词条 | Liquid breathing | |||||||||||
释义 |
}}{{Infobox interventions | Name = Liquid breathing | Image = | Caption = | ICD10 = | ICD9unlinked = | MeshID = D021061 | OPS301 = | OtherCodes = }} Liquid breathing is a form of respiration in which a normally air-breathing organism breathes an oxygen-rich liquid (such as a perfluorocarbon), rather than breathing air. This requires certain physical properties such as respiratory gas solubility, density, viscosity, vapor pressure, and lipid solubility which some, but not all, perfluorochemicals (perfluorocarbon) have.[1] Thus, it is critical to choose the appropriate PFC for a specific biomedical application, such as liquid ventilation, drug delivery or blood substitutes. The physical properties of PFC liquids vary substantially; however, the one common property is their high solubility for respiratory gases. In fact, these liquids carry more oxygen and carbon dioxide than blood.[2] In theory, liquid breathing could assist in the treatment of patients with severe pulmonary or cardiac trauma, especially in pediatric cases. Liquid breathing has also been proposed for use in deep diving[3][4][5] and space travel.[6][7] Despite some recent advances in liquid ventilation, a standard mode of application has not yet been established. Approaches
| footer = Computer models of three perfluorochemical molecules used for biomedical applications and for liquid ventilation studies: a) FC-75, b) perflubron, and c) perfluorodecalin. | align = center | image1 = FC-75 Molecule.png | width1 = {{#expr: (150 * 204 / 288) round 0}} | image2 = Perflubron Molecule.png | width2 = {{#expr: (150 * 288 / 189) round 0}} | image3 = Perfluorodecalin molecule.png | width3 = {{#expr: (150 * 288 / 216) round 0}} }} Because liquid breathing is still a highly experimental technique, there are several proposed approaches. Total liquid ventilationAlthough total liquid ventilation (TLV) with completely liquid-filled lungs can be beneficial,[8] the complex liquid-filled tube system required is a disadvantage compared to gas ventilation—the system must incorporate a membrane oxygenator, heater, and pumps to deliver to, and remove from the lungs tidal volume aliquots of conditioned perfluorocarbon (PFC). One research group led by Thomas H. Shaffer has maintained that with the use of microprocessors and new technology, it is possible to maintain better control of respiratory variables such as liquid functional residual capacity and tidal volume during TLV than with gas ventilation.[1][9][10][11] Consequently, the total liquid ventilation necessitates a dedicated liquid ventilator similar to a medical ventilator except that it uses a breathable liquid. Many prototypes are used for animal experimentation, but experts recommend continued development of a liquid ventilator toward clinical applications.[12] Specific preclinical liquid ventilator (Inolivent) is currently under joint development in Canada and France.[13] The main application of this liquid ventilator is the ultra-fast induction of therapeutic hypothermia after cardiac arrest. This has been demonstrated to be more protective than slower cooling method after experimental cardiac arrest.[14] Partial liquid ventilationIn contrast, partial liquid ventilation (PLV) is a technique in which a PFC is instilled into the lung to a volume approximating functional residual capacity (approximately 40% of total lung capacity). Conventional mechanical ventilation delivers tidal volume breaths on top of it. This mode of liquid ventilation currently seems technologically more feasible than total liquid ventilation, because PLV could utilise technology currently in place in many neonatal intensive-care units (NICU) worldwide. The influence of PLV on oxygenation, carbon dioxide removal and lung mechanics has been investigated in several animal studies using different models of lung injury.[15] Clinical applications of PLV have been reported in patients with acute respiratory distress syndrome (ARDS), meconium aspiration syndrome, congenital diaphragmatic hernia and respiratory distress syndrome (RDS) of neonates. In order to correctly and effectively conduct PLV, it is essential to
If PFC liquid is not maintained in the lung, PLV can not effectively protect the lung from biophysical forces associated with the gas ventilator. New application modes for PFC have been developed.[16] Partial liquid ventilation (PLV) involves filling the lungs with a fluid. This fluid is perfluorocarbon, also called Liquivent or Perflubron. The liquid has some unique properties. It has a very low surface tension, similar to surfactant, a substance that is produced in the lungs to prevent the alveoli from collapsing and sticking together during exhalation. It also has a high density, oxygen readily diffuses through it, and it may have some anti-inflammatory properties. In PLV, the lungs are filled with the liquid, the patient is then ventilated with a conventional ventilator using a protective lung ventilation strategy. This is called partial liquid ventilation. The hope is that the liquid will help the transport of oxygen to parts of the lung that are flooded and filled with debris, help remove this debris and open up more alveoli improving lung function. The study of PLV involves comparison to protocolized ventilator strategy designed to minimize lung damage.[17][18] PFC vaporVaporization of perfluorohexane with two anesthetic vaporizers calibrated for perfluorohexane has been shown to improve gas exchange in oleic acid-induced lung injury in sheep.[19]Predominantly PFCs with high vapor pressure are suitable for vaporization. Aerosol-PFCWith aerosolized perfluorooctane, significant improvement of oxygenation and pulmonary mechanics was shown in adult sheep with oleic acid-induced lung injury. In surfactant-depleted piglets, persistent improvement of gas exchange and lung mechanics was demonstrated with Aerosol-PFC.[20] The aerosol device is of decisive importance for the efficacy of PFC aerosolization, as aerosolization of PF5080 (a less purified FC77) has been shown to be ineffective using a different aerosol device in surfactant-depleted rabbits. Partial liquid ventilation and Aerosol-PFC reduced pulmonary inflammatory response.[21] Proposed usesDivingGas pressure increases with depth, rising 1 bar ({{convert|14.5|psi|kPa|abbr=on}}) every 10 meters to over 1,000 bar at the bottom of the Mariana Trench. Diving becomes more dangerous as depth increases, and deep diving presents many hazards. All surface-breathing animals are subject to decompression sickness, including aquatic mammals[22] and free-diving humans (see taravana). Breathing at depth can cause nitrogen narcosis and oxygen toxicity. Holding the breath while ascending after breathing at depth can cause air embolisms, burst lung, and collapsed lung. Special breathing gas mixes such as trimix or heliox ameliorate the risk of decompression illness but do not eliminate it. Heliox further eliminates the risk of nitrogen narcosis but introduces the risk of helium tremors below about {{convert|500|ft|m}}. Atmospheric diving suits maintain body and breathing pressure at 1 bar, eliminating most of the hazards of descending, ascending, and breathing at depth. However, the rigid suits are bulky, clumsy, and very expensive. Liquid breathing offers a third option,[3][23] promising the mobility available with flexible dive suits and the reduced risks of rigid suits. With liquid in the lungs, the pressure within the diver's lungs could accommodate changes in the pressure of the surrounding water without the huge gas partial pressure exposures required when the lungs are filled with gas. Liquid breathing would not result in the saturation of body tissues with high pressure nitrogen or helium that occurs with the use of non-liquids, thus would reduce or remove the need for slow decompression. A significant problem, however, arises from the high viscosity of the liquid and the corresponding reduction in its ability to remove CO2.[3][24] All uses of liquid breathing for diving must involve total liquid ventilation (see above). Total liquid ventilation, however, has difficulty moving enough liquid to carry away CO2, because no matter how great the total pressure is, the amount of partial CO2 gas pressure available to dissolve CO2 into the breathing liquid can never be much more than the pressure at which CO2 exists in the blood (about 40 mm of mercury (Torr)).[24] At these pressures, most fluorocarbon liquids require about 70 mL/kg minute-ventilation volumes of liquid (about 5 L/min for a 70 kg adult) to remove enough CO2 for normal resting metabolism.[25] This is a great deal of fluid to move, particularly as liquids are more viscous and denser than gases, (for example water is about 850 times the density of air[26]). Any increase in the diver's metabolic activity also increases CO2 production and the breathing rate, which is already at the limits of realistic flow rates in liquid breathing.[3][27][28] It seems unlikely that a person would move 10 liters/min of fluorocarbon liquid without assistance from a mechanical ventilator, so "free breathing" may be unlikely. However, it has been suggested that a liquid breathing system could be combined with a CO2 scrubber connected to the diver's blood supply; a US patent has been filed for such a method.[29][30] Medical treatmentIn order to explore drug delivery techniques that would be useful for both partial and total liquid ventilation, more recent studies have focused on PFC drug delivery using a nanocrystal suspension. The first image is a computer model of a PFC liquid (perflubron) combined with gentamicin molecules. The second image shows experimental results comparing both plasma and tissue levels of gentamicin after an intratracheal (IT) and intravenous (IV) dose of 5 mg/kg in a newborn lamb during gas ventilation. Note that the plasma levels of the IV dose greatly exceed the levels of the IT dose over the 4 hour study period; whereas, the lung tissue levels of gentamicin when delivered by an intratracheal (IT) suspension, uniformly exceed the intravenous (IV) delivery approach after 4 hours. Thus, the IT approach allows more effective delivery of the drug to the target organ while maintaining a safer level systemically. Both images represent the in-vivo time course over 4 hours. Numerous studies have now demonstrated the effectiveness of PFC liquids as a delivery vehicle to the lungs.[44][45][46][47][48][49][50][51][52][53] Clinical trials with premature infants, children and adults were conducted. Since the safety of the procedure and the effectiveness were apparent from an early stage, the US Food and Drug Administration (FDA) gave the product "fast track" status (meaning an accelerated review of the product, designed to get it to the public as quickly as is safely possible) due to its life-saving potential. Clinical trials showed that using perflubron with ordinary ventilators improved outcomes as much as using high frequency oscillating ventilation (HFOV). But because perflubron was not better than HFOV, the FDA did not approve perflubron, and Alliance is no longer pursuing the partial liquid ventilation application. Whether perflubron would improve outcomes when used with HFOV or has fewer long-term consequences than HFOV remains an open question. In 1996 Mike Darwin and Steven B. Harris proposed using cold liquid ventilation with perfluorocarbon to quickly lower the body temperature of victims of cardiac arrest and other brain trauma to allow the brain to better recover.[54] The technology came to be called gas/liquid ventilation (GLV), and was shown able to achieve a cooling rate of 0.5 °C per minute in large animals.[55] It has not yet been tried in humans. Most recently, hypothermic brain protection has been associated with rapid brain cooling. In this regard, a new therapeutic approach is the use of intranasal perfluorochemical spray for preferential brain cooling.[56] The nasopharyngeal (NP) approach is unique for brain cooling due to anatomic proximity to the cerebral circulation and arteries. Based on preclinical studies in adult sheep, it was shown that independent of region, brain cooling was faster during NP-perfluorochemical versus conventional whole body cooling with cooling blankets. To date, there have been four human studies including a completed randomized intra-arrest study (200 patients).[57][58] Results clearly demonstrated that prehospital intra-arrest transnasal cooling is safe, feasible and is associated with an improvement in cooling time. Space travelLiquid immersion provides a way to reduce the physical stress of G forces. Forces applied to fluids are distributed as omnidirectional pressures. Because liquids cannot be practically compressed, they do not change density under high acceleration such as performed in aerial maneuvers or space travel. A person immersed in liquid of the same density as tissue has acceleration forces distributed around the body, rather than applied at a single point such as a seat or harness straps. This principle is used in a new type of G-suit called the Libelle G-suit, which allows aircraft pilots to remain conscious and functioning at more than 10 G acceleration by surrounding them with water in a rigid suit. Acceleration protection by liquid immersion is limited by the differential density of body tissues and immersion fluid, limiting the utility of this method to about 15 to 20 G.[59] Extending acceleration protection beyond 20 G requires filling the lungs with fluid of density similar to water. An astronaut totally immersed in liquid, with liquid inside all body cavities, will feel little effect from extreme G forces because the forces on a liquid are distributed equally, and in all directions simultaneously. However effects will be felt because of density differences between different body tissues, so an upper acceleration limit still exists. Liquid breathing for acceleration protection may never be practical because of the difficulty of finding a suitable breathing medium of similar density to water that is compatible with lung tissue. Perfluorocarbon fluids are twice as dense as water, hence unsuitable for this application.[2] Examples in fiction{{Refimprove section|date=January 2013}}Literary works
Movies and series
Video games
See also
References1. ^1 {{Cite journal| last1 = Shaffer | first1 = Thomas H.| last2 = Wolfson | first2 = Marla R.| last3 = Clark | first3 = Leland C.| doi = 10.1002/ppul.1950140208| title = Liquid ventilation| journal = Pediatric Pulmonology| volume = 14| issue = 2| pages = 102–109|date=October 1992| pmid = 1437347}} 2. ^1 {{Cite journal| last1 = Gabriel | first1 = J. L.| last2 = Miller Jr | first2 = T. F.| last3 = Wolfson | first3 = M. R.| last4 = Shaffer | first4 = T. H.| title = Quantitative structure-activity relationships of perfluorinated hetero-hydrocarbons as potential respiratory media: application to oxygen solubility, partition coefficient, viscosity, vapor pressure, and density| journal = ASAIO Journal| volume = 42| issue = 6| pages = 968–973| year = 1996| pmid = 8959271| url = http://journals.lww.com/asaiojournal/Abstract/1996/42060/Quantitative_Structure_Activity_Relationships_of.9.aspx | doi=10.1097/00002480-199642060-00009}} 3. ^1 2 3 {{cite book |title=The Feasibility of Liquid Breathing in Man. |author=Kylstra JA |year=1977 |volume=Report to the US Office of Naval Research |publisher=Duke University |location=Durham, NC |url=http://archive.rubicon-foundation.org/4257 |accessdate=2008-05-05 }} 4. ^{{cite web |url=http://davidszondy.com/future/underwater/menfish.htm |title=menfish |accessdate=2008-05-17 |website= |deadurl=yes |archiveurl=https://web.archive.org/web/20080516182627/http://www.davidszondy.com/future/underwater/menfish.htm |archivedate=2008-05-16 |df= }} 5. ^Featured on the ABC television program That's Incredible, including a demonstration of a mouse surviving a prolonged dunking in perflourocarbon. 6. ^{{cite web|url=http://www.experiencefestival.com/a/Liquid_breathing_-_Medical_uses/id/1580110 |title=Liquid Breathing - Medical uses |accessdate=2008-05-17 |format= |website= |deadurl=yes |archiveurl=https://web.archive.org/web/20100415002959/http://www.experiencefestival.com/a/Liquid_breathing_-_Medical_uses/id/1580110 |archivedate=2010-04-15 |df= }} 7. ^Featured on the ABC television program That's Incredible. Cathy Lee Crosby describing diving and spaceflight applications. Voiceover with stock video. 8. ^{{cite journal | year = 2008 | title = Multicenter comparative study of conventional mechanical gas ventilation to tidal liquid ventilation in oleic acid injured sheep | url = | journal = | volume = 54 | issue = 3| pages = 236–269 |last1= Wolfson }} 9. ^{{cite journal | author = Cox CA, Stavis RL. Wolfson MR, Shaffer TH | year = 2003 | title = Long-term tidal liquid ventilation in premature lambs: Physiologic, biochemical and histological correlates | url = | journal = Biol. Neonate | volume = 84 | issue = 3| pages = 232–242 | doi=10.1159/000072307| pmid = 14504447 | last2 = Stavis | last3 = Wolfson | last4 = Shaffer }} 10. ^{{cite journal |last1= Libros |first1= R |last2= Philips |first2= CM |last3= Wolfson |first3= MR |last4= Shaffer |first4= TH | year = 2000 | title = A perfluorochemical loss/restoration (L/R) system for tidal liquid ventilation | url = | journal = Biomed Instrum & Technol | volume = 34 | issue = 5| pages = 351–360 }} 11. ^{{cite journal |last1= Heckman |first1= JL |last2= Hoffman |first2= J |last3= Shaffer |first3= TH |last4= Wolfson |first4= MR | year = 1999 | title = Software for real-time control of a tidal liquid ventilator | url = | journal = Biomedical Instrumentation & Technology | volume = 33 | issue = 3| pages = 268–276 }} 12. ^{{cite journal |first1= ML |last1= Costantino |first2= P |last2= Micheau |first3= TH |last3= Shaffer |first4= S |last4= Tredici |first5= MR |last5= Wolfson |displayauthors= 4| title = Clinical design functions: Round table discussions on bioengineering of liquid ventilators| journal = Asaio J. | volume = 55 | issue = 3 | year = 2009 | pages = 206–8 | url = http://journals.lww.com/asaiojournal/Abstract/2009/05000/Clinical_Design_Functions__Round_Table_Discussions.4.aspx | doi = 10.1097/MAT.0b013e318199c167 | pmid = 19282746 | author6 = 6th Internationl Symposium on Perfluorocarbon Application Liquid Ventilation}} 13. ^{{Cite web | url=http://www.inolivent.ca/?lang=en | title=Inolivent}} 14. ^{{cite journal |vauthors=Kohlhauer M, Lidouren F, Remy-Jouet I, Mongardon N, Adam C, Bruneval P, Hocini H, Levy Y, Blengio F, Carli P, Vivien B, Ricard JD, Micheau P, Walti H, Nadeau M, Robert R, Richard V, Mulder P, Maresca D, Demené C, Pernot M, Tanter M, Ghaleh B, Berdeaux A, Tissier R | year = 2015 | title = Hypothermic Total Liquid Ventilation Is Highly Protective Through Cerebral Hemodynamic Preservation and Sepsis-Like Mitigation After Asphyxial Cardiac Arrest | url = https://zenodo.org/record/895839/files/article.pdf| journal = Crit. Care Med. | volume = 43| issue = 10| pages = 420–30 | doi=10.1097/CCM.0000000000001160| pmid = 26110489}} 15. ^{{cite journal| title = Survival of mammals breathing organic liquids equilibrated with oxygen at atmospheric pressure| last = Clark| first = LC| authorlink = Leland Clark| last2 = Gollan| first2 = F| journal = Science| year = 1966| volume = 152| pages = 1755–6| doi = 10.1126/science.152.3730.1755| pmid = 5938414| issue = 3730| bibcode = 1966Sci...152.1755C}} 16. ^{{cite journal|quote= A significant positive step was the use of PFC-associated gas exchange, now termed partial liquid ventilation (PLV). |last1= Hlastala |first1= MP |first2= JE |title=Perfluorocarbon Enhanced Gas Exchange: The easy way|last2= Souders| journal=American Journal of Respiratory and Critical Care Medicine|date= July 1, 2001 |volume= 164|pages=1–2|url=http://ajrccm.atsjournals.org/cgi/content/full/164/1/1/|pmid= 11435228|issue= 1|doi=10.1164/ajrccm.164.1.2104021a}} 17. ^{{cite journal |last1=Hirschl |first1=RB |last2=Pranikoff |first2=T |last3=Wise |first3=C |last4=Overbeck |first4=MC |last5=Gauger |first5=P |last6=Schreiner |first6=RJ |last7=Dechert |first7=R |last8=Bartlett |first8=RH |displayauthors= 4 |year=1996 |title= Initial experience with partial liquid ventilation in adult patients With the acute respiratory distress syndrome |journal=JAMA |volume=275 |issue=5 |pages=383–389 |doi=10.1001/jama.1996.03530290053037}} 18. ^{{cite journal|last1=Verbrugge |first1=SJC |last2=Lachmann |first2=B |date=September 1, 1997 |title=Partial liquid ventilation |journal=European Respiratory Journal |volume=10 |issue=9 |pages=1937–9 |doi=10.1183/09031936.97.10091937 |pmid=9311481 |url=http://www.ersj.org.uk/content/10/9/1937.full.pdf }}{{dead link|date=November 2016 |bot=InternetArchiveBot |fix-attempted=yes }} (editorial) 19. ^"Vaporization is a new application technique for perfluorocarbon that significantly improved oxygenation and pulmonary function in oleic acid-induced lung injury."{{cite journal| title = Vaporized perfluorocarbon improves oxygenation and pulmonary function in an ovine model of acute respiratory distress syndrome| author = Bleyl JU| journal = Anesthesiology| year = 1999| volume = 91| pages = 340–2| doi = 10.1097/00000542-199908000-00021| pmid = 10443610| issue = 2| display-authors = 1| last2 = Ragaller| first2 = Maximilian| last3 = Tscho| first3 = Uwe| last4 = Regner| first4 = Mike| last5 = Kanzow| first5 = Maria| last6 = Hubler| first6 = Matthias| last7 = Rasche| first7 = Stefan| last8 = Albrecht| first8 = Michael}} 20. ^{{Cite journal| last1 = Kandler | first1 = Michael A.| last2 = Von Der Hardt | first2 = Katharina| last3 = Schoof | first3 = Ellen| last4 = Dötsch | first4 = Jörg R.| last5 = Rascher | first5 = Wolfgang| title = Persistent Improvement of Gas Exchange and Lung Mechanics by Aerosolized Perfluorocarbon| journal = American Journal of Respiratory and Critical Care Medicine| volume = 164| issue = 1| pages = 31–35| year = 2001| pmid = 11435235| quote = Aerosolized perfluorocarbon improved pulmonary gas exchange and lung mechanics as effectively as PLV did in surfactant-depleted piglets, and the improvement was sustained longer. | doi=10.1164/ajrccm.164.1.2010049}} 21. ^{{Cite journal| last1 = Von Der Hardt | first1 = Katharina| last2 = Schoof | first2 = Ellen| last3 = Kandler | first3 = Michael A.| last4 = Dötsch | first4 = Jörg R.| last5 = Rascher | first5 = Wolfgang| title = Aerosolized Perfluorocarbon Suppresses Early Pulmonary Inflammatory Response in a Surfactant-Depleted Piglet Model| doi = 10.1203/00006450-200202000-00009| journal = Pediatric Research| volume = 51| issue = 2| pages = 177–182| year = 2002| pmid = 11809911| quote = In a surfactant-depleted piglet model, aerosol therapy with perfluorocarbon but not LV-PLV reduces the initial pulmonary inflammatory reaction at least as potently as PLV at FRC volume. }} 22. ^{{cite journal |last=Lippsett |first=Lonny |title=Even Sperm Whales Get the Bends |journal=Oceanus |volume=44 |issue=1 |date=5 April 2005 |url=http://www.whoi.edu/oceanus/viewArticle.do?id=4720 |archiveurl=https://web.archive.org/web/20100605043855/http://www.whoi.edu/oceanus/viewArticle.do?id=4720 |archivedate=5 June 2010 |accessdate=3 August 2010 |deadurl=yes |df= }} 23. ^{{cite journal |author=Kylstra JA |title=Liquid breathing |journal=Undersea Biomed Res |volume=1 |issue=3 |pages=259–69 |date=September 1974 |pmid=4619862 |url=http://archive.rubicon-foundation.org/2665 |accessdate=2008-05-05 }} 24. ^1 {{cite journal |vauthors=Matthews WH, Kylstra JA |title=A fluorocarbon emulsion with a high solubility for CO2 |journal=Undersea Biomed Res |volume=3 |issue=2 |pages=113–20 |date=June 1976 |pmid=951821 |doi= |url=http://archive.rubicon-foundation.org/2764 |accessdate=2008-05-05 }} 25. ^{{cite journal |author1=Miyamoto Y. |author2=Mikami T. | year = 1976 | title = Maximum capacity of ventilation and efficiency of gas exchange during liquid breathing in guinea pigs | url = | journal = Jpn. J. Physiol. | volume = 26 | issue = 6| pages = 603–618 | pmid = 1030748 | doi = 10.2170/jjphysiol.26.603 }} 26. ^{{Cite book | last1 = Sherwood | first1 = Lauralee | last2 = Klandorf | first2 = Hillar | last3 = Yancey | first3 = Paul H. | year = 2005 | title = Animal Physiology: From Genes to Organisms | isbn = 978-0-534-55404-0 | publisher = Thomson/Brooks/Cole | location = Southbank, Victoria, Australia | oclc = 224468651 }} 27. ^{{cite journal |author1=Koen P. A. |author2=Wolfson M. R. |author3=Shaffer T. H. | year = 1988 | title = Fluorocarbon ventilation: maximal expiratory flows and CO2 elimination | url = | journal = Pediatr. Res. | volume = 24 | issue = 3| pages = 291–296 | pmid = 3145482 | doi=10.1203/00006450-198809000-00003}} 28. ^{{cite journal |vauthors=Matthews WH, Balzer RH, Shelburne JD, Pratt PC, Kylstra JA |title=Steady-state gas exchange in normothermic, anesthetized, liquid-ventilated dogs |journal=Undersea Biomed Res |volume=5 |issue=4 |pages=341–54 |date=December 1978 |pmid=153624 |url=http://archive.rubicon-foundation.org/2818 |accessdate=2008-05-05 }} 29. ^{{cite news|last1=Taylor|first1=Jerome|title=Into the abyss: The diving suit that turns men into fish|url=https://www.independent.co.uk/news/science/into-the-abyss-the-diving-suit-that-turns-men-into-fish-2139167.html|accessdate=20 October 2015|agency=The Independent|issue=20 November 2010|publisher=Independent Print Ltd|date=20 November 2010}} 30. ^Artificial gills for deep diving without incurring the bends and for scavenging O2 from and dispelling CO2 into water or thin air US Patent #8,631,788, published 21 Jan 2014. 31. ^{{cite journal|last1=Wolfson |title=Perfluorochemical rescue after surfactant treatment: Effect of perflubron dose and ventilatory frequency |journal=J Appl Physiol |volume=84 |issue=2 |pages=624–640 |year=1998 |url=http://www.jappl.org/content/84/2/624.short |archive-url=https://archive.is/20130415094058/http://www.jappl.org/content/84/2/624.short |dead-url=yes |archive-date=2013-04-15 |pmid=9475875 |first1=MR |first2=NE |last2=Kechner |last3=Roache |first3=RF |last4=Dechadarevian |first4=JP |last5=Friss |first5=HE |last6=Rubenstein |first6=SD |last7=Shaffer |first7=TH |displayauthors=4 |doi=10.1152/jappl.1998.84.2.624 }} 32. ^{{Cite journal| last1 = Stavis | first1 = RL| last2 = Wolfson | first2 = MR| last3 = Cox | first3 = C| last4 = Kechner | first4 = N| last5 = Shaffer | first5 = TH| title = Physiologic, biochemical, and histologic correlates associated with tidal liquid ventilation| doi = 10.1203/00006450-199801000-00020| journal = Pediatric Research| volume = 43| issue = 1| pages = 132–138|date=January 1998| pmid = 9432124}} 33. ^{{Cite journal |last1=Wolfson |first1=MR |last2=Shaffer |first2=TH |doi=10.1016/j.prrv.2005.03.010 |title=Pulmonary applications of perfluorochemical liquids: Ventilation and beyond |journal=Paediatric Respiratory Reviews |volume=6 |issue=2 |pages=117–127 |date=June 2005 |pmid=15911457 |url=http://cryoeuro.eu:8080/download/attachments/425990/LVandBeyondSchaffer.pdf |deadurl=yes |archiveurl=https://web.archive.org/web/20131217091530/http://cryoeuro.eu:8080/download/attachments/425990/LVandBeyondSchaffer.pdf |archivedate=2013-12-17 |df= }} 34. ^{{cite journal |title=Liquid ventilation of preterm baby |journal=The Lancet |volume=2 |issue=8671 |pages=1095 |year=1989 |pmid=2572810 |doi=10.1016/S0140-6736(89)91101-X |last1= Greenspan |first1= JS |last2= Wolfson |first2= MR |last3= Rubenstein |first3= SD |last4= Shaffer |first4= TH}} 35. ^{{cite journal |last1=Greenspan |first1= JS |last2= Wolfson |first2= MR |last3= Rubenstein |first3= SD |last4= Shaffer |first4= TH |title=Liquid ventilation of human preterm neonates |journal=The Journal of Pediatrics |volume=117 |issue=1 Pt 1 |pages=106–11 |date= July 1990 |pmid=2115078 |doi= 10.1016/S0022-3476(05)82457-6|url=}} 36. ^{{cite journal |last1=Leach |first1= CL |last2= Greenspan |first2= JS |last3= Rubenstein |first3= SD |last4= Shaffer |first4= TH |last5= Wolfson |first5= MR |last6= Jackson |first6= JC |last7= DeLemos |first7= R |last8= Fuhrman |first8= BP |displayauthors= 4 |title=Partial liquid ventilation with perflubron in premature infants with severe respiratory distress syndrome. The LiquiVent Study Group |journal=The New England Journal of Medicine |volume=335 |issue=11 |pages=761–7 |date=September 1996 |pmid=8778584 |doi=10.1056/NEJM199609123351101 |url=}} 37. ^{{cite journal |last1= Greenspan |first1= JS |last2= Fox |first2= WW |last3= Rubenstein |first3= SD |last4= Wolfson |first4= MR |last5= Spinner |first5= SS |last6= Shaffer |first6= TH | year = 1997 | title = Partial liquid ventilation in critically ill infants receiving extracorporeal life support. Philadelphia Liquid Ventilation Consortium | url = | journal = Pediatrics | volume = 99 | issue = 1| page = E2 | doi=10.1542/peds.99.1.e2 |pmid= 9096170}} 38. ^{{cite journal |last1= Brunelli |first1= L |last2= Hamilton |first2= E |last3= Davis |first3= JM |last4= Koo |first4= HC |last5= Joseph |first5= A |last6= Kazzaz |first6=JA |last7= Wolfson |first7= MR |last8= Shaffer |first8= TH |displayauthors= 4 | year = 2006 | title = Perfluorochemical liquids enhance delivery of superoxide dismutase to the lungs of juvenile rabbits | url = | journal = Pediatr Res | volume = 60 | issue = 1| pages = 65–70 | doi=10.1203/01.pdr.0000219392.73509.70 |pmid= 16690961}} 39. ^{{cite journal |year= 2001 |title= Perfluorochemical liquids modulate cell-mediated inflammatory responses |journal= Critical Care Medicine |volume= 29 |issue= 9 |pages= 1731–7 |pmid= 11546973 |doi=10.1097/00003246-200109000-00013|author1= Nakstad |first1= B |last2= Wolfson |first2= M. R |last3= Shaffer |first3= T. H |last4= Kähler |first4= H |last5= Lindemann |first5= R |last6= Fugelseth |first6= D |last7= Lyberg |first7= T }} 40. ^{{Cite journal| last1 = Ramesh Babu | first1 = PB| last2 = Chidekel | first2 = A| last3 = Shaffer | first3 = TH| doi = 10.1097/01.PCC.0000154944.67042.4F| title = Hyperoxia-induced changes in human airway epithelial cells: The protective effect of perflubron| journal = Pediatric Critical Care Medicine| volume = 6| issue = 2| pages = 188–194|date=March 2005| pmid = 15730607}} 41. ^Brunelli et al. 42. ^{{Cite journal| last1 = Cox | first1 = CA| last2 = Cullen | first2 = AB| last3 = Wolfson | first3 = MR| last4 = Shaffer | first4 = TH| title = Intratracheal administration of perfluorochemical-gentamicin suspension: A comparison to intravenous administration in normal and injured lungs| doi = 10.1002/ppul.1100| journal = Pediatric Pulmonology| volume = 32| issue = 2| pages = 142–151|date=August 2001| pmid = 11477731}} 43. ^{{Cite journal| last1 = Fox | first1 = WW| last2 = Weis | first2 = CM| last3 = Cox | first3 = C| last4 = Farina | first4 = C| last5 = Drott | first5 = H| last6 = Wolfson | first6 = MR| last7 = Shaffer | first7 = TH |displayauthors= 4| title = Pulmonary administration of gentamicin during liquid ventilation in a newborn lamb lung injury model| journal = Pediatrics| volume = 100| issue = 5| pages = E5|date=November 1997| pmid = 9346999 | doi=10.1542/peds.100.5.e5}} 44. ^Wolfson MR, Greenspan JS, Shaffer TH. Pulmonary adminis¬tration of vasoactive substances by perfluorochemical ventilation" Pediatrics 1996;97(4) 449-455. 45. ^Kimless Garber DB, Wolfson MR, Carlsson C, Shaffer TH. Halothane administration during liquid ventila¬tion. Respir Med. 1997; 91(5) 255-262. 46. ^{{cite journal |vauthors=Zelinka MA, Wolfson MR, Calligaro I, Rubenstein SD, Greenspan JS, Shaffer TH | year = 1997 | title = A comparison of intratracheal and intravenous administration of gentamicin during liquid ventilation | url = | journal = Eur J Pediatr | volume = 156 | issue = 5| pages = 401–404 | doi=10.1007/s004310050625}} 47. ^{{cite journal |vauthors=Lisby DA, Ballard PL, Fox WW, Wolfson MR, Shaffer TH, Gonzales LW | year = 1997 | title = Enhanced distribution of adenovirus-mediated gene transfer to lung parenchyma by perfluorochemical liquid | url = | journal = Hum Gene Ther. | volume = 8 | issue = 8| pages = 919–928 | doi=10.1089/hum.1997.8.8-919| pmid = 9195214 }} 48. ^{{cite journal |vauthors=Fox WW, Weis CM, Cox C, Farina C, Drott H, Wolfson MR, Shaffer TH | year = 1997 | title = Pulmonary administration of gentamicin during liquid ventilation in a newborn lamb lung injury model | url = | journal = Pediatrics | volume = 100 | issue = 5| page = E5 | doi=10.1542/peds.100.5.e5 | pmid=9346999}} 49. ^{{cite journal |vauthors=Cullen AB, Cox CA, Hipp SJ, Wolfson MR, Shaffer TH | year = 1999 | title = Intra-tracheal delivery strategy of gentamicin with partial liquid ventilation | url = | journal = Respir Med. | volume = 93 | issue = 11| pages = 770–778 | doi=10.1016/s0954-6111(99)90261-5}} 50. ^{{cite journal |vauthors=Cox CA, Cullen AB, Wolfson MR, Shaffer TH | year = 2001 | title = Intratracheal administration of perfluorochemical-gentamicin suspension: a comparison to intravenous administration in normal and injured lungs | url = | journal = Pediatr Pulmonol | volume = 32 | issue = 2| pages = 142–151 | doi=10.1002/ppul.1100 | pmid=11477731}} 51. ^{{cite journal |vauthors=Chappell SE, Wolfson MR, Shaffer TH | year = 2001 | title = A comparison of surfactant delivery with conventional mechanical ventilation and partial liquid ventilation in meconium aspiration injury | url = | journal = Respir Med. | volume = 95 | issue = 7| pages = 612–617 | doi=10.1053/rmed.2001.1114| pmid = 11453320 }} 52. ^{{cite journal |vauthors=Brunelli L, Hamilton E, Davis JM, Koo HC, Joseph A, Kazzaz JA, Wolfson MR, Shaffer TH | year = 2006 | title = Perfluorochemical liquids enhance delivery of superoxide dismutase to the lungs of juvenile rabbits | url = | journal = Pediatr. Res. | volume = 60 | issue = 1| pages = 65–70 | doi=10.1203/01.pdr.0000219392.73509.70 | pmid=16690961}} 53. ^{{cite journal |vauthors=Constantino ML, Shaffer TH, Wauer RR, Rudiger M | year = 2006 | title = The 5th European Symposium on Perfluorocarbon (PFC) Application | url = | journal = Asaio J. | volume = 52 | issue = 4| pages = 483–494 | doi = 10.1097/00002480-200607000-00021 }} 54. ^{{cite journal| last1= Darwin |first1= MG| title=Liquid ventilation: A bypass on the way to bypass| journal=BPI Tech Briefs| year=1996| volume=19| url=http://www.cryocare.org/index.cgi?subdir=bpi&url=tech19.txt}} 55. ^{{cite journal| last1= Harris |first1= SB| title=Rapid (0.5°C/min) minimally invasive induction of hypothermia using cold perfluorochemical lung lavage in dogs| journal=Resuscitation| year=2001| volume=50| pages=189–204| doi=10.1016/S0300-9572(01)00333-1| pmid=11719148| issue=2| display-authors= 4| last2=Darwin| first2=MG| last3=Russell| first3=SR| last4=O'Farrell| first4=JM| last5=Fletcher| first5=M| last6=Wowk| first6=B}} 56. ^{{cite journal | author = Wolfson| year = 2008 | title = Intranasal perfluorochemical spray for preferential brain cooling in sheep | url = | journal = Neurocrit Care. | volume = 8 | issue = 3| pages = 437–47 | doi=10.1007/s12028-008-9064-0| pmid = 18266110 |display-authors=etal}} 57. ^{{cite journal |vauthors=Castrén M, Nordberg P, Svensson L, etal |date=Aug 2010 | title = Intra-arrest transnasal evaporative cooling: a randomized, prehospital, multicenter study (PRINCE: Pre-ROSC IntraNasal Cooling Effectiveness) | url = | journal = Circulation | volume = 122 | issue = 7| pages = 729–36 | doi=10.1161/circulationaha.109.931691 | pmid=20679548}} 58. ^{{cite journal |vauthors=Busch HJ, Eichwede F, Födisch M, etal |date=Aug 2010 | title = Safety and feasibility of nasopharyngeal evaporative cooling in the emergency department setting in survivors of cardiac arrest | url = | journal = Resuscitation | volume = 81 | issue = 8| pages = 943–9 | doi=10.1016/j.resuscitation.2010.04.027 | pmid=20627524}} 59. ^{{cite book| title = Textbook of Medical Physiology |edition= 7th |chapter= Aviation, Space, and Deep Sea Diving Physiology| last = Guyton| first = Arthur C.| publisher = W. B. Saunders Company| year = 1986| page = 533}} 60. ^{{cite book|last=Westerfeld|first=Scott|year=2003|title=The Risen Empire|isbn=978-0-7653-0555-8|url=https://books.google.com/books?id=XsXmQYq0LiMC&pg=PT23}} 61. ^{{cite book|ref=harv|last=McNeill|first=Graham|year=2008|title=Mechanicum: war comes to Mars|others=Cover art & illustration by Neil Roberts; map by Adrian Wood|series=Horus Heresy|volume=9|publisher=Black Library|location=Nottingham, UK|edition=1st UK|pages=64, 149|isbn=978-1-84416-664-0|authorlink=Graham McNeill}} The {{em|amniotic}} tanks are referenced in several other places in the novel. 62. ^{{cite book|last=van Eekhout|first=Greg|year=2014|title=California Bones|isbn=978-0765328557|url=https://books.google.com/books?id=bMxiAwAAQBAJ}} 63. ^{{cite journal |first=Aljean |last=Harmetz |url=https://www.nytimes.com/1989/08/06/movies/film-the-abyss-a-foray-into-deep-waters.html |title='The Abyss': A Foray Into Deep Waters |newspaper=New York Times |date=August 6, 1989 }} 64. ^{{Cite web | url=https://forums.eveonline.com/default.aspx?g=posts&m=3479925#post3479925 | title=About Capsuleers - EVE Fiction - EVE Online Forums}} External links
7 : Liquids|Underwater diving procedures|Diving equipment|Respiration|University at Buffalo|Medical procedures|Respiratory system procedures |
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