You are on page 1of 6

Can history and physical examination reliably diagnose

pediatric obstructive sleep apnea/hypopnea syndrome?


A systematic review of the literature
SCOTT E. BRIETZKE, MD, MPH, MAJ, MC, USA, ELIOT S. KATZ, MD, and DAVID W. ROBERSON, MD, Boston, Massachusetts

OBJECTIVE: Using an evidence-based technique, cording to a recent survey of otolaryngologists, 59% of


systematically review the literature to evaluate the adenotonsillectomies were performed for “obstructed
accuracy of routine clinical history and physical breathing” and 39% specifically for OSAHS.1 How-
examination in the diagnosis of obstructive sleep ever, according to this same survey, less than 10% of
apnea/hypopnea syndrome (OSAHS) in the pedi- children underwent any objective testing prior to sur-
atric patient. gery and less than 5% underwent laboratory-based
STUDY DESIGN AND SETTING: The biomedical litera- polysomnogram (PSG). The use of the clinical evalua-
ture was systematically reviewed. Articles compar- tion alone (i.e., the clinical history and physical exam-
ing the results of clinical evaluation to polysomnog- ination) to diagnose OSAHS contradicts the evidence
raphy (PSG) were selected. The level of evidence presented in the literature of 4 different specialties
was assessed using established evidence-based (Pediatrics, Pediatric Pulmonology, Sleep Medicine,
medicine (EBM) guidelines. and Otolaryngology), which indicate that clinical eval-
RESULTS: Twelve articles were identified using the
uation for the diagnosis OSAHS is often inaccurate
search criteria. Eleven of 12 articles concluded that
compared to PSG. The purpose of this investigation
clinical evaluation is inaccurate in the diagnosis of
was to systematically review the biomedical literature
OSAHS. The level of evidence was good to very
using an evidence-based medicine (EBM) approach to
good (Grade B/Bⴙ).
compile and assess the current evidence addressing the
CONCLUSION/SIGNIFICANCE: Clinical history and
question of “Can the clinical history and/or routine
physical examination are not reliable for diagnos-
physical examination reliably diagnose OSAHS in the
ing OSAHS compared with overnight PSG. Compli-
pediatric patient?”
cating the interpretation of this work is the lack of a
validated PSG threshold of clinically significant dis-
ease. There is an urgent need for the development METHODS
of adequate screening tests with validated clinical The medical literature was reviewed using the
outcomes. EBM rating: B-3. (Otolaryngol Head PUBMED and Cochrane medical databases using key-
Neck Surg 2004;131:827-32.) words “pediatric sleep apnea,” “pediatric sleep-disor-
dered breathing,” “pediatric obstructive sleep apnea,”
O bstructive sleep apnea/hypopnea syndrome
and “diagnosis.” Only articles whose primary objective
was to evaluate the ability of the clinical history and/or
(OSAHS) has become a leading indication for pediatric
physical examination to accurately diagnose OSAHS
adenotonsillectomy. (The term OSAHS is used as it
were selected. Articles predominantly evaluating other
appropriately recognizes the importance of hypopneas
in pediatric sleep-disordered breathing [SDB].) Ac- diagnostic modalities (e.g., radiographs and pulse
oximetry) were excluded. Only articles using mul-
tichannel, nocturnal PSG as the “gold standard” refer-
From the Department of Otolaryngology (Drs Brietzke and Roberson) and
ence test compared to history and/or physical examina-
the Department of Pulmonology (Dr Katz), Boston Children’s Hospital,
Boston, MA. tion were selected. Searches were also restricted to
This work supported in part by a research award from the American Society of patients 0 to 18 years of age and to articles published in
Pediatric Otolaryngology. the English language only. Additional articles were
Dr Katz was supported by NIH/NHLBI HL 073238-01.
identified by reviewing the reference sections of previ-
The opinions and assertions of the authors contained herein are the private
views of the authors and are not to be construed as reflecting the views of
ously identified articles. Articles were separated into
the Department of Defense or the Department of the Army. those that evaluated both history and physical exami-
Reprint requests: Scott E. Brietzke, MD, MPH, Walter Reed Army Medical Center, nation versus those that evaluated only history. The
6900 Georgia Ave., Washington, DC 20307; e-mail, SEBrietzke@msn.com. study design of each article was then determined. A
0194-5998/$30.00
Copyright © 2004 by the American Academy of Otolaryngology–Head and
cohort study was distinguished from a case series by the
Neck Surgery Foundation, Inc. presence of a comparison group and more thorough
doi:10.1016/j.otohns.2004.07.002 follow-up. Statistical analysis was performed with the
827
Otolaryngology–
Head and Neck Surgery
828 BRIETZKE et al December 2004

Table 1. Evidence table


Evidence
Author Study design level n Significant findings Overall conclusion

History and physical examination:


Jain A, Sahni JK2 2002 Prospective cohort AHI ⬎ 5 3b 40 22 of 30 (73%) patients with “Found no significant
defined as OSAHS “obstructive symptoms” correlation of tonsil
found to have OSASH hypertrophy to AHI”
Nieminen P, et al.3 2000 Prospective cohort AHI ⬎ 1 1b 88 27 of 58 (46%) with “Not possible to establish the
defined as OSAHS OSAHS by clinical diagnosis without PSG”
evaluation with OSAHS
by PSG
Rosen CL4 1999 Retrospective cross:sectional 2b 326 192 of 326 (59%) with “Clinical evaluation has not
AHI ⬎ 1 defined as clinical concern for been shown to reliably
OSAHS OSAHS with OSAHS by distinguish primary snoring
PSG Questionnaire* with from OSAHS”
sensitivity of 47% and
specificity of 28%
Wang RC, et al.5 1998 Retrospective case series 2b 82 Overall accuracy of clinical “Multiple regression did not
AHI ⬎ 5 defined as suspicion was only 30% find an association between
OSAHS (25 of 82) clinical parameters and
OSAHS by PSG”
Nieminen P, et al.6 1997 Prospective cohort AHI ⬎1 1b 78 Parental report of “nightly “OSAHS cannot be reliably
defined as OSAHS apnea” with Risk Ratio ⫽ diagnosed without PSG”
3.6, “restless sleep” ⫽ 2.1
Sanchez-Armengol A, et Retrospective case series 3b 12 Formal OSAHS diagnosis “No association between PSG
al.7 1996 not established parameters and symptom
severity scores”
Suen JS, et al.8 1995 Prospective cohort AHI ⬎ 5 1b 69 35 of 69 (51%) with clinical “History and clinical features
defined as OSAHS concern for OSAHS with were not useful in predicting
OSAHS by PSG abnormal PSG”
Goldstein NA, et al.9 1994 Prospective cohort AHI ⬎ 1b 30 10 of 18 (56%) patients with “Clinical assessment of OSAHS
15 “definite OSAHS” by is sensitive but not specific”
clinical evaluation with
OSAHS by PSG
sensitivity ⫽ 92%
specificity ⫽ 29%
Leach J, et al.10 1992 Retrospective case series 3b 93 34 of 93 (37%) patients with “No significant differences in
PSG criteria ⫽ NR clinical concern for age, sex, symptoms between
OSAHS with OSAHS by OSAHS and normal PSG
PSG group”
History (questionnaire) only:
Preutthipan A, et al.11 Prospective cohort All 2b 65 Loud snoring, observed No observation(s) found to
2000 patients with OSAHS of apnea, shaking shaking have “high values for both
differing severity child more common in sensitivity and specificity”
severe OSAHS
Carroll JL, et al.12 1995 Retrospective case series 2b 83 Questionnaire* indeterminate “Primary snoring cannot be
AHI ⬎ 1 defined as in 48 patients (58%) distinguished from OSAHS”
OSAHS Correctly diagnosed 26 of
remaining 35 (74%)
Brouillette R, et al.13 1984 Case control Case ⫽ 4 92 Questionnaire (OSA Score) “Use of OSA Score should
OSAHS on PSG Control correctly identified all decrease need for PSG”
⫽ normal volunteer normal controls and 22 of
23 (96%) with OSAHS

*The “Questionnaire” evaluated in these studies included the instrument developed by Brouillette et al.
OSAHS, obstructive sleep apnea/hypopnea syndrome; PSG, polysomnogram; AHI, apnea/hypopnea index; NR, not reported.

assistance of computer software (STATA version 8, (www.cebm.net) under the heading of “Diagnosis”
STATA Corporation, College Station, TX). studies. The ratings that were used included: 1b: a
The level of evidence was assigned by applying the validating cohort study (goal was to test the quality of
Center for Evidence-Based Medicine (CEBM) criteria a specific diagnostic technique) with good reference
Otolaryngology–
Head and Neck Surgery
Volume 131 Number 6 BRIETZKE et al 829

standards, 2b: an exploratory cohort study (goal was to lette et al.13 As discussed above, this study compared
test associations of diagnostic categories) with good normal, nonsnoring children to children with OSAHS.
reference standards, 3b, a study without consistently The identical questionnaire (“OSA Score”) developed
applied reference standards, and 4, a case control study. in this study was applied to snoring children in 2 later
The study design, sample size, diagnostic criteria used studies,4,12 each of which demonstrated a much lower
for OSAHS, statistical highlights (prevalence of OS- level of PPV (58.8%4 and 74.3%12). The weighted
AHS in the cohort, sensitivity/specificity, etc.), and the average (weight ⫽ inverse of study variance ⫹ between
overall conclusion of the paper were compiled into an study variance) of the PPV for the combined 10 studies
evidence table. using a random effects model to account for between-
study variation was 55.8% (95% confidence interval,
RESULTS 42.1-69.6%). In general terms, this means that approx-
Twelve articles were identified using the stated cri- imately only 55% of patients with a “positive” clinical
teria (Table 1). Seven articles were from otolaryngol- evaluation for OSAHS were subsequently found to
ogy journals, 4 were from pediatric journals, and 1 have OSAHS by the specified PSG criteria. This sum-
article was from a sleep journal. Six articles were of a mary measure of PPV should be interpreted with ex-
prospective cohort design, 4 were retrospective case treme caution, given the highly significant heterogene-
series, 1 was a retrospective cross-sectional study, and ity amongst the studies (test of heterogeneity Q⫽
1 was a case control study. Sample sizes ranged from 153.392 P ⬍ 0.001), primarily in the area of the various
12 patients to 326 patients. The studies were very PSG criteria used to define OSAHS.
heterogeneous with different PSG-based diagnostic cri- To further delineate the diagnostic performance of
teria for OSAHS ranging from 1 event per hour to 15. history and physical examination, the 4 most common
The definitions of what constituted an actual “event” questions included in a typical sleep history and the
(e.g., apnea, hypopnea) were also very heterogeneous. most common component of the physical examination
A variety of data analysis techniques were employed (tonsil size) were separately tabulated. If sufficient raw
including logistic regression, receiver operating curve data were present in the given article, the sensitivity
analysis, formal calculations of sensitivity and speci- and specificity for that individual characteristic in pre-
ficity, and simple tests of association between the his-
torical features of those with OSAHS and those with-
out.
Despite the fact that the methodology of the articles
was quite varied, the overall conclusions of the articles
were very consistent. Eleven of 12 articles concluded
that history and/or physical examination cannot reliably
diagnose OSAHS in the pediatric patient in comparison
to PSG. The 1 article13 that did present a contrary view,
did so by developing a diagnostic questionnaire (“OSA
Score”) that was later invalidated by subsequent stud-
ies.4,12 This instrument was developed to distinguish
normal, nonsnoring patients from OSAHS patients, but
could not differentiate snoring children with and with-
out OSAHS.
The positive predictive value (PPV) of the clinical
evaluation in comparison to PSG results was extracted Fig 1. Forest plot of the positive predictive value (PPV %)
from the presented data in 10 of the 12 studies (Fig 1). of the clinical examination compared to PSG diagnosis.
The remaining 2 studies did not provide sufficient or Note that with a PPV far below 1.0, the clinical examina-
tion generally results in an over-diagnosis of OSAHS as
appropriate data for calculation of the PPV. The general
compared to PSG. Error bars reflect the 95% confidence
design of the 10 selected studies included presenting a interval for the diagnostic accuracy point estimate and
cohort of patients with a positive clinical evaluation the size of the box reflects the weight of the estimate
who where then evaluated with PSG. Very few subjects towards the summary estimate. The combined estimate
with a negative clinical evaluation were included in any represents a weighted average (weight⫽ inverse of the
study variance ⫹ between study variance) of the individ-
of the studies, which precluded the calculation of sen-
ual values of PPV using a random effects model. Note:
sitivity, specificity, or negative predictive value. The Sanchez-Armengol A, et al.7 and Preutthipan A, et al.11
PPV ranged from 30.5%5 to 95.7%.13 The study that did not provide sufficient or appropriate data for this
demonstrated the highest PPV (95.7%) was by Brouil- calculation and have been excluded.
Otolaryngology–
Head and Neck Surgery
830 BRIETZKE et al December 2004

Table 2. Diagnostic characteristics of various components of the clinical evaluation


Nieminen et al3 Wang et al5 Nieminen et al6

Characteristic Sensitivity Specificity Sensitivity Specificity Sensitivity Specificity

Snores nightly 74% 52% 44% 58% 76% 49%


Witnessed apnea 59% 90% 88% 17% 55% 86%
Mouth-breathing 78% 27% 36% 56%
Severe daytime somnolence 23% 0% 20% 81% 21% 92%
Tonsil size greater than 3⫹ 4⫹ 93% 35% 12% 89% 93% 35%

*In this study, the clinical characteristics were evaluated in their ability to distinguish severe OSAHS from nonsevere OSAHS.

dicting the presence of OSAHS were calculated (Table sign is not present given the disease is not present).
2). Six articles provided sufficient raw data to calculate Thus, the clinical evaluation would be expected to have
individual sensitivities and specificities. No component a high false positive rate (reflected by a low specificity)
of the clinical evaluation in any article was found to and a lower false negative rate (reflected by a higher
have a sensitivity and specificity greater than 65%. sensitivity).
The overall level of evidence was good to excellent. If it can reasonably be assumed that the majority of
There were 4 level 1b studies, 4 level 2b studies, 3 level children referred to the otolaryngologist for SDB are
3b studies, and 1 level 4 study. This conservatively going to have a “positive” clinical evaluation, then it
constitutes Grade B evidence (consistent level 2 and follows that a sizable proportion of these clinically
level 3 studies) according to the Center of Evidence- “positive” patients will not actually have OSAHS by
Based Medicine (CEBM) criteria. However, one could PSG. Thus, the use of the clinical evaluation alone can
very reasonably consider the overall grade of evidence be expected to “overdiagnose” OSAHS. This circum-
to be even higher (B⫹/A–), given that there were 4 of stance was repeatedly demonstrated in the articles se-
4 level 1b studies all concluding the clinical examina- lected for this review, which typically presented a co-
tion was inadequate (grade A evidence) and that the hort of patients all considered to have OSAHS by
only dissenting study was a level 4 study. clinical evaluation. Subsequently, only a proportion
(positive predictive value range 30%5 to 96%13) were
DISCUSSION actually found to have PSG findings consistent with
This systematic review of the literature clearly dem- OSAHS (Fig 1). Furthermore, if it is reasonably as-
onstrates that the use of the clinical history and physical sumed that the majority of patients with “positive”
examination alone in comparison to overnight PSG is clinical exams and thus, “clinical OSAHS,” will pro-
not adequate to diagnose OSAHS. The level of evi- ceed to undergo adenotonsillectomy, then it must fol-
dence supporting this conclusion is high. The general- low that a significant portion of patients who undergo
izability of this conclusion is also high given the het- adenotonsillectomy for the indication of OSAHS will
erogeneity of the populations studied and the varying not have OSAHS by PSG criteria.
diagnostic criteria for OSAHS used amongst the differ- As is often the case, however, things are not neces-
ent studies. The ability of the history and physical sarily as simple as they may appear. The underlying
examination to adequately diagnose OSAHS by any of basis of the argument against the use of the clinical
several different PSG criteria within several different evaluation alone for the diagnosis of OSAHS has 2
study populations was uniformly poor. major assumptions. Both of these assumptions have
What are the consequences of the inaccuracy of the recently been seriously questioned. First, it assumed
clinical evaluation? To fully evaluate these conse- that PSG is the gold standard test for SDB. However,
quences, we must first consider the manner in which outcomes data are severely lacking in pediatric SDB.
patients are typically being misclassified by the use of No study has linked diagnostic thresholds on PSG with
clinical evaluation alone. Table 2 shows the pooled untoward outcomes in SDB, particularly in the area of
sensitivity and specificity of the common components neurocognitive dysfunction, which may be the most
of the clinical evaluation extracted from the studies that common sequelae of SDB. Thus, PSG cannot be un-
presented sufficient raw data to allow their calculation. equivocally considered the “gold standard test” for
Although there is considerable variation, the general SDB if the results cannot predict harmful outcomes.
trend is that of high sensitivity (probability that the Either appropriate PSG thresholds must be defined, or
symptom or sign is present given the disease is present) new methods of testing that can be linked to neurocog-
and lower specificity (probability that the symptom or nitive outcomes must be developed. The second as-
Otolaryngology–
Head and Neck Surgery
Volume 131 Number 6 BRIETZKE et al 831

Table 2. (Continued)
Carroll et al12 Leach et al10 Preutthipan et al11*

Sensitivity Specificity Sensitivity Specificity Sensitivity Specificity

97% 4% 76% 27% 86% 27%


74% 54% 47% 25% 61% 65%
61% 15% 29% 46%
17% 93% 18% 86%
76% 59%

sumption that has been recently questioned is the as- icantly overdiagnose OSAHS. Objective testing should
sumption that only the more severe forms of SDB, be used with greater frequency to increase diagnostic
including OSAHS and upper airway resistance syn- accuracy. However, otolaryngologists should recognize
drome (UARS), require aggressive (surgical) treatment. the limitations of PSG and the lack of outcomes data
A growing body of evidence suggests that snoring associated with PSG findings. A normal PSG does not
alone, even without OSAHS or hypoxemia, may be necessarily indicate that no therapy is indicated. Mild
associated with neurocognitive impairment, particu- SDB in the form of primary snoring alone may produce
larly attention deficit hyperactivity disorder (ADHD) negative effects, particularly in the area of neurobehav-
and learning disorders.14-16 Thus, the unfortunate cur- ioral dysfunction. However, the utility of early, aggres-
rent circumstance is that a snoring child may undergo sive treatment has not been conclusively proven.17,18
the best diagnostic test available (PSG) and be found to Therefore, the judgment of the evaluating otolaryngol-
have no apnea, hypopnea, or hypoxemia, yet may still ogist may still be paramount in the decision to proceed
be at risk for a poor outcome. with adenotonsillectomy. More study into this area
Further complicating the issue is that the benefit of should be undertaken and should be a high priority for
adenotonsillectomy in treatment of the more mild forms our specialty.
of SDB (i.e., primary snoring) has not been fully sub- Despite the potential diagnostic benefits, obtaining a
stantiated. There is some evidence that the neurocog- PSG on every child who is evaluated for OSAHS is
nitive impairments of SDB may not be completely obviously not feasible or practical. Yet, the current
reversible with adenotonsillectomy.17,18 However, practice of using the clinical evaluation alone is also not
these conclusions are based on early, limited evidence. sufficient. A simple, inexpensive screening test that can
Further study linking SDB outcomes and PSG findings be linked to SDB outcomes would be an ideal solution
in mild SDB should be a pediatric public health prior- to this dilemma. Unfortunately, the simple screening
ity. tests that have been evaluated to date have not been
Aside from eliminating diagnostic uncertainty, there successful. Audiotaping and videotaping are highly
are other important reasons to objectively measure the variable in quality and require strong parental motiva-
level of SDB in pediatric patients. In patients with tion.20 Home pulse oximetry has not been conclusively
OSAHS, the severity of OSAHS is prognostically im- shown to be useful.21 More sophisticated screening
portant. Pediatric patients with moderate to severe OS- tests such as pulse transit time (PTT),22 arterial tonog-
AHS have been shown to have greater risk of periop- raphy,23 and dynamic CT scan24 are under intense
erative complications that may warrant increased investigation but are not yet available or have not been
anesthetic precautions and careful postoperative obser- studied extensively in children. The informed otolaryn-
vation.19 Perhaps most importantly, patients with mod- gologist would be well-advised to recognize the limits
erate and severe OSAHS are more likely to have per- of both the clinical evaluation and objective testing
sistent disease after adenotonsillectomy that may with PSG.
require continued observation and/or possible interven-
tion (e.g., CPAP.)8 These patients should be strongly CONCLUSIONS
considered for postoperative PSG to assess for persis- Routine history and physical examination are not
tent SDB if symptoms persist. adequate to reliably diagnose OSAHS in snoring chil-
Where does the concerned otolaryngologist go from dren who present to the otolaryngologist for evaluation.
here? Clearly, the first step is to recognize the diagnos- The level of evidence for this conclusion is high despite
tic limitations of the history and physical examination. inconsistent diagnostic criteria for OSAHS. Overnight
As has been suggested in this systematic review, the PSG is the best available objective test, but no specific
use of the clinical evaluation alone will tend to signif- threshold of disease has been linked to neurobehavioral
Otolaryngology–
Head and Neck Surgery
832 BRIETZKE et al December 2004

dysfunction. Early, limited evidence may indicate the clinical findings in children with obstructive sleep apnea. Arch
Otolaryngol Head Neck Surg 1992;118:741-4.
need for early aggressive surgical therapy in children
11. Preutthipan A, Chantarojanasiri , Suwanjutha S, et al. Can par-
with mild SDB. Therefore, the clinical judgment of the ents predict the severity of childhood obstructive sleep apnea?
otolaryngologist to evaluate the overall clinical presen- Acta Paediatr 2000;89:708-12.
tation of the patient, consider objective diagnostic tests, 12. Carroll J, McColley SA, Marcus CL, et al. Inability of clinical
history to distinguish primary snoring from obstructive sleep
and weigh the risks and benefits of therapy remains apnea syndrome. Chest 1995;108:610-18.
paramount in the decision to proceed with surgical 13. Brouilette R, Hanson D, David R, et al. A diagnostic approach to
therapy. Collection of outcomes data and development suspected obstructive sleep apnea in children. J Pediatr 1984;
105:10-14.
of a simple screening test linked to neurobehavioral 14. O’Brien LM, Holbrook CR, Mervis CB, et al. Sleep and neu-
outcomes should be a pediatric public health priority. robehavioral characteristics of 5- to 7-year-old children with
parentally reported symptoms of attention-deficit/hyperactivity
disorder. Pediatrics 2003;111:554-63.
REFERENCES 15. Chervin RD, Archbold KH, Dillon JE, et al. Inattention, hyper-
activity, and symptoms of sleep-disordered breathing. Pediatrics
1. Weatherly RA, Mai EF, Ruzicka DL, et al. Identification and 2002;109:449-56.
evaluation of obstructive sleep apnea prior to adenotonsillectomy 16. Chervin RD, Dillon JE, Bassetti C, et al. Symptoms of sleep
in children: a survey of practice patterns. Sleep Med 2003;4:297- disorders, inattention, and hyperactivity in children. Sleep 1997;
307. 20:1185-92.
2. Jain A, Sahni JK. Polysomnographic studies in children under- 17. Gozal D, Pope DW, Jr. Snoring during early childhood and
going adenoidectomy and/or tonsillectomy. J Laryngol Otol academic performance at ages thirteen to fourteen years. Pediat-
2002;116:711-5. rics 2001;107:1394-9.
3. Nieminen P, Tolonen U, Lopponen H. Snoring and obstructive 18. Gozal D. Sleep-disordered breathing and school performance in
sleep apnea in children: a 6-month follow-up study. Arch Oto- children. Pediatrics 1998;102:616-20.
laryngol Head Neck Surg 2000;124:481-6.
19. Brown KA, Morin I, Hickey C, et al. Urgent tonsillectomy: an
4. Rosen CL. Clinical features of obstructive sleep apnea hypoven-
analysis of risk factors associated with post-operative respiratory
tilation syndrome in otherwise healthy children. Ped Pulm 1999;
morbidity. Anesthesiology 2003;99:586-95.
27:403-9.
20. Section on Pediatric Pulmonology, Subcommittee on Obstructive
5. Wang RC, Elkins TP, Keech D, et al. Accuracy of clinical
evaluation in pediatric obstructive sleep apnea. Otolaryngol Sleep Apnea Syndrome. Clinical practice guideline: Diagnosis
Head Neck Surg 1998;118:69-73. and management of childhood obstructive sleep apnea syndrome.
6. Nieminen P, Tolonen U, Lopponen H, et al. Snoring children: Pediatrics 2002;109:704-12.
factors predicting sleep apnea. Acta Otolaryngol (Stockh) 1997; 21. Brouillette RT, Morielli A, Leimanis A, et al. Nocturnal pulse
529(Suppl):190-4. oximetry as an abbreviated testing modality for pediatric obstruc-
7. Sanchez-Armengol A, Capote-Gil F, Cano-Gomez S, et al. Poly- tive sleep apnea. Pediatrics 2000;105:405-12.
somnographic studies in children with adenotonsillar hypertro- 22. Katz ES, Lutz J, Black C, et al. Pulse transit time as a measure
phy and suspected obstructive sleep apnea. Pediatric Pulm 1996; of arousal and respiratory effort in children with sleep disordered
22:1010-5. breathing. Ped Res 2003;3:580-8.
8. Suen JS, Arnold JE, Brooks LJ. Adenotonsillectomy for treat- 23. Ayas NT, Pittman S, MacDonald M, et al. Assessment of a
ment of obstructive sleep apnea in children. Arch Otolaryngol wrist-worn device in the detection of obstructive sleep apnea.
Head Neck Surg 1995;121:525-30. Sleep Med 2003;4:435-42.
9. Goldstein NA, Sculerati N, Walsleben JA, et al. Clinical diag- 24. Bhattacharyya N, Blake SP, Fried MP. Assessment of the airway
nosis of pediatric obstructive sleep apnea validated by polysom- in obstructive sleep apnea syndrome with 3-dimensional airway
nography. Otolaryngol Head Neck Surg 1994;111:611-7. computed tomography. Otolaryngol Head Neck Surg 2000;123:
10. Leach J, Olson J, Hermann J, et al. Polysomnographic and 444-9.

You might also like