Inhaler

Types of inhalers

Meter-dosed inhaler (MDI)

The most common type of inhaler is the pressurized metered-dose inhaler (MDI) which is made up of 3 standard components- a metal canister, plastic actuator, and a metering valve. The medication is typically stored in solution in a pressurized canister that contains a propellant or suspension. The MDI canister is attached to a plastic, hand-operated actuator. On activation, the metered-dose inhaler releases a fixed dose of medication in aerosol form through the actuator and into a patient's lungs. These devices require significant coordination as a person must discharge the medication at or near the same time that they inhale in order for the medication to be effective. This problem is mitigated by the use of a spacer chamber, which allows the fine particle suspension to slow down and be more effectively inhaled into the lower airways . It is preferable that a spacer chamber is used for delivering medication by MDI for all age groups.

Dry powder inhaler (DPI)

Dry powder inhalers release a metered or device-measured dose of powdered medication that is inhaled through a DPI device. This device usually contains a chamber in which the powdered medication is deposited prior to each dosage. The powder can then be inhaled with a quick breath. This allows for medication to be delivered to the lungs without the need for use of propellant/suspension.

Soft mist inhaler (SMI)

Soft mist inhalers release a light mist containing medication without the need for a propellant/suspension. Upon pressing a button, the inhaler creates a mist of medication, allowing for inhalation into the lungs. SMIs suspend inhaled medications for roughly 1.2 seconds, which is longer than the average MDI inhaler suspension time period. This requires less coordination when using and may be helpful for young patients or patients that find the MDI inhalers difficult to use.

Nebulizer

Nebulizers are designed to deliver medications over an extended period of time over multiple breaths through a mouthpiece or face mask. They generate a continuous mist with aerosolized medication, allowing a patient to breathe normally and receive medications. They are commonly used in infants and toddlers requiring inhaled medications or in patients in the hospital who require inhaled medications.

Smart inhaler

The smart-inhaler is an inhaler that will automatically update an app with information that includes the time of day, air quality, and how many times it has been used through sensor technology on the device. The first smart-inhaler was approved in 2019 by the FDA, its purpose is to track patient use of the device and some other circumstantial factors that could affect the effectiveness of the dosage. This information is sent via Bluetooth to a mobile device app, and is later shared with their physician to determine what kind of things can trigger issues with asthma and other problems. This technology presents a great way to cut down on medical costs associated with asthma and also help patients better manage their condition with fewer emergencies.

The Teva ProAir Digihaler was the first FDA approved smart inhaler. It shows how effective the device is at aiding patients in using the proper dose amount for their asthma. In a study published by the European Respiratory Journal, the ProAir Digihaler accurately identified when patients were using their inhalers and whether they were effectively administering the dose in a 370 patient trial with the device. This study further gives an overview on the technology regarding applications and devices that help aid in the tracking and medication management for asthma and other lung conditions. Another study showed that smart inhalers accurately recorded all doses administered by patients with their technology, which signifies their importance in providing accurate dosage information to patients and their physicians.

Propellants

In 2009, the FDA banned the use of inhalers that use chlorofluorocarbons (CFC) as propellants. In their place, inhalers now use hydrofluorocarbons (HFCs), which are also called hydrofluoroalkanes (HFAs). HFCs are greenhouse gases, but do not deplete the ozone layer. While some people with asthma and advocacy groups contend that HFC inhalers are not as effective, published clinical studies indicate CFC and HFC inhalers are equally effective in controlling asthma.

While the impact of CFCs from inhalers on the ozone layer had been minuscule (dwarfed by industrial processes using CFCs), the FDA in its interpretation of the Montreal Protocol mandated the switch in propellants. Patients expressed concern about the high price of the HFA inhalers as there were initially no generic versions, whereas generic CFC inhalers had been available.

Proper use

It is important to use proper techniques when administering medications through inhalers.

Proper use of inhalers often involves initial deep breathing (which involves mostly the diaphragm's movements), and then rapid breathing (which involves most of the muscles of respiration, such as external and internal intercostal muscles) during intake of one or more puffs from the inhalers.

Improper use of inhalers is very common, can lead to distribution of the medicine into the mouth or throat where it cannot create its desired effect and may cause harm. Education on the correct use of inhalers for delivery of medications is a commonly cited topic in medical studies and a great deal of thought has been put into how best to help people learn to use their inhalers effectively. Below is a description of proper inhaler technique for each different type of inhaler as well as a helpful video explaining what the text states.

Meter-dosed inhalers

1. The mouthpiece is removed and the inhaler is shaken for 5–10 seconds.
2. The inhaler is gripped with mouthpiece on the bottom and canister on top. A finger is placed on the canister to allow for delivery of medicine.
3. Deep inhalation is done until no more air can be taken into the lungs.
4. Deep exhalation is done until most of the air is out of the lungs.
5. Once deep exhalation is done, mouth is placed over mouthpiece.
6. As the next deep inhalation begins, the canister is pressed down to release the medicine into the lungs.
7. Slow deep breathing is continued and breath is held for 5–10 seconds, keeping the medicine in the lungs for a longer time period and preventing escape of aerosolized form of the medicine.
8. Complete exhalation is done again. If multiple puffs of the medicine have to be taken, steps 1–5 are repeated after waiting for 15–30 seconds.
9. Mouthpiece is replaced.

With spacer

Spacer is placed at the mouthpiece of a meter-dosed inhaler while keeping mouth at the end of the spacer. After pressing the canister of the inhaler, the medicine will linger inside the spacer, allowing for the user of the inhaler to directly absorb medicine into their lungs. Deep breathing is done to be ready for the delivery of the medicine to the lungs; this minimizes need for coordination of breathing with inhaler activation. Cleanage of the spacer regularly with warm soapy water is recommended.

Dry powder inhalers

1. Inhaler medication chamber is prepared (this will be different based on the type of inhaler but will involve preparing and opening the chamber with the medication)
2. The inhaler is held with the chamber pointing towards the patient and complete exhalation is done with their head turned away from the inhaler.
3. Mouth is placed over the chamber and a quick, deep breath is taken allowing medication to dispense in the lungs.
4. Breath is held for 5–10 seconds and then slow exhalation is done.
5. After waiting for a few minutes, steps 1-4 are repeated if another dose is needed.

Soft mist inhalers

1. The inhaler is primed by loading the cartridge and discharging the inhaler until a fine mist is visible (more explanation in the video).
2. Once complete exhalation is done, mouth is placed around the mouthpiece while leaving space for the small holes on the side of the mouthpiece.
3. Slow inhalation is done while simultaneously pressing the button to release the medication.
4. Breath is held for 5–10 seconds.
5. Slow exhalation is done and steps 1-4 are repeated if another dose of medication is required after waiting for a few minutes.

If the inhaler is used every day, it usually has to be primed the first time using a new cartridge, and it may need to be primed again if it has not been used in multiple days.

After use

If using inhaled corticosteroids, one should wash the mouth out directly after use of an inhaler. This helps to prevent mouth infections that can occur due to immunosuppressant effects of corticosteroids.

Nebulizer

1. Mouth is placed over mouthpiece or face mask is placed over nose and mouth
2. The nebulizer machine is turned on.
3. Normal breathing is done for 10-20 min (or time allotted for treatment).
4. Machine is turned off and face mask/mouthpiece remove is removed.

Price and availability

In the United States, pharmaceutical manufacturers use legal and regulatory strategies to keep inhaler prices artificially high. There has been little innovation in inhaler technology for decades — the most recent drug to be approved by the FDA for treating asthma or COPD via a novel target of action was Ipratropium bromide in 1986. Since then, manufacturers have used small changes to drug delivery mechanisms, or have switched active ingredients from one inhaler device to another (a strategy known as a "device hop") to keep patents active. This has the effect of limiting competition, keeping inhalers expensive. Because of high prices, patients sometimes skip doses or give up using their inhalers.

History

The idea of directly delivering medication into the lungs was based on ancient traditional cures that involved the use of aromatic and medicinal vapors. These did not involve any special devices beyond the apparatus used for burning or heating to produce fumes. Early inhalation devices included one devised by John Mudge in 1778. It had a pewter mug with a hole allowing attachment of a flexible tube. Mudge used it for the treatment of coughs using opium. These devices evolved with modifications by Wolfe, Mackenzie (1872) and better mouth attachments such as by Beigel in 1866. Many of these early inhalers needed heat to vaporize the active chemical ingredient. The benefits of forced expiration and inspiration to treat asthma were noted by J. S. Monell in 1865. Chemicals used in inhalers included ammonia, chlorine, iodine, tar, balsams, turpentine camphor and numerous others in combinations. Julius Mount Bleyer used a variation in 1890 in New York.

In 1968, Robert Wexler of Abbott Laboratories developed the Analgizer, a disposable inhaler that allowed the self-administration of methoxyflurane vapor in air for analgesia. The Analgizer consisted of a polyethylene cylinder 5 inches long and 1 inch in diameter with a 1 inch long mouthpiece. The device contained a rolled wick of polypropylene felt which held 15 milliliters of methoxyflurane.

Because of the simplicity of the Analgizer and the pharmacological characteristics of methoxyflurane, it was easy for patients to self-administer the drug and rapidly achieve a level of conscious analgesia which could be maintained and adjusted as necessary over a period of time lasting from a few minutes to several hours. The 15 milliliter supply of methoxyflurane would typically last for two to three hours, during which time the user would often be partly amnesic to the sense of pain; the device could be refilled if necessary.

The Analgizer was found to be safe, effective, and simple to administer in obstetric patients during childbirth, as well as for patients with bone fractures and joint dislocations, and for dressing changes on burn patients. When used for labor analgesia, the Analgizer allows labor to progress normally and with no apparent adverse effect on Apgar scores. All vital signs remain normal in obstetric patients, newborns, and injured patients. The Analgizer was widely utilized for analgesia and sedation until the early 1970s, in a manner that foreshadowed the patient-controlled analgesia infusion pumps of today. The Analgizer inhaler was withdrawn in 1974, but use of methoxyflurane as a sedative and analgesic continues in Australia and New Zealand in the form of the Penthrox inhaler.