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1.
J Perinatol ; 42(6): 714-722, 2022 06.
Article in English | MEDLINE | ID: mdl-34471215

ABSTRACT

OBJECTIVE: To explore how the fathers experience their role as a support for their partner and the relationship with them during their preterm infant's stay in the NICU. STUDY DESIGN: Multi-method longitudinal study involving ethnographic observation, semi-structured interviews, self-report questionnaires, and clinical information. Twenty fathers of preterm infants hospitalized in a level-III-NICU were included. Data were analyzed using thematic continent analysis. RESULTS: Three main themes were identified: support for mother (subthemes: putting mother's and infant's needs first; hiding worries and negative emotions; counteracting the sense of guilt; fear that the mother would reject the child), mother's care for the infant (subthemes: observing mother engaged in caregiving; mother has "something extra"), and couple relationship (subthemes: collaboration; bond). CONCLUSION: Fathers supporting their partners during the stay in the NICU experience emotional distress and the need for being supported that often are hidden. This demands a great deal of emotional and physical energy.


Subject(s)
Infant, Premature , Intensive Care Units, Neonatal , Child , Female , Humans , Infant , Infant, Newborn , Longitudinal Studies , Mothers/psychology , Qualitative Research
2.
J Adv Nurs ; 74(5): 1090-1098, 2018 May.
Article in English | MEDLINE | ID: mdl-29350787

ABSTRACT

AIM: The aim of this study was to investigate fathers' emotional experiences of their infant's preterm birth and subsequent stay in neonatal intensive care unit. BACKGROUND: When a baby is born preterm, there is also the premature interruption of the process of preparation for fatherhood. As a result, the impact on fathers of the preterm birth can bring negative consequences for the development of father-infant relationship. DESIGN: A multi-method approach was used which included ethnographic observation, semi-structured interviews with fathers, a self-report questionnaire and clinical information between September 2015-March 2017. METHOD: Data were analysed using a mixed-method: a thematic analysis of data from the interviews and quantitative analyses to detect possible clusters of fathers' emotional experiences and associations between clusters and fathers' and/or infants' characteristics. RESULTS: Two clusters were identified. The "fathers-of-preterm-infants" touched their baby as soon as they were given the opportunity and without fear that they would harm their infant. They were struck by their baby's physical appearance. In contrast, the "preterm fathers" preferred not to touch their baby when first given the chance, for fear of breaking/damaging/infecting her/him. They were struck both by the baby's physical appearance and by the technology/equipment around her/him and were afraid that their infant would die. All the "fathers-of-preterm-infants", but only just over half of the "preterm fathers", were actively engaged in their infant's care. Clusters were associated with the infant's gestational age. CONCLUSION: Fathers of preterm infants should receive personalized support specifically addressed to them and based on the infant's gestational age.


Subject(s)
Father-Child Relations , Fathers/psychology , Infant, Premature/psychology , Intensive Care, Neonatal/psychology , Parenting/psychology , Adult , Hospitalization , Humans , Infant, Newborn , Male , Qualitative Research
3.
Acta Ophthalmol ; 95(2): 158-164, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27320903

ABSTRACT

PURPOSE: To evaluate sensitivity, specificity and the safest cut-offs of three predictive algorithms (WINROP, ROPScore and CHOP ROP) for retinopathy of prematurity (ROP). METHODS: A retrospective study was conducted in three centres from 2012 to 2014; 445 preterms with gestational age (GA) ≤ 30 weeks and/or birthweight (BW) ≤ 1500 g, and additional unstable cases, were included. No-ROP, mild and type 1 ROP were categorized. The algorithms were analysed for infants with all parameters (GA, BW, weight gain, oxygen therapy, blood transfusion) needed for calculation (399 babies). RESULTS: Retinopathy of prematurity (ROP) was identified in both eyes in 116 patients (26.1%), and 44 (9.9%) had type 1 ROP. Gestational age and BW were significantly lower in ROP group compared with no-ROP subjects (GA: 26.7 ± 2.2 and 30.2 ± 1.9, respectively, p < 0.0001; BW: 839.8 ± 287.0 and 1288.1 ± 321.5 g, respectively, p = 0.0016). Customized alarms of ROPScore and CHOP ROP correctly identified all infants having any ROP or type 1 ROP. WINROP missed 19 cases of ROP, including three type 1 ROP. ROPScore and CHOP ROP provided the best performances with an area under the receiver operating characteristic curve for the detection of severe ROP of 0.93 (95% CI, 0.90-0.96, and 95% CI, 0.89-0.96, respectively), and WINROP obtained 0.83 (95% CI, 0.77-0.87). Median time from alarm to treatment was 11.1, 5.1 and 9.1 weeks, for WINROP, ROPScore and CHOP ROP, respectively. CONCLUSION: ROPScore and CHOP ROP showed 100% sensitivity to identify sight-threatening ROP. Predictive algorithms are a reliable tool for early identification of infants requiring referral to an ophthalmologist, for reorganizing resources and reducing stressful procedures to preterm babies.


Subject(s)
Algorithms , Early Diagnosis , Neonatal Screening/methods , Ophthalmoscopy/methods , Retina/diagnostic imaging , Retinopathy of Prematurity/diagnosis , Female , Gestational Age , Humans , Incidence , Infant, Newborn , Italy/epidemiology , Male , ROC Curve , Retinopathy of Prematurity/epidemiology , Retrospective Studies , Risk Factors
4.
J Thromb Thrombolysis ; 24(2): 153-5, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17510751

ABSTRACT

BACKGROUND: The diagnostic approach to haemostatic defects in the newborn is challenging and requires appropriate interpretation of coagulation tests according to reference values dependent on the postnatal age. METHODS: This investigation was designed to study the postnatal development of the human coagulation system in newborn infants and to develop appropriate reference ranges for prothrombin time (PT), activated partial thromboplastin time (APTT) and fibrinogen (FBG) according at the day of birth and for the following postnatal period (days 1, 2, 3, 4, 5, 6, from 7 to 10 and from 11 to 44). RESULTS: The mean FBG value was already within the adult reference range in newborns at birth, the mean PT value fell within the adult reference range in infants aged 4 days or more, whereas the mean APTT value was still higher than the upper limit of the adult reference range in infants aged between 11 and 20 days. The prevalence of infants with pathological values according to the actual adult reference ranges was limited for FBG (from 24 to 7%), decreased from 92 to 8% in infants aged 0 and 11-20 days for PT, but remained elevated throughout the observational period for APTT (from 94 to 71%). CONCLUSIONS: The results of the present investigation demonstrate that the actual adult reference ranges for coagulation screening tests, especially PT and APTT, cannot be applied to newborns and young infants.


Subject(s)
Blood Coagulation Tests/standards , Mass Screening , Adult , Blood Coagulation/physiology , Fibrinogen , Humans , Infant , Infant, Newborn , Partial Thromboplastin Time , Prothrombin Time , Reference Values
5.
Acta Paediatr ; 94(7): 971-4, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16188825

ABSTRACT

UNLABELLED: We describe a premature twin born at 30 wk of gestational age, affected with familial haemophagocytic lymphohistiocytosis. Two different mutations were identified in his DNA: one inherited from the mother and one from the father. Haemophagocytosis had been confirmed in his twin brother, who died soon after birth, as well as in the re-evaluation of the autopsy of his older sister, who died 1 y earlier. At 26 d of age, chemotherapy and immune-suppressive treatment were started according to the HLH-94 protocol. At 6 mo of age, a bone marrow transplant from an HLA-identical, unrelated volunteer was performed. Now at 32 mo of age, the infant is healthy and without signs of graft-versus-host disease. CONCLUSION: This case report shows that immuno-chemotherapy and allogenic bone marrow transplant are feasible even in premature infants affected with familial haemophagocytic lymphohistiocytosis, which should be ruled out in unknown bleeding disorders of neonates.


Subject(s)
Bone Marrow Transplantation , Diseases in Twins/genetics , Immunosuppressive Agents/therapeutic use , Infant, Premature, Diseases/genetics , Infant, Premature, Diseases/therapy , Lymphohistiocytosis, Hemophagocytic/genetics , Lymphohistiocytosis, Hemophagocytic/therapy , Cyclosporine/administration & dosage , Diseases in Twins/therapy , Drug Therapy, Combination , Humans , Infant, Newborn , Infant, Premature , Lymphohistiocytosis, Hemophagocytic/diagnosis , Male , Transplantation Conditioning
6.
Arch Gynecol Obstet ; 271(4): 320-4, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15168131

ABSTRACT

MATERIALS AND METHODS: The maternal and neonatal outcome of 27 triplet and 1 quadruplet gestations was studied at the University Hospital of Verona. RESULTS: Mean maternal age was 31.7+/-3.7 years; 24 women (85.7%) were nulliparous. Six (21.4%) patients had conceived spontaneously. Common maternal complications were: preterm labor (78.6%), anemia (57.1%), preeclampsia (25.0%). Thirteen patients (46.4%) had cervical cerclage, 21(75%) received tocolysis, 20 (71.4%) corticosteroid prophylaxis, 4 (14.3%) unfractionated heparin. All patients underwent Caesarean section with mean gestational age of 32+/-2.5 weeks and mean postoperative stay was 9 days. Three patients were treated in ICU after delivery, 1 was hysterectomized and 6 received blood transfusions. The live newborns were 80, the stillborns 5. Mean birth weight was 1,520+/-516 g (range 650-2,665), 95.0% being LBW. The following neonatal complications were observed: RDS (28.7%), cerebral hemorrhage (26.2% of II degrees and 1.2% of III degrees ), anemia (20%), PDA (12.5%), ROP (6.5%), polyglobulia (3.75%), NEC (2.5%). Mean hospitalization time was 30.6 days (range 2-132). DISCUSSION: Iatrogenic multiple births are increasing as the use of assisted conception techniques expands. Gynecologists should be aware of maternal complications and neonatal outcome of triplet pregnancies and infertility management strategies should try to avoid iatrogenic multiple gestations.


Subject(s)
Pregnancy Complications , Pregnancy Outcome , Pregnancy, Multiple , Adult , Anemia/epidemiology , Anemia/etiology , Cerclage, Cervical/statistics & numerical data , Cesarean Section/statistics & numerical data , Female , Gestational Age , Heparin/administration & dosage , Hospitalization , Humans , Infant, Newborn , Infant, Newborn, Diseases/epidemiology , Infant, Newborn, Diseases/therapy , Intensive Care Units, Neonatal , Male , Pre-Eclampsia/epidemiology , Pre-Eclampsia/etiology , Pregnancy , Pregnancy Complications/epidemiology , Pregnancy Complications/etiology , Premature Birth/epidemiology , Premature Birth/etiology , Tocolysis/statistics & numerical data , Triplets
7.
J Perinatol ; 24(5): 315-6, 2004 May.
Article in English | MEDLINE | ID: mdl-15116127

ABSTRACT

Total anomalous pulmonary venous return (TAPVR) is a rare congenital heart defect that occurs when all four pulmonary veins connect to the systemic venous circulation. We describe a full-term male neonate who presented with cyanosis and mild tachypnea shortly after birth. One umbilical artery and the umbilical vein were catheterized, and oxygen treatment was provided. Four echocardiograms indicated severe pulmonary hypertension and were negative for any congenital heart defects. After the umbilical artery catheter was removed, high partial pressure of oxygen was detected in blood samples drawn from the umbilical venous catheter that was positioned below the diaphragm. Based on this finding, TAPVR was suspected and confirmed with angiography through a central venous catheter. The neonate underwent a successful surgical repair to correct the cardiac defect.


Subject(s)
Heart Defects, Congenital/diagnosis , Pulmonary Veins/abnormalities , Blood Gas Analysis , Catheterization, Central Venous , Catheterization, Peripheral , Heart Defects, Congenital/diagnostic imaging , Heart Defects, Congenital/surgery , Humans , Hypertension, Pulmonary/congenital , Hypertension, Pulmonary/diagnostic imaging , Infant, Newborn , Male , Oxygen Inhalation Therapy , Pulmonary Veins/diagnostic imaging , Ultrasonography
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