ELECTRONIC ARTICLE |


* Department of Pediatrics, Pennsylvania State College of Medicine, Hershey, Pennsylvania
Baker-Cederberg Museum and Archives, Rochester General Hospital, Rochester, New York
Department of Pediatrics, William Beaumont Hospital, Royal Oak, Michigan
| ABSTRACT |
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Parmalee said that the AL "certainly locks the infant up, safe from meddlesome and unintelligent treatment." When clear plastic versions of the AL became commercially available, it received widespread use in delivery rooms and newborn nurseries throughout the United States. In 1953, Apgar and Kreiselman produced apnea in adult dogs using pentobarbital and a muscle relaxant, and found that the AL device was unsuccessful with the oxygenation and ventilation of the animals.
In 1954, Townsend in Rochester, New York, reported on his experience with the AL in 150 premature infants. He concluded that the AL should be "more accurately referred to as an oxygenator" and that, "the truly apneic infant cannot be maintained in a acyanotic state by the AL." The AL was finally subjected to the scrutiny of a randomized, controlled clinical trial that was published in 1956. Reichelderfer and Nitowski at Johns Hopkins randomized 171 infants to receive care in the AL or in an Isolette. Routine resuscitation, including positive pressure ventilation, was administered, as needed, to both study groups before placement into the AL or Isolette (Air Shields Inc, Hatboro, PA). They did not find any differences in the outcomes of the 2 study groups. By the mid 1950s, new information linking oxygen therapy and retrolental fibroplasia, led to a rapid decline in the use of the AL, even before the publication of the randomized trial.
Key Words: Bloxsom air lock neonatal resuscitation prematurity
Abbreviations: AL, air lock
| DEVELOPMENT OF THE POSITIVE PRESSURE OXYGEN AIR LOCK (AL) DEVICE |
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Bloxsoms positive pressure oxygen AL was designed to replicate the alternating pressure changes produced by the contracting uterus during labor. He constructed his original AL (Fig 1) by sawing an aluminum pressure cooker in half and welding in a center cylinder of sheet aluminum, resulting in a chamber 37 inches in length and 12 inches in diameter. Heating and humidification units and an array of pressure gauges, switches, and motors were added to create what must have been a noisy and frightening juggernaut in the premature nursery. The entire body of a distressed infant was placed into the AL device immediately after delivery, and the cylindrical chamber was infused with humidified 60% oxygen. The pressures within the chamber were then cycled between 1 and 3 lb/in2 at 1-minute intervals to simulate the intrauterine contractions of labor. It is important to point out that Bloxsoms device was not a negative pressure ventilator or an "iron lung" device.
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| UNCONTROLLED TRIALS AND EXPERIENCE WITH THE AL |
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"Dr Bloxsoms method accomplishes at least 2 things that are advantageous to the infant. First, it favors absorption of oxygen through the skin and mucous membranes of the upper respiratory tract, sufficient perhaps to tide the infant over until such time as respirations may spontaneously begin. Second, it certainly locks the infant up, safe from meddlesome and unintelligent treatment."
Dr Robert A. Johnston of Houston remarked that: "With the use of the lock resuscitation, one can dispense, in practically all cases, with the tracheal catheter and its attendant danger."
The medical editor of Newsweek attended that convention and featured the Bloxsom AL, complete with a photograph, in the July 10, 1950 issue.4 This article described the AL as "the Plexiglass Mother" and credited it with a 25% reduction in the infant mortality rate at the St Joseph Infirmary in Houston.
Two years later, Drs John Zelenik and Harry Prystowsky,5 obstetricians at the United States Army Hospital at Fort Benning, Georgia, reported their experience with 153 infants who were placed in the positive pressure oxygen AL between May 23, 1951, and January 12, 1952. They concluded that the AL "was a valuable adjunct in resuscitation and seemed to be lifesaving for the occasional depressed and/or premature infant."
In 1954, Dr Edward (Ted) H. Townsend, Jr,6 a practicing pediatrician and Director of the Regional Premature Center at the Rochester General Hospital in Rochester, New York, reported his experience with 150 infants placed in the AL during the preceding 18 months. He reported that 72 of the treated infants failed to show any demonstrable benefits from the AL device. He pointed out that the AL should be referred to as an "oxygenator" and that "the truly apneic infant cannot be maintained in an acyanotic state by the AL." Based on his studies with the AL, Townsend claimed that:
"The improvement in color is not due to passive diffusion of oxygen into the infants skin because of a higher pressure gradient; it is due to an improvement in general oxygenation of the infant. Proof of this lies in the fact that it is accompanied not only by an improvement in color but also by a reduction in the apparent degree of respiratory distress, which is in turn followed by an improvement in the infants general clinical condition."
In a second paper published a year later, Townsend7 presented detailed clinical descriptions of 9 patients who improved after treatment in the AL. Here, he proposed that the AL was capable of promoting "antiatelectatic action." He attributed the observed clinical improvement to the "ability of the AL to induce expansion of collapsed segments of the pulmonary tissue."
In 1953, Drs Virginia Apgar and Joseph Kreiselman8 from the Department of Anesthesiology at the Columbia University College of Physicians and Surgeons, New York City, reported their laboratory studies with the Bloxsom AL device. They found that the device was ineffective for the resuscitation of adult dogs that were made apneic by the intravenous infusion of pentobarbital. They concluded:
}"Indeed, the condition of any anoxic patient should be improved by placing him in an atmosphere of at least 50% oxygen, under a tension of more than 50 mm Hg above atmospheric pressures. There is no evidence that any improvement in the infants is related to the alternating pressures simulating uterine contractions."
In an article published in 1954, Dr Bloxsom and Sister Mary Angelique9 from the St Josephs Maternity Hospital responded to Dr Apgars evaluation of their device as follows:
"In January 1953, an adverse critical evaluation of the AL from New York City appeared, based on attempts to make the AL function as a barospirator for apneic adult dogs. Such a function, of course, was never intended or claimed for the AL."
They went on to report that the 48-hour mortality rate for term infants delivered at their hospital decreased from 63 per 10 000 in 1949 to 37 per 10 000 in 1952, a 41% reduction. They attributed this decline, in part, to the use of the AL. They also suggested that the AL pressure helped to induce a flattening of the alveolar cuboidal epithelial cells, providing a greater surface for the exchange of O2 and CO2.
Finally, in 1956, 6 years after the introduction of the Bloxsom AL device, a randomized, controlled clinical trail of the device was reported from Johns Hopkins Hospital by Reichelderfer and Nitowsky.10 Seventy-two infants were randomized to the AL and 71 to standard treatment in an Isolette brand of incubator. They found no differences in mortality rates or relief of respiratory distress between the 2 groups.
| EPILOGUE |
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Despite its bulky size and loud noise, the Bloxsom AL was readily accepted by the nurses who were in charge of the many new premature nurseries that were established in the 1950s. For very important reasons of infection control, the premature nursery nurses from that era viewed themselves as the guardians of the fragile preterm infants. Physicians, house officers, and parents were typically locked out of the premature nursery. Thus, these nurses viewed the AL device as an additional barrier with which they could exclude others and protect the fragile infants from "meddlesome treatment."
By the late 1950s, use of the Bloxsom AL rapidly declined, particularly after cases of retrolental fibroplasia were reported in preterm infants and the association between RLF and oxygen therapy was established. There were a few outposts where use of the AL continued into the early 1970s. One small hospital located in the mountains of northern Pennsylvania, for instance, was still using the device in 1972. The only remaining device known to the authors is located at the Medical Museum of the University of Iowa Hospital and Clinics, Iowa City, Iowa. In retrospect, the Bloxsom AL was an anomaly. Its introduction was not based on any previous technology and it did not lead to the development of similar new technological devices for the care of the newborn. However, it did call national attention to the concurrent development of the special care nurseries and their role in the treatment of distressed newborn infants.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Address correspondence to James W. Kendig, MD, Division of Newborn Medicine-H085, Department of Pediatrics, Milton S. Hershey Medical Center, Box 850, Hershey, PA 17033-0850. E-mail: jkendig{at}psu.edu
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