A dissertation submitted to the Faculty of Health Sciences, University of Witwatersrand, Johannesburg, in fulfilment of requirements for the degree of Masters of Science. Johannesburg 2012 / Background: The detrimental effects of prolonged mechanical ventilation (MV) on the respiratory muscles, especially the diaphragm, are well documented and it is crucial that MV should be discontinued as soon as possible to prevent added complications and additional risks to patients with critical illness. The spontaneous breathing stage of MV can be managed as a rehabilitation and conditioning phase for the respiratory muscles due to the fact that the respiratory muscles are more active during this stage of MV. Weaning strategies that provide insufficient respiratory work, too high a respiratory muscle load or insufficient respiratory muscle rest may lead to respiratory muscle fatigue and consequently failed weaning and extubation. The aim of this research project was to develop an individualised continuous positive airway pressure (CPAP) weaning programme and test its effects on the outcomes of extubation in the adult ventilated patient. Method: An experimental, prospective, non-randomised, sequential study of two groups of subjects was performed. Forty eight subjects [group one: n =24 (control) and group two: n = 24 (intervention)], who were mechanically ventilated for longer than 48 hours, in an open adult, general intensive care unit were recruited. Subjects in the control group were weaned according to the standard weaning programme of the test setting at the time; and those in the intervention group were weaned according to an individualised CPAP programme. This weaning programme was developed utilising three principles of muscle rehabilitation namely; daily stepwise progression, sufficient rest and recovery periods and adapted to the individual needs and progression of each subject. Objective measurements such as the rapid shallow breathing index (RSBI), RSBI rate and the maximum inspiratory pressure (MIP) were used to determine the subjects in group two’s readiness for a spontaneous breathing trial. The primary outcomes assessed were time spent in the different stages of MV, rate of failure to sustain spontaneous breathing in stage 3 of MV, successful extubation and mortality rate. Results and Discussion: The difference in rate of failure to sustain spontaneous breathing between the two groups was statistically significant (p = 0.01) with 10 events of failure in group one and three in group two. The rate of successful extubation from MV between groups one and two was 70.8% and 91.7% iv respectively (p=0.52). The mortality rate was 33.3% for group one and 8.3% for group two (p = 0.02). The difference in the total time spent on MV (days) did not differ significantly (group one = 8.6 (± 0.40) days; group two = 9.3 (±0.32) days; p = 0.75). The results yielded from this study suggest that the use of a multidisciplinary team model and an individualised CPAP programme aids successful extubation from MV as the success rate was much higher in the intervention group than in the control group without adding additional time on MV. Conclusion: Results from this study showed that the implementation of an individualised CPAP programme during the spontaneous breathing stage of MV may improve the outcomes of extubation in adult ventilated patients.

No description available.

No description available.

With the rapid somatic growth and development in infants, simultaneous accurate measurements of lung volume and airway function are essential. Raised volume rapid thoracoabdominal compression (RTC) is widely used to generate forced expiration from an airway opening pressure of 30 cmH2O (V30). The (dynamic) functional residual capacity (FRCdyn) remains the lung volume most routinely measured. The aim of this study was to develop comprehensive integrated spirometry that included all subdivisions of lung volume at V30 or total lung capacity (TLC30). Measurements were performed on 17 healthy infants aged 8.6-119.7 weeks. A commercial system for multiple-breath nitrogen washout (MBNW) to measure lung volumes and a custom made system to perform RTC were used in unison. A refined automated raised volume RTC and the following two novel single maneuvers with dual volume measurements were performed from V30 during a brief post-hyperventilation apneic pause: (1) the passive expiratory flow was integrated to produce the inspiratory capacity (IC) and the static (passive) FRC (FRCst) was estimated by initiating MBNW after end-passive expiration; (2) RTC was initiated late during passive expiration, flow was integrated to produce the slow vital capacity (jSVC) and the residual volume (RV) was measured by initiating MBNW after end-expiration while the jacket (j) was inflated. Intrasubject FRCdyn and FRCst measurements overlapped (p = 0.6420) but neither did with the RV (p < 0.0001). Means (95% confidence interval) of FRCdyn, IC, FRCst, jSVC, RV, forced vital capacity and tidal volume were 21.2 (19.7-22.7), 36.7 (33.0-40.4), 21.2 (19.6-22.8), 40.7 (37.2-44.2), 18.1 (16.6-19.7), 40.7 (37.1-44.2) and 10.2 (9.6-10.7) ml/kg, respectively. Static lung volumes and capacities at V30 and variables from the best forced expiratory flow-volume curve were dependent on age, body length and weight. In conclusion, we developed a comprehensive physiologically integrated approach for in-depth investigation of lung function at V30 in infants.

Astma är en kronisk inflammatorisk sjukdom som leder till obstruktion av luftvägarna. Cirka 10% av Sveriges befolkning är diagnostiserade med astma och intresset av icke-farmakologisk behandling är stort. En sådan behandling är inspiratorisk muskelträning. Syftet med den här systematiska litteraturstudien är att kritiskt granska kvaliteten av vetenskaplig litteratur samt undersöka det vetenskapliga underlaget för effekten av inspiratorisk muskelträning (IMT) på styrka i andningsmuskulatur, pulmonell funktion och symtombild utifrån funktionell kapacitet, dyspné och livskvalitet hos astmatiker.  Artikelsökningen utfördes i PubMed och Cinahl, urvalsprocessen utgick från förbestämda inklusionskriterier baserade på PRISMA guidelines. Utifrån 23 sökträffar i databas och 7 träffar genom manuell sökning i referenslistor inkluderades 9 artiklar i kvalitetsgranskningen. Studierna kvalitetsgranskades enligt PEDro skalan individuellt av författarna innan gemensam bedömning gjordes. Resultatet jämfördes med granskningen av databasen PEDro.  I kvalitetsgranskningen bedömdes tre artiklar vara av medelhög kvalitet, resterande sex hade en hög kvalitet. Samtliga artiklar som bedömde utfallsmåttet muskelstyrka visade signifikant ökning efter IMT. Signifikant ökning av pulmonell funktion fann två av nio inkluderade artiklar. Funktionell kapacitet, dyspné och livskvalitet utvärderades i fåtal inkluderade studier, majoriteten visade signifikanta förbättringar.  IMT ensamt eller kombinerat med annan behandling kan ha gynnsamma effekter för personer med astma framförallt för inspiratorisk muskelstyrka. Ytterligare forskning krävs för slutsatser kring interventionens effekt på pulmonell funktion och symtombild. Det sammantagna forskningsunderlaget kan anses begränsat men av relativt hög kvalitét. De positiva effekterna antyder visst vetenskapligt stöd för IMT vid astma. För framtida forskning föreslås mer standardiserade metoder, träningsinstrument, dosering för IMT och beskrivning av deltagarnas träningsnivå och astmatyp.

Our study focuses on the connection between existence of a punctum fixum (or point of support) and respiratory muscle strength. Respiratory muscles execute both respiratory and postural function. Therefore, their strength defines both of these functions. We summarize contemporary knowledge about respiratory and postural functions of the respiratory muscles, their interactions and the connection to postural stability. We used a spirometry assesment of maximal respiratory pressures (PImax and PEmax). The values of PImax (PEmax respectively) retrieved in stance and during water immersion without stable support were compared. We found statistically significant differences. PImax was lower in the water immersion situation (p=0,0009; p≤0,05) and so was PEmax (p=0,0076; p≤0,05). Regarding the results, we suppose a significant influence of punctum fixum presence/absence on maximal respiratory muscle strength. Possible reasons are discussed.

Bibliographic identification HAVLIŠTOVÁ, Michaela. Respiratory physiotherapy affects the quality of life of children with SMA - how, when and why? Prague: Charles University, 2nd Faculty of Medicine, Department of rehabilitation and sport medicine, 2012. 81 p. Supervisor Doc. PaedDr. Libuše Smolíková, Ph. D. Annotation This thesis deals with the influence respiratory function in children with spinal muscular atrophy (SMA). The theoretical part provides an overview of respiratory physiotherapy techniques that can be used in the care of the airways in people with SMA. The practical part deals with the question whether it is possible using the selected techniques of respiratory physiotherapy after six weeks of training to affect ventilatory parameters in children with SMA. The group of six probands with SMA I. - III. type in the range of the age from 3.5 to 12 years participated in this study. To objectively assess changes was performed spirometry efore the beginning of the therapy and after its conclusion. The main therapy was daily training with inspiratory breath simulator CliniFlo. After the finishing of therapy there was a positive change in all measured parameters except for vital capacity (VC) and maximal expiratory flow at 75% of FVC (MEF75), where the values didn't change. Statistically significant...

Pacientes com insuficiência cardíaca (IC) podem apresentar fraqueza da musculatura inspiratória. O treinamento da musculatura inspiratória (TMI) vem sendo utilizado nesta população para melhorar a capacidade cardiorrespiratória, porém, não se conhece a segurança e as alterações hemodinâmicas que possam ocorrer durante uma sessão deste modelo de exercício. Portanto, nosso objetivo foi avaliar a resposta cardiovascular durante o exercício agudo da musculatura inspiratória (ExAMI) em pacientes com IC associada a cardiomiopatia hipertensiva (CMHAS) ou chagásica (CMCH). Inicialmente, os pacientes responderam ao Questionário de Qualidade de Vida de Minnesota e na seqüência realizaram teste de força muscular respiratória por meio do equipamento manovacuômetro digital MVD300. Os pacientes que apresentaram fraqueza da musculatura inspiratória (valores 70% do predito da pressão inspiratória máxima - Pimáx) realizaram o ExAMI. Durante os momentos basal (repouso) e ExAMI registramos de forma indireta e não-invasiva, curvas da pressão arterial (PA) batimento a batimento com o equipamento Finometer. Também monitoramos o ritmo cardíaco por meio do eletrocardiograma e a frequência respiratória com uso da cinta respiratória. O protocolo foi realizado com todos os pacientes sentados e teve duração de 25 minutos (10 min basal, 10 min ExAMI e 5 min de recuperação). O exercício foi executado com o equipamento Threshold inspiratório com carga de 30% da Pimáx. O protocolo do ExAMI foi realizado por 27 pacientes com CMHAS e 9 pacientes com CMCH (FEVE<45%), porém, 7 pacientes (26%) do grupo CMHAS não finalizaram o protocolo por apresentarem elevação da PA sistólica > 20mmHg e referirem exaustão. Todos os pacientes do grupo CMCH concluíram o tempo previsto do ExAMI, mas relataram intenso cansaço ao final do exercício. Quando comparamos o basal vs. exercício (valor ) para ambos os grupos (CMHAS e CMCH), encontramos aumentos significativos da: PA sistólica ( = 9 ± 2 e = 7,6 ± 3 mmHg), diastólica ( = 4,8 ± 1 e = 4,2 ± 1 mmHg), FC ( = 5,5 ± 1,2 e = 6,6 ± 3 bpm) e DP ( = 1327 ± 208 e = 1319 ± 373 mmHg.bpm); o grupo CMHAS também apresentou aumento significativo do DC ( = 0,36 ± 0,1 l/min), Ic ( = 0,2 ± 0,1 l/min/m2), dp/dt ( = 118 ± 35 mmHg/s) e SPTI ( = 1,98 ± 0,6 mmHg.s). A modulação autonômica foi semelhante em ambos os grupos no momento basal e durante o exercício ocorreu um aumento da modulação vagal no grupo CMHAS ( = 258 ± 115 ms2). Os nossos resultados demonstraram que o ExAMI provocou alterações hemodinâmicas significativas nos pacientes dos dois grupos estudados, mas sem repercussão clínica na maioria deles. Um quarto (26%) dos pacientes com CMHAS apresentaram resposta exacerbada da PAS, referiram exaustão e portanto, não conseguiram realizar o tempo pré-determinado (10 min) do ExAMI. Sendo assim, concluímos que antes da indicação do TMI (3 séries de 10 min/dia) faz-se necessário a realização de uma sessão do exercício com monitorização cardíaca e respiratória, para avaliar se há ou não segurança da indicação deste modelo de exercício para pacientes com IC de diferentes etiologias / Patients with heart failure (HF) may show weakness of respiratory muscles. The inspiratory muscle training (IMT) has been used in this population to improve cardiorespiratory fitness, however, does not know the safety and hemodynamic changes that may occur during a session of exercise model. Therefore, our objective was to evaluate the cardiovascular response during acute inspiratory muscle exercise (AIME) in patients with HF associated with hypertensive cardiomyopathy (HCM) or Chagas (CCM). Initially, the patients responded to the questionnaire of quality of life of Minnesota and the test sequence performed by respiratory muscle strength equipment MVD300 digital manometer. Those patients who had inspiratory muscle weakness (values 70% predicted maximal inspiratory pressure - MIP) were AIME. During the basal (resting) and AIME recorded indirectly and non-invasive blood pressure curves (BP) beat to beat with the equipment Finometer. We also monitor the heart rate by electrocardiogram and respiration using the respiratory belt. The protocol was performed with patients sitting and lasted 25 minutes (10 min baseline, 10 min AIME and 5 min recovery). The exercise was carried out with the equipment inspiratory threshold load of 30% of MIP. The protocol of the AIME was performed for 27 patients with HCM and 9 patients with CCM (LVEF <45%), however, seven patients (26%) in group HCM not finalized the protocol for having elevated systolic BP 20mmHg and refer exhaustion. All patients in CCM group completed the scheduled time of the AIME, but reported heavy fatigue at the end of the exercise. When comparing the basal. vs. exercise (value ) for both groups (HCM and CCM), we found significant increases in: Systolic BP ( = 9 ± 2 e = 7,6 ± 3 mmHg), diastolic BP ( = 4,8 ± 1 e = 4,2 ± 1 mmHg), HR ( = 5,5 ± 1,2 e = 6,6 ± 3 bpm) e PD ( = 1327 ± 208 e = 1319 ± 373 mmHg.bpm); the HCM group also showed a significant increase in CO ( = 0,36 ± 0,1 l/min), CI ( = 0,2 ± 0,1 l/min/m2), dp/dt ( = 118 ± 35 mmHg/s) e SPTI ( = 1,98 ± 0,6 mmHg.s). The autonomic modulation was similar in both groups at baseline and during exercise there was an increase in vagal modulation in the group HCM ( = 258 ± 115 ms2). Our results demonstrate that the AIME caused significant hemodynamic changes in patients of both groups, but no clinical significance in most areas. A quarter (26%) patients with HCM showed exacerbated response of SBP, reported exhaustion and therefore could not perform the predetermined time (10 min) of the AIME. Thus, we conclude that before the indications of IMT (3 x 10 min / day) is necessary to carry out an exercise session with cardiac and respiratory monitoring, to evaluate whether or not the security alert to this type of exercise patients with HF of different etiologies

Pacientes com Insuficiência Cardíaca (IC) e fraqueza da musculatura inspiratória (FMI) apresentam limitação na realização de atividades da vida diária devido à dispnéia e cansaço. Objetivo. Avaliar em pacientes com miocardiopatia hipertensiva e FMI o efeito do treinamento da musculatura inspiratória (TMI) sobre a força e resistência dos músculos respiratórios, bem como na atividade simpática, hemodinâmica e a qualidade de vida. Métodos. Vinte e sete pacientes foram alocados em seqüência em dois grupos: Grupo Controle (não realizavam o treinamento) e Grupo TMI. Os pacientes incluídos no Grupo TMI participaram de um programa de exercícios respiratórios com o Threshold Inspiratório durante 12 semanas, sete sessões por semana com duração de 30 minutos por sessão, com carga de 30% da pressão inspiratória máxima (Pimáx) de repouso, ajustada mensalmente. Antes e após 12 semanas ambos os grupos foram avaliados quanto a Pimáx de repouso, variáveis hemodinâmicas em repouso: pressão arterial sistólica (PAS) e diastólica (PAD), freqüência cardíaca (FC), resistência vascular periférica (RVP) e débito cardíaco (DC); capacidade funcional cardiorrespiratória: consumo de oxigênio (VO2), quociente respiratório de produção de gás carbônico (VCO2), limiar anaeróbio (LA), ponto de compensação respiratório (PCR) e duração da atividade física, atividade simpática nervosa periférica (ANSP- microneurografia) e central (variabilidade da FC- componentes LF e HF), fluxo de sangue para o antebraço (FSA) e qualidade de vida (Questionário de Minessota). Resultados. Após 12 semanas não foram encontradas alterações significativas em qualquer parâmetro avaliado nos pacientes incluídos no Grupo Controle. Nos pacientes alocados no Grupo TMI foi possível observar alterações significativas nos seguintes parâmetros: aumento da Pimáx (basal 59,2 cmH2O ± 4,9 vs pós 87,5cmH2O ± 6,5); aumento do VO2 pico (14,4 ml/kg/min ± 1,0 vs 18,9 ml/kg/min ± 1,16); diminuição do VE/VCO2 pico (35,8 ml/kg/min ± 0,4 vs 32,5 ml/kg/min ± 0,8); diminuição do componente LF em valor absoluto (607,2 mms2 ± 153,9 vs 263,5 mms2 ± 53,6), e do componente LF em valor normalizado (6,2 mms2 ± 1,7 vs 5,0 mms2 ± 1,1) e aumento do componente HF em valor absoluto (48,41 mms2 ± 4,4 vs 56,7 mms2 ± 4,4); diminuição da ANSP (37,1 ± 3 disparos /min. vs 29,5 ± 2,3 disparos por minuto) e diminuição na pontuação nos domínio físico (20,2 pontos ± 3,5 vs 7,6 pontos ± 2,2) e geral (23,6 pontos ± 3,8 vs 9,2 pontos ± 2,4) do Questionário de Minessota. Conclusão. O TMI correlacionou-se com o aumento de força e resistência dos músculos respiratórios, melhora da capacidade cardiorrespiratória, diminuição da atividade simpática cardíaca e periférica, acarretando uma melhora na qualidade de vida de pacientes com IC hipertensiva. O TMI pode ser considerado um método seguro, prático e eficaz e uma alternativa no tratamento de pacientes com IC de etiologia hipertensiva / Patients with heart failure and inspiratory muscle weakness (IMW) experience limitations in performing their routine activities due to dyspnea and fatigue. Methods and Results: Twenty-seven patients were sequentially allocated to one of two groups: a control group in which inspiratory muscle training (IMT) was not provided and the IMT group. Patients included in the IMT group participated in a program of respiratory exercises with inspiratory threshold loading consisting of seven 30-minute sessions a week for a period of 12 weeks, with a monthly increase of 30% in maximal inspiratory pressure (Pimax) at rest. Prior to and following the 12-week evaluation period, both groups were assessed for Pimax measured at rest; oxygen consumption (VO2), ratio of ventilation to carbon dioxide production (VE/VCO2), peripheral and cardiac nervous sympathetic activity, and quality of life. Results: In the patients allocated to the IMT group, significant alterations were recorded: an increase in Pimax (59,2 ± 4,9 cmH2O at baseline compared to 87,5 ± 6,5 cmH2O following therapy),; an increase in peak oxygen consumption (14,4 ± 1,03 versus 18,9 ± 1,16 ml/kg/min); a reduction in peak VE/VCO2 (35,8 ± 0,4 versus 32,5 ± 0,8 ml/kg/min), a reduction in the low-frequency (LF) component (6,18 ± 1,7 versus 5,04 ± 1,1 mms2) and an increase in the normalized value of the high frequency (HF) component (48,4 ± 4,4 versus 56,7 ± 4,4 mms2), a reduction in peripheral sympathetic activity (37,1 ± 3 versus 29,5 ± 2,3 bursts/minute) and a reduction in the physical domain (20,2 ± 3,5 versus 7,6 ± 2,2 points) and general scores (23,6 ± 3,8 versus 9,2 ± 2,4 points) of the Minnesota instrument. Conclusion: IMT is associated with an increase in respiratory muscle strength and endurance, an improvement in cardiorespiratory capacity and a reduction in central and peripheral sympathetic activity, resulting in an improvement in the quality of life of patients with hypertensive heart disease

Background: Positive expiratory pressure (PEP) and continuous positive airway pressure (CPAP) are two forms of resistance breathing used in spontaneously breathing patients. With a threshold resistor or a flow resistor, both PEP and CPAP provide a positive (elevated) pressure level during the expiratory phase. With PEP, inspiratory pressure is negative, i.e. lower than ambient air pressure, as during a normal inspiration, but with CPAP, the inspiratory pressure is positive, i.e. higher than ambient air pressure. Methods: This thesis is based on four separate studies in which four different breathing devices, a PEP-bottle (threshold resistor device), a PEP-mask (flow resistor device), a threshold resistor CPAP and a flow resistor device were investigated. Paper I, II and III are based on studies in healthy volunteers. Paper IV is a bench study performed in a hypobaric chamber. Paper I examined differences between two PEP devices, the PEP-bottle and the PEP-mask. Paper II evaluated the performance of a flow resistor CPAP device, (Boussignac CPAP). Paper III investigated the effect of two PEP-devices, a PEP-bottle and a PEP-mask and two CPAP devices, a threshold resistor CPAP and a flow resistor CPAP, on inspiratory capacity (IC). In paper IV, the effect of changes in ambient pressure on preset CPAP levels in two different CPAP devices was compared. Results: With the PEP bottle, both expiration and inspiration began with a zero-flow period during which airway pressure changed rapidly. With the PEP-mask, the zero-flow period was very short and the change in airway pressure almost non-existent (paper I). During normal breathing with the Boussignac CPAP, changes in airway pressure were never large enough to reduce airway pressure below zero. During forced breathing, as airflow increased, both the drop in inspiratory airway pressure and the increase in expiratory airway pressure were potentiated (paper II). IC decreased significantly with three of the breathing devices, the PEP-mask and the two CPAP devices (paper III). With the threshold resistor CPAP, measured pressure levels were close to the preset CPAP level. With the flow resistor CPAP, as the altitude increased CPAP produced pressure levels increased (paper IV). Conclusion: The effect on airway pressure, airflow, IC and the effect of changes in ambient air pressure differ between different kinds of resistance breathing devices. These differences in device performance should be taken into consideration when choosing the optimal resistance breathing device for each patient.