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BackgroundDiagnostic testing for primary ciliary dyskinesia (PCD) started in 2013 in Palestine. We aimed to describe the diagnostic, genetic and clinical spectrum of the Palestinian PCD population.MethodsIndividuals with symptoms suggestive of PCD were opportunistically considered for diagnostic testing: nasal nitric oxide (nNO) measurement, transmission electron microscopy (TEM) and/or PCD genetic panel or whole-exome testing. Clinical characteristics of those with a positive diagnosis were collected close to testing including forced expiratory volume in 1 s (FEV1) Global Lung Index z-scores and body mass index z-scores.Results68 individuals had a definite positive PCD diagnosis, 31 confirmed by genetic and TEM results, 23 by TEM results alone, and 14 by genetic variants alone. 45 individuals from 40 families had 17 clinically actionable variants and four had variants of unknown significance in 14 PCD genes. CCDC39,DNAH11andDNAAF11were the most commonly mutated genes. 100% of variants were homozygous. Patients had a median age of 10.0 years at diagnosis, were highly consanguineous (93%) and 100% were of Arabic descent. Clinical features included persistent wet cough (99%), neonatal respiratory distress (84%) and situs inversus (43%). Lung function at diagnosis was already impaired (FEV1z-score median −1.90 (−5.0–1.32)) and growth was mostly within the normal range (z-score mean −0.36 (−3.03–2.57). 19% individuals had finger clubbing.ConclusionsDespite limited local resources in Palestine, detailed geno- and phenotyping forms the basis of one of the largest national PCD populations globally. There was notable familial homozygosity within the context of significant population heterogeneity.

Refereed/Peer-reviewed Nasal nitric oxide (nNO) is extremely low in most people with primary ciliary dyskinesia (PCD) and its measurement is an important contributor to making the diagnosis. Existing guidelines and technical standards focus on nNO measurements in older, cooperative children using chemiluminescence analysers. However, measurements of nNO in pre-school-age children (age 2–5 years) may facilitate early diagnosis and electrochemical rather than chemiluminescence analysers are widely used. Pre-schoolers often need different methods to be employed when measuring nNO. Hence, a European Respiratory Society Task Force has developed this technical standard as the first step towards standardising sampling, analysis and reporting of nNO measured as part of the diagnostic testing for PCD in all age groups, including pre-school-age children. Furthermore, we considered both chemiluminescence and electrochemical analysers that are in use worldwide. There was a paucity of quality evidence for electrochemical analysers and sampling methods used in young children, and the Task Force proposes future research priorities to allow updates of this technical standard.

Ciliopathies may be classed as primary or motile depending on the underlying ciliary defect and are usually considered distinct clinical entities. Primary ciliopathies are associated with multisystem syndromes typically affecting the brain, kidney, and eye, as well as other organ systems such as the liver, skeleton, auditory system, and metabolism. Motile ciliopathies are a heterogenous group of disorders with defects in specialised motile ciliated tissues found within the lung, brain, and reproductive system, and are associated with primary ciliary dyskinesia, bronchiectasis, infertility and rarely hydrocephalus. Primary and motile cilia share defined core ultra-structures with an overlapping proteome, and human disease phenotypes can reflect both primary and motile ciliopathies. CEP164 encodes a centrosomal distal appendage protein vital for primary ciliogenesis. Human CEP164 mutations are typically described in patients with nephronophthisis-related primary ciliopathies but have also been implicated in motile ciliary dysfunction. Here we describe a patient with an atypical motile ciliopathy phenotype and biallelic CEP164 variants. This work provides further evidence that CEP164 mutations can contribute to both primary and motile ciliopathy syndromes, supporting their functional and clinical overlap, and informs the investigation and management of CEP164 ciliopathy patients.

Introduction In primary ciliary dyskinesia (PCD) impaired mucociliary clearance leads to recurrent airway infections and progressive lung destruction, and concern over chronic airway infection and patient-to-patient transmission is considerable. So far, there has been no defined consensus on how to control infection across centres caring for patients with PCD. Within the BEAT-PCD network, COST Action and ERS CRC together with the ERN-Lung PCD core a first initiative has now been taken towards creating such a consensus statement. Methods A multidisciplinary international PCD expert panel was set up to create a consensus statement for infection prevention and control (IP&C) for PCD, covering diagnostic microbiology, infection prevention for specific pathogens considered indicated for treatment and segregation aspects. Using a modified Delphi process, consensus to a statement demanded at least 80% agreement within the PCD expert panel group. Patient organisation representatives were involved throughout the process. Results We present a consensus statement on 20 IP&C statements for PCD including suggested actions for microbiological identification, indications for treatment of Pseudomonas aeruginosa, Burkholderia cepacia and nontuberculous mycobacteria and suggested segregation aspects aimed to minimise patient-to-patient transmission of infections whether in-hospital, in PCD clinics or wards, or out of hospital at meetings between people with PCD. The statement also includes segregation aspects adapted to the current coronavirus disease 2019 (COVID-19) pandemic. Conclusion The first ever international consensus statement on IP&C intended specifically for PCD is presented and is targeted at clinicians managing paediatric and adult patients with PCD, microbiologists, patient organisations and not least the patients and their families., For the first time ever, an international consensus statement for infection prevention and control in PCD is presented. A total of 20 statements were developed in a collaboration of BEAT-PCD, COST Action, ERS CRC and ERN-LUNG PCD Core Network. https://bit.ly/3yuahKt

Background It is estimated that 1–13% of cases of bronchiectasis in adults globally are attributable to primary ciliary dyskinesia (PCD) but many adult patients with bronchiectasis have not been investigated for PCD. PCD is a disorder caused by mutations in genes required for motile cilium structure or function, resulting in impaired mucociliary clearance. Symptoms appear in infancy but diagnosis is often late or missed, often due to the lack of a “gold standard” diagnostic tool and non-specific symptoms. Mutations in > 50 genes account for around 70% of cases, with additional genes, and non-coding, synonymous, missense changes or structural variants (SVs) in known genes presumed to account for the missing heritability. Methods UK patients with no identified genetic confirmation for the cause of their PCD or bronchiectasis were eligible for whole genome sequencing (WGS) in the Genomics England Ltd 100,000 Genomes Project. 21 PCD probands and 52 non-cystic fibrosis (CF) bronchiectasis probands were recruited in Wessex Genome Medicine Centre (GMC). We carried out analysis of single nucleotide variants (SNVs) and SVs in all families recruited in Wessex GMC. Results 16/21 probands in the PCD cohort received confirmed (n = 9), probable (n = 4) or possible (n = 3) diagnosis from WGS, although 13/16 of these could have been picked up by current standard of care gene panel testing. In the other cases, SVs were identified which were missed by panel testing. We identified variants in novel PCD candidate genes (IFT140 and PLK4) in 2 probands in the PCD cohort. 3/52 probands in the non-CF bronchiectasis cohort received a confirmed (n = 2) or possible (n = 1) diagnosis of PCD. We identified variants in novel PCD candidate genes (CFAP53 and CEP164) in 2 further probands in the non-CF bronchiectasis cohort. Conclusions Genetic testing is an important component of diagnosing PCD, especially in cases of atypical disease history. WGS is effective in cases where prior gene panel testing has found no variants or only heterozygous variants. In these cases it may detect SVs and is a powerful tool for novel gene discovery.

Primary ciliary dyskinesia is an incurable, rare, inherited, chronic condition. Treatment includes regular clearing of airway mucus, aggressive treatment of infections and management of hearing loss. Caregiver burden has not been explored, hence we interviewed 18 English speaking mothers and 6 English speaking fathers of children under 6 years who were diagnosed with PCD around the world. The parents described how the child’s diagnosis, treatment regimen, and health status impacted their life. They discussed the impact of the COVID-19 pandemic and they talked about the different ways they cope with challenges that arise. The need for integrated social care is discussed.

Background: nNO, alongside clinical history, is established in PCD screening. We describe our experience measuring nNO across the age range comparing methods, analysers, PCD diagnostic status & outliers. Methods: 856 patients (0.4-82.8yrs) referred to Southampton had nNO measured. Technically acceptable measurements were obtained using chemiluminescent analysers Niox Flex (2006-14)/ Ecomedics CLD88sp (2014-20) or electrochemical analysers Niox Mino (2013-17)/ Niox Vero (2017-2020). Cut-off 77nL/min was used for all measurements although this is defined only for velum closure, chemiluminescent measurements. Diagnostic status followed ERS Diagnostic Guideline (2016). Results: 9/113 (8%) positive patients had normal nNO. 17% of patients who were diagnosed ‘PCD unlikely’ had nNO We obtained reproducible measurements in 110 children CLD88sp & Vero provided acceptable velum closure measurements but were more difficult for patients to achieve on Vero. Pursed lip TB was acceptable using both instruments allowing for measurement in younger children. Nasal TB can be measured using CLD88sp. Conclusions: nNO is a good screening tool for PCD but should not be used diagnostically alone. nNO can be measured across age range on CLD88 & Vero with age appropriate method. nNO Historical data review against current standards may highlight missed cases.

Primary ciliary dyskinesia (PCD) is an autosomal recessive condition characterized by dysmotile cilia. Typically associated with defects in the cilia structure, it results in impaired mucociliary clearance of pathogens from the lungs and sinuses. Consequently, patients suffer from recurrent sinopulmonary and middle ear infections. We report on the management of a 5-year-old boy who presented with increased work of breathing, fever and crepitations, with an existing diagnosis of PCD with situs inversus totalis. Chest X-ray imaging revealed right lower lobe collapse. He was managed with intensive physiotherapy, nebulized mucolytic agents and antibiotics. However, due to a poor response, he underwent flexible bronchoscopy, which allowed removal of a mucus plug and subsequent re-expansion of his collapsed lobe. Although there is limited evidence for the management of PCD, here we discuss the accepted strategies for its management, based on expert opinion and guidelines for other suppurative lung diseases.

Primary ciliary dyskinesia (PCD) is a rare heterogeneous disorder, usually inherited as an autosomal recessive condition but X-linked inheritance is also described. Abnormal ciliary function in childhood leads to neonatal respiratory distress in term infants, persistent wet cough, bronchiectasis, chronic rhinosinusitis, and hearing impairment; approximately 50% of patients have situs inversus. There is a paucity of evidence for treating PCD, hence consensus guidelines are predominantly influenced by knowledge from cystic fibrosis (CF). Extrapolation of evidence from other diseases is inappropriate since differences in pathophysiology, morbidity and prognosis risk treatment failure and lack of adherence. Areas covered: Review authors searched PubMed and Cochrane databases for publications relating to management of children with PCD. Because of the paucity of data, we emphasise the need for well-designed clinical trials with PCD patients rather than reliance on evidence from other diseases. Expert commentary: The evidence for treatment of PCD is poor, and management is often extrapolated from studies of patients with CF or chronic rhinosinusitis. However, much work is underway to improve the situation and international consortia and networks are conducting well-designed projects to inform the management of children with PCD.

Background: To review children and their family’s experiences of PCD care provided by the 4 specialist teams commissioned to deliver PCD care in England, and establish if the current service meets their needs. Methods: Satisfaction surveys were developed: one for teenagers (12–18yrs), another for parents/carers. These were available in electronic (online) and paper form. Teenagers/families were approached at clinic, by telephone and via email and the survey was also publicised through the UK PCD Family Support Group. Responses were collected between March and October 2018. Results: 407 patients (176 teenagers) from 324 families were under the care of this Service at the time of the surveys. Of these 324 families, 93 parents/carers and 38 teenagers participated. In general, those who responded felt access to the specialist PCD team met their ideals however 51% would like access to a psychologist with only 22% having been offered a review by one and 20% would like input from a social worker. Attitudes towards research were positive, with 87% agreeing it was important to have access to participate in research studies. Of note, 40% of parents/carers reported having problems accessing antibiotics in the community. Encouragingly, 93% of parents/carers and 94% of teenagers believed the specialist PCD service had improved their care. Conclusions: >93% of parents/carers and teenagers felt that the specialist PCD service had improved their PCD care and the current service for the most part met their ideals. Access to psychology and social work services and difficulties obtaining antibiotics in the community were highlighted as issues to be addressed.

BackgroundPrimary ciliary dyskinesia (PCD), a genetically heterogeneous condition enriched in some consanguineous populations, results from recessive mutations affecting cilia biogenesis and motility. Currently, diagnosis requires multiple expert tests.MethodsThe diagnostic utility of multigene panel next-generation sequencing (NGS) was evaluated in 161 unrelated families from multiple population ancestries.ResultsMost (82%) families had affected individuals with biallelic or hemizygous (75%) or single (7%) pathogenic causal alleles in known PCD genes. Loss-of-function alleles dominate (73% frameshift, stop-gain, splice site), most (58%) being homozygous, even in non-consanguineous families. Although 57% (88) of the total 155 diagnostic disease variants were novel, recurrent mutations and mutated genes were detected. These differed markedly between white European (52% of families carry DNAH5 or DNAH11 mutations), Arab (42% of families carry CCDC39 or CCDC40 mutations) and South Asian (single LRRC6 or CCDC103 mutations carried in 36% of families) patients, revealing a striking genetic stratification according to population of origin in PCD. Genetics facilitated successful diagnosis of 81% of families with normal or inconclusive ultrastructure and 67% missing prior ultrastructure results.ConclusionsThis study shows the added value of high-throughput targeted NGS in expediting PCD diagnosis. Therefore, there is potential significant patient benefit in wider and/or earlier implementation of genetic screening.

Introduction: Primary ciliary dyskinesia (PCD) is a rare condition where impaired mucociliary clearance leads to recurrent sinopulmonary infection & bronchiectasis. A National Children9s PCD management service was commissioned in England in 2012 across 4 Centres. The aim of this study was to describe the characteristics of all children in England within this new service. Methods: Detailed diagnostic, phenotypic & management data were collected at annual review assessments for all children seen in 2014. Results: 334 children underwent annual review. Median age at review was 9.8yrs. Median age at diagnosis was 2.6yrs, however was significantly lower in patients with dextrocardia (1.0yr vs 6.2yrs, p Conclusion We provide evidence that, far from being a mild respiratory condition, children with PCD have worse lung function than those with CF. This highlights the need for intensive management of PCD by a multi-professional specialist team.

Primary ciliary dyskinesia (PCD) generally causes symptoms from the first weeks of life, but diagnosis is usually delayed for years or can be missed altogether. Referral for diagnostic testing is often late because key symptoms, such as wet cough, chronic rhinitis and recurrent upper and lower respiratory tract infection, are non-specific. An international survey of patients reported that 37% had >40 visits to medical professionals due to PCD-related symptoms before being referred for diagnostic testing [1]. Approximately 50% of children with PCD have situs inversus, a rare condition in the general population, and it is therefore not surprising that these patients are investigated earlier. A European survey found that age of diagnosis was at 3.5 years in those with situs inversus and 5.8 years in children with normal situs [2]. Assuming a prevalence of 1 in 10 000 [3], we expect ∼1180 diagnosed children in England (childhood population ∼11.8 million); however, there are currently only ∼340 children in the National Paediatric PCD Service. This highlights a huge proportion of undiagnosed patients even in a country with a national PCD service [4]. This is in stark contrast to cystic fibrosis (CF) where neonatal screening programmes ensure that diagnosis occurs in early infancy in many countries, with positive impact on clinical outcome [5]. Young children with PCD have similarly impaired forced expiratory volume in 1 s to children with CF [6], and require multidisciplinary treatment. Early diagnosis facilitates a management plan, including regular airway clearance physiotherapy, surveillance for airway pathogens with treatment of respiratory exacerbations, genetic counselling for families, audiology monitoring and management of conductive hearing loss [7, 8]. We expect that early diagnosis would delay respiratory decline and ensure specialist treatment of ear, hearing and nasal issues, thereby optimising health, psychological, social and educational outcomes. There is no single gold standard test for PCD diagnosis. Presently, the diagnosis is made in patients with a compatible medical history following a demanding combination of tests including nasal nitric oxide (nNO), high-speed video microscopy, transmission electron microscopy, genetics, and culture of respiratory epithelial cells [7, 9–12]. These tests are costly and need experienced staff using sophisticated equipment, hence testing is restricted to reference centres which may be geographically distant from the patient. Identifying the correct patients for testing is therefore important and screening tools are needed. Although individual symptoms are non-specific, the pattern of symptoms is often characteristic. A typical history might include neonatal respiratory distress in an infant with no risk factors, a daily wet cough starting in early infancy, recurrent chest infections, persistent rhinitis and serous otitis media. Screening tools (e.g. PICADAR) to identify patients based on their clinical history are helpful but require a history that might not yet have evolved in young infants [13, 14].

Primary ciliary dyskinesia (PCD) is a rare, heterogeneous genetic disorder where impaired mucociliary clearance is caused by dysfunctional motile cilia leading to bronchiectasis. There is limited evidence characterising the nutritional status of children with PCD, although lower body mass index (BMI) z-score has been associated with worse lung function (FEVAll children (n = 43) with PCD, aged16 years, from a single tertiary centre were prospectively enrolled. Information on clinical phenotype and nutritional status including bioelectrical impedance spectroscopy (BIS) phase-angle was collected.There was a weak positive association between height-for-age z-score (HAZ) and FEVWe have characterised the nutritional phenotype of a cohort of children with PCD. Monitoring vitamin D levels is important in PCD patients. There is a weak association between lung function and nutritional status, and measures of BIS phase-angle. The use of BIS phase-angle may allow for early identification of at risk children and may therefore be of benefit for nutritional assessments in the clinical setting. These findings will help inform a future nutritional intervention strategy in children with PCD.

RationalePrimary ciliary dyskinesia is a genetically heterogeneous inherited condition characterised by progressive lung disease arising from abnormal cilia function. Approximately half of patients have situs inversus. The estimated prevalence of primary ciliary dyskinesia in the UK South Asian population is 1:2265. Early, accurate diagnosis is key to implementing appropriate management but clinical diagnostic tests can be equivocal.ObjectivesTo determine the importance of genetic screening for primary ciliary dyskinesia in a UK South Asian population with a typical clinical phenotype, where standard testing is inconclusive.MethodsNext-generation sequencing was used to screen 86 South Asian patients who had a clinical history consistent with primary ciliary dyskinesia. The effect of a CCDC103 p.His154Pro missense variant compared with other dynein arm-associated gene mutations on diagnostic/phenotypic variability was tested. CCDC103 p.His154Pro variant pathogenicity was assessed by oligomerisation assay.ResultsSixteen of 86 (19%) patients carried a homozygous CCDC103 p.His154Pro mutation which was found to disrupt protein oligomerisation. Variable diagnostic test results were obtained including normal nasal nitric oxide levels, normal ciliary beat pattern and frequency and a spectrum of partial and normal dynein arm retention. Fifteen (94%) patients or their sibling(s) had situs inversus suggesting CCDC103 p.His154Pro patients without situs inversus are missed.ConclusionsThe CCDC103 p.His154Pro mutation is more prevalent than previously thought in the South Asian community and causes primary ciliary dyskinesia that can be difficult to diagnose using pathology-based clinical tests. Genetic testing is critical when there is a strong clinical phenotype with inconclusive standard diagnostic tests.

Background Airway NO synthase (NOS) isoenzymes are responsible for rapid and localised nitric oxide (NO) production and are expressed in airway epithelium. We sought to determine the localisation of neuronal NOS (nNOS) in airway epithelium due to the paucity of evidence. Methods and results Sections of healthy human bronchial tissue in glycol methacrylate resin and human nasal polyps in paraffin wax were immunohistochemically labelled and reproducibly demonstrated nNOS immunoreactivity, particularly at the proximal portion of cilia; this immunoreactivity was blocked by a specific nNOS peptide fragment. Healthy human epithelial cells differentiated at an air–liquid interface (ALI) confirmed the presence of all three NOS isoenzymes by immunofluorescence labelling. Only nNOS immunoreactivity was specific to the ciliary axonemeand co-localised with the cilia marker β-tubulin in the proximal part of the ciliary axoneme. Conclusions We report a novel localisation of nNOS at the proximal portion of cilia in airway epithelium and conclude that its independent and local regulation of NO levels is crucial for normal cilia function.

Background: PCD is an inherited heterogenous disorder of impaired mucociliary clearance. Early colonisation of the lower airways with non-typeable Haemophilus influenzae (NTHi) is common. Chronic inflammation and recurrent infections inevitably lead to irreversible bronchiectasis. It is unknown whether epithelial dysfunction contributes to morbidity. We compared the host responses of healthy and PCD respiratory epithelium to NTHi biofilm using proteomic approaches. Method: Nasal epithelial cells were cultured from 5 PCD subjects with DNAH11 mutations and 3 healthy volunteers. Differentiated ciliated cells were co-cultured with a clinical isolate of NTHi for 72 hours in order to colonise the epithelium with biofilm. Following Label-free LC/MS proteomic analyses, proteins were analysed using the Gene Ontology (GO) PANTHER analysis tool. Results: Differences in protein expression between PCD and healthy epithelial cells included upregulation of the following pathways in PCD: “sodium ion export from cell” (adjusted p=0.045) and “cell-cell adhesion” (adj p=0.001). Downregulated PCD pathways were “positive regulation of substrate adhesion-dependent cell spreading” (adj p=0.020) and “cytoskeletal organisation” (adj p Conclusions: We found epithelial dysfunction in PCD in the form of aberrant responses to colonising NTHi. Our data provide potential mechanistic insights into this dysfunction.

Background: Primary ciliary dyskinesia (PCD) is a rare genetic disease that impedes ciliary function, leading to recurrent upper and lower airway infections. The Southampton PCD Diagnostic Centre has been commissioned by NHS England since 2006. We aimed to describe the characteristics of patients diagnosed at the centre. Methods: We conducted a cross-sectional study using data from local PCD registry, electronic health records and medical notes for all patients diagnosed with PCD in Southampton from 2006 to 2016. Results: Of 1,720 referrals, we diagnosed 142 patients with PCD (8%). Diagnosis was always based on at least one diagnostic test. The number of tests has increased in the last 5 years particularly in genotyping (65% vs 56% before 2011). Nasal nitric oxide was measured in 82% of patients over 5 years of age. Overall, 84% had high-speed video analysis, of which 70% showed predominantly static cilia, with the remainder exhibiting a variety of beat patterns; 131 patients had transmission electron microscopy, which showed ‘hallmark’ defects in 70% of cases; and 59% were genotyped. Median age at initial assessment was 10 years, younger for the 43% with situs abnormalities (7 vs 12 years, p=0.062). 11% had congenital heart disease, considerably higher than previously reported (3-6%). 72% reported neonatal respiratory symptoms, of which 58% needed respiratory support. Mean FEV1% was low in both children and adults (79% vs 71% respectively, p=0.26) at the time of diagnosis. Conclusion: We found a high prevalence of congenital heart disease and neonatal respiratory symptoms. Lung function was impaired in both children and adults. These findings highlight the need for early care for PCD in specialised centres.

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous condition characterised by progressive lung disease arising from abnormal motile ciliary function. Approximately half of patients have situs inversus. The estimated prevalence of PCD in the UK South Asian population is 1:2,265. Early, accurate diagnosis is key to implementing appropriate management but clinical diagnostic tests can be equivocal. The aim of this study was to determine the importance of genetic screening for primary ciliary dyskinesia in a UK South Asian population with a typical clinical phenotype, where standard testing is inconclusive. Next-generation sequencing was used to screen 86 South Asian patients who had a clinical history consistent with PCD. The effect of a CCDC103 c.461A>C p.His154Pro missense variant on phenotypic variability was tested and variant pathogenicity was assessed by oligomerisation assay. Sixteen of 86(19%) patients carried a homozygous CCDC103 p.His154Pro mutation which was found to disrupt protein oligomerisation. Variable diagnostic test results were obtained including normal nasal nitric oxide levels (7/15 patients tested), normal ciliary beat pattern or frequency (9/16 cases) and a spectrum of partial and normal dynein arm retention (9/16 cases). Fifteen (94%) patients or their sibling (s) had situs inversus suggesting in CCDC103 p.His154Pro patients without situs inversus the diagnosis is missed. In conclusion, the CCDC103 p.His154Pro mutation is more prevalent than previously thought in the South Asian community and causes PCD that can be difficult to diagnose using pathology-based clinical tests. Genetic testing is critical when there is a strong clinical phenotype with inconclusive or normal diagnostic tests

Non-typeable

Nasal nitric oxide (nNO) concentrations are low in patients with primary ciliary dyskinesia (PCD) providing a noninvasive screening test.We conducted a systematic review of the literature to examine the utility of nNO in screening for PCD, in particular 1) different respiratory manoeuvres during sampling (velum closure, tidal breathing, etc.), 2) accuracy in screening young/uncooperative children, 3) stationary versus portable analysers, and 4) nNO in “atypical” PCD.96 papers were assessed according to modified PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) criteria and 22 were included in this review.Meta-analysis of 11 studies comparing nNO during a velum closure breath hold gave a mean±sd nNO of 19.4±18.6 nL·min-1 in PCD (n = 478) and 265.0±118.9 nL·min-1 in healthy controls (n = 338). Weighted mean difference for PCD versus healthy controls was 231.1 nL·min-1 (95% CI 193.3–268.9; n = 338) and 114.1 nL·min-1 (95% CI 101.5–126.8; n = 415) for PCD versus cystic fibrosis. Five studies of nNO measurement during tidal breathing demonstrated that this is an acceptable manoeuvre in young children where velum closure is not possible, but the discriminatory value was reduced. Four small studies of portable NO analysers suggest these are reliable tools for screening for PCD. However, nNO must be interpreted alongside clinical suspicion. Future studies should focus on standardising sampling techniques and reporting.

Primary ciliary dyskinesia (PCD) is an autosomal recessive disease associated with bronchiectasis, chronic rhinosinusitis, infertility and situs inversus. Estimates of prevalence vary widely, but is probably between 1:10,000- 1:40,000 in most populations. A number of observational studies indicate that access to services to diagnose and manage patients with PCD vary both between and within countries. Diagnosis is often delayed and frequently missed completely. The prognosis of patients with PCD is variable, but evidence suggests that it is improved by early diagnosis and specialist care. This article briefly reviews the literature concerning PCD and the evidence that specialist care will improve healthcare outcomes. The article specifically refers to a new national service in the UK.

BACKGROUND: We report on a follow-up clinical and serological investigation of 274 children who received seasonal influenza vaccine (trivalent inactivated vaccine [TIV]) 1 year after receipt of either AS03(B)-adjuvanted subunit or whole virus monovalent A(H1N1)pdm09 vaccine and describe the antibody responses to the H3N2 A/Perth/16/2009 and B/Brisbane/60/2008 components of TIV. METHODS: Vaccine responses were analyzed using hemagglutination inhibition (HAI) assays. In children aged 3 years, responses to the H3 and B components of TIV were similar between vaccine groups. Sera taken before and after the pandemic vaccine were also analyzed by HAI using A/Perth/16/2009 virus. This analysis showed that 11.1% of children receiving the AS03(B)-adjuvanted vaccine but only 1.4% in the nonadjuvanted group had a 4-fold rise to A/Perth/16/2009. CONCLUSION: AS03B-adjuvanted A(H1N1)pdm09 influenza vaccine generates a cross-reactive antibody response to H3N2 in children and enhances responses to heterologous subtypes in children aged

Background Allergic rhinitis (AR) is a significant issue in children. Treatment options include allergen avoidance, pharmacotherapy and immunotherapy. The use of nasal saline douching (NSD) in children has recently gained acceptability. However, there is limited data regarding the acceptability and tolerability of NSD in children with AR. Methods A search was conducted using Medline and Embase databases from January 1946 until June 2015 on the use of NSD in children aged 4–12 years with AR. All publications identified that assessed the beneficial effects, acceptability and tolerability were included. Results 40 studies were analyzed. Data varied considerably in terms of saline solutions used, modality of application, participant numbers, study design, follow up and outcomes. Factors that appear to influence the acceptability and tolerability of NSD include parental and health professionals' preconceptions, and characteristics of the solution. Conclusions Nasal saline douching appears to be effective, being accepted and tolerated in the majority of children (78–100%). NSD has a significant positive impact on the quality of life in children with allergic rhinitis. When used as an adjunctive treatment having mainly a cleansing property, NSD potentiates the effects and may reduce the dose required of AR medications. Among the principal factors that influence the acceptability and tolerability of NSD are the child's age, delivery system and method, and tonicity. Nasal saline douching provides an accessible, low cost, low morbidity, easy to use treatment in children with allergic rhinitis.

Introduction: Cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) both cause recurrent pulmonary infections resulting in bronchiectasis. CF is considered the more severe condition. Nutritional status is fundamental to outcome in CF but there is little evidence about its importance in PCD. Aim: To compare BMI and lung function of pancreatic sufficient (PS) and insufficient (PI) CF children to those with PCD. Methods: Cross sectional data (2015) from 204 CF (189 PI, 15 PS) and 46 PCD children, obtained at annual review at our Paediatric Respiratory Centre were compared. Results: Age, sex and mean BMI centile were comparable across the three groups. Mean age (SD) at diagnosis was significantly older in the PCD compared to the PI-CF cohort (4.8yrs (4.6) vs 0.6yrs (1.3) P 1 % did not vary significantly with BMI centile in PS-CF, a lower BMI centile was associated with a lower FEV 1 % in both PI-CF and PCD cohorts, even when adjusted by age. FEV 1 declined similarly in the PS-CF and PCD groups with increasing age although the rate of decline was greater in the PI-CF cohort. Of note, the mean (SD) FEV 1 % was significantly lower in the PCD cohort than both PI-CF and PS-CF children (73.8% (19.4), 84.9% (21.2), 96.1% (15.9) P Conclusion: Similar to PI-CF, a lower BMI centile was associated with a lower FEV 1 % in our PCD cohort. Whilst a greater decline in FEV 1 % with increasing age was observed in the PI-CF patients, the mean FEV 1 % in the PCD patients was significantly lower and they were significantly older at diagnosis. Optimising nutritional status and earlier diagnosis might be of importance in improving lung function amongst PCD patients.

Two doses of AS03B-adjuvanted pandemic influenza vaccine may be sufficient to maintain seroprotection across 2 influenza seasons. Administration of trivalent influenza vaccine to children who previously received 2 doses of pandemic influenza vaccine is safe and is immunogenic for the H1N1 strain., Background. We investigated antibody persistence in children 1 year after 2 doses of either an AS03B-adjuvanted split-virion or nonadjuvanted whole-virion monovalent pandemic influenza vaccine and assessed the immunogenicity and reactogenicity of a subsequent dose of trivalent influenza vaccine (TIV). Methods. Children previously immunized at age 6 months to 12 years in the original study were invited to participate. After a blood sample was obtained to assess persistence of antibody against swine influenza A/H1N1(2009) pandemic influenza, children received 1 dose of 2010/2011 TIV, reactogenicity data were collected for 7 days, and another blood sample was obtained 21 days after vaccination. Results. Of 323 children recruited, 302 received TIV. Antibody persistence (defined as microneutralization [MN] titer ≥1:40) 1 year after initial vaccination was significantly higher in the AS03B-adjuvanted compared with the whole-virion vaccine group, 100% (95% confidence interval [CI], 94.1%–100%) vs 32.4% (95% CI, 21.5%–44.8%) in children immunized

Chronic Obstructive Pulmonary Disease (COPD) has a high mortality. Many indices have been developed to classify disease severity including the 2007 and 2011 GOLD classification and BODE index. However, no study has compared the prediction of mortality by those indices. This is an observational study of 96 patients with COPD and followed prospectively for a median of 60 months. We performed at baseline pulmonary function tests, 6-minute walking test, dyspnea scale mMRC, anthropometric and questionnaire measures of exacerbations. BODE index and GOLD 2007 and GOLD 2011 classification was calculated. The capacity of all indices to predict mortality was compared using Cox proportional hazard analysis and Kaplan Meier survival cruves. A total of 55 men and 41 women were studied, of whom 50% died during a follow-up time mean of 69 +/- 37 months. The mean FEV1 was 27% +/- 5%. Statistically significant associations were observed between mortality and BODE index (p = 0.024) and male sex (p = 0.021). Cox regression analysisshowed that the only statistically significant association was with BODE (p=0,037; IC: 95% 1,024-2,17). The Kaplan-Meier curves for BODE, 2007 GOLD and GOLD ABCD were calculated and are The BODE index predicts all cause mortality better than the old GOLD classification based on FEV1 and the new ABCD grading . We also observed that patients classified as GOLD B has higher mortality than those classified as GOLD C.

Background: Nasal nitric oxide (nNO) is usually low in primary ciliary dyskinesia (PCD) and measurement is part of a complex diagnostic work-up. Previous research has failed to define the accuracy of nNO testing in differing patient populations. Aims: Use accuracy data of nNO testing in patients referred to a UK national diagnostic service to calculate the predictive value of nNO testing in children with persistent wet cough (estimated 5% PCD prevalence) and in the general population (1:10,000 prevalence). Methods: From June 2006 to January 2014, 282 consecutive referrals (aged 6-79 years) had nNO measured by breath hold technique on the chemiluminescent NIOX Flex analyser. PCD was diagnosed by high resolution video microscopy and quantitative electron microscopy. Sensitivity and specificity was calculated and used to derive positive and negative predictive values (PPV & NPV) for each population. Results: 31 patients were PCD positive. Using a published cut-off of 77 nl/min (256 parts per billion on NIOX Flex), sensitivity was 93.6% (95% CI 78.5-99.0) and specificity 84.1% (95% CI 78.9-88.4). PPV was 42% (30.2-54.5%) and NPV 99.1% (96.6-99.9%) for referrals (prevalence of PCD 11%). PPV was 23.6% for persistent wet cough and Conclusion: PPV is poor and diminishes rapidly with lower PCD prevalence therefore screening should be targeted at those with high clinical suspicion of PCD. Whilst NPV is excellent, it must be interpreted alongside clinical history given published cases of PCD with normal nNO. These findings highlight the importance of using clinical features to select those who undergo nNO testing.

Robust diagnosis of primary ciliary dyskinesia (PCD) is important if patients are to receive appropriate specialist management before irreversible deterioration of lung function occurs. Early diagnosis also enables patients and their families to receive appropriate genetic counseling, disease-specific management of ear and rhino-sinus disease, and screening for PCD-associated problems (e.g., cardiac problems) (1, 2). The association of extremely low levels of nasal nitric oxide (nNO) in PCD has been recognized for over 15 years, and measurement of nNO is increasingly used as a screening test for PCD in Europe (1). The manuscript by Leigh and coworkers in this edition of AnnalsATS (3) provides an important advance in the use of nNO for clinical and research purposes. Their data confirm that nNO is a reliable investigation for PCD in the North American population and setting, including identification of “atypical” patients with PCD who might otherwise be missed due to normal ciliary ultrastructure. The authors provide evidence that a standardized protocol using different NO analyzers can be used to reliably differentiate patients with PCD from patients without PCD and from healthy children, in geographically dispersed centers. They have additionally developed cutoff values using data from their large study population, which can now be validated in other populations. There is no “gold standard” diagnostic test to identify all PCD phenotypes, and diagnostic workup requires access to a number of specialist investigations. Previously, ciliary ultrastructure analyzed by electron microscopy (EM) was considered diagnostic, but there is an increasing literature on normal ciliary ultrastructure, at EM resolution, in PCD. This indicates that PCD will be missed in centers where diagnosis depends solely on EM (2, 4). It is also recognized that certain EM defects previously considered diagnostic might on occasion represent secondary changes that resolve on repeat testing (4, 5). In Europe, assessment of ciliary beat frequency (CBF) and pattern (CBP) by high-resolution, high-speed video microscopy (HSVm) is recommended as a functional test for PCD (1, 6). If HSVm analysis is abnormal, re-differentiation of basal epithelial cells at an air–liquid interface (ALI) in cell culture enables reassessment of ciliary function and ultrastructure to differentiate primary from secondary dyskinesia (1). Alternatively, immunoflorescent (IF) staining of ciliary proteins can support diagnosis of PCD (7). EM, HSVm, ALI-culture, and IF all require a high degree of expertise in addition to expensive equipment and infrastructure. These techniques are therefore restricted to a few highly specialized centers, limiting easy access to diagnostic testing (8). Diagnosis supported by bi-allelic mutations in genes known to be associated with PCD is promising; currently genotyping detects only 50–65% of patients (2), but as new genes are rapidly identified this will become increasingly sensitive. The evidence provided by Leigh and coleagues (3) is therefore to be welcomed by clinicians, researchers, and in particular families who are unable to travel to a highly specialized center. It is to be hoped that the U.S. Food and Drug Administration and other regulatory authorities will approve nNO analyzers for clinical use given the evidence that nNO is a reliable screening test for PCD and that valid measurements can be taken at sites geographically distant from a diagnostic center using standardized protocols. Leigh and coworkers report a cutoff value for nNO of 77 nL/min providing sensitivity of 0.98 and specificity greater than 0.999. This cutoff value was validated across six other sites, identifying 70 of the 71 (98.6%) participants with confirmed PCD. A previous study used a cutoff for nNO of 105 parts per billion and reported a specificity of 88%, a sensitivity of 100%, and a positive predictive value of 89% for correctly diagnosing PCD (9). While there are now substantial data to demonstrate that nNO measurement is helpful in guiding the diagnostic pathway, we need to recognize limitations of this measurement. Standardized methods (10) to measure nNO are not appropriate for younger children, precisely the age group that need targeting for diagnostic measurement. Tidal measurements allow levels to be measured in young infants, although there is limited experience in this younger age group (1, 11, 12). Patients with other with upper and lower airway diseases have been reported to have reduced nNO levels, although usually not as low as in PCD; such diseases include cystic fibrosis, nasal polyps and chronic sinusitis. A few groups have recently reported normal levels of nasal NO in a minority of patients with PCD (1, 11, 13). These studies highlight that patients with a history strongly suggestive of PCD should not be excluded from further diagnostic evaluation on the basis of nNO, and also that, while providing an excellent screening test, nNO is not diagnostic and low levels should trigger referral to a highly specialized diagnostic center. A priority for researchers is to understand the cause of the extraordinarily low nNO observed in PCD (14). From a clinical perspective, the next hurdle to overcome is the lack of regulatory approvals of nNO analyzers for PCD diagnosis, as well as the cost and therefore availability of devices. Until recently, the only commercially available analyzers for measuring nNO were nonportable desktop analyzers, which are extremely expensive. More reasonably priced portable machines (15) are now available, although they are not yet fully validated nor approved for clinical use. Manufacturers should be encouraged to develop, validate, and seek approvals for user-friendly, reasonably priced nNO analyzers. This will lead to a step change in the diagnosis of PCD by reliably identifying patients for referral to specialist diagnostic centers.

Before routine infant pneumococcal immunisation and improved access to neuroimaging, around 25% of children with pneumococcal meningitis (PM) suffered ischaemic stroke (IS).1 ,2 In a population-based retrospective audit (UHS ZAUD2053), we investigated the postimmunisation prevalence of stroke/cerebrovascular disease (CVD), and compared features of children with and without IS/CVD. We included all cases of PM in children 5 white cells in the CSF and/or signs of meningism and/or focal neurology and/or meningeal enhancement on CT with contrast. Stroke and/or CVD were identified on CT …

Objective: To determine the quality of life in individuals with corrected tetralogy of Fallot. Methods and subjects: Questionnaires concerning quality of life were sent to all 87 surviving patients aged between 16 and 40 years who had undergone intracardiac repair of tetralogy of Fallot and follow-up in the Wessex Cardiothoracic Unit, and to 87 age and sex matched controls, with medically treated haemodynamically insignificant ventricular septal defects. Results: The only significant difference found between the cases and controls was in requirements for schooling, where those with tetralogy of Fallot were more likely to require additional educational help at school (p = 0.044). For all other aspects of quality of life examined by the questionnaire, including social and genetic history, exercise ability, and health related quality of life, no significant differences were found. Different operative techniques, such as transjunctional patching, right ventriculotomy, and previous palliative shunting, did not affect the quality of life of our population with Tetralogy of Fallot, on average twenty years after their surgery, although the range of operative techniques was limited. Neither age at surgery, nor time since surgery, was correlated with measurements of quality of life. Conclusions: Those who have undergone surgical correction of tetralogy of Fallot have a normal quality of life, with few differences compared to controls.

The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link. Non-typeable Haemophilus influenzae (NTHi) is the most common pathogen in primary ciliary dyskinesia (PCD) patients. We hypothesised that abnormal ciliary motility and low airway nitric oxide (NO) levels on airway epithelial cells from PCD patients might be permissive for NTHi colonisation and biofilm development. We used a primary epithelial cell co-culture model to investigate NTHi infection. Primary airway epithelial cells from PCD and non-PCD patients were differentiated to ciliation using an air–liquid interface culture and then co-cultured with NTHi. NTHi adherence was greater on PCD epithelial cells compared to non-PCD cells ( p

1article. The study was approved by the Southampton and South West Hampshire Research Ethics Committee (06/Q1702/109). Airway epithelium from patients with PCD and control patients without PCD was obtained by nasal brushing and was cultured at the air-liquid interface until differentiated and ciliated. We quantifi ed the presence of NO using a total NO detection assay (Enzo Life Sciences, Inc) within phosphate-buffered saline washes applied to the apical surface of air-liquid interface cultures. NO levels were measured before and after epithelial cells were apically cocultured for 72 h with NTHi at a multiplicity of infection of 100 to evaluate biofi lm infection. Cell viability was demonstrated by daily stable transepithelial electrical resistance (PCD and non-PCD) and ciliary beat frequency measurements (control subjects without PCD). We also measured levels following an 18-h incubation with a cocktail of proinflammatory cytokines (10 ng/mL each of IL-1 b /interferon- g /tumor necrosis factor- a ) applied basolaterally to the cells (n 5 14 for each experiment). Our baseline data were consistent with that of Smith et al, 1

Primary ciliary dyskinesia (PCD) is a genetic disease characterized by abnormalities in ciliary function, leading to compromised airway clearance and chronic bacterial infection of the upper and lower airways. The compositions of these infections and the relationships between their characteristics and disease presentation are poorly defined. We describe here the first systematic culture-independent evaluation of lower airway bacteriology in PCD. Thirty-three airway samples (26 from sputum, 7 from bronchoalveolar lavage [BAL] fluid) were collected from 24 PCD patients aged 4 to 73 years. 16S rRNA quantitative PCR and pyrosequencing were used to determine the bacterial loads and community compositions of the samples. Bacterial loads, which ranged from 1.3 × 10 4 to 5.2 × 10 9 CFU/ml, were positively correlated with age ( P = 0.002) but not lung function. An analysis of ∼7,000 16S rRNA sequences per sample identified bacterial species belonging to 128 genera. The concurrently collected paired samples showed high bacterial community similarity. The mean relative abundance of the dominant genera was 64.5% (standard deviation [SD], 24.5), including taxa reported through standard diagnostic microbiology (members of the genera Pseudomonas , Haemophilus , and Streptococcus ) and those requiring specific ex vivo growth conditions (members of the genera Prevotella and Porphyromonas ). The significant correlations observed included a positive relationship between Pseudomonas aeruginosa relative abundance and age and a negative relationship between P. aeruginosa relative abundance and lung function. Members of the genus Ralstonia were also found to contribute substantially to the bacterial communities in a number of patients. Follow-up samples from a subset of patients revealed high levels of bacterial community temporal stability. The detailed microbiological characterization presented here provides a basis for the reassessment of the clinical management of PCD airway infections.

Background Nasal nitric oxide (nNO) levels are very low in primary ciliary dyskinesia (PCD) and it is used as a screening test. Methods We assessed the reliability and usability of a hand-held analyser in comparison to a stationary nitric oxide (NO) analyser in 50 participants (15 healthy, 13 PCD, 22 other respiratory diseases; age 6–79 years). Nasal NO was measured using a stationary NO analyser during a breath-holding maneuver, and using a hand-held analyser during tidal breathing, sampling at 2 ml/sec or 5 ml/sec. The three methods were compared for their specificity and sensitivity as a screen for PCD, their success rate in different age groups, within subject repeatability and acceptability. Correlation between methods was assessed. Results Valid nNO measurements were obtained in 94% of participants using the stationary analyser, 96% using the hand-held analyser at 5 ml/sec and 76% at 2 ml/sec. The hand-held device at 5 ml/sec had excellent sensitivity and specificity as a screening test for PCD during tidal breathing (cut-off of 30 nL/min,100% sensitivity, >95% specificity). The cut-off using the stationary analyser during breath-hold was 38 nL/min (100% sensitivity, 95% specificity). The stationary and hand-held analyser (5 ml/sec) showed reasonable within-subject repeatability(% coefficient of variation = 15). Conclusion The hand-held NO analyser provides a promising screening tool for PCD.

Nitric oxide is continually synthesized in the respiratory epithelium and is upregulated in response to infection or inflammation. Primary ciliary dyskinesia is characterized by recurrent sinopulmonary infections due to impaired mucociliary clearance. Despite chronic infections, nasal nitric oxide in such patients is markedly reduced and is used as a screening test for this condition. These low levels were first described over 15 years ago but the underlying mechanisms have yet to be fully elucidated. We review epithelial nitric oxide synthesis, release and measurement in the upper airways with particular reference to primary ciliary dyskinesia. The key hypotheses that have been proposed to explain the low levels in this condition are explored and the potential benefits of augmenting airway nitric oxide levels are considered. Further work in these patients clarifying both whether the respiratory epithelium is able to biosynthesise normal levels of nitric oxide and the role played by abnormalities in the anatomy of the paranasal sinuses is essential. While nitric oxide augmentation is unlikely to be beneficial in common primary ciliary dyskinesia phenotypes, it has potential in the treatment of secondary dyskinesias and may also improve treatment of bacterial infections, particularly where biofilms are implicated.

Primary ciliary dyskinesia (PCD) is an autosomal recessive disease with an incidence estimated between 1:2,000 and 1:40,000. Ciliated epithelia line the airways, nasal and sinus cavities, Eustachian tube and fallopian tubes. Congenital abnormalities of ciliary structure and function impair mucociliary clearance. As a consequence, patients present with chronic sinopulmonary infections, recurrent glue ear and female subfertility. Similarities in the ultrastructure of respiratory cilia, nodal cilia and sperm result in patients with PCD also presenting with male infertility, abnormalities of left-right asymmetry (most commonly situs inversus totalis) and congenital heart disease. Early diagnosis is essential to ensure specialist management of the respiratory and otological complications of PCD. Diagnostic tests focus on analysis of ciliary function and electron microscopy structure. Analysis is technically difficult and labour intensive. It requires expertise for interpretation, restricting diagnosis to specialist centres. Management is currently based on the consensus of experts, and there is a pressing need for randomised clinical trials to inform treatment.

The first cases of pandemic influenza A (H1N1) 2009 infection were seen in Mexico in March 2009. Since then, it is thought to have been responsible for at least 18,337 deaths globally. Owing to the young age of fatalities, there have been an estimated 2 million years of life lost, which is comparable to the previous pandemics of 1957 and 1968. In this article, we consider the available data on a monovalent inactivated split-virion AS03-adjuvanted pandemic influenza A (H1N1) vaccine, Pandemrix™ (GlaxoSmithKline, Rixensart, Belgium). At present, Pandemrix appears to be highly immunogenic in all age groups, including children and infants under 3 years of age, with an acceptable safety profile in the context of an influenza pandemic. However, owing to the novel adjuvant, further studies on the safety, immunogenicity and vaccine effectiveness of Pandemrix together with robust post-marketing surveillance are required.