Published online May 6, 2009
PEDIATRICS
Vol. 123
Supplement
May 2009, pp.
S236-S238
(doi:10.1542/peds.2008-2952H)
Initiating Noninvasive Management of Respiratory Insufficiency in Neuromuscular Disease
Joshua O. Benditt, MD
University of Washington Medical Center, Pulmonary and Critical Care Medicine, Seattle, Washington
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ABSTRACT
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This is a summary of the presentation on initiating noninvasive
management of respiratory insufficiency in neuromuscular disease,
presented as part of the program on pulmonary management of
pediatric patients with neuromuscular disorders at the 30th
annual Carrell-Krusen Neuromuscular Symposium on February 20,
2008.
Abbreviations: DMD—Duchenne muscular dystrophy NPPV—noninvasive positive-pressure ventilation
Respiratory insufficiency is one of the leading causes of morbidity and mortality in patients with neuromuscular disease. Recent advances in respiratory support technologies have led to devices that are able to support respiration and improve quality of life and survival in individuals with neuromuscular disease and, in particular, Duchenne muscular dystrophy (DMD).1–3
Respiratory failure in neuromuscular disease consists of several major functional problems (Fig 1 www.pediatrics.org/content/vol123/Supplement_4) that can lead to ventilatory failure, pneumonia, and death: (1) inspiratory failure (ventilatory failure) that occurs because of weakness of the diaphragm, external intercostals, and accessory muscles of breathing; (2) expiratory (cough) failure that occurs because of weakness of the abdominal and internal intercostal muscles; and (3) swallowing failure that can result from involvement with the bulbar muscles. In this article I concentrate primarily on ventilatory failure, the methods to support it, and factors around initiation of those support measures.
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NOCTURNAL VENTILATORY FAILURE
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Inspiratory failure is most commonly seen first at night because
during rapid eye movement sleep, atony of muscles other than
the diaphragm occurs and weakness of the diaphragm is exposed.
In addition, upper airway muscles may also be weak, leading
to obstructive sleep apnea. Individuals with neuromuscular disease
are at risk for a wide variety of sleep-disordered breathing
types including central and obstructive sleep apnea leading
to hypercarbia and hypoxemia. Treatment of nocturnal sleep disturbance
can result in improved quality of life, reduced daytime hypercarbia,
and increased survival rates.
3–5
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INDICATIONS FOR INITIATING NOCTURNAL VENTILATORY SUPPORT
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Nocturnal ventilatory support should be initiated when the presence
of sleep-disordered breathing is detected. Symptoms of nocturnal
hypoventilation should be sought for but can be subtle and include
frequent nocturnal awakenings, morning headaches, fatigue, daytime
hypersomnolence, and difficulty with concentration and schoolwork.
The finding of hypercarbia during the daytime is a predictor
of nocturnal sleep-disordered breathing and, if present, should
prompt further investigation. In terms of evaluation of sleep-disordered
breathing, the American Thoracic Society has published a position
paper on the respiratory care of individuals with DMD.
2 They
suggested the following:
- Review sleep quality and symptoms of sleep-disordered breathing at every patient encounter.
- Perform an annual evaluation for sleep-disordered breathing in patients with DMD, starting from the time they are wheelchair users and/or when clinically indicated.
- When available, it is ideal to perform annual polysomnography with continuous CO2 monitoring.
- In areas where full polysomnography is not readily available, perform overnight pulse oximetry with continuous CO2 monitoring, which provides useful information about nighttime gas exchange, although sleep-disordered breathing not associated with desaturation or CO2 retention will not be detected.
A consensus conference of the American College of Physicians6 has established generally accepted criteria for reimbursement for devices for nocturnal ventilatory support that most insurers follow that include the following criteria: symptoms of sleep-disordered breathing such as morning headache, daytime fatigue or dyspnea, and 1 of the following: (1) a PaCO2 level of
45 mm Hg; (2) nocturnal oximetry demonstrating oxygen saturation at
88% for 5 consecutive minutes; (3) a maximal inspiratory pressure of <60 cm H2O; or (4) a forced vital capacity of <50% predicted. It should be noted that these are criteria for reimbursement only and that the astute clinician must look for more subtle symptoms and signs of sleep-disordered breathing.
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CONTRAINDICATIONS TO NONINVASIVE VENTILATORY SUPPORT
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Although there are few contraindications to noninvasive positive-pressure
ventilation (NPPV), inability to fit or tolerate the mask interfaces
is an absolute contraindication. Relative contraindications
include bulbar involvement and swallowing dysfunction, lack
of patient motivation, and inability to clear secretions (despite
assisted coughing maneuvers).
7,8
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EQUIPMENT FOR NOCTURNAL VENTILATORY SUPPORT
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The equipment for nocturnal noninvasive ventilatory support
consists of 2 major pieces of equipment: a pressure/volume generator
that supplies the forces to provide ventilation (Fig
2 www.pediatrics.org/content/vol123/Supplement_4)
and an interface that connects the ventilator to the patient
(Fig
3 www.pediatrics.org/content/vol123/Supplement_4). In most
cases, the pressure/volume generators are pressure-support bilevel-type
devices that are adjusted for a set expiratory positive airway
pressure that functions to prevent airway obstructions and a
set inspiratory positive airway pressure that serves to ventilate
the individual. In almost all cases, because of the presence
of central sleep apnea in patients with neuromuscular disease,
a back-up rate is supplied that functions to deliver a breath
if the patient does not trigger an inspiratory effort. Volume-type
ventilators can also be used for nocturnal ventilation.
9 They
have the advantage of being able to supply higher pressures
if needed but are not able to compensate for leaks as the pressure-support
devices are.

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FIGURE 3 Interfaces for noninvasive mask ventilation. A, nasal mask; B, full face mask; C, nasal pillows; D, oral interface with lip seal.
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The second major piece of equipment is the interface that connects
the ventilator to the patient. Interfaces are available in a
wide variety of forms including nasal mask, nasal pillows, full
face mask, and oral interfaces (Fig
3 www.pediatrics.org/content/vol123/Supplement_4).
The type of interface used will depend on the preference of
the patient. We have found that many patients prefer starting
with the nasal mask. If mouth leak is present, a chin strap
can be used. Alternatively, a full mask device can be used.
Some individuals who have trouble fitting the mask to their
nose or who suffer from claustrophobia may prefer an oral interface.
Proper fitting of the mask is of utmost importance in the overall
success of the ventilator-support venture. It is crucial to
have an experienced therapist with a wide array of masks available
for the patient to try on. We often spend an hour or more in
the clinic during the fitting procedure.
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WHERE TO INITIATE NPPV
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Nocturnal NPPV may be initiated in a number of locations. Often,
it will be started in the sleep laboratory and can be accomplished
by using part of the night for diagnosis and part for treatment
application, a so-called split-night protocol. On some occasions,
individuals will be admitted to the hospital for initiation
of NPPV or will be transitioned off of invasive ventilation
to nocturnal NPPV during a hospital stay. In our practice, once
diagnostic criteria for sleep-disordered breathing are met,
we will acclimatize the patient to the device and begin initial
titration of the ventilator in the office. Once the patient
has had a chance to become used to the device, final titration
occurs in the sleep laboratory or in the home with oximetry
and CO
2 monitoring.
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DIURNAL NONINVASIVE VENTILATION
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When to Initiate Diurnal Noninvasive Ventilatory Support
Many neuromuscular diseases such as DMD are progressive; therefore,
even with optimal management of nocturnal hypoventilation daytime
respiratory insufficiency is bound to develop. Three possibilities
for management of this situation are to (1) do nothing and let
nature take its course, (2) consider tracheostomy, or (3) use
a noninvasive ventilator device during the daytime. In our clinic,
we have chosen the latter and found it to be quite successful,
as has been reported in the literature.
10–12 The criteria
for timing the initiation of daytime support have not been well
defined; however, we have used the following triggers to initiate
diurnal support: (1) if diurnal hypercarbia develops despite
maximal nocturnal ventilatory support; (2) development of daytime
dyspnea; and (3) increasing infections despite adequate cough
therapy.
Equipment for Diurnal Ventilatory Support
There are 2 major methods of performing diurnal positive pressure with either mask or mouthpiece ventilation on a continuous basis. Mouthpiece ventilation (Fig 4 www.pediatrics.org/content/vol123/Supplement_4) is a methodology that has been available for the past 50 years or more. It involves the use of a portable volume ventilator set in the assist-control mode. The ventilator is attached to a standard ventilator circuit (Figs 2 and 4 www.pediatrics.org/content/vol123/Supplement_4), at the distal end of which is attached a mouthpiece that has either a narrow bore or an angled bend that allows back pressure in the circuit to prevent the ventilator from activating the low-pressure alarm. The circuit is open, but the pressure in the circuit prevents alarming. The respiratory rate is generally set on the lowest possible setting so that the patient may take breaths as needed without the machine cycling when a breath is not needed. The patient activates the breath by placing his or her mouth on the mouthpiece and creating a small negative pressure in the circuit by "sipping" or inhaling. Some of the breath is lost in a leak through the lips; therefore, tidal volumes are set higher than those that would be set for tracheostomy ventilation. Tidal-volume values are set per the patient's comfort but generally range between 700 and 1200 mL.
It is also possible to use nasal-mask ventilation during the
day for those who cannot tolerate mouthpiece ventilation or
chose not to use it. No direct comparison studies between diurnal
mouthpiece and mask ventilation have been performed. The use
of the device will depend in part on the experience of the health
care team taking care of the patients.
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COUGH SUPPORT
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Although the focus of this article is on the initiation of noninvasive
ventilation modalities, the importance of implementing cough
support in parallel cannot be underestimated. In fact, some
have considered adequate cough support to be the most important
factor in maintaining lung health. In almost all cases we will
initiate cough support in parallel with noninvasive ventilatory
support.
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FOOTNOTES
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Accepted Jan 5, 2009.
Address correspondence to Joshua O. Benditt, MD, University of Washington Medical Center, Pulmonary and Critical Care Medicine, Box 356522, Seattle, WA 98195-6522. E-mail: benditt{at}u.washington.edu
All figures for this article appear online at: www.pediatrics.org/content/vol123/Supplement_4
The author has indicated he has no financial relationships relevant to this article to disclose.
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REFERENCES
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- Benditt JO, Boitano L. Respiratory support of individuals with Duchenne muscular dystrophy: toward a standard of care.
Phys Med Rehabil Clin N Am. 2005;16
(4):1125
–1139, xii[Medline]
- Finder JD, Birnkrant D, Carl J, et al. Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement.
Am J Respir Crit Care Med. 2004;170
(4):456
–465[Free Full Text]
- Simonds AK. Home ventilation.
Eur Respir J Suppl. 2003;47
:38s
–46s[CrossRef][Medline]
- Bach JR, Campagnolo DI, Hoeman S. Life satisfaction of individuals with Duchenne muscular dystrophy using long-term mechanical ventilatory support.
Am J Phys Med Rehabil. 1991;70
(3):129
–135[Web of Science][Medline]
- Simonds AK, Muntoni F, Heather S, Fielding S. Impact of nasal ventilation on survival in hypercapnic Duchenne muscular dystrophy.
Thorax. 1998;53
(11):949
–952[Abstract/Free Full Text]
- Clinical indications for noninvasive positive pressure ventilation in chronic respiratory failure due to restrictive lung disease, COPD, and nocturnal hypoventilation: a consensus conference report.
Chest. 1999;116
(2):521
–534[CrossRef][Web of Science][Medline]
- Mehta S, Hill NS. Noninvasive ventilation.
Am J Respir Crit Care Med. 2001;163
(2):540
–577[Free Full Text]
- Simonds AK. Nasal ventilation in progressive neuromuscular disease: experience in adults and adolescents.
Monaldi Arch Chest Dis. 2000;55
(3):237
–241[Medline]
- Bach JR.
Noninvasive Mechanical Ventilation. Philadelphia, PA: Hanley & Belfus; 2002
- Gomez-Merino E, Bach JR. Duchenne muscular dystrophy: prolongation of life by noninvasive ventilation and mechanically assisted coughing.
Am J Phys Med Rehabil. 2002;81
(6):411
–415[CrossRef][Web of Science][Medline]
- Bach JR. Noninvasive ventilation is more than mask ventilation.
Chest. 2003;123
(6):2156
–2157[CrossRef][Medline]
- Toussaint M, Steens M, Wasteels G, Soudon P. Diurnal ventilation via mouthpiece: survival in end-stage Duchenne patients.
Eur Respir J. 2006;28
(3):549
–555[Abstract/Free Full Text]
PEDIATRICS (ISSN 1098-4275). ©2009 by the American Academy of Pediatrics

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