately reported in a clinic setting. There is no data on the validity of cough quality in spite its use in management and diagnostic guidelines [11, 27, 28] and cough being the most common symptom seen by general practitioners [1–3]. The level of agreement recommended for symptoms and signs to be used in clinical prediction rules is kappa value of ≥ 0.6 . The kappa values we obtained in this study well exceeded 0.6. Specifically, intra and inter-clinician evaluation was very good and parental reporting of cough quality (wet/dry) also related well to clinicians' evaluation.
When compared to bronchoscopic findings, this study showed that a wet cough is always associated with BS grades of 3 or more. Dry cough is less valid; the presence of dry cough does not necessary indicate absence of secretions. However BS grades are less in dry cough as shown in the ROC curve. The generation of cough sounds and some factors that influence cough sounds have been examined in the laboratory [16, 30]. Using cough sound analysis (spectrogram and time-expanded waveform), productive and non-productive cough can be differentiated in the laboratory . However to date there is no data on its clinical reliability and its relationship to quantification of airway secretions. In humans, it is not known how much mucus is required and where it has to be located for the human ear to detect presence of a moist cough. It is likely that mucus in the large airways is required for detectable difference in cough quality as the sound of cough is generated from vibration of larger airways and laryngeal structures during turbulent flow in expiration [16, 17]. Laminar airflow, which occurs in smaller airways, is inaudible . In an animal model, Korpas and colleagues showed that a certain amount of mucus is required to alter cough sound; 0.5 ml of mucus instilled into the trachea of cats altered cough sound, too little mucin had no effect on cough quality whilst too much mucin impaired breathing . Our study findings support this and it is not surprising that when the cough is dry, BS grades were less. The rheological properties of airway mucus also influence cough sound . It is not known how airway secretions in the more peripheral airways influences the sound of cough.
One possible limiting factor of our study is the choice of cut offs for BS grades in determining presence or absence of significant secretions. We chose to use a cut off of 3 as a minor amount of bubbles in the airways can be present from trickling of lignocaine into the airways or spillage from the upper airways. BS cut-off at grade 4 resulted in improved specificity but decreased sensitivity. Children grouped by both BS cut-offs (3 and 4) had significantly different airway cellular profile. The clinical significance of minimal BS grades and appropriate cut-offs can only be determined in a prospective follow-up study which is not an aim of this study. This study did determine that our BS scoring method was easy to use (most done in real time) and had very good inter-rater agreement. The clinical outcomes of wet and dry cough were not the aims of this study and thus cannot be determined here. To relate clinical outcomes to cough descriptors would ideally require a randomised controlled trial with dry and wet cough as entry criteria. A follow-up cohort study with strict clinical diagnostic categories would be useful and we have shown in a preliminary study that dry cough was significantly more likely to naturally resolve than wet cough .
In addition to the limitation of quantifying airway secretions using a bronchoscopic method, this study is also limited by a number of factors. Firstly, clinical repeatability or agreement of cough sounds was assessed by doctors in a tertiary setting. Whether or not these findings can be extrapolated to the secondary and primary setting can only be speculated. Hay and colleagues showed that inter-observer agreement for clinical signs of fever, tachypnoea and chest signs were poor to fair (kappa of 0.12–0.39) in the primary care setting but these signs are known to have good agreement in secondary care settings . However as parents were almost as good as clinicians in our study and are 'untrained' compared to medical practitioners, we would expect that this data can be extrapolated to most primary and secondary settings. Secondly, anaesthesia and atropine could possibly influence mucus quantity and properties. However this influence, if any, is likely to be small as both bronchoscopists (ABC, IBM) are experienced (our recorded average total theatre time is relatively short at 22 mins) , and atropine is given just immediately prior to commencement of bronchoscopy.
Determining the validity of cough quality in children is important not only because of the commonality of the clinical problem of cough but also its use in guidelines and research studies [11, 27, 28]. A particularly important finding is the presence of small amounts of secretions in children with dry cough which may have implications in the management of suppurative lung disease; a dry cough may represent early disease process where only a small amount of mucous is present.
We conclude that the description of a cough as wet or dry cough as determined by clinicians and parents has good clinical validity as it has good agreement with, and relates to, quantification of airway secretions. However as minimal amount of secretions may be present in children with dry cough, clinicians should be cognisant that a dry cough may eventually become wet if airway secretions increase. Thus it should not be assumed that airway secretions are absent in children with chronic dry cough and cough quality in these children should be reviewed. We also conclude that the brassy cough determined by respiratory physicians is highly specific for presence of tracheomalacia.
Negative predictive value
Positive predictive value
receiver operating characteristic
Britt H, Miller GC, Knox S, Charles J, Valenti L, Henderson J, Pan Y, Sutton S, Harrison C: Bettering the Evaluation and Care of Health – A Study of General Practice Activity. In (AIHW Cat. No. GEP-10). Australian Institue of Health and Welfare; 2002.
Cherry DK, Burt CW, Woodwell DA: National Ambulatory Medical Care Survey: 2001 summary. Adv Data 2003, 337:1–44.
Morice AH: Epidemiology of cough. Pulm Pharmacol Ther 2002, 15:253–259.
Jalaludin BB, O'Toole BI, Leeder SR: Acute effects of urban ambient air pollution on respiratory symptoms, asthma medication use, and doctor visits for asthma in a cohort of Australian children. Environ Res 2004, 95:32–42.
Spengler JD, Jaakkola JJ, Parise H, Katsnelson BA, Privalova LI, Kosheleva AA: Housing characteristics and children's respiratory health in the Russian Federation. Am J Public Health 2004, 94:657–662.
Robertson CF, Heycock E, Bishop J, Nolan T, Olinsky A, Phelan PD: Prevalence of asthma in Melbourne schoolchildren: changes over 26 years. BMJ 1991, 302:1116–1118.
Soto-Quiros ME, Soto-Martinez M, Hanson LA: Epidemiological studies of the very high prevalence of asthma and related symptoms among school children in Costa Rica from 1989 to 1998. Pediatr Allergy Immunol 2002, 13:342–349.
Chang AB, Phelan PD, Sawyer SM, Robertson CF: Airway hyperresponsiveness and cough-receptor sensitivity in children with recurrent cough. Am J Respir Crit Care Med 1997, 155:1935–1939.
Coren ME, Ng V, Rubens M, Rosenthal M, Bush A: The value of ultrafast computed tomography in the investigation of pediatric chest disease. Pediatr Pulmonol 1998, 26:389–395.
De Jongste JC, Shields MD: Chronic cough in children. Thorax 2003, 58:998–1003.
Chang AB, Asher MI: A review of cough in children. J Asthma 2001, 38:299–309.
Wubbel C, Faro A: Chronic cough in children. Pediatr Case Rev 2003, 3:95–104.
Chang AB, Masel JP, Boyce NC, Wheaton G, Torzillo PJ: Non-CF bronchiectasis-clinical and HRCT evaluation. Pediatr Pulmonol 2003, 35:477–483.
Chang AB, Newman RG, Carlin J, Phelan PD, Robertson CF: Subjective scoring of cough in children: parent-completed vs child-completed diary cards vs an objective method. Eur Respir J 1998, 11:462–466.
Hsu JY, Stone RA, Logan-Sinclair RB, Worsdell M, Busst CM, Chung KF: Coughing frequency in patients with persistent cough: assessment using a 24 hour ambulatory recorder. Eur Respir J 1994, 7:1246–1253.
Korpas J, Sadlonova J, Salat D, Masarova E: The origin of cough sounds. Bull Eur Physiopathol Respir 1987,23(Suppl 10):47s-50s.
Hashimoto Y, Murata A, Mikami M, Nakamura S, Yamanaka E, Kudoh S: Influence of the rheological properties of airway mucus on cough sound generation. Respirology 2003, 8:45–51.
Foster WM: Mucus secretion and cough. In Cough: Causes, Mechanisms and Therapy. Edited by: Chung FK, Widdicombe JG, Boushey HA. London: Blackwell Science; 2003:207–216.
Nunn JF: Functional anatomy of the respiratory tract. In Applied Respiratory Physiology. London: Butterworths; 1993:18–21.
Chang AB, Boyce NC, Masters IB, Torzillo PJ, Masel JP: Bronchoscopic findings in children with non-cystic fibrosis chronic suppurative lung disease. Thorax 2002, 57:935–938.
Masters IB, Chang AB, Patterson L, Wainwright C, Buntain H, Dean BW, Francis PW: Series of laryngomalacia, tracheomalacia, and bronchomalacia disorders and their associations with other conditions in children. Pediatr Pulmonol 2002, 34:189–195.
Chang AB, Moloney GE, Harms PJ, Masters IB: Endoscopic intratracheal carbon dioxide measurements during pediatric flexible bronchoscopy. Paediatr Anaesth 2004, 14:650–655.
Altman DG: Some common problems in medical research. In Practical statistics for medical research. London: Chapman & Hall; 1991:396–439.
Eng J: ROC analysis: web-based calculator for ROC curves. [http://www.rad.jhmi.edu/roc]
Cane RS, McKenzie SA: Parents' interpretations of children's respiratory symptoms on video. Arch Dis Child 2001, 84:31–34.
Cane RS, Ranganathan SC, McKenzie SA: What do parents of wheezy children understand by "wheeze"? Arch Dis Child 2000, 82:327–332.
British Guideline on the Management of AsthmaThorax 2003, 58:i1-i94i.
Morice AH, Committee M: The diagnosis and management of chronic cough. Eur Respir J 2004, 24:481–492.
Laupacis A, Sekar N, Stiell IG: Clinical prediction rules. A review and suggested modifications of methodological standards. JAMA 1997, 277:488–494.
Murata A, Taniguchi Y, Hashimoto Y, Kaneko Y, Takasaki Y, Kudoh S: Discrimination of productive and non-productive cough by sound analysis. Intern Med 1998, 37:732–735.
Nunn JF: Non-elastic resistance to gas flow. In Applied Respiratory Physiology. 4th edition. London: Butterworths; 1993:61–89.
Korpas J, Widdicombe JG, Vrabec M: Influence of simulated mucus on cough sounds in cats. Respiratory Medicine 1993, 87:49–54.
Marchant JM, Masters IB, Chang AB: Defining paediatric chronic bronchitis. Respirology 2004,9(Suppl):A61.
Hay AD, Wilson A, Fahey T, Peters TJ: The inter-observer agreement of examining pre-school children with acute cough: a nested study. BMC Fam Pract 2004, 5:4.
We thank members of the anaesthetic department, Royal Children's Hospital for their help, in particular Dr. L Patterson and Dr. J Wuth. We also thank Dr M McElrea for proof reading the manuscript and Barry Dean for providing the images used in the bronchoscopic secretion card (figure 1). ABC is supported by the National Health and Medical Research Council and the Royal Children's Hospital Foundation.
AC conceived the idea, designed the study, performed the data analysis and drafted the manuscript. JG participated in data acquisition and coordination of project. ME participated in electronic acquisition of data and software for sound recordings. JF and NC designed the microbiology and cytological components respectively and both helped draft the manuscript. IBM helped in formulation of overall study design, data acquisition and drafting of the manuscript. All authors read and approved the manuscript.
Electronic supplementary material
Additional File 2: Table 4: Assessment of cough quality vs bronchoscopic findings in children grouped by indication for bronchoscopy 4a: Assessment of cough quality vs bronchoscopic findings in children whose indication for bronchoscopy was cough 4b: Assessment of cough quality vs bronchoscopic findings in children whose indication for bronchoscopy was others (ie not cough) Table 5: Assessment of cough quality vs bronchoscopic findings in children grouped by age 5a: Assessment of cough quality vs bronchoscopic findings in children aged ≤ 2 years 5b: Assessment of cough quality vs bronchoscopic findings in children aged > 2 years (DOC 52 KB)
About this article
Cite this article
Chang, B.A., Gaffney, J.T., Eastburn, M.M. et al. Cough quality in children: a comparison of subjective vs. bronchoscopic findings. Respir Res 6, 3 (2005). https://doi.org/10.1186/1465-9921-6-3
- Receiver Operating Characteristic Curve
- Data Additional File
- Large Airway
- Productive Cough
- Airway Secretion